Praxis Data Lab · Variable History

Variable history and harmonization report.

Review variable definitions, cycle chronology, survey design, laboratory methods, method-change boundaries, detection limits, and evidence-backed harmonization actions.

3,394matching variable codes

14,173 release records across 900 datasets and 12 cycles.

Search scope

Filtered NHANES variable history

Component: Laboratory.

Harmonization summary

2,067 label-stable codes

Label changes detected
942
Multiple dataset contexts
679
Unique codes
3,394
Enriched codes in this report
0

Scientific safeguard

Qualified assessment is authoritative; chronology remains supporting evidence.

Praxis separates source-stated method or instrument changes from automated differences in CDC/NCHS method text. The qualified harmonization assessment below is the researcher-facing conclusion; method chronology explains the underlying evidence and does not override that adjudication.

Variable-by-variable chronology

Qualified harmonization assessment and indexed evidence

Each variable first shows the current qualified assessment used by Study Builder, followed by cycle-specific source evidence and method chronology.

AADBDSPEvidence developing

Bed Space Vacuumed (square inches)

Observed years
20052006
Release records
1
Datasets
1
Components
Laboratory
Qualified Praxis harmonization assessment

Evidence developing · low confidence

No normalized longitudinal change evidence is available for this variable. Absence of events must not be interpreted as proof of cross-cycle equivalence.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Variable names / labels over time
  • Bed Space Vacuumed (square inches)2005-2006
Cycle-by-cycle release history
  • 2005-2006: ALDUST_D — Bed Space Vacuumed (square inches) — Allergens - Household Dust (Laboratory)
AADBDTIMEvidence developing

Bed Vacuum Time (seconds)

Observed years
20052006
Release records
1
Datasets
1
Components
Laboratory
Qualified Praxis harmonization assessment

Evidence developing · low confidence

No normalized longitudinal change evidence is available for this variable. Absence of events must not be interpreted as proof of cross-cycle equivalence.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Variable names / labels over time
  • Bed Vacuum Time (seconds)2005-2006
Cycle-by-cycle release history
AADBDTYPEvidence developing

Type of Bed

Observed years
20052006
Release records
1
Datasets
1
Components
Laboratory
Qualified Praxis harmonization assessment

Evidence developing · low confidence

No normalized longitudinal change evidence is available for this variable. Absence of events must not be interpreted as proof of cross-cycle equivalence.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Variable names / labels over time
  • Type of Bed2005-2006
Cycle-by-cycle release history
AADEXSTSEvidence developing

Status of Dust Allergen Data

Observed years
20052006
Release records
1
Datasets
1
Components
Laboratory
Qualified Praxis harmonization assessment

Evidence developing · low confidence

No normalized longitudinal change evidence is available for this variable. Absence of events must not be interpreted as proof of cross-cycle equivalence.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Variable names / labels over time
  • Status of Dust Allergen Data2005-2006
Cycle-by-cycle release history
  • 2005-2006: ALDUST_D — Status of Dust Allergen Data — Allergens - Household Dust (Laboratory)
AADFLSPEvidence developing

Floor Space Vacuumed (square inches)

Observed years
20052006
Release records
1
Datasets
1
Components
Laboratory
Qualified Praxis harmonization assessment

Evidence developing · low confidence

No normalized longitudinal change evidence is available for this variable. Absence of events must not be interpreted as proof of cross-cycle equivalence.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Variable names / labels over time
  • Floor Space Vacuumed (square inches)2005-2006
Cycle-by-cycle release history
  • 2005-2006: ALDUST_D — Floor Space Vacuumed (square inches) — Allergens - Household Dust (Laboratory)
AADFLTIMEvidence developing

Floor Vacuum Time (seconds)

Observed years
20052006
Release records
1
Datasets
1
Components
Laboratory
Qualified Praxis harmonization assessment

Evidence developing · low confidence

No normalized longitudinal change evidence is available for this variable. Absence of events must not be interpreted as proof of cross-cycle equivalence.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Variable names / labels over time
  • Floor Vacuum Time (seconds)2005-2006
Cycle-by-cycle release history
  • 2005-2006: ALDUST_D — Floor Vacuum Time (seconds) — Allergens - Household Dust (Laboratory)
AADMOVEEvidence developing

Have you/any of the SPs listed below moved since the time when you were last interviewed in your household?

Observed years
20052006
Release records
1
Datasets
1
Components
Laboratory
Qualified Praxis harmonization assessment

Evidence developing · low confidence

No normalized longitudinal change evidence is available for this variable. Absence of events must not be interpreted as proof of cross-cycle equivalence.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Variable names / labels over time
  • Have you/any of the SPs listed below moved since the time when you were last interviewed in your household?2005-2006
Cycle-by-cycle release history
  • 2005-2006: ALDUST_D — Have you/any of the SPs listed below moved since the time when you were last interviewed in your household? — Allergens - Household Dust (Laboratory)
AAXBDMATEvidence developing

Impermeable Mattress Cover

Observed years
20052006
Release records
1
Datasets
1
Components
Laboratory
Qualified Praxis harmonization assessment

Evidence developing · low confidence

No normalized longitudinal change evidence is available for this variable. Absence of events must not be interpreted as proof of cross-cycle equivalence.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Variable names / labels over time
  • Impermeable Mattress Cover2005-2006
Cycle-by-cycle release history
AAXBDPLWEvidence developing

Impermeable Pillow Cover

Observed years
20052006
Release records
1
Datasets
1
Components
Laboratory
Qualified Praxis harmonization assessment

Evidence developing · low confidence

No normalized longitudinal change evidence is available for this variable. Absence of events must not be interpreted as proof of cross-cycle equivalence.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Variable names / labels over time
  • Impermeable Pillow Cover2005-2006
Cycle-by-cycle release history
AAXBDSTEvidence developing

Bed Sample Status

Observed years
20052006
Release records
1
Datasets
1
Components
Laboratory
Qualified Praxis harmonization assessment

Evidence developing · low confidence

No normalized longitudinal change evidence is available for this variable. Absence of events must not be interpreted as proof of cross-cycle equivalence.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Variable names / labels over time
  • Bed Sample Status2005-2006
Cycle-by-cycle release history
AAXBDSUREvidence developing

Bed Surface Vacuumed

Observed years
20052006
Release records
1
Datasets
1
Components
Laboratory
Qualified Praxis harmonization assessment

Evidence developing · low confidence

No normalized longitudinal change evidence is available for this variable. Absence of events must not be interpreted as proof of cross-cycle equivalence.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Variable names / labels over time
  • Bed Surface Vacuumed2005-2006
Cycle-by-cycle release history
AAXFLSTEvidence developing

Floor Sample Status

Observed years
20052006
Release records
1
Datasets
1
Components
Laboratory
Qualified Praxis harmonization assessment

Evidence developing · low confidence

No normalized longitudinal change evidence is available for this variable. Absence of events must not be interpreted as proof of cross-cycle equivalence.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Variable names / labels over time
  • Floor Sample Status2005-2006
Cycle-by-cycle release history
AAXFLTYPEvidence developing

Type of Floor Covering

Observed years
20052006
Release records
1
Datasets
1
Components
Laboratory
Qualified Praxis harmonization assessment

Evidence developing · low confidence

No normalized longitudinal change evidence is available for this variable. Absence of events must not be interpreted as proof of cross-cycle equivalence.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Variable names / labels over time
  • Type of Floor Covering2005-2006
Cycle-by-cycle release history
AAXRMDESEvidence developing

Room Description

Observed years
20052006
Release records
1
Datasets
1
Components
Laboratory
Qualified Praxis harmonization assessment

Evidence developing · low confidence

No normalized longitudinal change evidence is available for this variable. Absence of events must not be interpreted as proof of cross-cycle equivalence.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Variable names / labels over time
  • Room Description2005-2006
Cycle-by-cycle release history
AAXRMHUMEvidence developing

Room Humidity (%)

Observed years
20052006
Release records
1
Datasets
1
Components
Laboratory
Qualified Praxis harmonization assessment

Evidence developing · low confidence

No normalized longitudinal change evidence is available for this variable. Absence of events must not be interpreted as proof of cross-cycle equivalence.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Variable names / labels over time
  • Room Humidity (%)2005-2006
Cycle-by-cycle release history
AAXRMTMPEvidence developing

Room Temperature (F)

Observed years
20052006
Release records
1
Datasets
1
Components
Laboratory
Qualified Praxis harmonization assessment

Evidence developing · low confidence

No normalized longitudinal change evidence is available for this variable. Absence of events must not be interpreted as proof of cross-cycle equivalence.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Variable names / labels over time
  • Room Temperature (F)2005-2006
Cycle-by-cycle release history
DCD030Compatible with harmonization

Room where samples taken

Observed years
19992004
Release records
3
Datasets
3
Components
Laboratory
Qualified Praxis harmonization assessment

Compatible with harmonization · moderate confidence

No blocking method discontinuity is identified inside the selected cycle span, but one or more longitudinal changes require explicit harmonization conditions before pooling.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 1999-2000 → 2001-2002 · 2001-2002 → 2003-2004

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Review the adjacent codebooks/methods. Keep this boundary as documentation variation unless source evidence confirms a substantive method or instrument change.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • Room where samples taken1999-2000 · 2001-2002 · 2003-2004
Cycle-by-cycle release history
DCD070ACompatible with harmonization

Indicates whether floor was carpeted in room-floor sample

Observed years
19992004
Release records
3
Datasets
3
Components
Laboratory
Qualified Praxis harmonization assessment

Compatible with harmonization · moderate confidence

No blocking method discontinuity is identified inside the selected cycle span, but one or more longitudinal changes require explicit harmonization conditions before pooling.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 1999-2000 → 2001-2002 · 2001-2002 → 2003-2004

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Review the adjacent codebooks/methods. Keep this boundary as documentation variation unless source evidence confirms a substantive method or instrument change.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • Indicates whether floor was carpeted in room-floor sample1999-2000 · 2001-2002 · 2003-2004
Cycle-by-cycle release history
  • 1999-2000: LAB20 — Indicates whether floor was carpeted in room-floor sample — Lead - Dust (Laboratory)
  • 2001-2002: L20_B — Indicates whether floor was carpeted in room-floor sample — Lead - Dust (Laboratory)
  • 2003-2004: L20_C — Indicates whether floor was carpeted in room-floor sample — Lead - Dust (Laboratory)
DCDINDEXCompatible with harmonization

Observed years
19992004
Release records
3
Datasets
3
Components
Laboratory
Qualified Praxis harmonization assessment

Compatible with harmonization · moderate confidence

No blocking method discontinuity is identified inside the selected cycle span, but one or more longitudinal changes require explicit harmonization conditions before pooling.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 1999-2000 → 2001-2002 · 2001-2002 → 2003-2004

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Review the adjacent codebooks/methods. Keep this boundary as documentation variation unless source evidence confirms a substantive method or instrument change.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • 1999-2000 · 2001-2002 · 2003-2004
Cycle-by-cycle release history
DCDSTATCompatible with harmonization

Observed years
19992004
Release records
3
Datasets
3
Components
Laboratory
Qualified Praxis harmonization assessment

Compatible with harmonization · moderate confidence

No blocking method discontinuity is identified inside the selected cycle span, but one or more longitudinal changes require explicit harmonization conditions before pooling.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 1999-2000 → 2001-2002 · 2001-2002 → 2003-2004

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Review the adjacent codebooks/methods. Keep this boundary as documentation variation unless source evidence confirms a substantive method or instrument change.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • 1999-2000 · 2001-2002 · 2003-2004
Cycle-by-cycle release history
DCQ070BCompatible with harmonization

Indicates whether mat was found in room-floor sample

Observed years
19992004
Release records
3
Datasets
3
Components
Laboratory
Qualified Praxis harmonization assessment

Compatible with harmonization · moderate confidence

No blocking method discontinuity is identified inside the selected cycle span, but one or more longitudinal changes require explicit harmonization conditions before pooling.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 1999-2000 → 2001-2002 · 2001-2002 → 2003-2004

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Review the adjacent codebooks/methods. Keep this boundary as documentation variation unless source evidence confirms a substantive method or instrument change.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • Indicates whether mat was found in room-floor sample1999-2000 · 2001-2002 · 2003-2004
Cycle-by-cycle release history
  • 1999-2000: LAB20 — Indicates whether mat was found in room-floor sample — Lead - Dust (Laboratory)
  • 2001-2002: L20_B — Indicates whether mat was found in room-floor sample — Lead - Dust (Laboratory)
  • 2003-2004: L20_C — Indicates whether mat was found in room-floor sample — Lead - Dust (Laboratory)
DCQ070CCompatible with harmonization

Indicates whether area rug was found in room-floor sample

Observed years
19992004
Release records
3
Datasets
3
Components
Laboratory
Qualified Praxis harmonization assessment

Compatible with harmonization · moderate confidence

No blocking method discontinuity is identified inside the selected cycle span, but one or more longitudinal changes require explicit harmonization conditions before pooling.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 1999-2000 → 2001-2002 · 2001-2002 → 2003-2004

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Review the adjacent codebooks/methods. Keep this boundary as documentation variation unless source evidence confirms a substantive method or instrument change.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • Indicates whether area rug was found in room-floor sample1999-2000 · 2001-2002 · 2003-2004
Cycle-by-cycle release history
  • 1999-2000: LAB20 — Indicates whether area rug was found in room-floor sample — Lead - Dust (Laboratory)
  • 2001-2002: L20_B — Indicates whether area rug was found in room-floor sample — Lead - Dust (Laboratory)
  • 2003-2004: L20_C — Indicates whether area rug was found in room-floor sample — Lead - Dust (Laboratory)
DCQ070DCompatible with harmonization

If there was wall to wall carpet-floor sample

Observed years
19992004
Release records
3
Datasets
3
Components
Laboratory
Qualified Praxis harmonization assessment

Compatible with harmonization · moderate confidence

No blocking method discontinuity is identified inside the selected cycle span, but one or more longitudinal changes require explicit harmonization conditions before pooling.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 1999-2000 → 2001-2002 · 2001-2002 → 2003-2004

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Review the adjacent codebooks/methods. Keep this boundary as documentation variation unless source evidence confirms a substantive method or instrument change.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • If there was wall to wall carpet-floor sample1999-2000 · 2001-2002 · 2003-2004
Cycle-by-cycle release history
  • 1999-2000: LAB20 — If there was wall to wall carpet-floor sample — Lead - Dust (Laboratory)
  • 2001-2002: L20_B — If there was wall to wall carpet-floor sample — Lead - Dust (Laboratory)
  • 2003-2004: L20_C — If there was wall to wall carpet-floor sample — Lead - Dust (Laboratory)
DCQ090Compatible with harmonization

Depth of carpeting-floor sample

Observed years
19992004
Release records
3
Datasets
3
Components
Laboratory
Qualified Praxis harmonization assessment

Compatible with harmonization · moderate confidence

No blocking method discontinuity is identified inside the selected cycle span, but one or more longitudinal changes require explicit harmonization conditions before pooling.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 1999-2000 → 2001-2002 · 2001-2002 → 2003-2004

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Review the adjacent codebooks/methods. Keep this boundary as documentation variation unless source evidence confirms a substantive method or instrument change.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • Depth of carpeting-floor sample1999-2000 · 2001-2002 · 2003-2004
Cycle-by-cycle release history
  • 1999-2000: LAB20 — Depth of carpeting-floor sample — Lead - Dust (Laboratory)
  • 2001-2002: L20_B — Depth of carpeting-floor sample — Lead - Dust (Laboratory)
  • 2003-2004: L20_C — Depth of carpeting-floor sample — Lead - Dust (Laboratory)
DCQ160Compatible with harmonization

Surface condition for floor dust sample

Observed years
19992004
Release records
3
Datasets
3
Components
Laboratory
Qualified Praxis harmonization assessment

Compatible with harmonization · moderate confidence

No blocking method discontinuity is identified inside the selected cycle span, but one or more longitudinal changes require explicit harmonization conditions before pooling.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 1999-2000 → 2001-2002 · 2001-2002 → 2003-2004

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Review the adjacent codebooks/methods. Keep this boundary as documentation variation unless source evidence confirms a substantive method or instrument change.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • Surface condition for floor dust sample1999-2000 · 2001-2002 · 2003-2004
Cycle-by-cycle release history
  • 1999-2000: LAB20 — Surface condition for floor dust sample — Lead - Dust (Laboratory)
  • 2001-2002: L20_B — Surface condition for floor dust sample — Lead - Dust (Laboratory)
  • 2003-2004: L20_C — Surface condition for floor dust sample — Lead - Dust (Laboratory)
DCQ240Compatible with harmonization

Window sill finished

Observed years
19992004
Release records
3
Datasets
3
Components
Laboratory
Qualified Praxis harmonization assessment

Compatible with harmonization · moderate confidence

No blocking method discontinuity is identified inside the selected cycle span, but one or more longitudinal changes require explicit harmonization conditions before pooling.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 1999-2000 → 2001-2002 · 2001-2002 → 2003-2004

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Review the adjacent codebooks/methods. Keep this boundary as documentation variation unless source evidence confirms a substantive method or instrument change.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • Window sill finished1999-2000 · 2001-2002 · 2003-2004
Cycle-by-cycle release history
DCQ250Compatible with harmonization

Surface condition for sill dust sample

Observed years
19992004
Release records
3
Datasets
3
Components
Laboratory
Qualified Praxis harmonization assessment

Compatible with harmonization · moderate confidence

No blocking method discontinuity is identified inside the selected cycle span, but one or more longitudinal changes require explicit harmonization conditions before pooling.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 1999-2000 → 2001-2002 · 2001-2002 → 2003-2004

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Review the adjacent codebooks/methods. Keep this boundary as documentation variation unless source evidence confirms a substantive method or instrument change.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • Surface condition for sill dust sample1999-2000 · 2001-2002 · 2003-2004
Cycle-by-cycle release history
  • 1999-2000: LAB20 — Surface condition for sill dust sample — Lead - Dust (Laboratory)
  • 2001-2002: L20_B — Surface condition for sill dust sample — Lead - Dust (Laboratory)
  • 2003-2004: L20_C — Surface condition for sill dust sample — Lead - Dust (Laboratory)
DCQ400Compatible with harmonization

INTERVIEWER OBSERVATION: ROOM CLEANLINESS

Observed years
19992004
Release records
3
Datasets
3
Components
Laboratory
Qualified Praxis harmonization assessment

Compatible with harmonization · moderate confidence

No blocking method discontinuity is identified inside the selected cycle span, but one or more longitudinal changes require explicit harmonization conditions before pooling.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 1999-2000 → 2001-2002 · 2001-2002 → 2003-2004

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Review the adjacent codebooks/methods. Keep this boundary as documentation variation unless source evidence confirms a substantive method or instrument change.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • INTERVIEWER OBSERVATION: ROOM CLEANLINESS1999-2000 · 2001-2002 · 2003-2004
Cycle-by-cycle release history
  • 1999-2000: LAB20 — INTERVIEWER OBSERVATION: ROOM CLEANLINESS — Lead - Dust (Laboratory)
  • 2001-2002: L20_B — INTERVIEWER OBSERVATION: ROOM CLEANLINESS — Lead - Dust (Laboratory)
  • 2003-2004: L20_C — INTERVIEWER OBSERVATION: ROOM CLEANLINESS — Lead - Dust (Laboratory)
DCQ410Compatible with harmonization

INTERVIEWER OBSERVATION: ROOM CLUTTER

Observed years
19992004
Release records
3
Datasets
3
Components
Laboratory
Qualified Praxis harmonization assessment

Compatible with harmonization · moderate confidence

No blocking method discontinuity is identified inside the selected cycle span, but one or more longitudinal changes require explicit harmonization conditions before pooling.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 1999-2000 → 2001-2002 · 2001-2002 → 2003-2004

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Review the adjacent codebooks/methods. Keep this boundary as documentation variation unless source evidence confirms a substantive method or instrument change.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • INTERVIEWER OBSERVATION: ROOM CLUTTER1999-2000 · 2001-2002 · 2003-2004
Cycle-by-cycle release history
  • 1999-2000: LAB20 — INTERVIEWER OBSERVATION: ROOM CLUTTER — Lead - Dust (Laboratory)
  • 2001-2002: L20_B — INTERVIEWER OBSERVATION: ROOM CLUTTER — Lead - Dust (Laboratory)
  • 2003-2004: L20_C — INTERVIEWER OBSERVATION: ROOM CLUTTER — Lead - Dust (Laboratory)
DSDAA1LCEvidence developing

Fungus Alternaria alternata 1 (Alt a 1) dust antigen, comment code

Observed years
20052006
Release records
1
Datasets
1
Components
Laboratory
Qualified Praxis harmonization assessment

Evidence developing · low confidence

No normalized longitudinal change evidence is available for this variable. Absence of events must not be interpreted as proof of cross-cycle equivalence.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Variable names / labels over time
  • Fungus Alternaria alternata 1 (Alt a 1) dust antigen, comment code2005-2006
Cycle-by-cycle release history
  • 2005-2006: ALDUST_D — Fungus Alternaria alternata 1 (Alt a 1) dust antigen, comment code — Allergens - Household Dust (Laboratory)
DSDAF1LCEvidence developing

Fungus Aspergillus fumigatus dust antigen, comment code

Observed years
20052006
Release records
1
Datasets
1
Components
Laboratory
Qualified Praxis harmonization assessment

Evidence developing · low confidence

No normalized longitudinal change evidence is available for this variable. Absence of events must not be interpreted as proof of cross-cycle equivalence.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Variable names / labels over time
  • Fungus Aspergillus fumigatus dust antigen, comment code2005-2006
Cycle-by-cycle release history
  • 2005-2006: ALDUST_D — Fungus Aspergillus fumigatus dust antigen, comment code — Allergens - Household Dust (Laboratory)
DSDBG1LCEvidence developing

German cockroach Blattella germanica 1 (Bla g 1) dust antigen, comment code

Observed years
20052006
Release records
1
Datasets
1
Components
Laboratory
Qualified Praxis harmonization assessment

Evidence developing · low confidence

No normalized longitudinal change evidence is available for this variable. Absence of events must not be interpreted as proof of cross-cycle equivalence.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Variable names / labels over time
  • German cockroach Blattella germanica 1 (Bla g 1) dust antigen, comment code2005-2006
Cycle-by-cycle release history
  • 2005-2006: ALDUST_D — German cockroach Blattella germanica 1 (Bla g 1) dust antigen, comment code — Allergens - Household Dust (Laboratory)
DSDBG2LCEvidence developing

German cockroach Blattella germanica 2 (Bla g 2) dust antigen, comment code

Observed years
20052006
Release records
1
Datasets
1
Components
Laboratory
Qualified Praxis harmonization assessment

Evidence developing · low confidence

No normalized longitudinal change evidence is available for this variable. Absence of events must not be interpreted as proof of cross-cycle equivalence.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Variable names / labels over time
  • German cockroach Blattella germanica 2 (Bla g 2) dust antigen, comment code2005-2006
Cycle-by-cycle release history
  • 2005-2006: ALDUST_D — German cockroach Blattella germanica 2 (Bla g 2) dust antigen, comment code — Allergens - Household Dust (Laboratory)
DSDCF1LCEvidence developing

Dog allergen Canis familiaris 1 (Can f 1) dust antigen, comment code

Observed years
20052006
Release records
1
Datasets
1
Components
Laboratory
Qualified Praxis harmonization assessment

Evidence developing · low confidence

No normalized longitudinal change evidence is available for this variable. Absence of events must not be interpreted as proof of cross-cycle equivalence.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Variable names / labels over time
  • Dog allergen Canis familiaris 1 (Can f 1) dust antigen, comment code2005-2006
Cycle-by-cycle release history
  • 2005-2006: ALDUST_D — Dog allergen Canis familiaris 1 (Can f 1) dust antigen, comment code — Allergens - Household Dust (Laboratory)
DSDDF1LCEvidence developing

Dust mite Dermatophagoides farinae 1 (Der f 1) dust antigen, comment code

Observed years
20052006
Release records
1
Datasets
1
Components
Laboratory
Qualified Praxis harmonization assessment

Evidence developing · low confidence

No normalized longitudinal change evidence is available for this variable. Absence of events must not be interpreted as proof of cross-cycle equivalence.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Variable names / labels over time
  • Dust mite Dermatophagoides farinae 1 (Der f 1) dust antigen, comment code2005-2006
Cycle-by-cycle release history
  • 2005-2006: ALDUST_D — Dust mite Dermatophagoides farinae 1 (Der f 1) dust antigen, comment code — Allergens - Household Dust (Laboratory)
DSDDP1LCEvidence developing

Dust mite Dermatophagoides pteronyssinus 1 (Der p 1) dust antigen, comment code

Observed years
20052006
Release records
1
Datasets
1
Components
Laboratory
Qualified Praxis harmonization assessment

Evidence developing · low confidence

No normalized longitudinal change evidence is available for this variable. Absence of events must not be interpreted as proof of cross-cycle equivalence.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Variable names / labels over time
  • Dust mite Dermatophagoides pteronyssinus 1 (Der p 1) dust antigen, comment code2005-2006
Cycle-by-cycle release history
  • 2005-2006: ALDUST_D — Dust mite Dermatophagoides pteronyssinus 1 (Der p 1) dust antigen, comment code — Allergens - Household Dust (Laboratory)
DSDENXLCEvidence developing

Endotoxin dust, comment code

Observed years
20052006
Release records
1
Datasets
1
Components
Laboratory
Qualified Praxis harmonization assessment

Evidence developing · low confidence

No normalized longitudinal change evidence is available for this variable. Absence of events must not be interpreted as proof of cross-cycle equivalence.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Variable names / labels over time
  • Endotoxin dust, comment code2005-2006
Cycle-by-cycle release history
  • 2005-2006: ALDUST_D — Endotoxin dust, comment code — Allergens - Household Dust (Laboratory)
DSDFD1LCEvidence developing

Cat allergen Felis domesticus 1 (Fel d 1) dust allergen, comment code

Observed years
20052006
Release records
1
Datasets
1
Components
Laboratory
Qualified Praxis harmonization assessment

Evidence developing · low confidence

No normalized longitudinal change evidence is available for this variable. Absence of events must not be interpreted as proof of cross-cycle equivalence.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Variable names / labels over time
  • Cat allergen Felis domesticus 1 (Fel d 1) dust allergen, comment code2005-2006
Cycle-by-cycle release history
  • 2005-2006: ALDUST_D — Cat allergen Felis domesticus 1 (Fel d 1) dust allergen, comment code — Allergens - Household Dust (Laboratory)
DSDMM1LCEvidence developing

Mouse urinary protein (Mus m 1) dust antigen, comment code

Observed years
20052006
Release records
1
Datasets
1
Components
Laboratory
Qualified Praxis harmonization assessment

Evidence developing · low confidence

No normalized longitudinal change evidence is available for this variable. Absence of events must not be interpreted as proof of cross-cycle equivalence.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Variable names / labels over time
  • Mouse urinary protein (Mus m 1) dust antigen, comment code2005-2006
Cycle-by-cycle release history
  • 2005-2006: ALDUST_D — Mouse urinary protein (Mus m 1) dust antigen, comment code — Allergens - Household Dust (Laboratory)
DSDRN1LCEvidence developing

Rat urinary protein (Rat n 1) dust antigen, comment code

Observed years
20052006
Release records
1
Datasets
1
Components
Laboratory
Qualified Praxis harmonization assessment

Evidence developing · low confidence

No normalized longitudinal change evidence is available for this variable. Absence of events must not be interpreted as proof of cross-cycle equivalence.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Variable names / labels over time
  • Rat urinary protein (Rat n 1) dust antigen, comment code2005-2006
Cycle-by-cycle release history
  • 2005-2006: ALDUST_D — Rat urinary protein (Rat n 1) dust antigen, comment code — Allergens - Household Dust (Laboratory)
DSXAA1Evidence developing

Fungus Alternaria alternata 1 (Alt a 1) dust antigen, result (ng/mL dust)

Observed years
20052006
Release records
1
Datasets
1
Components
Laboratory
Qualified Praxis harmonization assessment

Evidence developing · low confidence

No normalized longitudinal change evidence is available for this variable. Absence of events must not be interpreted as proof of cross-cycle equivalence.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Variable names / labels over time
  • Fungus Alternaria alternata 1 (Alt a 1) dust antigen, result (ng/mL dust)2005-2006
Cycle-by-cycle release history
  • 2005-2006: ALDUST_D — Fungus Alternaria alternata 1 (Alt a 1) dust antigen, result (ng/mL dust) — Allergens - Household Dust (Laboratory)
DSXAA1LDEvidence developing

Fungus Alternaria alternata 1 (Alt a 1) dust antigen, limit of detection (ng/mL dust)

Observed years
20052006
Release records
1
Datasets
1
Components
Laboratory
Qualified Praxis harmonization assessment

Evidence developing · low confidence

No normalized longitudinal change evidence is available for this variable. Absence of events must not be interpreted as proof of cross-cycle equivalence.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Variable names / labels over time
  • Fungus Alternaria alternata 1 (Alt a 1) dust antigen, limit of detection (ng/mL dust)2005-2006
Cycle-by-cycle release history
  • 2005-2006: ALDUST_D — Fungus Alternaria alternata 1 (Alt a 1) dust antigen, limit of detection (ng/mL dust) — Allergens - Household Dust (Laboratory)
DSXAF1Evidence developing

Fungus Aspergillus fumigatus dust antigen, result (ng/mL dust)

Observed years
20052006
Release records
1
Datasets
1
Components
Laboratory
Qualified Praxis harmonization assessment

Evidence developing · low confidence

No normalized longitudinal change evidence is available for this variable. Absence of events must not be interpreted as proof of cross-cycle equivalence.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Variable names / labels over time
  • Fungus Aspergillus fumigatus dust antigen, result (ng/mL dust)2005-2006
Cycle-by-cycle release history
  • 2005-2006: ALDUST_D — Fungus Aspergillus fumigatus dust antigen, result (ng/mL dust) — Allergens - Household Dust (Laboratory)
DSXAF1LDEvidence developing

Fungus Aspergillus fumigatus dust antigen, limit of detection (ng/mL dust)

Observed years
20052006
Release records
1
Datasets
1
Components
Laboratory
Qualified Praxis harmonization assessment

Evidence developing · low confidence

No normalized longitudinal change evidence is available for this variable. Absence of events must not be interpreted as proof of cross-cycle equivalence.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Variable names / labels over time
  • Fungus Aspergillus fumigatus dust antigen, limit of detection (ng/mL dust)2005-2006
Cycle-by-cycle release history
  • 2005-2006: ALDUST_D — Fungus Aspergillus fumigatus dust antigen, limit of detection (ng/mL dust) — Allergens - Household Dust (Laboratory)
DSXBG1Evidence developing

German cockroach Blattella germanica 1 (Bla g 1) dust antigen, result (U/mL dust)

Observed years
20052006
Release records
1
Datasets
1
Components
Laboratory
Qualified Praxis harmonization assessment

Evidence developing · low confidence

No normalized longitudinal change evidence is available for this variable. Absence of events must not be interpreted as proof of cross-cycle equivalence.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Variable names / labels over time
  • German cockroach Blattella germanica 1 (Bla g 1) dust antigen, result (U/mL dust)2005-2006
Cycle-by-cycle release history
  • 2005-2006: ALDUST_D — German cockroach Blattella germanica 1 (Bla g 1) dust antigen, result (U/mL dust) — Allergens - Household Dust (Laboratory)
DSXBG1LDEvidence developing

German cockroach Blattella germanica 1 (Bla g 1) dust antigen, limit of detection (U/mL dust)

Observed years
20052006
Release records
1
Datasets
1
Components
Laboratory
Qualified Praxis harmonization assessment

Evidence developing · low confidence

No normalized longitudinal change evidence is available for this variable. Absence of events must not be interpreted as proof of cross-cycle equivalence.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Variable names / labels over time
  • German cockroach Blattella germanica 1 (Bla g 1) dust antigen, limit of detection (U/mL dust)2005-2006
Cycle-by-cycle release history
  • 2005-2006: ALDUST_D — German cockroach Blattella germanica 1 (Bla g 1) dust antigen, limit of detection (U/mL dust) — Allergens - Household Dust (Laboratory)
DSXBG2Evidence developing

German cockroach Blattella germanica 2 (Bla g 2) dust antigen, result (ng/mL dust)

Observed years
20052006
Release records
1
Datasets
1
Components
Laboratory
Qualified Praxis harmonization assessment

Evidence developing · low confidence

No normalized longitudinal change evidence is available for this variable. Absence of events must not be interpreted as proof of cross-cycle equivalence.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Variable names / labels over time
  • German cockroach Blattella germanica 2 (Bla g 2) dust antigen, result (ng/mL dust)2005-2006
Cycle-by-cycle release history
  • 2005-2006: ALDUST_D — German cockroach Blattella germanica 2 (Bla g 2) dust antigen, result (ng/mL dust) — Allergens - Household Dust (Laboratory)
DSXBG2LDEvidence developing

German cockroach Blattella germanica 2 (Bla g 2) dust antigen, limit of detection (ng/mL dust)

Observed years
20052006
Release records
1
Datasets
1
Components
Laboratory
Qualified Praxis harmonization assessment

Evidence developing · low confidence

No normalized longitudinal change evidence is available for this variable. Absence of events must not be interpreted as proof of cross-cycle equivalence.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Variable names / labels over time
  • German cockroach Blattella germanica 2 (Bla g 2) dust antigen, limit of detection (ng/mL dust)2005-2006
Cycle-by-cycle release history
  • 2005-2006: ALDUST_D — German cockroach Blattella germanica 2 (Bla g 2) dust antigen, limit of detection (ng/mL dust) — Allergens - Household Dust (Laboratory)
DSXCF1Evidence developing

Dog allergen Canis familiaris 1 (Can f 1) dust antigen, result (ng/mL dust)

Observed years
20052006
Release records
1
Datasets
1
Components
Laboratory
Qualified Praxis harmonization assessment

Evidence developing · low confidence

No normalized longitudinal change evidence is available for this variable. Absence of events must not be interpreted as proof of cross-cycle equivalence.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Variable names / labels over time
  • Dog allergen Canis familiaris 1 (Can f 1) dust antigen, result (ng/mL dust)2005-2006
Cycle-by-cycle release history
  • 2005-2006: ALDUST_D — Dog allergen Canis familiaris 1 (Can f 1) dust antigen, result (ng/mL dust) — Allergens - Household Dust (Laboratory)
DSXCF1LDEvidence developing

Dog allergen Canis familiaris 1 (Can f 1) dust antigen, limit of detection (ng/mL dust)

Observed years
20052006
Release records
1
Datasets
1
Components
Laboratory
Qualified Praxis harmonization assessment

Evidence developing · low confidence

No normalized longitudinal change evidence is available for this variable. Absence of events must not be interpreted as proof of cross-cycle equivalence.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Variable names / labels over time
  • Dog allergen Canis familiaris 1 (Can f 1) dust antigen, limit of detection (ng/mL dust)2005-2006
Cycle-by-cycle release history
  • 2005-2006: ALDUST_D — Dog allergen Canis familiaris 1 (Can f 1) dust antigen, limit of detection (ng/mL dust) — Allergens - Household Dust (Laboratory)
DSXDF1Evidence developing

Dust mite Dermatophagoides farinae 1 (Der f 1) dust antigen, result (ng/mL dust)

Observed years
20052006
Release records
1
Datasets
1
Components
Laboratory
Qualified Praxis harmonization assessment

Evidence developing · low confidence

No normalized longitudinal change evidence is available for this variable. Absence of events must not be interpreted as proof of cross-cycle equivalence.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Variable names / labels over time
  • Dust mite Dermatophagoides farinae 1 (Der f 1) dust antigen, result (ng/mL dust)2005-2006
Cycle-by-cycle release history
  • 2005-2006: ALDUST_D — Dust mite Dermatophagoides farinae 1 (Der f 1) dust antigen, result (ng/mL dust) — Allergens - Household Dust (Laboratory)
DSXDF1LDEvidence developing

Dust mite Dermatophagoides farinae 1 (Der f 1) dust allergen, limit of detection (ng/mL dust)

Observed years
20052006
Release records
1
Datasets
1
Components
Laboratory
Qualified Praxis harmonization assessment

Evidence developing · low confidence

No normalized longitudinal change evidence is available for this variable. Absence of events must not be interpreted as proof of cross-cycle equivalence.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Variable names / labels over time
  • Dust mite Dermatophagoides farinae 1 (Der f 1) dust allergen, limit of detection (ng/mL dust)2005-2006
Cycle-by-cycle release history
  • 2005-2006: ALDUST_D — Dust mite Dermatophagoides farinae 1 (Der f 1) dust allergen, limit of detection (ng/mL dust) — Allergens - Household Dust (Laboratory)
DSXDP1Evidence developing

Dust mite Dermatophagoides pteronyssinus 1 (Der p 1) dust antigen, result (ng/mL dust)

Observed years
20052006
Release records
1
Datasets
1
Components
Laboratory
Qualified Praxis harmonization assessment

Evidence developing · low confidence

No normalized longitudinal change evidence is available for this variable. Absence of events must not be interpreted as proof of cross-cycle equivalence.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Variable names / labels over time
  • Dust mite Dermatophagoides pteronyssinus 1 (Der p 1) dust antigen, result (ng/mL dust)2005-2006
Cycle-by-cycle release history
  • 2005-2006: ALDUST_D — Dust mite Dermatophagoides pteronyssinus 1 (Der p 1) dust antigen, result (ng/mL dust) — Allergens - Household Dust (Laboratory)
DSXDP1LDEvidence developing

Dust mite Dermatophagoides pteronyssinus 1 (Der p 1) dust antigen, limit of detection (ng/mL dust)

Observed years
20052006
Release records
1
Datasets
1
Components
Laboratory
Qualified Praxis harmonization assessment

Evidence developing · low confidence

No normalized longitudinal change evidence is available for this variable. Absence of events must not be interpreted as proof of cross-cycle equivalence.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Variable names / labels over time
  • Dust mite Dermatophagoides pteronyssinus 1 (Der p 1) dust antigen, limit of detection (ng/mL dust)2005-2006
Cycle-by-cycle release history
  • 2005-2006: ALDUST_D — Dust mite Dermatophagoides pteronyssinus 1 (Der p 1) dust antigen, limit of detection (ng/mL dust) — Allergens - Household Dust (Laboratory)
DSXENXEvidence developing

Endotoxin dust, result (EU/mL dust)

Observed years
20052006
Release records
1
Datasets
1
Components
Laboratory
Qualified Praxis harmonization assessment

Evidence developing · low confidence

No normalized longitudinal change evidence is available for this variable. Absence of events must not be interpreted as proof of cross-cycle equivalence.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Variable names / labels over time
  • Endotoxin dust, result (EU/mL dust)2005-2006
Cycle-by-cycle release history
  • 2005-2006: ALDUST_D — Endotoxin dust, result (EU/mL dust) — Allergens - Household Dust (Laboratory)
DSXENXLDEvidence developing

Endotoxin dust, limit of detection (EU/mL dust)

Observed years
20052006
Release records
1
Datasets
1
Components
Laboratory
Qualified Praxis harmonization assessment

Evidence developing · low confidence

No normalized longitudinal change evidence is available for this variable. Absence of events must not be interpreted as proof of cross-cycle equivalence.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Variable names / labels over time
  • Endotoxin dust, limit of detection (EU/mL dust)2005-2006
Cycle-by-cycle release history
  • 2005-2006: ALDUST_D — Endotoxin dust, limit of detection (EU/mL dust) — Allergens - Household Dust (Laboratory)
DSXFD1Evidence developing

Cat allergen Felis domesticus 1 (Fel d 1) dust allergen, result (ng/mL dust)

Observed years
20052006
Release records
1
Datasets
1
Components
Laboratory
Qualified Praxis harmonization assessment

Evidence developing · low confidence

No normalized longitudinal change evidence is available for this variable. Absence of events must not be interpreted as proof of cross-cycle equivalence.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Variable names / labels over time
  • Cat allergen Felis domesticus 1 (Fel d 1) dust allergen, result (ng/mL dust)2005-2006
Cycle-by-cycle release history
  • 2005-2006: ALDUST_D — Cat allergen Felis domesticus 1 (Fel d 1) dust allergen, result (ng/mL dust) — Allergens - Household Dust (Laboratory)
DSXFD1LDEvidence developing

Cat allergen Felis domesticus 1 (Fel d 1) dust allergen, limit of detection (ng/mL dust)

Observed years
20052006
Release records
1
Datasets
1
Components
Laboratory
Qualified Praxis harmonization assessment

Evidence developing · low confidence

No normalized longitudinal change evidence is available for this variable. Absence of events must not be interpreted as proof of cross-cycle equivalence.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Variable names / labels over time
  • Cat allergen Felis domesticus 1 (Fel d 1) dust allergen, limit of detection (ng/mL dust)2005-2006
Cycle-by-cycle release history
  • 2005-2006: ALDUST_D — Cat allergen Felis domesticus 1 (Fel d 1) dust allergen, limit of detection (ng/mL dust) — Allergens - Household Dust (Laboratory)
DSXMM1Evidence developing

Mouse urinary protein (Mus m 1) dust antigen, result (ng/mL dust)

Observed years
20052006
Release records
1
Datasets
1
Components
Laboratory
Qualified Praxis harmonization assessment

Evidence developing · low confidence

No normalized longitudinal change evidence is available for this variable. Absence of events must not be interpreted as proof of cross-cycle equivalence.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Variable names / labels over time
  • Mouse urinary protein (Mus m 1) dust antigen, result (ng/mL dust)2005-2006
Cycle-by-cycle release history
  • 2005-2006: ALDUST_D — Mouse urinary protein (Mus m 1) dust antigen, result (ng/mL dust) — Allergens - Household Dust (Laboratory)
DSXMM1LDEvidence developing

Mouse urinary protein (Mus m 1) dust antigen, limit of detection (ng/mL dust)

Observed years
20052006
Release records
1
Datasets
1
Components
Laboratory
Qualified Praxis harmonization assessment

Evidence developing · low confidence

No normalized longitudinal change evidence is available for this variable. Absence of events must not be interpreted as proof of cross-cycle equivalence.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Variable names / labels over time
  • Mouse urinary protein (Mus m 1) dust antigen, limit of detection (ng/mL dust)2005-2006
Cycle-by-cycle release history
  • 2005-2006: ALDUST_D — Mouse urinary protein (Mus m 1) dust antigen, limit of detection (ng/mL dust) — Allergens - Household Dust (Laboratory)
DSXRN1Evidence developing

Rat urinary protein (Rat n 1) dust antigen, result (ng/mL dust)

Observed years
20052006
Release records
1
Datasets
1
Components
Laboratory
Qualified Praxis harmonization assessment

Evidence developing · low confidence

No normalized longitudinal change evidence is available for this variable. Absence of events must not be interpreted as proof of cross-cycle equivalence.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Variable names / labels over time
  • Rat urinary protein (Rat n 1) dust antigen, result (ng/mL dust)2005-2006
Cycle-by-cycle release history
  • 2005-2006: ALDUST_D — Rat urinary protein (Rat n 1) dust antigen, result (ng/mL dust) — Allergens - Household Dust (Laboratory)
DSXRN1LDEvidence developing

Rat urinary protein (Rat n 1) dust antigen, limit of detection (ng/mL dust)

Observed years
20052006
Release records
1
Datasets
1
Components
Laboratory
Qualified Praxis harmonization assessment

Evidence developing · low confidence

No normalized longitudinal change evidence is available for this variable. Absence of events must not be interpreted as proof of cross-cycle equivalence.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Variable names / labels over time
  • Rat urinary protein (Rat n 1) dust antigen, limit of detection (ng/mL dust)2005-2006
Cycle-by-cycle release history
  • 2005-2006: ALDUST_D — Rat urinary protein (Rat n 1) dust antigen, limit of detection (ng/mL dust) — Allergens - Household Dust (Laboratory)
ELISAEvidence developing

ELISA result interpretation

Observed years
20032004
Release records
1
Datasets
1
Components
Laboratory
Qualified Praxis harmonization assessment

Evidence developing · low confidence

No normalized longitudinal change evidence is available for this variable. Absence of events must not be interpreted as proof of cross-cycle equivalence.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Variable names / labels over time
  • ELISA result interpretation2003-2004
Cycle-by-cycle release history
  • 2003-2004: SSQFEV_C — ELISA result interpretation — Coxiella Burnetii (Q Fever) Antibodies - Serum (Surplus) (Laboratory)
ETHNICTYCompatible with harmonization

Ethnicity - Recode

Observed years
20052008
Release records
8
Datasets
8
Components
Laboratory
Qualified Praxis harmonization assessment

Compatible with harmonization · moderate confidence

No blocking method discontinuity is identified inside the selected cycle span, but one or more longitudinal changes require explicit harmonization conditions before pooling.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 2005-2006 → 2007-2008

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Review the adjacent codebooks/methods. Keep this boundary as documentation variation unless source evidence confirms a substantive method or instrument change.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • Ethnicity - Recode2005-2006 · 2007-2008
Cycle-by-cycle release history
  • 2005-2006: BFRPOL_D — Ethnicity - Recode — Brominated Flame Retardants (BFRs) - Pooled Samples (Laboratory)
  • 2005-2006: DOXPOL_D — Ethnicity - Recode — Polychlorinated dibenzo-p-dioxins (PCDDs), Dibenzofurans (PCDFs) & Coplanar Polychlorinated Biphenyls (cPCBs) - Pooled Samples (Laboratory)
  • 2005-2006: PCBPOL_D — Ethnicity - Recode — Non-dioxin-like Polychlorinated Biphenyls & Mono-ortho-substituted Polychlorinated Biphenyls - Pooled Samples (Laboratory)
  • 2005-2006: PSTPOL_D — Ethnicity - Recode — Pesticides - Organochlorine Pesticides - Pooled Samples (Laboratory)
  • 2007-2008: BFRPOL_E — Ethnicity - Recode — Brominated Flame Retardants (BFRs) - Pooled Samples (Laboratory)
  • 2007-2008: DOXPOL_E — Ethnicity - Recode — Polychlorinated dibenzo-p-dioxins (PCDDs), Dibenzofurans (PCDFs) & Coplanar Polychlorinated Biphenyls (cPCBs) - Pooled Samples (Laboratory)
  • 2007-2008: PCBPOL_E — Ethnicity - Recode — Non-dioxin-like Polychlorinated Biphenyls & Mono-ortho-substituted Polychlorinated Biphenyls - Pooled Samples (Laboratory)
  • 2007-2008: PSTPOL_E — Ethnicity - Recode — Pesticides - Organochlorine Pesticides - Pooled Samples (Laboratory)
GTDBL2MNAdjustment required

Time from fasting glucose & OGTT (min)

Observed years
20072016
Release records
5
Datasets
5
Components
Laboratory
Qualified Praxis harmonization assessment

Adjustment required · high confidence

A methodological discontinuity falls inside the selected cycle span. Naive pooling of raw values across the flagged boundary is not recommended unless CDC/NCHS provides a defensible calibration or comparability procedure.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 2007-2008 → 2009-2010 · 2009-2010 → 2011-2012 · 2011-2012 → 2013-2014 · 2013-2014 → 2015-2016

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Review the adjacent codebooks/methods. Keep this boundary as documentation variation unless source evidence confirms a substantive method or instrument change.
  • Select the weight appropriate to each cycle and subsample; when pooling cycles, construct the combined weight according to NHANES guidance rather than reusing a single-cycle weight unchanged.
  • Apply CDC/NCHS comparability or calibration guidance where available. If equivalence is not established, preserve separate method periods or perform sensitivity analyses rather than naively pooling raw values.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • Time from fasting glucose & OGTT (min)2007-2008 · 2009-2010 · 2011-2012 · 2013-2014 · 2015-2016
Cycle-by-cycle release history
  • 2007-2008: OGTT_E — Time from fasting glucose & OGTT (min) — Oral Glucose Tolerance Test (Laboratory)
  • 2009-2010: OGTT_F — Time from fasting glucose & OGTT (min) — Oral Glucose Tolerance Test (Laboratory)
  • 2011-2012: OGTT_G — Time from fasting glucose & OGTT (min) — Oral Glucose Tolerance Test (Laboratory)
  • 2013-2014: OGTT_H — Time from fasting glucose & OGTT (min) — Oral Glucose Tolerance Test (Laboratory)
  • 2015-2016: OGTT_I — Time from fasting glucose & OGTT (min) — Oral Glucose Tolerance Test (Laboratory)
GTDCODEAdjustment required

Incomplete OGTT Comment Code

Observed years
20072016
Release records
5
Datasets
5
Components
Laboratory
Qualified Praxis harmonization assessment

Adjustment required · high confidence

A methodological discontinuity falls inside the selected cycle span. Naive pooling of raw values across the flagged boundary is not recommended unless CDC/NCHS provides a defensible calibration or comparability procedure.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 2007-2008 → 2009-2010 · 2009-2010 → 2011-2012 · 2011-2012 → 2013-2014 · 2013-2014 → 2015-2016

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Review the adjacent codebooks/methods. Keep this boundary as documentation variation unless source evidence confirms a substantive method or instrument change.
  • Select the weight appropriate to each cycle and subsample; when pooling cycles, construct the combined weight according to NHANES guidance rather than reusing a single-cycle weight unchanged.
  • Apply CDC/NCHS comparability or calibration guidance where available. If equivalence is not established, preserve separate method periods or perform sensitivity analyses rather than naively pooling raw values.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • Incomplete OGTT Comment Code2007-2008 · 2009-2010 · 2011-2012 · 2013-2014 · 2015-2016
Cycle-by-cycle release history
  • 2007-2008: OGTT_E — Incomplete OGTT Comment Code — Oral Glucose Tolerance Test (Laboratory)
  • 2009-2010: OGTT_F — Incomplete OGTT Comment Code — Oral Glucose Tolerance Test (Laboratory)
  • 2011-2012: OGTT_G — Incomplete OGTT Comment Code — Oral Glucose Tolerance Test (Laboratory)
  • 2013-2014: OGTT_H — Incomplete OGTT Comment Code — Oral Glucose Tolerance Test (Laboratory)
  • 2015-2016: OGTT_I — Incomplete OGTT Comment Code — Oral Glucose Tolerance Test (Laboratory)
GTDDR1MNAdjustment required

Time from fast glucose & challenge (min)

Observed years
20072016
Release records
5
Datasets
5
Components
Laboratory
Qualified Praxis harmonization assessment

Adjustment required · high confidence

A methodological discontinuity falls inside the selected cycle span. Naive pooling of raw values across the flagged boundary is not recommended unless CDC/NCHS provides a defensible calibration or comparability procedure.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 2007-2008 → 2009-2010 · 2009-2010 → 2011-2012 · 2011-2012 → 2013-2014 · 2013-2014 → 2015-2016

Praxis harmonization actions
  • Confirm that the construct and coding are unchanged before pooling or recoding.
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Review the adjacent codebooks/methods. Keep this boundary as documentation variation unless source evidence confirms a substantive method or instrument change.
  • Select the weight appropriate to each cycle and subsample; when pooling cycles, construct the combined weight according to NHANES guidance rather than reusing a single-cycle weight unchanged.
  • Apply CDC/NCHS comparability or calibration guidance where available. If equivalence is not established, preserve separate method periods or perform sensitivity analyses rather than naively pooling raw values.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • Time from fast glucose & challenge (min)2007-2008
  • Time from fast glucose & challenge(min)2009-2010 · 2011-2012 · 2013-2014 · 2015-2016
Cycle-by-cycle release history
  • 2007-2008: OGTT_E — Time from fast glucose & challenge (min) — Oral Glucose Tolerance Test (Laboratory)
  • 2009-2010: OGTT_F — Time from fast glucose & challenge(min) — Oral Glucose Tolerance Test (Laboratory)
  • 2011-2012: OGTT_G — Time from fast glucose & challenge(min) — Oral Glucose Tolerance Test (Laboratory)
  • 2013-2014: OGTT_H — Time from fast glucose & challenge(min) — Oral Glucose Tolerance Test (Laboratory)
  • 2015-2016: OGTT_I — Time from fast glucose & challenge(min) — Oral Glucose Tolerance Test (Laboratory)
GTDDR2MNAdjustment required

Time from glucose challenge & OGTT(min)

Observed years
20072016
Release records
5
Datasets
5
Components
Laboratory
Qualified Praxis harmonization assessment

Adjustment required · high confidence

A methodological discontinuity falls inside the selected cycle span. Naive pooling of raw values across the flagged boundary is not recommended unless CDC/NCHS provides a defensible calibration or comparability procedure.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 2007-2008 → 2009-2010 · 2009-2010 → 2011-2012 · 2011-2012 → 2013-2014 · 2013-2014 → 2015-2016

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Review the adjacent codebooks/methods. Keep this boundary as documentation variation unless source evidence confirms a substantive method or instrument change.
  • Select the weight appropriate to each cycle and subsample; when pooling cycles, construct the combined weight according to NHANES guidance rather than reusing a single-cycle weight unchanged.
  • Apply CDC/NCHS comparability or calibration guidance where available. If equivalence is not established, preserve separate method periods or perform sensitivity analyses rather than naively pooling raw values.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • Time from glucose challenge & OGTT(min)2007-2008 · 2009-2010 · 2011-2012 · 2013-2014 · 2015-2016
Cycle-by-cycle release history
  • 2007-2008: OGTT_E — Time from glucose challenge & OGTT(min) — Oral Glucose Tolerance Test (Laboratory)
  • 2009-2010: OGTT_F — Time from glucose challenge & OGTT(min) — Oral Glucose Tolerance Test (Laboratory)
  • 2011-2012: OGTT_G — Time from glucose challenge & OGTT(min) — Oral Glucose Tolerance Test (Laboratory)
  • 2013-2014: OGTT_H — Time from glucose challenge & OGTT(min) — Oral Glucose Tolerance Test (Laboratory)
  • 2015-2016: OGTT_I — Time from glucose challenge & OGTT(min) — Oral Glucose Tolerance Test (Laboratory)
GTDSCMMNAdjustment required

Glucose challenge Administer Time in minutes

Observed years
20072016
Release records
5
Datasets
5
Components
Laboratory
Qualified Praxis harmonization assessment

Adjustment required · high confidence

A methodological discontinuity falls inside the selected cycle span. Naive pooling of raw values across the flagged boundary is not recommended unless CDC/NCHS provides a defensible calibration or comparability procedure.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 2007-2008 → 2009-2010 · 2009-2010 → 2011-2012 · 2011-2012 → 2013-2014 · 2013-2014 → 2015-2016

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Review the adjacent codebooks/methods. Keep this boundary as documentation variation unless source evidence confirms a substantive method or instrument change.
  • Select the weight appropriate to each cycle and subsample; when pooling cycles, construct the combined weight according to NHANES guidance rather than reusing a single-cycle weight unchanged.
  • Apply CDC/NCHS comparability or calibration guidance where available. If equivalence is not established, preserve separate method periods or perform sensitivity analyses rather than naively pooling raw values.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • Glucose challenge Administer Time in minutes2007-2008 · 2009-2010 · 2011-2012 · 2013-2014 · 2015-2016
Cycle-by-cycle release history
  • 2007-2008: OGTT_E — Glucose challenge Administer Time in minutes — Oral Glucose Tolerance Test (Laboratory)
  • 2009-2010: OGTT_F — Glucose challenge Administer Time in minutes — Oral Glucose Tolerance Test (Laboratory)
  • 2011-2012: OGTT_G — Glucose challenge Administer Time in minutes — Oral Glucose Tolerance Test (Laboratory)
  • 2013-2014: OGTT_H — Glucose challenge Administer Time in minutes — Oral Glucose Tolerance Test (Laboratory)
  • 2015-2016: OGTT_I — Glucose challenge Administer Time in minutes — Oral Glucose Tolerance Test (Laboratory)
GTXDRANKAdjustment required

Amount of glucose challenge drank

Observed years
20072016
Release records
5
Datasets
5
Components
Laboratory
Qualified Praxis harmonization assessment

Adjustment required · high confidence

A methodological discontinuity falls inside the selected cycle span. Naive pooling of raw values across the flagged boundary is not recommended unless CDC/NCHS provides a defensible calibration or comparability procedure.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 2007-2008 → 2009-2010 · 2009-2010 → 2011-2012 · 2011-2012 → 2013-2014 · 2013-2014 → 2015-2016

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Review the adjacent codebooks/methods. Keep this boundary as documentation variation unless source evidence confirms a substantive method or instrument change.
  • Select the weight appropriate to each cycle and subsample; when pooling cycles, construct the combined weight according to NHANES guidance rather than reusing a single-cycle weight unchanged.
  • Apply CDC/NCHS comparability or calibration guidance where available. If equivalence is not established, preserve separate method periods or perform sensitivity analyses rather than naively pooling raw values.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • Amount of glucose challenge drank2007-2008 · 2009-2010 · 2011-2012 · 2013-2014 · 2015-2016
Cycle-by-cycle release history
  • 2007-2008: OGTT_E — Amount of glucose challenge drank — Oral Glucose Tolerance Test (Laboratory)
  • 2009-2010: OGTT_F — Amount of glucose challenge drank — Oral Glucose Tolerance Test (Laboratory)
  • 2011-2012: OGTT_G — Amount of glucose challenge drank — Oral Glucose Tolerance Test (Laboratory)
  • 2013-2014: OGTT_H — Amount of glucose challenge drank — Oral Glucose Tolerance Test (Laboratory)
  • 2015-2016: OGTT_I — Amount of glucose challenge drank — Oral Glucose Tolerance Test (Laboratory)
HRDHGEvidence developing

Total Hair Mercury as ug mercury/gram hair (ppm): MDL is Detection Limit (See Documentation for Definitions)

Observed years
19992000
Release records
1
Datasets
1
Components
Laboratory
Qualified Praxis harmonization assessment

Evidence developing · low confidence

No normalized longitudinal change evidence is available for this variable. Absence of events must not be interpreted as proof of cross-cycle equivalence.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Variable names / labels over time
  • Total Hair Mercury as ug mercury/gram hair (ppm): MDL is Detection Limit (See Documentation for Definitions)1999-2000
Cycle-by-cycle release history
  • 1999-2000: LAB22 — Total Hair Mercury as ug mercury/gram hair (ppm): MDL is Detection Limit (See Documentation for Definitions) — Mercury - Hair (Laboratory)
HRDHGLCEvidence developing

The comment code associated with the value of the HRXHG variable (see Documentation for definitions)

Observed years
19992000
Release records
1
Datasets
1
Components
Laboratory
Qualified Praxis harmonization assessment

Evidence developing · low confidence

No normalized longitudinal change evidence is available for this variable. Absence of events must not be interpreted as proof of cross-cycle equivalence.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Variable names / labels over time
  • The comment code associated with the value of the HRXHG variable (see Documentation for definitions)1999-2000
Cycle-by-cycle release history
  • 1999-2000: LAB22 — The comment code associated with the value of the HRXHG variable (see Documentation for definitions) — Mercury - Hair (Laboratory)
HRDHGLC2Evidence developing

The comment code associated with the value of the HRDHG variable (see Documentation for definitions)

Observed years
19992000
Release records
1
Datasets
1
Components
Laboratory
Qualified Praxis harmonization assessment

Evidence developing · low confidence

No normalized longitudinal change evidence is available for this variable. Absence of events must not be interpreted as proof of cross-cycle equivalence.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Variable names / labels over time
  • The comment code associated with the value of the HRDHG variable (see Documentation for definitions)1999-2000
Cycle-by-cycle release history
  • 1999-2000: LAB22 — The comment code associated with the value of the HRDHG variable (see Documentation for definitions) — Mercury - Hair (Laboratory)
HRQ010Evidence developing

Has your hair been given a permanent or been treated with a hair dye or a hair straightener within the last month?

Observed years
19992000
Release records
1
Datasets
1
Components
Laboratory
Qualified Praxis harmonization assessment

Evidence developing · low confidence

No normalized longitudinal change evidence is available for this variable. Absence of events must not be interpreted as proof of cross-cycle equivalence.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Variable names / labels over time
  • Has your hair been given a permanent or been treated with a hair dye or a hair straightener within the last month?1999-2000
Cycle-by-cycle release history
  • 1999-2000: LAB22 — Has your hair been given a permanent or been treated with a hair dye or a hair straightener within the last month? — Mercury - Hair (Laboratory)
HRXHGEvidence developing

Total Hair Mercury as ug mercury/gram hair (ppm): MQL is Detection Limit (See Documentation for Definitions)

Observed years
19992000
Release records
1
Datasets
1
Components
Laboratory
Qualified Praxis harmonization assessment

Evidence developing · low confidence

No normalized longitudinal change evidence is available for this variable. Absence of events must not be interpreted as proof of cross-cycle equivalence.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Variable names / labels over time
  • Total Hair Mercury as ug mercury/gram hair (ppm): MQL is Detection Limit (See Documentation for Definitions)1999-2000
Cycle-by-cycle release history
  • 1999-2000: LAB22 — Total Hair Mercury as ug mercury/gram hair (ppm): MQL is Detection Limit (See Documentation for Definitions) — Mercury - Hair (Laboratory)
KID221Adjustment required

How old {were you/was SP} when {you were/he was} first told that {you/he} had prostate cancer?

Observed years
20032010
Release records
3
Datasets
3
Components
Laboratory
Qualified Praxis harmonization assessment

Adjustment required · high confidence

A methodological discontinuity falls inside the selected cycle span. Naive pooling of raw values across the flagged boundary is not recommended unless CDC/NCHS provides a defensible calibration or comparability procedure.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 2003-2004 → 2005-2006 · 2005-2006 → 2009-2010

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Review the adjacent codebooks/methods. Keep this boundary as documentation variation unless source evidence confirms a substantive method or instrument change.
  • Apply CDC/NCHS comparability or calibration guidance where available. If equivalence is not established, preserve separate method periods or perform sensitivity analyses rather than naively pooling raw values.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • How old {were you/was SP} when {you were/he was} first told that {you/he} had prostate cancer?2003-2004 · 2005-2006 · 2009-2010
Cycle-by-cycle release history
  • 2003-2004: L11PSA_C — How old {were you/was SP} when {you were/he was} first told that {you/he} had prostate cancer? — Prostate Specific Antigen (PSA) (Laboratory)
  • 2005-2006: PSA_D — How old {were you/was SP} when {you were/he was} first told that {you/he} had prostate cancer? — Prostate Specific Antigen (PSA) (Laboratory)
  • 2009-2010: PSA_F — How old {were you/was SP} when {you were/he was} first told that {you/he} had prostate cancer? — Prostate Specific Antigen (PSA) (Laboratory)
KIQ110Adjustment required

Are you willing to have your blood tested for PSA?

Observed years
20012010
Release records
5
Datasets
5
Components
Laboratory
Qualified Praxis harmonization assessment

Adjustment required · high confidence

A methodological discontinuity falls inside the selected cycle span. Naive pooling of raw values across the flagged boundary is not recommended unless CDC/NCHS provides a defensible calibration or comparability procedure.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 2001-2002 → 2003-2004 · 2003-2004 → 2005-2006 · 2005-2006 → 2007-2008 · 2007-2008 → 2009-2010

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Review the adjacent codebooks/methods. Keep this boundary as documentation variation unless source evidence confirms a substantive method or instrument change.
  • Apply CDC/NCHS comparability or calibration guidance where available. If equivalence is not established, preserve separate method periods or perform sensitivity analyses rather than naively pooling raw values.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • Are you willing to have your blood tested for PSA?2001-2002 · 2003-2004 · 2005-2006 · 2007-2008 · 2009-2010
Cycle-by-cycle release history
  • 2001-2002: L11PSA_B — Are you willing to have your blood tested for PSA? — Prostate specific antigen (PSA) (Laboratory)
  • 2003-2004: L11PSA_C — Are you willing to have your blood tested for PSA? — Prostate Specific Antigen (PSA) (Laboratory)
  • 2005-2006: PSA_D — Are you willing to have your blood tested for PSA? — Prostate Specific Antigen (PSA) (Laboratory)
  • 2007-2008: PSA_E — Are you willing to have your blood tested for PSA? — Prostate Specific Antigen (PSA) (Laboratory)
  • 2009-2010: PSA_F — Are you willing to have your blood tested for PSA? — Prostate Specific Antigen (PSA) (Laboratory)
KIQ115Adjustment required

{Do you/does SP} have an infection or inflammation of the prostate gland at the present time?

Observed years
20012010
Release records
5
Datasets
5
Components
Laboratory
Qualified Praxis harmonization assessment

Adjustment required · high confidence

A methodological discontinuity falls inside the selected cycle span. Naive pooling of raw values across the flagged boundary is not recommended unless CDC/NCHS provides a defensible calibration or comparability procedure.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 2001-2002 → 2003-2004 · 2003-2004 → 2005-2006 · 2005-2006 → 2007-2008 · 2007-2008 → 2009-2010

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Review the adjacent codebooks/methods. Keep this boundary as documentation variation unless source evidence confirms a substantive method or instrument change.
  • Apply CDC/NCHS comparability or calibration guidance where available. If equivalence is not established, preserve separate method periods or perform sensitivity analyses rather than naively pooling raw values.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • {Do you/does SP} have an infection or inflammation of the prostate gland at the present time?2001-2002 · 2003-2004 · 2005-2006 · 2007-2008 · 2009-2010
Cycle-by-cycle release history
  • 2001-2002: L11PSA_B — {Do you/does SP} have an infection or inflammation of the prostate gland at the present time? — Prostate specific antigen (PSA) (Laboratory)
  • 2003-2004: L11PSA_C — {Do you/does SP} have an infection or inflammation of the prostate gland at the present time? — Prostate Specific Antigen (PSA) (Laboratory)
  • 2005-2006: PSA_D — {Do you/does SP} have an infection or inflammation of the prostate gland at the present time? — Prostate Specific Antigen (PSA) (Laboratory)
  • 2007-2008: PSA_E — {Do you/does SP} have an infection or inflammation of the prostate gland at the present time? — Prostate Specific Antigen (PSA) (Laboratory)
  • 2009-2010: PSA_F — {Do you/does SP} have an infection or inflammation of the prostate gland at the present time? — Prostate Specific Antigen (PSA) (Laboratory)
KIQ185Adjustment required

{Have you/Has SP} had a rectal exam in the last 7 days?

Observed years
20012010
Release records
5
Datasets
5
Components
Laboratory
Qualified Praxis harmonization assessment

Adjustment required · high confidence

A methodological discontinuity falls inside the selected cycle span. Naive pooling of raw values across the flagged boundary is not recommended unless CDC/NCHS provides a defensible calibration or comparability procedure.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 2001-2002 → 2003-2004 · 2003-2004 → 2005-2006 · 2005-2006 → 2007-2008 · 2007-2008 → 2009-2010

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Review the adjacent codebooks/methods. Keep this boundary as documentation variation unless source evidence confirms a substantive method or instrument change.
  • Apply CDC/NCHS comparability or calibration guidance where available. If equivalence is not established, preserve separate method periods or perform sensitivity analyses rather than naively pooling raw values.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • {Have you/Has SP} had a rectal exam in the last 7 days?2001-2002 · 2003-2004 · 2005-2006 · 2007-2008 · 2009-2010
Cycle-by-cycle release history
  • 2001-2002: L11PSA_B — {Have you/Has SP} had a rectal exam in the last 7 days? — Prostate specific antigen (PSA) (Laboratory)
  • 2003-2004: L11PSA_C — {Have you/Has SP} had a rectal exam in the last 7 days? — Prostate Specific Antigen (PSA) (Laboratory)
  • 2005-2006: PSA_D — {Have you/Has SP} had a rectal exam in the last 7 days? — Prostate Specific Antigen (PSA) (Laboratory)
  • 2007-2008: PSA_E — {Have you/Has SP} had a rectal exam in the last 7 days? — Prostate Specific Antigen (PSA) (Laboratory)
  • 2009-2010: PSA_F — {Have you/Has SP} had a rectal exam in the last 7 days? — Prostate Specific Antigen (PSA) (Laboratory)
KIQ190Compatible with harmonization

{Have you/Has SP} had a prostate biopsy in the last 4 weeks?

Observed years
20012004
Release records
2
Datasets
2
Components
Laboratory
Qualified Praxis harmonization assessment

Compatible with harmonization · moderate confidence

No blocking method discontinuity is identified inside the selected cycle span, but one or more longitudinal changes require explicit harmonization conditions before pooling.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 2001-2002 → 2003-2004

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Review the adjacent codebooks/methods. Keep this boundary as documentation variation unless source evidence confirms a substantive method or instrument change.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • {Have you/Has SP} had a prostate biopsy in the last 4 weeks?2001-2002 · 2003-2004
Cycle-by-cycle release history
  • 2001-2002: L11PSA_B — {Have you/Has SP} had a prostate biopsy in the last 4 weeks? — Prostate specific antigen (PSA) (Laboratory)
  • 2003-2004: L11PSA_C — {Have you/Has SP} had a prostate biopsy in the last 4 weeks? — Prostate Specific Antigen (PSA) (Laboratory)
KIQ191Adjustment required

{Have you/Has SP} had a prostate biopsy or other prostate surgery in the last 4 weeks?

Observed years
20052010
Release records
3
Datasets
3
Components
Laboratory
Qualified Praxis harmonization assessment

Adjustment required · high confidence

A methodological discontinuity falls inside the selected cycle span. Naive pooling of raw values across the flagged boundary is not recommended unless CDC/NCHS provides a defensible calibration or comparability procedure.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 2005-2006 → 2007-2008 · 2007-2008 → 2009-2010

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Apply CDC/NCHS comparability or calibration guidance where available. If equivalence is not established, preserve separate method periods or perform sensitivity analyses rather than naively pooling raw values.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • {Have you/Has SP} had a prostate biopsy or other prostate surgery in the last 4 weeks?2005-2006 · 2007-2008 · 2009-2010
Cycle-by-cycle release history
  • 2005-2006: PSA_D — {Have you/Has SP} had a prostate biopsy or other prostate surgery in the last 4 weeks? — Prostate Specific Antigen (PSA) (Laboratory)
  • 2007-2008: PSA_E — {Have you/Has SP} had a prostate biopsy or other prostate surgery in the last 4 weeks? — Prostate Specific Antigen (PSA) (Laboratory)
  • 2009-2010: PSA_F — {Have you/Has SP} had a prostate biopsy or other prostate surgery in the last 4 weeks? — Prostate Specific Antigen (PSA) (Laboratory)
KIQ195Adjustment required

{Have you/Has SP} had a cystoscopy in the last 4 weeks? (Cystoscopy is an internal examination of the prostate and bladder using a flexible tube-like instrument with a lens inserted through the penis.)

Observed years
20012010
Release records
5
Datasets
5
Components
Laboratory
Qualified Praxis harmonization assessment

Adjustment required · high confidence

A methodological discontinuity falls inside the selected cycle span. Naive pooling of raw values across the flagged boundary is not recommended unless CDC/NCHS provides a defensible calibration or comparability procedure.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 2001-2002 → 2003-2004 · 2003-2004 → 2005-2006 · 2005-2006 → 2007-2008 · 2007-2008 → 2009-2010

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Review the adjacent codebooks/methods. Keep this boundary as documentation variation unless source evidence confirms a substantive method or instrument change.
  • Apply CDC/NCHS comparability or calibration guidance where available. If equivalence is not established, preserve separate method periods or perform sensitivity analyses rather than naively pooling raw values.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • {Have you/Has SP} had a cystoscopy in the last 4 weeks? (Cystoscopy is an internal examination of the prostate and bladder using a flexible tube-like instrument with a lens inserted through the penis.)2001-2002 · 2003-2004 · 2005-2006 · 2007-2008 · 2009-2010
Cycle-by-cycle release history
  • 2001-2002: L11PSA_B — {Have you/Has SP} had a cystoscopy in the last 4 weeks? (Cystoscopy is an internal examination of the prostate and bladder using a flexible tube-like instrument with a lens inserted through the penis.) — Prostate specific antigen (PSA) (Laboratory)
  • 2003-2004: L11PSA_C — {Have you/Has SP} had a cystoscopy in the last 4 weeks? (Cystoscopy is an internal examination of the prostate and bladder using a flexible tube-like instrument with a lens inserted through the penis.) — Prostate Specific Antigen (PSA) (Laboratory)
  • 2005-2006: PSA_D — {Have you/Has SP} had a cystoscopy in the last 4 weeks? (Cystoscopy is an internal examination of the prostate and bladder using a flexible tube-like instrument with a lens inserted through the penis.) — Prostate Specific Antigen (PSA) (Laboratory)
  • 2007-2008: PSA_E — {Have you/Has SP} had a cystoscopy in the last 4 weeks? (Cystoscopy is an internal examination of the prostate and bladder using a flexible tube-like instrument with a lens inserted through the penis.) — Prostate Specific Antigen (PSA) (Laboratory)
  • 2009-2010: PSA_F — {Have you/Has SP} had a cystoscopy in the last 4 weeks? (Cystoscopy is an internal examination of the prostate and bladder using a flexible tube-like instrument with a lens inserted through the penis.) — Prostate Specific Antigen (PSA) (Laboratory)
KIQ201Adjustment required

{Have you/Has SP} ever been told by a doctor or health professional that {you/he} had prostate cancer?

Observed years
20012010
Release records
5
Datasets
5
Components
Laboratory
Qualified Praxis harmonization assessment

Adjustment required · high confidence

A methodological discontinuity falls inside the selected cycle span. Naive pooling of raw values across the flagged boundary is not recommended unless CDC/NCHS provides a defensible calibration or comparability procedure.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 2001-2002 → 2003-2004 · 2003-2004 → 2005-2006 · 2005-2006 → 2007-2008 · 2007-2008 → 2009-2010

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Review the adjacent codebooks/methods. Keep this boundary as documentation variation unless source evidence confirms a substantive method or instrument change.
  • Apply CDC/NCHS comparability or calibration guidance where available. If equivalence is not established, preserve separate method periods or perform sensitivity analyses rather than naively pooling raw values.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • {Have you/Has SP} ever been told by a doctor or health professional that {you/he} had prostate cancer?2001-2002 · 2003-2004 · 2005-2006 · 2007-2008 · 2009-2010
Cycle-by-cycle release history
  • 2001-2002: L11PSA_B — {Have you/Has SP} ever been told by a doctor or health professional that {you/he} had prostate cancer? — Prostate specific antigen (PSA) (Laboratory)
  • 2003-2004: L11PSA_C — {Have you/Has SP} ever been told by a doctor or health professional that {you/he} had prostate cancer? — Prostate Specific Antigen (PSA) (Laboratory)
  • 2005-2006: PSA_D — {Have you/Has SP} ever been told by a doctor or health professional that {you/he} had prostate cancer? — Prostate Specific Antigen (PSA) (Laboratory)
  • 2007-2008: PSA_E — {Have you/Has SP} ever been told by a doctor or health professional that {you/he} had prostate cancer? — Prostate Specific Antigen (PSA) (Laboratory)
  • 2009-2010: PSA_F — {Have you/Has SP} ever been told by a doctor or health professional that {you/he} had prostate cancer? — Prostate Specific Antigen (PSA) (Laboratory)
KIQ221Adjustment required

How old {were you/was SP} when {you were/he was} first told that {you/he} had prostate cancer?

Observed years
20012008
Release records
2
Datasets
2
Components
Laboratory
Qualified Praxis harmonization assessment

Adjustment required · high confidence

A methodological discontinuity falls inside the selected cycle span. Naive pooling of raw values across the flagged boundary is not recommended unless CDC/NCHS provides a defensible calibration or comparability procedure.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 2001-2002 → 2007-2008

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Apply CDC/NCHS comparability or calibration guidance where available. If equivalence is not established, preserve separate method periods or perform sensitivity analyses rather than naively pooling raw values.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • How old {were you/was SP} when {you were/he was} first told that {you/he} had prostate cancer?2001-2002 · 2007-2008
Cycle-by-cycle release history
  • 2001-2002: L11PSA_B — How old {were you/was SP} when {you were/he was} first told that {you/he} had prostate cancer? — Prostate specific antigen (PSA) (Laboratory)
  • 2007-2008: PSA_E — How old {were you/was SP} when {you were/he was} first told that {you/he} had prostate cancer? — Prostate Specific Antigen (PSA) (Laboratory)
KIQ241Adjustment required

{Have you/Has SP} ever had surgery on {your/his} prostate?

Observed years
20012010
Release records
5
Datasets
5
Components
Laboratory
Qualified Praxis harmonization assessment

Adjustment required · high confidence

A methodological discontinuity falls inside the selected cycle span. Naive pooling of raw values across the flagged boundary is not recommended unless CDC/NCHS provides a defensible calibration or comparability procedure.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 2001-2002 → 2003-2004 · 2003-2004 → 2005-2006 · 2005-2006 → 2007-2008 · 2007-2008 → 2009-2010

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Review the adjacent codebooks/methods. Keep this boundary as documentation variation unless source evidence confirms a substantive method or instrument change.
  • Apply CDC/NCHS comparability or calibration guidance where available. If equivalence is not established, preserve separate method periods or perform sensitivity analyses rather than naively pooling raw values.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • {Have you/Has SP} ever had surgery on {your/his} prostate?2001-2002 · 2003-2004 · 2005-2006 · 2007-2008 · 2009-2010
Cycle-by-cycle release history
  • 2001-2002: L11PSA_B — {Have you/Has SP} ever had surgery on {your/his} prostate? — Prostate specific antigen (PSA) (Laboratory)
  • 2003-2004: L11PSA_C — {Have you/Has SP} ever had surgery on {your/his} prostate? — Prostate Specific Antigen (PSA) (Laboratory)
  • 2005-2006: PSA_D — {Have you/Has SP} ever had surgery on {your/his} prostate? — Prostate Specific Antigen (PSA) (Laboratory)
  • 2007-2008: PSA_E — {Have you/Has SP} ever had surgery on {your/his} prostate? — Prostate Specific Antigen (PSA) (Laboratory)
  • 2009-2010: PSA_F — {Have you/Has SP} ever had surgery on {your/his} prostate? — Prostate Specific Antigen (PSA) (Laboratory)
KIQ281Compatible with harmonization

Was the surgery for cancer of the prostate gland?

Observed years
20012004
Release records
2
Datasets
2
Components
Laboratory
Qualified Praxis harmonization assessment

Compatible with harmonization · moderate confidence

No blocking method discontinuity is identified inside the selected cycle span, but one or more longitudinal changes require explicit harmonization conditions before pooling.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 2001-2002 → 2003-2004

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Review the adjacent codebooks/methods. Keep this boundary as documentation variation unless source evidence confirms a substantive method or instrument change.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • Was the surgery for cancer of the prostate gland?2001-2002 · 2003-2004
Cycle-by-cycle release history
  • 2001-2002: L11PSA_B — Was the surgery for cancer of the prostate gland? — Prostate specific antigen (PSA) (Laboratory)
  • 2003-2004: L11PSA_C — Was the surgery for cancer of the prostate gland? — Prostate Specific Antigen (PSA) (Laboratory)
KIQ282Adjustment required

{Have you/Has SP} had surgery for prostate cancer?

Observed years
20052010
Release records
3
Datasets
3
Components
Laboratory
Qualified Praxis harmonization assessment

Adjustment required · high confidence

A methodological discontinuity falls inside the selected cycle span. Naive pooling of raw values across the flagged boundary is not recommended unless CDC/NCHS provides a defensible calibration or comparability procedure.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 2005-2006 → 2007-2008 · 2007-2008 → 2009-2010

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Apply CDC/NCHS comparability or calibration guidance where available. If equivalence is not established, preserve separate method periods or perform sensitivity analyses rather than naively pooling raw values.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • {Have you/Has SP} had surgery for prostate cancer?2005-2006 · 2007-2008 · 2009-2010
Cycle-by-cycle release history
  • 2005-2006: PSA_D — {Have you/Has SP} had surgery for prostate cancer? — Prostate Specific Antigen (PSA) (Laboratory)
  • 2007-2008: PSA_E — {Have you/Has SP} had surgery for prostate cancer? — Prostate Specific Antigen (PSA) (Laboratory)
  • 2009-2010: PSA_F — {Have you/Has SP} had surgery for prostate cancer? — Prostate Specific Antigen (PSA) (Laboratory)
KIQ301Adjustment required

{Have you/Has SP} ever had radiation treatments for prostate cancer?

Observed years
20012010
Release records
5
Datasets
5
Components
Laboratory
Qualified Praxis harmonization assessment

Adjustment required · high confidence

A methodological discontinuity falls inside the selected cycle span. Naive pooling of raw values across the flagged boundary is not recommended unless CDC/NCHS provides a defensible calibration or comparability procedure.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 2001-2002 → 2003-2004 · 2003-2004 → 2005-2006 · 2005-2006 → 2007-2008 · 2007-2008 → 2009-2010

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Review the adjacent codebooks/methods. Keep this boundary as documentation variation unless source evidence confirms a substantive method or instrument change.
  • Apply CDC/NCHS comparability or calibration guidance where available. If equivalence is not established, preserve separate method periods or perform sensitivity analyses rather than naively pooling raw values.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • {Have you/Has SP} ever had radiation treatments for prostate cancer?2001-2002 · 2003-2004 · 2005-2006 · 2007-2008 · 2009-2010
Cycle-by-cycle release history
  • 2001-2002: L11PSA_B — {Have you/Has SP} ever had radiation treatments for prostate cancer? — Prostate specific antigen (PSA) (Laboratory)
  • 2003-2004: L11PSA_C — {Have you/Has SP} ever had radiation treatments for prostate cancer? — Prostate Specific Antigen (PSA) (Laboratory)
  • 2005-2006: PSA_D — {Have you/Has SP} ever had radiation treatments for prostate cancer? — Prostate Specific Antigen (PSA) (Laboratory)
  • 2007-2008: PSA_E — {Have you/Has SP} ever had radiation treatments for prostate cancer? — Prostate Specific Antigen (PSA) (Laboratory)
  • 2009-2010: PSA_F — {Have you/Has SP} ever had radiation treatments for prostate cancer? — Prostate Specific Antigen (PSA) (Laboratory)
KIQ311Adjustment required

{Have you/Has SP} ever taken prescribed medicines for prostate cancer?

Observed years
20012010
Release records
5
Datasets
5
Components
Laboratory
Qualified Praxis harmonization assessment

Adjustment required · high confidence

A methodological discontinuity falls inside the selected cycle span. Naive pooling of raw values across the flagged boundary is not recommended unless CDC/NCHS provides a defensible calibration or comparability procedure.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 2001-2002 → 2003-2004 · 2003-2004 → 2005-2006 · 2005-2006 → 2007-2008 · 2007-2008 → 2009-2010

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Review the adjacent codebooks/methods. Keep this boundary as documentation variation unless source evidence confirms a substantive method or instrument change.
  • Apply CDC/NCHS comparability or calibration guidance where available. If equivalence is not established, preserve separate method periods or perform sensitivity analyses rather than naively pooling raw values.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • {Have you/Has SP} ever taken prescribed medicines for prostate cancer?2001-2002 · 2003-2004 · 2005-2006 · 2007-2008 · 2009-2010
Cycle-by-cycle release history
  • 2001-2002: L11PSA_B — {Have you/Has SP} ever taken prescribed medicines for prostate cancer? — Prostate specific antigen (PSA) (Laboratory)
  • 2003-2004: L11PSA_C — {Have you/Has SP} ever taken prescribed medicines for prostate cancer? — Prostate Specific Antigen (PSA) (Laboratory)
  • 2005-2006: PSA_D — {Have you/Has SP} ever taken prescribed medicines for prostate cancer? — Prostate Specific Antigen (PSA) (Laboratory)
  • 2007-2008: PSA_E — {Have you/Has SP} ever taken prescribed medicines for prostate cancer? — Prostate Specific Antigen (PSA) (Laboratory)
  • 2009-2010: PSA_F — {Have you/Has SP} ever taken prescribed medicines for prostate cancer? — Prostate Specific Antigen (PSA) (Laboratory)
LB2ALCEvidence developing

alpha-carotene(ug/dL)

Observed years
20012002
Release records
1
Datasets
1
Components
Laboratory
Qualified Praxis harmonization assessment

Evidence developing · low confidence

No normalized longitudinal change evidence is available for this variable. Absence of events must not be interpreted as proof of cross-cycle equivalence.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Variable names / labels over time
  • alpha-carotene(ug/dL)2001-2002
Cycle-by-cycle release history
  • 2001-2002: VIT_2_B — alpha-carotene(ug/dL) — Vitamin A, Vitamin E, & Carotenoids, Second Exam (Laboratory)
LB2ALCSIEvidence developing

alpha-carotene(umol/L)

Observed years
20012002
Release records
1
Datasets
1
Components
Laboratory
Qualified Praxis harmonization assessment

Evidence developing · low confidence

No normalized longitudinal change evidence is available for this variable. Absence of events must not be interpreted as proof of cross-cycle equivalence.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Variable names / labels over time
  • alpha-carotene(umol/L)2001-2002
Cycle-by-cycle release history
  • 2001-2002: VIT_2_B — alpha-carotene(umol/L) — Vitamin A, Vitamin E, & Carotenoids, Second Exam (Laboratory)
LB2B12Compatible with harmonization

Vitamin B12, serum (pg/mL)

Observed years
20002002
Release records
2
Datasets
2
Components
Laboratory
Qualified Praxis harmonization assessment

Compatible with harmonization · moderate confidence

No blocking method discontinuity is identified inside the selected cycle span, but one or more longitudinal changes require explicit harmonization conditions before pooling.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 1999-2000 → 2001-2002

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Review the adjacent codebooks/methods. Keep this boundary as documentation variation unless source evidence confirms a substantive method or instrument change.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • Vitamin B12, serum (pg/mL)1999-2000 · 2001-2002
Cycle-by-cycle release history
  • 1999-2000: L06_2_00 — Vitamin B12, serum (pg/mL) — Cadmium, Lead, Ferritin, Serum Folate, RBC Folate, Vitamin B12, Homocysteine, Methylmalonic acid, Cotinine & Other Selected Nutritional Biochemistries - Blood, Second Exam (Laboratory) — Note: RDC Only
  • 2001-2002: L06_2_B — Vitamin B12, serum (pg/mL) — Cadmium, Lead, Total Mercury, Ferritin, Serum Folate, RBC Folate, Vitamin B12, Homocysteine, Methylmalonic acid, Cotinine - Blood, Second Exam (Laboratory)
LB2B12SICompatible with harmonization

Vitamin B12, serum (pmol/L)

Observed years
20002002
Release records
2
Datasets
2
Components
Laboratory
Qualified Praxis harmonization assessment

Compatible with harmonization · moderate confidence

No blocking method discontinuity is identified inside the selected cycle span, but one or more longitudinal changes require explicit harmonization conditions before pooling.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 1999-2000 → 2001-2002

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Review the adjacent codebooks/methods. Keep this boundary as documentation variation unless source evidence confirms a substantive method or instrument change.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • Vitamin B12, serum (pmol/L)1999-2000 · 2001-2002
Cycle-by-cycle release history
  • 1999-2000: L06_2_00 — Vitamin B12, serum (pmol/L) — Cadmium, Lead, Ferritin, Serum Folate, RBC Folate, Vitamin B12, Homocysteine, Methylmalonic acid, Cotinine & Other Selected Nutritional Biochemistries - Blood, Second Exam (Laboratory) — Note: RDC Only
  • 2001-2002: L06_2_B — Vitamin B12, serum (pmol/L) — Cadmium, Lead, Total Mercury, Ferritin, Serum Folate, RBC Folate, Vitamin B12, Homocysteine, Methylmalonic acid, Cotinine - Blood, Second Exam (Laboratory)
LB2BANOCompatible with harmonization

Basophils number (1000 cells/uL)

Observed years
20002002
Release records
2
Datasets
2
Components
Laboratory
Qualified Praxis harmonization assessment

Compatible with harmonization · moderate confidence

No blocking method discontinuity is identified inside the selected cycle span, but one or more longitudinal changes require explicit harmonization conditions before pooling.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 1999-2000 → 2001-2002

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • Basophils number (1000 cells/uL)1999-2000 · 2001-2002
Cycle-by-cycle release history
  • 1999-2000: l25_2_r — Basophils number (1000 cells/uL) — Complete Blood Count with 5-part Differential - Whole Blood, Second Exam (Laboratory) — Note: RDC Only
  • 2001-2002: l25_2_b — Basophils number (1000 cells/uL) — Complete Blood Count with 5-part Differential - Whole Blood, Second Exam (Laboratory)
LB2BAPCompatible with harmonization

Bone alkaline phosphotase (ug/L)

Observed years
20002002
Release records
2
Datasets
2
Components
Laboratory
Qualified Praxis harmonization assessment

Compatible with harmonization · moderate confidence

No blocking method discontinuity is identified inside the selected cycle span, but one or more longitudinal changes require explicit harmonization conditions before pooling.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 1999-2000 → 2001-2002

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Review the adjacent codebooks/methods. Keep this boundary as documentation variation unless source evidence confirms a substantive method or instrument change.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • Bone alkaline phosphotase (ug/L)1999-2000 · 2001-2002
Cycle-by-cycle release history
  • 1999-2000: L11_2_R — Bone alkaline phosphotase (ug/L) — C-Reactive Protein & Others, Second Exam (Laboratory) — Note: RDC Only
  • 2001-2002: L11_2_b — Bone alkaline phosphotase (ug/L) — C-Reactive Protein & Others, Second Exam (Laboratory)
LB2BAPCTCompatible with harmonization

Basophils percent (%)

Observed years
20002002
Release records
2
Datasets
2
Components
Laboratory
Qualified Praxis harmonization assessment

Compatible with harmonization · moderate confidence

No blocking method discontinuity is identified inside the selected cycle span, but one or more longitudinal changes require explicit harmonization conditions before pooling.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 1999-2000 → 2001-2002

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • Basophils percent (%)1999-2000 · 2001-2002
Cycle-by-cycle release history
  • 1999-2000: l25_2_r — Basophils percent (%) — Complete Blood Count with 5-part Differential - Whole Blood, Second Exam (Laboratory) — Note: RDC Only
  • 2001-2002: l25_2_b — Basophils percent (%) — Complete Blood Count with 5-part Differential - Whole Blood, Second Exam (Laboratory)
LB2BCDCompatible with harmonization

Cadmium (ug/L)

Observed years
20002002
Release records
2
Datasets
2
Components
Laboratory
Qualified Praxis harmonization assessment

Compatible with harmonization · moderate confidence

No blocking method discontinuity is identified inside the selected cycle span, but one or more longitudinal changes require explicit harmonization conditions before pooling.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 1999-2000 → 2001-2002

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Review the adjacent codebooks/methods. Keep this boundary as documentation variation unless source evidence confirms a substantive method or instrument change.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • Cadmium (ug/L)1999-2000 · 2001-2002
Cycle-by-cycle release history
  • 1999-2000: L06_2_00 — Cadmium (ug/L) — Cadmium, Lead, Ferritin, Serum Folate, RBC Folate, Vitamin B12, Homocysteine, Methylmalonic acid, Cotinine & Other Selected Nutritional Biochemistries - Blood, Second Exam (Laboratory) — Note: RDC Only
  • 2001-2002: L06_2_B — Cadmium (ug/L) — Cadmium, Lead, Total Mercury, Ferritin, Serum Folate, RBC Folate, Vitamin B12, Homocysteine, Methylmalonic acid, Cotinine - Blood, Second Exam (Laboratory)
LB2BCDSICompatible with harmonization

Cadmium (umol/L)

Observed years
20002002
Release records
2
Datasets
2
Components
Laboratory
Qualified Praxis harmonization assessment

Compatible with harmonization · moderate confidence

No blocking method discontinuity is identified inside the selected cycle span, but one or more longitudinal changes require explicit harmonization conditions before pooling.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 1999-2000 → 2001-2002

Praxis harmonization actions
  • Confirm that the construct and coding are unchanged before pooling or recoding.
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Review the adjacent codebooks/methods. Keep this boundary as documentation variation unless source evidence confirms a substantive method or instrument change.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • Cadmium (umol/L)1999-2000
  • Cadmium (nmol/L)2001-2002
Cycle-by-cycle release history
  • 1999-2000: L06_2_00 — Cadmium (umol/L) — Cadmium, Lead, Ferritin, Serum Folate, RBC Folate, Vitamin B12, Homocysteine, Methylmalonic acid, Cotinine & Other Selected Nutritional Biochemistries - Blood, Second Exam (Laboratory) — Note: RDC Only
  • 2001-2002: L06_2_B — Cadmium (nmol/L) — Cadmium, Lead, Total Mercury, Ferritin, Serum Folate, RBC Folate, Vitamin B12, Homocysteine, Methylmalonic acid, Cotinine - Blood, Second Exam (Laboratory)
LB2BECEvidence developing

trans-beta-carotene(ug/dL)

Observed years
20012002
Release records
1
Datasets
1
Components
Laboratory
Qualified Praxis harmonization assessment

Evidence developing · low confidence

No normalized longitudinal change evidence is available for this variable. Absence of events must not be interpreted as proof of cross-cycle equivalence.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Variable names / labels over time
  • trans-beta-carotene(ug/dL)2001-2002
Cycle-by-cycle release history
  • 2001-2002: VIT_2_B — trans-beta-carotene(ug/dL) — Vitamin A, Vitamin E, & Carotenoids, Second Exam (Laboratory)
LB2BECSIEvidence developing

trans-beta-carotene(umol/L)

Observed years
20012002
Release records
1
Datasets
1
Components
Laboratory
Qualified Praxis harmonization assessment

Evidence developing · low confidence

No normalized longitudinal change evidence is available for this variable. Absence of events must not be interpreted as proof of cross-cycle equivalence.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Variable names / labels over time
  • trans-beta-carotene(umol/L)2001-2002
Cycle-by-cycle release history
  • 2001-2002: VIT_2_B — trans-beta-carotene(umol/L) — Vitamin A, Vitamin E, & Carotenoids, Second Exam (Laboratory)
LB2BPBCompatible with harmonization

Lead (ug/dL)

Observed years
20002002
Release records
2
Datasets
2
Components
Laboratory
Qualified Praxis harmonization assessment

Compatible with harmonization · moderate confidence

No blocking method discontinuity is identified inside the selected cycle span, but one or more longitudinal changes require explicit harmonization conditions before pooling.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 1999-2000 → 2001-2002

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Review the adjacent codebooks/methods. Keep this boundary as documentation variation unless source evidence confirms a substantive method or instrument change.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • Lead (ug/dL)1999-2000 · 2001-2002
Cycle-by-cycle release history
  • 1999-2000: L06_2_00 — Lead (ug/dL) — Cadmium, Lead, Ferritin, Serum Folate, RBC Folate, Vitamin B12, Homocysteine, Methylmalonic acid, Cotinine & Other Selected Nutritional Biochemistries - Blood, Second Exam (Laboratory) — Note: RDC Only
  • 2001-2002: L06_2_B — Lead (ug/dL) — Cadmium, Lead, Total Mercury, Ferritin, Serum Folate, RBC Folate, Vitamin B12, Homocysteine, Methylmalonic acid, Cotinine - Blood, Second Exam (Laboratory)
LB2BPBSICompatible with harmonization

Lead (umol/L)

Observed years
20002002
Release records
2
Datasets
2
Components
Laboratory
Qualified Praxis harmonization assessment

Compatible with harmonization · moderate confidence

No blocking method discontinuity is identified inside the selected cycle span, but one or more longitudinal changes require explicit harmonization conditions before pooling.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 1999-2000 → 2001-2002

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Review the adjacent codebooks/methods. Keep this boundary as documentation variation unless source evidence confirms a substantive method or instrument change.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • Lead (umol/L)1999-2000 · 2001-2002
Cycle-by-cycle release history
  • 1999-2000: L06_2_00 — Lead (umol/L) — Cadmium, Lead, Ferritin, Serum Folate, RBC Folate, Vitamin B12, Homocysteine, Methylmalonic acid, Cotinine & Other Selected Nutritional Biochemistries - Blood, Second Exam (Laboratory) — Note: RDC Only
  • 2001-2002: L06_2_B — Lead (umol/L) — Cadmium, Lead, Total Mercury, Ferritin, Serum Folate, RBC Folate, Vitamin B12, Homocysteine, Methylmalonic acid, Cotinine - Blood, Second Exam (Laboratory)
LB2CBCEvidence developing

cis-beta-carotene(ug/dL)

Observed years
20012002
Release records
1
Datasets
1
Components
Laboratory
Qualified Praxis harmonization assessment

Evidence developing · low confidence

No normalized longitudinal change evidence is available for this variable. Absence of events must not be interpreted as proof of cross-cycle equivalence.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Variable names / labels over time
  • cis-beta-carotene(ug/dL)2001-2002
Cycle-by-cycle release history
  • 2001-2002: VIT_2_B — cis-beta-carotene(ug/dL) — Vitamin A, Vitamin E, & Carotenoids, Second Exam (Laboratory)
LB2CBCSIEvidence developing

cis-beta-carotene(umol/L)

Observed years
20012002
Release records
1
Datasets
1
Components
Laboratory
Qualified Praxis harmonization assessment

Evidence developing · low confidence

No normalized longitudinal change evidence is available for this variable. Absence of events must not be interpreted as proof of cross-cycle equivalence.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Variable names / labels over time
  • cis-beta-carotene(umol/L)2001-2002
Cycle-by-cycle release history
  • 2001-2002: VIT_2_B — cis-beta-carotene(umol/L) — Vitamin A, Vitamin E, & Carotenoids, Second Exam (Laboratory)
LB2COTCompatible with harmonization

Cotinine (ng/mL)

Observed years
20002002
Release records
2
Datasets
2
Components
Laboratory
Qualified Praxis harmonization assessment

Compatible with harmonization · moderate confidence

No blocking method discontinuity is identified inside the selected cycle span, but one or more longitudinal changes require explicit harmonization conditions before pooling.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 1999-2000 → 2001-2002

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Review the adjacent codebooks/methods. Keep this boundary as documentation variation unless source evidence confirms a substantive method or instrument change.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • Cotinine (ng/mL)1999-2000 · 2001-2002
Cycle-by-cycle release history
  • 1999-2000: L06_2_00 — Cotinine (ng/mL) — Cadmium, Lead, Ferritin, Serum Folate, RBC Folate, Vitamin B12, Homocysteine, Methylmalonic acid, Cotinine & Other Selected Nutritional Biochemistries - Blood, Second Exam (Laboratory) — Note: RDC Only
  • 2001-2002: L06_2_B — Cotinine (ng/mL) — Cadmium, Lead, Total Mercury, Ferritin, Serum Folate, RBC Folate, Vitamin B12, Homocysteine, Methylmalonic acid, Cotinine - Blood, Second Exam (Laboratory)
LB2COTLCEvidence developing

Cotinine comment code

Observed years
20012002
Release records
1
Datasets
1
Components
Laboratory
Qualified Praxis harmonization assessment

Evidence developing · low confidence

No normalized longitudinal change evidence is available for this variable. Absence of events must not be interpreted as proof of cross-cycle equivalence.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Variable names / labels over time
  • Cotinine comment code2001-2002
Cycle-by-cycle release history
  • 2001-2002: L06_2_B — Cotinine comment code — Cadmium, Lead, Total Mercury, Ferritin, Serum Folate, RBC Folate, Vitamin B12, Homocysteine, Methylmalonic acid, Cotinine - Blood, Second Exam (Laboratory)
LB2COTSIEvidence developing

Cotinine (nmol/L)

Observed years
20002000
Release records
1
Datasets
1
Components
Laboratory
Qualified Praxis harmonization assessment

Evidence developing · low confidence

No normalized longitudinal change evidence is available for this variable. Absence of events must not be interpreted as proof of cross-cycle equivalence.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Variable names / labels over time
  • Cotinine (nmol/L)1999-2000
Cycle-by-cycle release history
  • 1999-2000: L06_2_00 — Cotinine (nmol/L) — Cadmium, Lead, Ferritin, Serum Folate, RBC Folate, Vitamin B12, Homocysteine, Methylmalonic acid, Cotinine & Other Selected Nutritional Biochemistries - Blood, Second Exam (Laboratory) — Note: RDC Only
LB2CPCompatible with harmonization

C-peptide: pmol/mL

Observed years
20002002
Release records
2
Datasets
2
Components
Laboratory
Qualified Praxis harmonization assessment

Compatible with harmonization · moderate confidence

No blocking method discontinuity is identified inside the selected cycle span, but one or more longitudinal changes require explicit harmonization conditions before pooling.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 1999-2000 → 2001-2002

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Review the adjacent codebooks/methods. Keep this boundary as documentation variation unless source evidence confirms a substantive method or instrument change.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • C-peptide: pmol/mL1999-2000 · 2001-2002
Cycle-by-cycle release history
  • 1999-2000: l10_2_00 — C-peptide: pmol/mL — Glycohemoglobin, Plasma Glucose, Serum C-peptide, & Insulin, Second Exam (Laboratory) — Note: RDC Only
  • 2001-2002: L10_2_B — C-peptide: pmol/mL — Glycohemoglobin, Plasma Glucose, Serum C-peptide, & Insulin, Second Exam (Laboratory)
LB2CPSICompatible with harmonization

C-peptide SI(nmol/L)

Observed years
20002002
Release records
2
Datasets
2
Components
Laboratory
Qualified Praxis harmonization assessment

Compatible with harmonization · moderate confidence

No blocking method discontinuity is identified inside the selected cycle span, but one or more longitudinal changes require explicit harmonization conditions before pooling.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 1999-2000 → 2001-2002

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Review the adjacent codebooks/methods. Keep this boundary as documentation variation unless source evidence confirms a substantive method or instrument change.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • C-peptide SI(nmol/L)1999-2000
  • C-peptide (nmol/L) in SI units2001-2002
Cycle-by-cycle release history
  • 1999-2000: l10_2_00 — C-peptide SI(nmol/L) — Glycohemoglobin, Plasma Glucose, Serum C-peptide, & Insulin, Second Exam (Laboratory) — Note: RDC Only
  • 2001-2002: L10_2_B — C-peptide (nmol/L) in SI units — Glycohemoglobin, Plasma Glucose, Serum C-peptide, & Insulin, Second Exam (Laboratory)
LB2CRPCompatible with harmonization

C-reactive protein(mg/dL)

Observed years
20002002
Release records
2
Datasets
2
Components
Laboratory
Qualified Praxis harmonization assessment

Compatible with harmonization · moderate confidence

No blocking method discontinuity is identified inside the selected cycle span, but one or more longitudinal changes require explicit harmonization conditions before pooling.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 1999-2000 → 2001-2002

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Review the adjacent codebooks/methods. Keep this boundary as documentation variation unless source evidence confirms a substantive method or instrument change.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • C-reactive protein(mg/dL)1999-2000
  • C-reactive protein (mg/dL)2001-2002
Cycle-by-cycle release history
  • 1999-2000: L11_2_R — C-reactive protein(mg/dL) — C-Reactive Protein & Others, Second Exam (Laboratory) — Note: RDC Only
  • 2001-2002: L11_2_b — C-reactive protein (mg/dL) — C-Reactive Protein & Others, Second Exam (Laboratory)
LB2CRYEvidence developing

beta-cryptoxanthin(ug/dL)

Observed years
20012002
Release records
1
Datasets
1
Components
Laboratory
Qualified Praxis harmonization assessment

Evidence developing · low confidence

No normalized longitudinal change evidence is available for this variable. Absence of events must not be interpreted as proof of cross-cycle equivalence.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Variable names / labels over time
  • beta-cryptoxanthin(ug/dL)2001-2002
Cycle-by-cycle release history
  • 2001-2002: VIT_2_B — beta-cryptoxanthin(ug/dL) — Vitamin A, Vitamin E, & Carotenoids, Second Exam (Laboratory)
LB2CRYSIEvidence developing

beta-cryptoxanthin(umol/L)

Observed years
20012002
Release records
1
Datasets
1
Components
Laboratory
Qualified Praxis harmonization assessment

Evidence developing · low confidence

No normalized longitudinal change evidence is available for this variable. Absence of events must not be interpreted as proof of cross-cycle equivalence.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Variable names / labels over time
  • beta-cryptoxanthin(umol/L)2001-2002
Cycle-by-cycle release history
  • 2001-2002: VIT_2_B — beta-cryptoxanthin(umol/L) — Vitamin A, Vitamin E, & Carotenoids, Second Exam (Laboratory)
LB2DAYAdjustment required

Days between 1st and 2nd exam

Observed years
20002002
Release records
23
Datasets
23
Components
Laboratory
Qualified Praxis harmonization assessment

Adjustment required · high confidence

A methodological discontinuity falls inside the selected cycle span. Naive pooling of raw values across the flagged boundary is not recommended unless CDC/NCHS provides a defensible calibration or comparability procedure.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 1999-2000 → 2001-2002

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Review the adjacent codebooks/methods. Keep this boundary as documentation variation unless source evidence confirms a substantive method or instrument change.
  • Apply CDC/NCHS comparability or calibration guidance where available. If equivalence is not established, preserve separate method periods or perform sensitivity analyses rather than naively pooling raw values.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • Days between 1st and 2nd exam1999-2000 · 2001-2002
  • The number of days between the first and second collections1999-2000
  • Days between first and second exams1999-2000 · 2001-2002
  • Days between the 1st and 2nd exams1999-2000 · 2001-2002
  • The number of days between the collection of the first and second exam1999-2000 · 2001-2002
  • Days between first and second exam1999-2000 · 2001-2002
  • 2001-2002
  • number of days between the collection of the first and second exam2001-2002
  • The number of days between the collections of first and second exams2001-2002
Cycle-by-cycle release history
  • 1999-2000: L06_2_00 — The number of days between the first and second collections — Cadmium, Lead, Ferritin, Serum Folate, RBC Folate, Vitamin B12, Homocysteine, Methylmalonic acid, Cotinine & Other Selected Nutritional Biochemistries - Blood, Second Exam (Laboratory) — Note: RDC Only
  • 1999-2000: l10_2_00 — Days between the 1st and 2nd exams — Glycohemoglobin, Plasma Glucose, Serum C-peptide, & Insulin, Second Exam (Laboratory) — Note: RDC Only
  • 1999-2000: L11_2_R — Days between 1st and 2nd exam — C-Reactive Protein & Others, Second Exam (Laboratory) — Note: RDC Only
  • 1999-2000: l13_2_r — Days between 1st and 2nd exam — Cholesterol - Total, HDL, LDL & Triglycerides, Second Exam (Laboratory) — Note: RDC Only
  • 1999-2000: L16_2_R — The number of days between the collection of the first and second exam — Creatinine & Albumin - Urine, Second Exam (Laboratory) — Note: RDC Only
  • 1999-2000: l18_2_00 — The number of days between the collection of the first and second exam — Standard Biochemistry Profile & Hormones, Second Exam (Laboratory) — Note: RDC Only
  • 1999-2000: L19_2_R — The number of days between the collection of the first and second exam — Measles, Rubella, & Varicella, Second Exam (Laboratory) — Note: RDC Only
  • 1999-2000: l25_2_r — Days between first and second exam — Complete Blood Count with 5-part Differential - Whole Blood, Second Exam (Laboratory) — Note: RDC Only
  • 1999-2000: VID_2_00 — Days between first and second exams — Vitamin D, Second Exam (Laboratory) — Note: RDC Only
  • 1999-2000: VIT_2_R — The number of days between the collection of the first and second exam — Vitamin A & Vitamin E, Second Exam (Laboratory) — Note: RDC Only
  • 2001-2002: HP2_01_R — Days between the 1st and 2nd exams — Helicobacter pylori (HP1), Second Exam (Laboratory) — Note: RDC Only
  • 2001-2002: L06_2_B — The number of days between the collections of first and second exams — Cadmium, Lead, Total Mercury, Ferritin, Serum Folate, RBC Folate, Vitamin B12, Homocysteine, Methylmalonic acid, Cotinine - Blood, Second Exam (Laboratory)
  • 2001-2002: L10_2_B — Days between the 1st and 2nd exams — Glycohemoglobin, Plasma Glucose, Serum C-peptide, & Insulin, Second Exam (Laboratory)
  • 2001-2002: L11_2_b — number of days between the collection of the first and second exam — C-Reactive Protein & Others, Second Exam (Laboratory)
  • 2001-2002: l11p_2_b — — Prostate-specific Antigen (PSA), Second Exam (Laboratory)
  • 2001-2002: l13_2_b — The number of days between the collection of the first and second exam — Cholesterol - Total, HDL, LDL & Triglycerides, Second Exam (Laboratory)
  • 2001-2002: L16_2_B — The number of days between the collection of the first and second exam — Creatinine & Albumin - Urine, Second Exam (Laboratory)
  • 2001-2002: L19_2_B — The number of days between the collection of the first and second exam — Measles, Rubella, & Varicella, Second Exam (Laboratory)
  • 2001-2002: l25_2_b — Days between first and second exam — Complete Blood Count with 5-part Differential - Whole Blood, Second Exam (Laboratory)
  • 2001-2002: l39_2_b — Days between 1st and 2nd exam — Erythrocyte Protoporphyrin (Laboratory)
  • 2001-2002: L40_2_B — The number of days between the collection of the first and second exam — Standard Biochemistry Profile, Follicle Stimulating Hormone & Luteinizing Hormone, Second Exam (Laboratory)
  • 2001-2002: VID_2_B — Days between first and second exams — Vitamin D, Second Exam (Laboratory)
  • 2001-2002: VIT_2_B — The number of days between the collection of the first and second exam — Vitamin A, Vitamin E, & Carotenoids, Second Exam (Laboratory)
LB2EONOCompatible with harmonization

Eosinophils number (1000 cells/uL)

Observed years
20002002
Release records
2
Datasets
2
Components
Laboratory
Qualified Praxis harmonization assessment

Compatible with harmonization · moderate confidence

No blocking method discontinuity is identified inside the selected cycle span, but one or more longitudinal changes require explicit harmonization conditions before pooling.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 1999-2000 → 2001-2002

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • Eosinophils number (1000 cells/uL)1999-2000 · 2001-2002
Cycle-by-cycle release history
  • 1999-2000: l25_2_r — Eosinophils number (1000 cells/uL) — Complete Blood Count with 5-part Differential - Whole Blood, Second Exam (Laboratory) — Note: RDC Only
  • 2001-2002: l25_2_b — Eosinophils number (1000 cells/uL) — Complete Blood Count with 5-part Differential - Whole Blood, Second Exam (Laboratory)
LB2EOPCTCompatible with harmonization

Eosinophils percent (%)

Observed years
20002002
Release records
2
Datasets
2
Components
Laboratory
Qualified Praxis harmonization assessment

Compatible with harmonization · moderate confidence

No blocking method discontinuity is identified inside the selected cycle span, but one or more longitudinal changes require explicit harmonization conditions before pooling.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 1999-2000 → 2001-2002

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • Eosinophils percent (%)1999-2000 · 2001-2002
Cycle-by-cycle release history
  • 1999-2000: l25_2_r — Eosinophils percent (%) — Complete Blood Count with 5-part Differential - Whole Blood, Second Exam (Laboratory) — Note: RDC Only
  • 2001-2002: l25_2_b — Eosinophils percent (%) — Complete Blood Count with 5-part Differential - Whole Blood, Second Exam (Laboratory)
LB2EPPCompatible with harmonization

Erythrocyte protoporphyrin (ug/dL RBC)

Observed years
20002002
Release records
2
Datasets
2
Components
Laboratory
Qualified Praxis harmonization assessment

Compatible with harmonization · moderate confidence

No blocking method discontinuity is identified inside the selected cycle span, but one or more longitudinal changes require explicit harmonization conditions before pooling.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 1999-2000 → 2001-2002

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Review the adjacent codebooks/methods. Keep this boundary as documentation variation unless source evidence confirms a substantive method or instrument change.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • Erythrocyte protoporphyrin (ug/dL RBC)1999-2000 · 2001-2002
Cycle-by-cycle release history
  • 1999-2000: L06_2_00 — Erythrocyte protoporphyrin (ug/dL RBC) — Cadmium, Lead, Ferritin, Serum Folate, RBC Folate, Vitamin B12, Homocysteine, Methylmalonic acid, Cotinine & Other Selected Nutritional Biochemistries - Blood, Second Exam (Laboratory) — Note: RDC Only
  • 2001-2002: l39_2_b — Erythrocyte protoporphyrin (ug/dL RBC) — Erythrocyte Protoporphyrin (Laboratory)
LB2EPPSICompatible with harmonization

Erythrocyte protoporphyrin (umol/L RBC)

Observed years
20002002
Release records
2
Datasets
2
Components
Laboratory
Qualified Praxis harmonization assessment

Compatible with harmonization · moderate confidence

No blocking method discontinuity is identified inside the selected cycle span, but one or more longitudinal changes require explicit harmonization conditions before pooling.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 1999-2000 → 2001-2002

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Review the adjacent codebooks/methods. Keep this boundary as documentation variation unless source evidence confirms a substantive method or instrument change.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • Erythrocyte protoporphyrin (umol/L RBC)1999-2000 · 2001-2002
Cycle-by-cycle release history
  • 1999-2000: L06_2_00 — Erythrocyte protoporphyrin (umol/L RBC) — Cadmium, Lead, Ferritin, Serum Folate, RBC Folate, Vitamin B12, Homocysteine, Methylmalonic acid, Cotinine & Other Selected Nutritional Biochemistries - Blood, Second Exam (Laboratory) — Note: RDC Only
  • 2001-2002: l39_2_b — Erythrocyte protoporphyrin (umol/L RBC) — Erythrocyte Protoporphyrin (Laboratory)
LB2FBCompatible with harmonization

Fibrinogen (mg/dL)

Observed years
20002002
Release records
2
Datasets
2
Components
Laboratory
Qualified Praxis harmonization assessment

Compatible with harmonization · moderate confidence

No blocking method discontinuity is identified inside the selected cycle span, but one or more longitudinal changes require explicit harmonization conditions before pooling.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 1999-2000 → 2001-2002

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Review the adjacent codebooks/methods. Keep this boundary as documentation variation unless source evidence confirms a substantive method or instrument change.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • Fibrinogen (mg/dL)1999-2000 · 2001-2002
Cycle-by-cycle release history
  • 1999-2000: L11_2_R — Fibrinogen (mg/dL) — C-Reactive Protein & Others, Second Exam (Laboratory) — Note: RDC Only
  • 2001-2002: L11_2_b — Fibrinogen (mg/dL) — C-Reactive Protein & Others, Second Exam (Laboratory)
LB2FBSICompatible with harmonization

Fibrinogen (g/L)

Observed years
20002002
Release records
2
Datasets
2
Components
Laboratory
Qualified Praxis harmonization assessment

Compatible with harmonization · moderate confidence

No blocking method discontinuity is identified inside the selected cycle span, but one or more longitudinal changes require explicit harmonization conditions before pooling.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 1999-2000 → 2001-2002

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Review the adjacent codebooks/methods. Keep this boundary as documentation variation unless source evidence confirms a substantive method or instrument change.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • Fibrinogen (g/L)1999-2000 · 2001-2002
Cycle-by-cycle release history
  • 1999-2000: L11_2_R — Fibrinogen (g/L) — C-Reactive Protein & Others, Second Exam (Laboratory) — Note: RDC Only
  • 2001-2002: L11_2_b — Fibrinogen (g/L) — C-Reactive Protein & Others, Second Exam (Laboratory)
LB2FERCompatible with harmonization

Ferritin (ng/mL)

Observed years
20002002
Release records
2
Datasets
2
Components
Laboratory
Qualified Praxis harmonization assessment

Compatible with harmonization · moderate confidence

No blocking method discontinuity is identified inside the selected cycle span, but one or more longitudinal changes require explicit harmonization conditions before pooling.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 1999-2000 → 2001-2002

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Review the adjacent codebooks/methods. Keep this boundary as documentation variation unless source evidence confirms a substantive method or instrument change.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • Ferritin (ng/mL)1999-2000 · 2001-2002
Cycle-by-cycle release history
  • 1999-2000: L06_2_00 — Ferritin (ng/mL) — Cadmium, Lead, Ferritin, Serum Folate, RBC Folate, Vitamin B12, Homocysteine, Methylmalonic acid, Cotinine & Other Selected Nutritional Biochemistries - Blood, Second Exam (Laboratory) — Note: RDC Only
  • 2001-2002: L06_2_B — Ferritin (ng/mL) — Cadmium, Lead, Total Mercury, Ferritin, Serum Folate, RBC Folate, Vitamin B12, Homocysteine, Methylmalonic acid, Cotinine - Blood, Second Exam (Laboratory)
LB2FERSICompatible with harmonization

Ferritin (ug/L)

Observed years
20002002
Release records
2
Datasets
2
Components
Laboratory
Qualified Praxis harmonization assessment

Compatible with harmonization · moderate confidence

No blocking method discontinuity is identified inside the selected cycle span, but one or more longitudinal changes require explicit harmonization conditions before pooling.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 1999-2000 → 2001-2002

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Review the adjacent codebooks/methods. Keep this boundary as documentation variation unless source evidence confirms a substantive method or instrument change.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • Ferritin (ug/L)1999-2000 · 2001-2002
Cycle-by-cycle release history
  • 1999-2000: L06_2_00 — Ferritin (ug/L) — Cadmium, Lead, Ferritin, Serum Folate, RBC Folate, Vitamin B12, Homocysteine, Methylmalonic acid, Cotinine & Other Selected Nutritional Biochemistries - Blood, Second Exam (Laboratory) — Note: RDC Only
  • 2001-2002: L06_2_B — Ferritin (ug/L) — Cadmium, Lead, Total Mercury, Ferritin, Serum Folate, RBC Folate, Vitamin B12, Homocysteine, Methylmalonic acid, Cotinine - Blood, Second Exam (Laboratory)
LB2FOLCompatible with harmonization

Folate, serum (ng/mL)

Observed years
20002002
Release records
2
Datasets
2
Components
Laboratory
Qualified Praxis harmonization assessment

Compatible with harmonization · moderate confidence

No blocking method discontinuity is identified inside the selected cycle span, but one or more longitudinal changes require explicit harmonization conditions before pooling.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 1999-2000 → 2001-2002

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Review the adjacent codebooks/methods. Keep this boundary as documentation variation unless source evidence confirms a substantive method or instrument change.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • Folate, serum (ng/mL)1999-2000 · 2001-2002
Cycle-by-cycle release history
  • 1999-2000: L06_2_00 — Folate, serum (ng/mL) — Cadmium, Lead, Ferritin, Serum Folate, RBC Folate, Vitamin B12, Homocysteine, Methylmalonic acid, Cotinine & Other Selected Nutritional Biochemistries - Blood, Second Exam (Laboratory) — Note: RDC Only
  • 2001-2002: L06_2_B — Folate, serum (ng/mL) — Cadmium, Lead, Total Mercury, Ferritin, Serum Folate, RBC Folate, Vitamin B12, Homocysteine, Methylmalonic acid, Cotinine - Blood, Second Exam (Laboratory)
LB2FOLSICompatible with harmonization

Folate, serum (nmol/L)

Observed years
20002002
Release records
2
Datasets
2
Components
Laboratory
Qualified Praxis harmonization assessment

Compatible with harmonization · moderate confidence

No blocking method discontinuity is identified inside the selected cycle span, but one or more longitudinal changes require explicit harmonization conditions before pooling.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 1999-2000 → 2001-2002

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Review the adjacent codebooks/methods. Keep this boundary as documentation variation unless source evidence confirms a substantive method or instrument change.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • Folate, serum (nmol/L)1999-2000 · 2001-2002
Cycle-by-cycle release history
  • 1999-2000: L06_2_00 — Folate, serum (nmol/L) — Cadmium, Lead, Ferritin, Serum Folate, RBC Folate, Vitamin B12, Homocysteine, Methylmalonic acid, Cotinine & Other Selected Nutritional Biochemistries - Blood, Second Exam (Laboratory) — Note: RDC Only
  • 2001-2002: L06_2_B — Folate, serum (nmol/L) — Cadmium, Lead, Total Mercury, Ferritin, Serum Folate, RBC Folate, Vitamin B12, Homocysteine, Methylmalonic acid, Cotinine - Blood, Second Exam (Laboratory)
LB2FSHAdjustment required

Follicle stimulating hormone (mIU/mL)

Observed years
20002002
Release records
2
Datasets
2
Components
Laboratory
Qualified Praxis harmonization assessment

Adjustment required · high confidence

A methodological discontinuity falls inside the selected cycle span. Naive pooling of raw values across the flagged boundary is not recommended unless CDC/NCHS provides a defensible calibration or comparability procedure.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 1999-2000 → 2001-2002

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Apply CDC/NCHS comparability or calibration guidance where available. If equivalence is not established, preserve separate method periods or perform sensitivity analyses rather than naively pooling raw values.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • Follicle stimulating hormone (mIU/mL)1999-2000 · 2001-2002
Cycle-by-cycle release history
  • 1999-2000: l18_2_00 — Follicle stimulating hormone (mIU/mL) — Standard Biochemistry Profile & Hormones, Second Exam (Laboratory) — Note: RDC Only
  • 2001-2002: L40_2_B — Follicle stimulating hormone (mIU/mL) — Standard Biochemistry Profile, Follicle Stimulating Hormone & Luteinizing Hormone, Second Exam (Laboratory)
LB2FSHSIAdjustment required

Follicle stimulating hormone (IU/L)

Observed years
20002002
Release records
2
Datasets
2
Components
Laboratory
Qualified Praxis harmonization assessment

Adjustment required · high confidence

A methodological discontinuity falls inside the selected cycle span. Naive pooling of raw values across the flagged boundary is not recommended unless CDC/NCHS provides a defensible calibration or comparability procedure.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 1999-2000 → 2001-2002

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Apply CDC/NCHS comparability or calibration guidance where available. If equivalence is not established, preserve separate method periods or perform sensitivity analyses rather than naively pooling raw values.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • Follicle stimulating hormone (IU/L)1999-2000 · 2001-2002
Cycle-by-cycle release history
  • 1999-2000: l18_2_00 — Follicle stimulating hormone (IU/L) — Standard Biochemistry Profile & Hormones, Second Exam (Laboratory) — Note: RDC Only
  • 2001-2002: L40_2_B — Follicle stimulating hormone (IU/L) — Standard Biochemistry Profile, Follicle Stimulating Hormone & Luteinizing Hormone, Second Exam (Laboratory)
LB2GHCompatible with harmonization

Glycohemoglobin (%)

Observed years
20002002
Release records
2
Datasets
2
Components
Laboratory
Qualified Praxis harmonization assessment

Compatible with harmonization · moderate confidence

No blocking method discontinuity is identified inside the selected cycle span, but one or more longitudinal changes require explicit harmonization conditions before pooling.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 1999-2000 → 2001-2002

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Review the adjacent codebooks/methods. Keep this boundary as documentation variation unless source evidence confirms a substantive method or instrument change.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • Glycohemoglobin (%)1999-2000 · 2001-2002
Cycle-by-cycle release history
  • 1999-2000: l10_2_00 — Glycohemoglobin (%) — Glycohemoglobin, Plasma Glucose, Serum C-peptide, & Insulin, Second Exam (Laboratory) — Note: RDC Only
  • 2001-2002: L10_2_B — Glycohemoglobin (%) — Glycohemoglobin, Plasma Glucose, Serum C-peptide, & Insulin, Second Exam (Laboratory)
LB2GLUCompatible with harmonization

Plasma glucose (mg/dL)

Observed years
20002002
Release records
2
Datasets
2
Components
Laboratory
Qualified Praxis harmonization assessment

Compatible with harmonization · moderate confidence

No blocking method discontinuity is identified inside the selected cycle span, but one or more longitudinal changes require explicit harmonization conditions before pooling.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 1999-2000 → 2001-2002

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Review the adjacent codebooks/methods. Keep this boundary as documentation variation unless source evidence confirms a substantive method or instrument change.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • Plasma glucose (mg/dL)1999-2000 · 2001-2002
Cycle-by-cycle release history
  • 1999-2000: l10_2_00 — Plasma glucose (mg/dL) — Glycohemoglobin, Plasma Glucose, Serum C-peptide, & Insulin, Second Exam (Laboratory) — Note: RDC Only
  • 2001-2002: L10_2_B — Plasma glucose (mg/dL) — Glycohemoglobin, Plasma Glucose, Serum C-peptide, & Insulin, Second Exam (Laboratory)
LB2GLUSICompatible with harmonization

Plasma glucose: SI(mmol/L)

Observed years
20002002
Release records
2
Datasets
2
Components
Laboratory
Qualified Praxis harmonization assessment

Compatible with harmonization · moderate confidence

No blocking method discontinuity is identified inside the selected cycle span, but one or more longitudinal changes require explicit harmonization conditions before pooling.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 1999-2000 → 2001-2002

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Review the adjacent codebooks/methods. Keep this boundary as documentation variation unless source evidence confirms a substantive method or instrument change.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • Plasma glucose: SI(mmol/L)1999-2000 · 2001-2002
Cycle-by-cycle release history
  • 1999-2000: l10_2_00 — Plasma glucose: SI(mmol/L) — Glycohemoglobin, Plasma Glucose, Serum C-peptide, & Insulin, Second Exam (Laboratory) — Note: RDC Only
  • 2001-2002: L10_2_B — Plasma glucose: SI(mmol/L) — Glycohemoglobin, Plasma Glucose, Serum C-peptide, & Insulin, Second Exam (Laboratory)
LB2GTCCompatible with harmonization

Gamma tocopherol (ug/dL)

Observed years
20002002
Release records
3
Datasets
3
Components
Laboratory
Qualified Praxis harmonization assessment

Compatible with harmonization · moderate confidence

No blocking method discontinuity is identified inside the selected cycle span, but one or more longitudinal changes require explicit harmonization conditions before pooling.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 1999-2000 → 2001-2002

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • Gamma tocopherol (ug/dL)1999-2000
  • gamma-tocopherol(ug/dL)1999-2000 · 2001-2002
Cycle-by-cycle release history
  • 1999-2000: L06_2_00 — Gamma tocopherol (ug/dL) — Cadmium, Lead, Ferritin, Serum Folate, RBC Folate, Vitamin B12, Homocysteine, Methylmalonic acid, Cotinine & Other Selected Nutritional Biochemistries - Blood, Second Exam (Laboratory) — Note: RDC Only
  • 1999-2000: VIT_2_R — gamma-tocopherol(ug/dL) — Vitamin A & Vitamin E, Second Exam (Laboratory) — Note: RDC Only
  • 2001-2002: VIT_2_B — gamma-tocopherol(ug/dL) — Vitamin A, Vitamin E, & Carotenoids, Second Exam (Laboratory)
LB2GTCSICompatible with harmonization

Gamma tocopherol (umol/L)

Observed years
20002002
Release records
3
Datasets
3
Components
Laboratory
Qualified Praxis harmonization assessment

Compatible with harmonization · moderate confidence

No blocking method discontinuity is identified inside the selected cycle span, but one or more longitudinal changes require explicit harmonization conditions before pooling.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 1999-2000 → 2001-2002

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • Gamma tocopherol (umol/L)1999-2000
  • gamma-tocopherol(umol/L)1999-2000 · 2001-2002
Cycle-by-cycle release history
  • 1999-2000: L06_2_00 — Gamma tocopherol (umol/L) — Cadmium, Lead, Ferritin, Serum Folate, RBC Folate, Vitamin B12, Homocysteine, Methylmalonic acid, Cotinine & Other Selected Nutritional Biochemistries - Blood, Second Exam (Laboratory) — Note: RDC Only
  • 1999-2000: VIT_2_R — gamma-tocopherol(umol/L) — Vitamin A & Vitamin E, Second Exam (Laboratory) — Note: RDC Only
  • 2001-2002: VIT_2_B — gamma-tocopherol(umol/L) — Vitamin A, Vitamin E, & Carotenoids, Second Exam (Laboratory)
LB2HCTCompatible with harmonization

Hematocrit (%)

Observed years
20002002
Release records
2
Datasets
2
Components
Laboratory
Qualified Praxis harmonization assessment

Compatible with harmonization · moderate confidence

No blocking method discontinuity is identified inside the selected cycle span, but one or more longitudinal changes require explicit harmonization conditions before pooling.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 1999-2000 → 2001-2002

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • Hematocrit (%)1999-2000 · 2001-2002
Cycle-by-cycle release history
  • 1999-2000: l25_2_r — Hematocrit (%) — Complete Blood Count with 5-part Differential - Whole Blood, Second Exam (Laboratory) — Note: RDC Only
  • 2001-2002: l25_2_b — Hematocrit (%) — Complete Blood Count with 5-part Differential - Whole Blood, Second Exam (Laboratory)
LB2HCYCompatible with harmonization

Homocysteine (umol/L)

Observed years
20002002
Release records
2
Datasets
2
Components
Laboratory
Qualified Praxis harmonization assessment

Compatible with harmonization · moderate confidence

No blocking method discontinuity is identified inside the selected cycle span, but one or more longitudinal changes require explicit harmonization conditions before pooling.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 1999-2000 → 2001-2002

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Review the adjacent codebooks/methods. Keep this boundary as documentation variation unless source evidence confirms a substantive method or instrument change.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • Homocysteine (umol/L)1999-2000
  • Homocysteine(umol/L)2001-2002
Cycle-by-cycle release history
  • 1999-2000: L06_2_00 — Homocysteine (umol/L) — Cadmium, Lead, Ferritin, Serum Folate, RBC Folate, Vitamin B12, Homocysteine, Methylmalonic acid, Cotinine & Other Selected Nutritional Biochemistries - Blood, Second Exam (Laboratory) — Note: RDC Only
  • 2001-2002: L06_2_B — Homocysteine(umol/L) — Cadmium, Lead, Total Mercury, Ferritin, Serum Folate, RBC Folate, Vitamin B12, Homocysteine, Methylmalonic acid, Cotinine - Blood, Second Exam (Laboratory)
LB2HDLAdjustment required

HDL-cholesterol (mg/dL)

Observed years
20002002
Release records
2
Datasets
2
Components
Laboratory
Qualified Praxis harmonization assessment

Adjustment required · high confidence

A methodological discontinuity falls inside the selected cycle span. Naive pooling of raw values across the flagged boundary is not recommended unless CDC/NCHS provides a defensible calibration or comparability procedure.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 1999-2000 → 2001-2002

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Apply CDC/NCHS comparability or calibration guidance where available. If equivalence is not established, preserve separate method periods or perform sensitivity analyses rather than naively pooling raw values.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • HDL-cholesterol (mg/dL)1999-2000 · 2001-2002
Cycle-by-cycle release history
  • 1999-2000: l13_2_r — HDL-cholesterol (mg/dL) — Cholesterol - Total, HDL, LDL & Triglycerides, Second Exam (Laboratory) — Note: RDC Only
  • 2001-2002: l13_2_b — HDL-cholesterol (mg/dL) — Cholesterol - Total, HDL, LDL & Triglycerides, Second Exam (Laboratory)
LB2HDLSIAdjustment required

HDL-cholesterol (mmol/L)

Observed years
20002002
Release records
2
Datasets
2
Components
Laboratory
Qualified Praxis harmonization assessment

Adjustment required · high confidence

A methodological discontinuity falls inside the selected cycle span. Naive pooling of raw values across the flagged boundary is not recommended unless CDC/NCHS provides a defensible calibration or comparability procedure.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 1999-2000 → 2001-2002

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Apply CDC/NCHS comparability or calibration guidance where available. If equivalence is not established, preserve separate method periods or perform sensitivity analyses rather than naively pooling raw values.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • HDL-cholesterol (mmol/L)1999-2000 · 2001-2002
Cycle-by-cycle release history
  • 1999-2000: l13_2_r — HDL-cholesterol (mmol/L) — Cholesterol - Total, HDL, LDL & Triglycerides, Second Exam (Laboratory) — Note: RDC Only
  • 2001-2002: l13_2_b — HDL-cholesterol (mmol/L) — Cholesterol - Total, HDL, LDL & Triglycerides, Second Exam (Laboratory)
LB2HGBCompatible with harmonization

Hemoglobin (g/dL)

Observed years
20002002
Release records
2
Datasets
2
Components
Laboratory
Qualified Praxis harmonization assessment

Compatible with harmonization · moderate confidence

No blocking method discontinuity is identified inside the selected cycle span, but one or more longitudinal changes require explicit harmonization conditions before pooling.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 1999-2000 → 2001-2002

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • Hemoglobin (g/dL)1999-2000 · 2001-2002
Cycle-by-cycle release history
  • 1999-2000: l25_2_r — Hemoglobin (g/dL) — Complete Blood Count with 5-part Differential - Whole Blood, Second Exam (Laboratory) — Note: RDC Only
  • 2001-2002: l25_2_b — Hemoglobin (g/dL) — Complete Blood Count with 5-part Differential - Whole Blood, Second Exam (Laboratory)
LB2HP1Evidence developing

Helicobacter pylori (HP1)

Observed years
20012001
Release records
1
Datasets
1
Components
Laboratory
Qualified Praxis harmonization assessment

Evidence developing · low confidence

No normalized longitudinal change evidence is available for this variable. Absence of events must not be interpreted as proof of cross-cycle equivalence.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Variable names / labels over time
  • Helicobacter pylori (HP1)2001-2002
Cycle-by-cycle release history
  • 2001-2002: HP2_01_R — Helicobacter pylori (HP1) — Helicobacter pylori (HP1), Second Exam (Laboratory) — Note: RDC Only
LB2INCompatible with harmonization

Insulin (uU/mL)

Observed years
20002002
Release records
2
Datasets
2
Components
Laboratory
Qualified Praxis harmonization assessment

Compatible with harmonization · moderate confidence

No blocking method discontinuity is identified inside the selected cycle span, but one or more longitudinal changes require explicit harmonization conditions before pooling.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 1999-2000 → 2001-2002

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Review the adjacent codebooks/methods. Keep this boundary as documentation variation unless source evidence confirms a substantive method or instrument change.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • Insulin (uU/mL)1999-2000 · 2001-2002
Cycle-by-cycle release history
  • 1999-2000: l10_2_00 — Insulin (uU/mL) — Glycohemoglobin, Plasma Glucose, Serum C-peptide, & Insulin, Second Exam (Laboratory) — Note: RDC Only
  • 2001-2002: L10_2_B — Insulin (uU/mL) — Glycohemoglobin, Plasma Glucose, Serum C-peptide, & Insulin, Second Exam (Laboratory)
LB2INSICompatible with harmonization

Insulin: SI(pmol/L)

Observed years
20002002
Release records
2
Datasets
2
Components
Laboratory
Qualified Praxis harmonization assessment

Compatible with harmonization · moderate confidence

No blocking method discontinuity is identified inside the selected cycle span, but one or more longitudinal changes require explicit harmonization conditions before pooling.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 1999-2000 → 2001-2002

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Review the adjacent codebooks/methods. Keep this boundary as documentation variation unless source evidence confirms a substantive method or instrument change.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • Insulin: SI(pmol/L)1999-2000 · 2001-2002
Cycle-by-cycle release history
  • 1999-2000: l10_2_00 — Insulin: SI(pmol/L) — Glycohemoglobin, Plasma Glucose, Serum C-peptide, & Insulin, Second Exam (Laboratory) — Note: RDC Only
  • 2001-2002: L10_2_B — Insulin: SI(pmol/L) — Glycohemoglobin, Plasma Glucose, Serum C-peptide, & Insulin, Second Exam (Laboratory)
LB2IRNEvidence developing

Iron (ug/dL)

Observed years
20002000
Release records
1
Datasets
1
Components
Laboratory
Qualified Praxis harmonization assessment

Evidence developing · low confidence

No normalized longitudinal change evidence is available for this variable. Absence of events must not be interpreted as proof of cross-cycle equivalence.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Variable names / labels over time
  • Iron (ug/dL)1999-2000
Cycle-by-cycle release history
  • 1999-2000: L06_2_00 — Iron (ug/dL) — Cadmium, Lead, Ferritin, Serum Folate, RBC Folate, Vitamin B12, Homocysteine, Methylmalonic acid, Cotinine & Other Selected Nutritional Biochemistries - Blood, Second Exam (Laboratory) — Note: RDC Only
LB2IRNSIEvidence developing

Iron (umol/L)

Observed years
20002000
Release records
1
Datasets
1
Components
Laboratory
Qualified Praxis harmonization assessment

Evidence developing · low confidence

No normalized longitudinal change evidence is available for this variable. Absence of events must not be interpreted as proof of cross-cycle equivalence.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Variable names / labels over time
  • Iron (umol/L)1999-2000
Cycle-by-cycle release history
  • 1999-2000: L06_2_00 — Iron (umol/L) — Cadmium, Lead, Ferritin, Serum Folate, RBC Folate, Vitamin B12, Homocysteine, Methylmalonic acid, Cotinine & Other Selected Nutritional Biochemistries - Blood, Second Exam (Laboratory) — Note: RDC Only
LB2LDLAdjustment required

LDL-cholesterol (mg/dL)

Observed years
20002002
Release records
2
Datasets
2
Components
Laboratory
Qualified Praxis harmonization assessment

Adjustment required · high confidence

A methodological discontinuity falls inside the selected cycle span. Naive pooling of raw values across the flagged boundary is not recommended unless CDC/NCHS provides a defensible calibration or comparability procedure.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 1999-2000 → 2001-2002

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Apply CDC/NCHS comparability or calibration guidance where available. If equivalence is not established, preserve separate method periods or perform sensitivity analyses rather than naively pooling raw values.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • LDL-cholesterol (mg/dL)1999-2000 · 2001-2002
Cycle-by-cycle release history
  • 1999-2000: l13_2_r — LDL-cholesterol (mg/dL) — Cholesterol - Total, HDL, LDL & Triglycerides, Second Exam (Laboratory) — Note: RDC Only
  • 2001-2002: l13_2_b — LDL-cholesterol (mg/dL) — Cholesterol - Total, HDL, LDL & Triglycerides, Second Exam (Laboratory)
LB2LDLSIAdjustment required

LDL-cholesterol (mmol/L)

Observed years
20002002
Release records
2
Datasets
2
Components
Laboratory
Qualified Praxis harmonization assessment

Adjustment required · high confidence

A methodological discontinuity falls inside the selected cycle span. Naive pooling of raw values across the flagged boundary is not recommended unless CDC/NCHS provides a defensible calibration or comparability procedure.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 1999-2000 → 2001-2002

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Apply CDC/NCHS comparability or calibration guidance where available. If equivalence is not established, preserve separate method periods or perform sensitivity analyses rather than naively pooling raw values.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • LDL-cholesterol (mmol/L)1999-2000 · 2001-2002
Cycle-by-cycle release history
  • 1999-2000: l13_2_r — LDL-cholesterol (mmol/L) — Cholesterol - Total, HDL, LDL & Triglycerides, Second Exam (Laboratory) — Note: RDC Only
  • 2001-2002: l13_2_b — LDL-cholesterol (mmol/L) — Cholesterol - Total, HDL, LDL & Triglycerides, Second Exam (Laboratory)
LB2LHAdjustment required

Luteinizing hormone (mIU/mL)

Observed years
20002002
Release records
2
Datasets
2
Components
Laboratory
Qualified Praxis harmonization assessment

Adjustment required · high confidence

A methodological discontinuity falls inside the selected cycle span. Naive pooling of raw values across the flagged boundary is not recommended unless CDC/NCHS provides a defensible calibration or comparability procedure.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 1999-2000 → 2001-2002

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Apply CDC/NCHS comparability or calibration guidance where available. If equivalence is not established, preserve separate method periods or perform sensitivity analyses rather than naively pooling raw values.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • Luteinizing hormone (mIU/mL)1999-2000 · 2001-2002
Cycle-by-cycle release history
  • 1999-2000: l18_2_00 — Luteinizing hormone (mIU/mL) — Standard Biochemistry Profile & Hormones, Second Exam (Laboratory) — Note: RDC Only
  • 2001-2002: L40_2_B — Luteinizing hormone (mIU/mL) — Standard Biochemistry Profile, Follicle Stimulating Hormone & Luteinizing Hormone, Second Exam (Laboratory)
LB2LHSIAdjustment required

Luteinizing hormone (IU/L)

Observed years
20002002
Release records
2
Datasets
2
Components
Laboratory
Qualified Praxis harmonization assessment

Adjustment required · high confidence

A methodological discontinuity falls inside the selected cycle span. Naive pooling of raw values across the flagged boundary is not recommended unless CDC/NCHS provides a defensible calibration or comparability procedure.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 1999-2000 → 2001-2002

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Apply CDC/NCHS comparability or calibration guidance where available. If equivalence is not established, preserve separate method periods or perform sensitivity analyses rather than naively pooling raw values.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • Luteinizing hormone (IU/L)1999-2000 · 2001-2002
Cycle-by-cycle release history
  • 1999-2000: l18_2_00 — Luteinizing hormone (IU/L) — Standard Biochemistry Profile & Hormones, Second Exam (Laboratory) — Note: RDC Only
  • 2001-2002: L40_2_B — Luteinizing hormone (IU/L) — Standard Biochemistry Profile, Follicle Stimulating Hormone & Luteinizing Hormone, Second Exam (Laboratory)
LB2LUZEvidence developing

Combined Lutein/zeaxanthin(ug/dL)

Observed years
20012002
Release records
1
Datasets
1
Components
Laboratory
Qualified Praxis harmonization assessment

Evidence developing · low confidence

No normalized longitudinal change evidence is available for this variable. Absence of events must not be interpreted as proof of cross-cycle equivalence.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Variable names / labels over time
  • Combined Lutein/zeaxanthin(ug/dL)2001-2002
Cycle-by-cycle release history
  • 2001-2002: VIT_2_B — Combined Lutein/zeaxanthin(ug/dL) — Vitamin A, Vitamin E, & Carotenoids, Second Exam (Laboratory)
LB2LUZSIEvidence developing

Combined Lutein/zeaxanthin(umol/L)

Observed years
20012002
Release records
1
Datasets
1
Components
Laboratory
Qualified Praxis harmonization assessment

Evidence developing · low confidence

No normalized longitudinal change evidence is available for this variable. Absence of events must not be interpreted as proof of cross-cycle equivalence.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Variable names / labels over time
  • Combined Lutein/zeaxanthin(umol/L)2001-2002
Cycle-by-cycle release history
  • 2001-2002: VIT_2_B — Combined Lutein/zeaxanthin(umol/L) — Vitamin A, Vitamin E, & Carotenoids, Second Exam (Laboratory)
LB2LYCEvidence developing

trans-lycopene(ug/dL)

Observed years
20012002
Release records
1
Datasets
1
Components
Laboratory
Qualified Praxis harmonization assessment

Evidence developing · low confidence

No normalized longitudinal change evidence is available for this variable. Absence of events must not be interpreted as proof of cross-cycle equivalence.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Variable names / labels over time
  • trans-lycopene(ug/dL)2001-2002
Cycle-by-cycle release history
  • 2001-2002: VIT_2_B — trans-lycopene(ug/dL) — Vitamin A, Vitamin E, & Carotenoids, Second Exam (Laboratory)
LB2LYCSIEvidence developing

trans-lycopene(umol/L)

Observed years
20012002
Release records
1
Datasets
1
Components
Laboratory
Qualified Praxis harmonization assessment

Evidence developing · low confidence

No normalized longitudinal change evidence is available for this variable. Absence of events must not be interpreted as proof of cross-cycle equivalence.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Variable names / labels over time
  • trans-lycopene(umol/L)2001-2002
Cycle-by-cycle release history
  • 2001-2002: VIT_2_B — trans-lycopene(umol/L) — Vitamin A, Vitamin E, & Carotenoids, Second Exam (Laboratory)
LB2LYMNOCompatible with harmonization

Lymphocyte number (1000 cells/uL)

Observed years
20002002
Release records
2
Datasets
2
Components
Laboratory
Qualified Praxis harmonization assessment

Compatible with harmonization · moderate confidence

No blocking method discontinuity is identified inside the selected cycle span, but one or more longitudinal changes require explicit harmonization conditions before pooling.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 1999-2000 → 2001-2002

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • Lymphocyte number (1000 cells/uL)1999-2000 · 2001-2002
Cycle-by-cycle release history
  • 1999-2000: l25_2_r — Lymphocyte number (1000 cells/uL) — Complete Blood Count with 5-part Differential - Whole Blood, Second Exam (Laboratory) — Note: RDC Only
  • 2001-2002: l25_2_b — Lymphocyte number (1000 cells/uL) — Complete Blood Count with 5-part Differential - Whole Blood, Second Exam (Laboratory)
LB2LYPCTCompatible with harmonization

Lymphocyte percent (%)

Observed years
20002002
Release records
2
Datasets
2
Components
Laboratory
Qualified Praxis harmonization assessment

Compatible with harmonization · moderate confidence

No blocking method discontinuity is identified inside the selected cycle span, but one or more longitudinal changes require explicit harmonization conditions before pooling.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 1999-2000 → 2001-2002

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • Lymphocyte percent (%)1999-2000 · 2001-2002
Cycle-by-cycle release history
  • 1999-2000: l25_2_r — Lymphocyte percent (%) — Complete Blood Count with 5-part Differential - Whole Blood, Second Exam (Laboratory) — Note: RDC Only
  • 2001-2002: l25_2_b — Lymphocyte percent (%) — Complete Blood Count with 5-part Differential - Whole Blood, Second Exam (Laboratory)
LB2MCCompatible with harmonization

MCHC (g/dL)

Observed years
20002002
Release records
2
Datasets
2
Components
Laboratory
Qualified Praxis harmonization assessment

Compatible with harmonization · moderate confidence

No blocking method discontinuity is identified inside the selected cycle span, but one or more longitudinal changes require explicit harmonization conditions before pooling.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 1999-2000 → 2001-2002

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • MCHC (g/dL)1999-2000 · 2001-2002
Cycle-by-cycle release history
  • 1999-2000: l25_2_r — MCHC (g/dL) — Complete Blood Count with 5-part Differential - Whole Blood, Second Exam (Laboratory) — Note: RDC Only
  • 2001-2002: l25_2_b — MCHC (g/dL) — Complete Blood Count with 5-part Differential - Whole Blood, Second Exam (Laboratory)
LB2MCHSICompatible with harmonization

Mean cell hemoglobin (pg)

Observed years
20002002
Release records
2
Datasets
2
Components
Laboratory
Qualified Praxis harmonization assessment

Compatible with harmonization · moderate confidence

No blocking method discontinuity is identified inside the selected cycle span, but one or more longitudinal changes require explicit harmonization conditions before pooling.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 1999-2000 → 2001-2002

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • Mean cell hemoglobin (pg)1999-2000 · 2001-2002
Cycle-by-cycle release history
  • 1999-2000: l25_2_r — Mean cell hemoglobin (pg) — Complete Blood Count with 5-part Differential - Whole Blood, Second Exam (Laboratory) — Note: RDC Only
  • 2001-2002: l25_2_b — Mean cell hemoglobin (pg) — Complete Blood Count with 5-part Differential - Whole Blood, Second Exam (Laboratory)
LB2MCVSICompatible with harmonization

Mean cell volume (fL)

Observed years
20002002
Release records
2
Datasets
2
Components
Laboratory
Qualified Praxis harmonization assessment

Compatible with harmonization · moderate confidence

No blocking method discontinuity is identified inside the selected cycle span, but one or more longitudinal changes require explicit harmonization conditions before pooling.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 1999-2000 → 2001-2002

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • Mean cell volume (fL)1999-2000 · 2001-2002
Cycle-by-cycle release history
  • 1999-2000: l25_2_r — Mean cell volume (fL) — Complete Blood Count with 5-part Differential - Whole Blood, Second Exam (Laboratory) — Note: RDC Only
  • 2001-2002: l25_2_b — Mean cell volume (fL) — Complete Blood Count with 5-part Differential - Whole Blood, Second Exam (Laboratory)
LB2MECompatible with harmonization

Measles

Observed years
20002002
Release records
2
Datasets
2
Components
Laboratory
Qualified Praxis harmonization assessment

Compatible with harmonization · moderate confidence

No blocking method discontinuity is identified inside the selected cycle span, but one or more longitudinal changes require explicit harmonization conditions before pooling.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 1999-2000 → 2001-2002

Praxis harmonization actions
  • Apply cycle-specific eligibility rules and restrict the pooled analytic population to a defensible common target population.
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • Measles1999-2000 · 2001-2002
Cycle-by-cycle release history
  • 1999-2000: L19_2_R — Measles — Measles, Rubella, & Varicella, Second Exam (Laboratory) — Note: RDC Only
  • 2001-2002: L19_2_B — Measles — Measles, Rubella, & Varicella, Second Exam (Laboratory)
LB2MMACompatible with harmonization

Methylmalonic acid (umol/L)

Observed years
20002002
Release records
2
Datasets
2
Components
Laboratory
Qualified Praxis harmonization assessment

Compatible with harmonization · moderate confidence

No blocking method discontinuity is identified inside the selected cycle span, but one or more longitudinal changes require explicit harmonization conditions before pooling.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 1999-2000 → 2001-2002

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Review the adjacent codebooks/methods. Keep this boundary as documentation variation unless source evidence confirms a substantive method or instrument change.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • Methylmalonic acid (umol/L)1999-2000 · 2001-2002
Cycle-by-cycle release history
  • 1999-2000: L06_2_00 — Methylmalonic acid (umol/L) — Cadmium, Lead, Ferritin, Serum Folate, RBC Folate, Vitamin B12, Homocysteine, Methylmalonic acid, Cotinine & Other Selected Nutritional Biochemistries - Blood, Second Exam (Laboratory) — Note: RDC Only
  • 2001-2002: L06_2_B — Methylmalonic acid (umol/L) — Cadmium, Lead, Total Mercury, Ferritin, Serum Folate, RBC Folate, Vitamin B12, Homocysteine, Methylmalonic acid, Cotinine - Blood, Second Exam (Laboratory)
LB2MONOCompatible with harmonization

Monocyte number (1000 cells/uL)

Observed years
20002002
Release records
2
Datasets
2
Components
Laboratory
Qualified Praxis harmonization assessment

Compatible with harmonization · moderate confidence

No blocking method discontinuity is identified inside the selected cycle span, but one or more longitudinal changes require explicit harmonization conditions before pooling.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 1999-2000 → 2001-2002

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • Monocyte number (1000 cells/uL)1999-2000 · 2001-2002
Cycle-by-cycle release history
  • 1999-2000: l25_2_r — Monocyte number (1000 cells/uL) — Complete Blood Count with 5-part Differential - Whole Blood, Second Exam (Laboratory) — Note: RDC Only
  • 2001-2002: l25_2_b — Monocyte number (1000 cells/uL) — Complete Blood Count with 5-part Differential - Whole Blood, Second Exam (Laboratory)
LB2MOPCTCompatible with harmonization

Monocyte percent (%)

Observed years
20002002
Release records
2
Datasets
2
Components
Laboratory
Qualified Praxis harmonization assessment

Compatible with harmonization · moderate confidence

No blocking method discontinuity is identified inside the selected cycle span, but one or more longitudinal changes require explicit harmonization conditions before pooling.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 1999-2000 → 2001-2002

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • Monocyte percent (%)1999-2000 · 2001-2002
Cycle-by-cycle release history
  • 1999-2000: l25_2_r — Monocyte percent (%) — Complete Blood Count with 5-part Differential - Whole Blood, Second Exam (Laboratory) — Note: RDC Only
  • 2001-2002: l25_2_b — Monocyte percent (%) — Complete Blood Count with 5-part Differential - Whole Blood, Second Exam (Laboratory)
LB2MPSICompatible with harmonization

Mean platelet volume (fL)

Observed years
20002002
Release records
2
Datasets
2
Components
Laboratory
Qualified Praxis harmonization assessment

Compatible with harmonization · moderate confidence

No blocking method discontinuity is identified inside the selected cycle span, but one or more longitudinal changes require explicit harmonization conditions before pooling.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 1999-2000 → 2001-2002

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • Mean platelet volume (fL)1999-2000 · 2001-2002
Cycle-by-cycle release history
  • 1999-2000: l25_2_r — Mean platelet volume (fL) — Complete Blood Count with 5-part Differential - Whole Blood, Second Exam (Laboratory) — Note: RDC Only
  • 2001-2002: l25_2_b — Mean platelet volume (fL) — Complete Blood Count with 5-part Differential - Whole Blood, Second Exam (Laboratory)
LB2NENOCompatible with harmonization

Segmented neutrophils num (1000 cell/uL)

Observed years
20002002
Release records
2
Datasets
2
Components
Laboratory
Qualified Praxis harmonization assessment

Compatible with harmonization · moderate confidence

No blocking method discontinuity is identified inside the selected cycle span, but one or more longitudinal changes require explicit harmonization conditions before pooling.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 1999-2000 → 2001-2002

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • Segmented neutrophils num (1000 cell/uL)1999-2000 · 2001-2002
Cycle-by-cycle release history
  • 1999-2000: l25_2_r — Segmented neutrophils num (1000 cell/uL) — Complete Blood Count with 5-part Differential - Whole Blood, Second Exam (Laboratory) — Note: RDC Only
  • 2001-2002: l25_2_b — Segmented neutrophils num (1000 cell/uL) — Complete Blood Count with 5-part Differential - Whole Blood, Second Exam (Laboratory)
LB2NEPCTCompatible with harmonization

Segmented neutrophils percent (%)

Observed years
20002002
Release records
2
Datasets
2
Components
Laboratory
Qualified Praxis harmonization assessment

Compatible with harmonization · moderate confidence

No blocking method discontinuity is identified inside the selected cycle span, but one or more longitudinal changes require explicit harmonization conditions before pooling.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 1999-2000 → 2001-2002

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • Segmented neutrophils percent (%)1999-2000 · 2001-2002
Cycle-by-cycle release history
  • 1999-2000: l25_2_r — Segmented neutrophils percent (%) — Complete Blood Count with 5-part Differential - Whole Blood, Second Exam (Laboratory) — Note: RDC Only
  • 2001-2002: l25_2_b — Segmented neutrophils percent (%) — Complete Blood Count with 5-part Differential - Whole Blood, Second Exam (Laboratory)
LB2P1Evidence developing

Prostate specific antigen, total (ng/mL)

Observed years
20012002
Release records
1
Datasets
1
Components
Laboratory
Qualified Praxis harmonization assessment

Evidence developing · low confidence

No normalized longitudinal change evidence is available for this variable. Absence of events must not be interpreted as proof of cross-cycle equivalence.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Variable names / labels over time
  • Prostate specific antigen, total (ng/mL)2001-2002
Cycle-by-cycle release history
  • 2001-2002: l11p_2_b — Prostate specific antigen, total (ng/mL) — Prostate-specific Antigen (PSA), Second Exam (Laboratory)
LB2P2Evidence developing

Prostate specific antigen (PSA), free (ng/mL)

Observed years
20012002
Release records
1
Datasets
1
Components
Laboratory
Qualified Praxis harmonization assessment

Evidence developing · low confidence

No normalized longitudinal change evidence is available for this variable. Absence of events must not be interpreted as proof of cross-cycle equivalence.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Variable names / labels over time
  • Prostate specific antigen (PSA), free (ng/mL)2001-2002
Cycle-by-cycle release history
  • 2001-2002: l11p_2_b — Prostate specific antigen (PSA), free (ng/mL) — Prostate-specific Antigen (PSA), Second Exam (Laboratory)
LB2P3Evidence developing

Prostate specific antigen ratio (%)

Observed years
20012002
Release records
1
Datasets
1
Components
Laboratory
Qualified Praxis harmonization assessment

Evidence developing · low confidence

No normalized longitudinal change evidence is available for this variable. Absence of events must not be interpreted as proof of cross-cycle equivalence.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Variable names / labels over time
  • Prostate specific antigen ratio (%)2001-2002
Cycle-by-cycle release history
  • 2001-2002: l11p_2_b — Prostate specific antigen ratio (%) — Prostate-specific Antigen (PSA), Second Exam (Laboratory)
LB2PCTEvidence developing

Transferrin saturation (%)

Observed years
20002000
Release records
1
Datasets
1
Components
Laboratory
Qualified Praxis harmonization assessment

Evidence developing · low confidence

No normalized longitudinal change evidence is available for this variable. Absence of events must not be interpreted as proof of cross-cycle equivalence.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Variable names / labels over time
  • Transferrin saturation (%)1999-2000
Cycle-by-cycle release history
  • 1999-2000: L06_2_00 — Transferrin saturation (%) — Cadmium, Lead, Ferritin, Serum Folate, RBC Folate, Vitamin B12, Homocysteine, Methylmalonic acid, Cotinine & Other Selected Nutritional Biochemistries - Blood, Second Exam (Laboratory) — Note: RDC Only
LB2PLTSICompatible with harmonization

Platelet count (1000 cells/uL)

Observed years
20002002
Release records
2
Datasets
2
Components
Laboratory
Qualified Praxis harmonization assessment

Compatible with harmonization · moderate confidence

No blocking method discontinuity is identified inside the selected cycle span, but one or more longitudinal changes require explicit harmonization conditions before pooling.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 1999-2000 → 2001-2002

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • Platelet count (1000 cells/uL)1999-2000 · 2001-2002
Cycle-by-cycle release history
  • 1999-2000: l25_2_r — Platelet count (1000 cells/uL) — Complete Blood Count with 5-part Differential - Whole Blood, Second Exam (Laboratory) — Note: RDC Only
  • 2001-2002: l25_2_b — Platelet count (1000 cells/uL) — Complete Blood Count with 5-part Differential - Whole Blood, Second Exam (Laboratory)
LB2RBCSICompatible with harmonization

Red blood cell count (million cells/uL)

Observed years
20002002
Release records
2
Datasets
2
Components
Laboratory
Qualified Praxis harmonization assessment

Compatible with harmonization · moderate confidence

No blocking method discontinuity is identified inside the selected cycle span, but one or more longitudinal changes require explicit harmonization conditions before pooling.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 1999-2000 → 2001-2002

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • Red blood cell count (million cells/uL)1999-2000 · 2001-2002
Cycle-by-cycle release history
  • 1999-2000: l25_2_r — Red blood cell count (million cells/uL) — Complete Blood Count with 5-part Differential - Whole Blood, Second Exam (Laboratory) — Note: RDC Only
  • 2001-2002: l25_2_b — Red blood cell count (million cells/uL) — Complete Blood Count with 5-part Differential - Whole Blood, Second Exam (Laboratory)
LB2RBFCompatible with harmonization

Folate (ng/mL RBC)

Observed years
20002002
Release records
2
Datasets
2
Components
Laboratory
Qualified Praxis harmonization assessment

Compatible with harmonization · moderate confidence

No blocking method discontinuity is identified inside the selected cycle span, but one or more longitudinal changes require explicit harmonization conditions before pooling.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 1999-2000 → 2001-2002

Praxis harmonization actions
  • Confirm that the construct and coding are unchanged before pooling or recoding.
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Review the adjacent codebooks/methods. Keep this boundary as documentation variation unless source evidence confirms a substantive method or instrument change.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • Folate (ng/mL RBC)1999-2000
  • Folate, RBC (ng/mL RBC)2001-2002
Cycle-by-cycle release history
  • 1999-2000: L06_2_00 — Folate (ng/mL RBC) — Cadmium, Lead, Ferritin, Serum Folate, RBC Folate, Vitamin B12, Homocysteine, Methylmalonic acid, Cotinine & Other Selected Nutritional Biochemistries - Blood, Second Exam (Laboratory) — Note: RDC Only
  • 2001-2002: L06_2_B — Folate, RBC (ng/mL RBC) — Cadmium, Lead, Total Mercury, Ferritin, Serum Folate, RBC Folate, Vitamin B12, Homocysteine, Methylmalonic acid, Cotinine - Blood, Second Exam (Laboratory)
LB2RBFSICompatible with harmonization

Folate (nmol/L RBC)

Observed years
20002002
Release records
2
Datasets
2
Components
Laboratory
Qualified Praxis harmonization assessment

Compatible with harmonization · moderate confidence

No blocking method discontinuity is identified inside the selected cycle span, but one or more longitudinal changes require explicit harmonization conditions before pooling.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 1999-2000 → 2001-2002

Praxis harmonization actions
  • Confirm that the construct and coding are unchanged before pooling or recoding.
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Review the adjacent codebooks/methods. Keep this boundary as documentation variation unless source evidence confirms a substantive method or instrument change.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • Folate (nmol/L RBC)1999-2000
  • Folate, RBC (nmol/L RBC)2001-2002
Cycle-by-cycle release history
  • 1999-2000: L06_2_00 — Folate (nmol/L RBC) — Cadmium, Lead, Ferritin, Serum Folate, RBC Folate, Vitamin B12, Homocysteine, Methylmalonic acid, Cotinine & Other Selected Nutritional Biochemistries - Blood, Second Exam (Laboratory) — Note: RDC Only
  • 2001-2002: L06_2_B — Folate, RBC (nmol/L RBC) — Cadmium, Lead, Total Mercury, Ferritin, Serum Folate, RBC Folate, Vitamin B12, Homocysteine, Methylmalonic acid, Cotinine - Blood, Second Exam (Laboratory)
LB2RDWCompatible with harmonization

Red cell distribution width (%)

Observed years
20002002
Release records
2
Datasets
2
Components
Laboratory
Qualified Praxis harmonization assessment

Compatible with harmonization · moderate confidence

No blocking method discontinuity is identified inside the selected cycle span, but one or more longitudinal changes require explicit harmonization conditions before pooling.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 1999-2000 → 2001-2002

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • Red cell distribution width (%)1999-2000 · 2001-2002
Cycle-by-cycle release history
  • 1999-2000: l25_2_r — Red cell distribution width (%) — Complete Blood Count with 5-part Differential - Whole Blood, Second Exam (Laboratory) — Note: RDC Only
  • 2001-2002: l25_2_b — Red cell distribution width (%) — Complete Blood Count with 5-part Differential - Whole Blood, Second Exam (Laboratory)
LB2RPLCompatible with harmonization

Retinyl palmitate (ug/dL)

Observed years
20002002
Release records
3
Datasets
3
Components
Laboratory
Qualified Praxis harmonization assessment

Compatible with harmonization · moderate confidence

No blocking method discontinuity is identified inside the selected cycle span, but one or more longitudinal changes require explicit harmonization conditions before pooling.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 1999-2000 → 2001-2002

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • Retinyl palmitate (ug/dL)1999-2000
  • Retinyl palmitate(ug/dL)1999-2000 · 2001-2002
Cycle-by-cycle release history
  • 1999-2000: L06_2_00 — Retinyl palmitate (ug/dL) — Cadmium, Lead, Ferritin, Serum Folate, RBC Folate, Vitamin B12, Homocysteine, Methylmalonic acid, Cotinine & Other Selected Nutritional Biochemistries - Blood, Second Exam (Laboratory) — Note: RDC Only
  • 1999-2000: VIT_2_R — Retinyl palmitate(ug/dL) — Vitamin A & Vitamin E, Second Exam (Laboratory) — Note: RDC Only
  • 2001-2002: VIT_2_B — Retinyl palmitate(ug/dL) — Vitamin A, Vitamin E, & Carotenoids, Second Exam (Laboratory)
LB2RPLSICompatible with harmonization

Retinyl palmitate (umol/L)

Observed years
20002002
Release records
3
Datasets
3
Components
Laboratory
Qualified Praxis harmonization assessment

Compatible with harmonization · moderate confidence

No blocking method discontinuity is identified inside the selected cycle span, but one or more longitudinal changes require explicit harmonization conditions before pooling.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 1999-2000 → 2001-2002

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • Retinyl palmitate (umol/L)1999-2000
  • Retinyl palmitate(umol/L)1999-2000 · 2001-2002
Cycle-by-cycle release history
  • 1999-2000: L06_2_00 — Retinyl palmitate (umol/L) — Cadmium, Lead, Ferritin, Serum Folate, RBC Folate, Vitamin B12, Homocysteine, Methylmalonic acid, Cotinine & Other Selected Nutritional Biochemistries - Blood, Second Exam (Laboratory) — Note: RDC Only
  • 1999-2000: VIT_2_R — Retinyl palmitate(umol/L) — Vitamin A & Vitamin E, Second Exam (Laboratory) — Note: RDC Only
  • 2001-2002: VIT_2_B — Retinyl palmitate(umol/L) — Vitamin A, Vitamin E, & Carotenoids, Second Exam (Laboratory)
LB2RSTCompatible with harmonization

Retinyl stearate (ug/dL)

Observed years
20002002
Release records
3
Datasets
3
Components
Laboratory
Qualified Praxis harmonization assessment

Compatible with harmonization · moderate confidence

No blocking method discontinuity is identified inside the selected cycle span, but one or more longitudinal changes require explicit harmonization conditions before pooling.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 1999-2000 → 2001-2002

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • Retinyl stearate (ug/dL)1999-2000
  • Retinyl stearate(ug/dL)1999-2000 · 2001-2002
Cycle-by-cycle release history
  • 1999-2000: L06_2_00 — Retinyl stearate (ug/dL) — Cadmium, Lead, Ferritin, Serum Folate, RBC Folate, Vitamin B12, Homocysteine, Methylmalonic acid, Cotinine & Other Selected Nutritional Biochemistries - Blood, Second Exam (Laboratory) — Note: RDC Only
  • 1999-2000: VIT_2_R — Retinyl stearate(ug/dL) — Vitamin A & Vitamin E, Second Exam (Laboratory) — Note: RDC Only
  • 2001-2002: VIT_2_B — Retinyl stearate(ug/dL) — Vitamin A, Vitamin E, & Carotenoids, Second Exam (Laboratory)
LB2RSTSICompatible with harmonization

Retinyl stearate (umol/L)

Observed years
20002002
Release records
3
Datasets
3
Components
Laboratory
Qualified Praxis harmonization assessment

Compatible with harmonization · moderate confidence

No blocking method discontinuity is identified inside the selected cycle span, but one or more longitudinal changes require explicit harmonization conditions before pooling.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 1999-2000 → 2001-2002

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • Retinyl stearate (umol/L)1999-2000
  • Retinyl stearate(umol/L)1999-2000 · 2001-2002
Cycle-by-cycle release history
  • 1999-2000: L06_2_00 — Retinyl stearate (umol/L) — Cadmium, Lead, Ferritin, Serum Folate, RBC Folate, Vitamin B12, Homocysteine, Methylmalonic acid, Cotinine & Other Selected Nutritional Biochemistries - Blood, Second Exam (Laboratory) — Note: RDC Only
  • 1999-2000: VIT_2_R — Retinyl stearate(umol/L) — Vitamin A & Vitamin E, Second Exam (Laboratory) — Note: RDC Only
  • 2001-2002: VIT_2_B — Retinyl stearate(umol/L) — Vitamin A, Vitamin E, & Carotenoids, Second Exam (Laboratory)
LB2RUCompatible with harmonization

Rubella

Observed years
20002002
Release records
2
Datasets
2
Components
Laboratory
Qualified Praxis harmonization assessment

Compatible with harmonization · moderate confidence

No blocking method discontinuity is identified inside the selected cycle span, but one or more longitudinal changes require explicit harmonization conditions before pooling.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 1999-2000 → 2001-2002

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • Rubella1999-2000 · 2001-2002
Cycle-by-cycle release history
  • 1999-2000: L19_2_R — Rubella — Measles, Rubella, & Varicella, Second Exam (Laboratory) — Note: RDC Only
  • 2001-2002: L19_2_B — Rubella — Measles, Rubella, & Varicella, Second Exam (Laboratory)
LB2RUIUCompatible with harmonization

Rubella antibody (international units)

Observed years
20002002
Release records
2
Datasets
2
Components
Laboratory
Qualified Praxis harmonization assessment

Compatible with harmonization · moderate confidence

No blocking method discontinuity is identified inside the selected cycle span, but one or more longitudinal changes require explicit harmonization conditions before pooling.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 1999-2000 → 2001-2002

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • Rubella antibody (international units)1999-2000 · 2001-2002
Cycle-by-cycle release history
  • 1999-2000: L19_2_R — Rubella antibody (international units) — Measles, Rubella, & Varicella, Second Exam (Laboratory) — Note: RDC Only
  • 2001-2002: L19_2_B — Rubella antibody (international units) — Measles, Rubella, & Varicella, Second Exam (Laboratory)
LB2SALAdjustment required

Albumin (g/dL)

Observed years
20002002
Release records
2
Datasets
2
Components
Laboratory
Qualified Praxis harmonization assessment

Adjustment required · high confidence

A methodological discontinuity falls inside the selected cycle span. Naive pooling of raw values across the flagged boundary is not recommended unless CDC/NCHS provides a defensible calibration or comparability procedure.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 1999-2000 → 2001-2002

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Apply CDC/NCHS comparability or calibration guidance where available. If equivalence is not established, preserve separate method periods or perform sensitivity analyses rather than naively pooling raw values.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • Albumin (g/dL)1999-2000 · 2001-2002
Cycle-by-cycle release history
  • 1999-2000: l18_2_00 — Albumin (g/dL) — Standard Biochemistry Profile & Hormones, Second Exam (Laboratory) — Note: RDC Only
  • 2001-2002: L40_2_B — Albumin (g/dL) — Standard Biochemistry Profile, Follicle Stimulating Hormone & Luteinizing Hormone, Second Exam (Laboratory)
LB2SALSIAdjustment required

Albumin (g/L)

Observed years
20002002
Release records
2
Datasets
2
Components
Laboratory
Qualified Praxis harmonization assessment

Adjustment required · high confidence

A methodological discontinuity falls inside the selected cycle span. Naive pooling of raw values across the flagged boundary is not recommended unless CDC/NCHS provides a defensible calibration or comparability procedure.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 1999-2000 → 2001-2002

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Apply CDC/NCHS comparability or calibration guidance where available. If equivalence is not established, preserve separate method periods or perform sensitivity analyses rather than naively pooling raw values.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • Albumin (g/L)1999-2000 · 2001-2002
Cycle-by-cycle release history
  • 1999-2000: l18_2_00 — Albumin (g/L) — Standard Biochemistry Profile & Hormones, Second Exam (Laboratory) — Note: RDC Only
  • 2001-2002: L40_2_B — Albumin (g/L) — Standard Biochemistry Profile, Follicle Stimulating Hormone & Luteinizing Hormone, Second Exam (Laboratory)
LB2SAPSIAdjustment required

Alkaline phosphotase (U/L)

Observed years
20002002
Release records
2
Datasets
2
Components
Laboratory
Qualified Praxis harmonization assessment

Adjustment required · high confidence

A methodological discontinuity falls inside the selected cycle span. Naive pooling of raw values across the flagged boundary is not recommended unless CDC/NCHS provides a defensible calibration or comparability procedure.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 1999-2000 → 2001-2002

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Apply CDC/NCHS comparability or calibration guidance where available. If equivalence is not established, preserve separate method periods or perform sensitivity analyses rather than naively pooling raw values.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • Alkaline phosphotase (U/L)1999-2000 · 2001-2002
Cycle-by-cycle release history
  • 1999-2000: l18_2_00 — Alkaline phosphotase (U/L) — Standard Biochemistry Profile & Hormones, Second Exam (Laboratory) — Note: RDC Only
  • 2001-2002: L40_2_B — Alkaline phosphotase (U/L) — Standard Biochemistry Profile, Follicle Stimulating Hormone & Luteinizing Hormone, Second Exam (Laboratory)
LB2SASSIAdjustment required

Aspartate aminotransferase (U/L)

Observed years
20002002
Release records
2
Datasets
2
Components
Laboratory
Qualified Praxis harmonization assessment

Adjustment required · high confidence

A methodological discontinuity falls inside the selected cycle span. Naive pooling of raw values across the flagged boundary is not recommended unless CDC/NCHS provides a defensible calibration or comparability procedure.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 1999-2000 → 2001-2002

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Apply CDC/NCHS comparability or calibration guidance where available. If equivalence is not established, preserve separate method periods or perform sensitivity analyses rather than naively pooling raw values.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • Aspartate aminotransferase (U/L)1999-2000 · 2001-2002
Cycle-by-cycle release history
  • 1999-2000: l18_2_00 — Aspartate aminotransferase (U/L) — Standard Biochemistry Profile & Hormones, Second Exam (Laboratory) — Note: RDC Only
  • 2001-2002: L40_2_B — Aspartate aminotransferase (U/L) — Standard Biochemistry Profile, Follicle Stimulating Hormone & Luteinizing Hormone, Second Exam (Laboratory)
LB2SATSIAdjustment required

Alanine aminotransferase (U/L)

Observed years
20002002
Release records
2
Datasets
2
Components
Laboratory
Qualified Praxis harmonization assessment

Adjustment required · high confidence

A methodological discontinuity falls inside the selected cycle span. Naive pooling of raw values across the flagged boundary is not recommended unless CDC/NCHS provides a defensible calibration or comparability procedure.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 1999-2000 → 2001-2002

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Apply CDC/NCHS comparability or calibration guidance where available. If equivalence is not established, preserve separate method periods or perform sensitivity analyses rather than naively pooling raw values.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • Alanine aminotransferase (U/L)1999-2000 · 2001-2002
Cycle-by-cycle release history
  • 1999-2000: l18_2_00 — Alanine aminotransferase (U/L) — Standard Biochemistry Profile & Hormones, Second Exam (Laboratory) — Note: RDC Only
  • 2001-2002: L40_2_B — Alanine aminotransferase (U/L) — Standard Biochemistry Profile, Follicle Stimulating Hormone & Luteinizing Hormone, Second Exam (Laboratory)
LB2SBUAdjustment required

Blood urea nitrogen (mg/dL)

Observed years
20002002
Release records
2
Datasets
2
Components
Laboratory
Qualified Praxis harmonization assessment

Adjustment required · high confidence

A methodological discontinuity falls inside the selected cycle span. Naive pooling of raw values across the flagged boundary is not recommended unless CDC/NCHS provides a defensible calibration or comparability procedure.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 1999-2000 → 2001-2002

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Apply CDC/NCHS comparability or calibration guidance where available. If equivalence is not established, preserve separate method periods or perform sensitivity analyses rather than naively pooling raw values.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • Blood urea nitrogen (mg/dL)1999-2000 · 2001-2002
Cycle-by-cycle release history
  • 1999-2000: l18_2_00 — Blood urea nitrogen (mg/dL) — Standard Biochemistry Profile & Hormones, Second Exam (Laboratory) — Note: RDC Only
  • 2001-2002: L40_2_B — Blood urea nitrogen (mg/dL) — Standard Biochemistry Profile, Follicle Stimulating Hormone & Luteinizing Hormone, Second Exam (Laboratory)
LB2SBUSIAdjustment required

Blood urea nitrogen (mmol/L)

Observed years
20002002
Release records
2
Datasets
2
Components
Laboratory
Qualified Praxis harmonization assessment

Adjustment required · high confidence

A methodological discontinuity falls inside the selected cycle span. Naive pooling of raw values across the flagged boundary is not recommended unless CDC/NCHS provides a defensible calibration or comparability procedure.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 1999-2000 → 2001-2002

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Apply CDC/NCHS comparability or calibration guidance where available. If equivalence is not established, preserve separate method periods or perform sensitivity analyses rather than naively pooling raw values.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • Blood urea nitrogen (mmol/L)1999-2000 · 2001-2002
Cycle-by-cycle release history
  • 1999-2000: l18_2_00 — Blood urea nitrogen (mmol/L) — Standard Biochemistry Profile & Hormones, Second Exam (Laboratory) — Note: RDC Only
  • 2001-2002: L40_2_B — Blood urea nitrogen (mmol/L) — Standard Biochemistry Profile, Follicle Stimulating Hormone & Luteinizing Hormone, Second Exam (Laboratory)
LB2SC3SIAdjustment required

Bicarbonate (mmol/L)

Observed years
20002002
Release records
2
Datasets
2
Components
Laboratory
Qualified Praxis harmonization assessment

Adjustment required · high confidence

A methodological discontinuity falls inside the selected cycle span. Naive pooling of raw values across the flagged boundary is not recommended unless CDC/NCHS provides a defensible calibration or comparability procedure.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 1999-2000 → 2001-2002

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Apply CDC/NCHS comparability or calibration guidance where available. If equivalence is not established, preserve separate method periods or perform sensitivity analyses rather than naively pooling raw values.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • Bicarbonate (mmol/L)1999-2000 · 2001-2002
Cycle-by-cycle release history
  • 1999-2000: l18_2_00 — Bicarbonate (mmol/L) — Standard Biochemistry Profile & Hormones, Second Exam (Laboratory) — Note: RDC Only
  • 2001-2002: L40_2_B — Bicarbonate (mmol/L) — Standard Biochemistry Profile, Follicle Stimulating Hormone & Luteinizing Hormone, Second Exam (Laboratory)
LB2SCAAdjustment required

Total calcium (mg/dL)

Observed years
20002002
Release records
2
Datasets
2
Components
Laboratory
Qualified Praxis harmonization assessment

Adjustment required · high confidence

A methodological discontinuity falls inside the selected cycle span. Naive pooling of raw values across the flagged boundary is not recommended unless CDC/NCHS provides a defensible calibration or comparability procedure.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 1999-2000 → 2001-2002

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Apply CDC/NCHS comparability or calibration guidance where available. If equivalence is not established, preserve separate method periods or perform sensitivity analyses rather than naively pooling raw values.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • Total calcium (mg/dL)1999-2000 · 2001-2002
Cycle-by-cycle release history
  • 1999-2000: l18_2_00 — Total calcium (mg/dL) — Standard Biochemistry Profile & Hormones, Second Exam (Laboratory) — Note: RDC Only
  • 2001-2002: L40_2_B — Total calcium (mg/dL) — Standard Biochemistry Profile, Follicle Stimulating Hormone & Luteinizing Hormone, Second Exam (Laboratory)
LB2SCASIAdjustment required

Total calcium (mmol/L)

Observed years
20002002
Release records
2
Datasets
2
Components
Laboratory
Qualified Praxis harmonization assessment

Adjustment required · high confidence

A methodological discontinuity falls inside the selected cycle span. Naive pooling of raw values across the flagged boundary is not recommended unless CDC/NCHS provides a defensible calibration or comparability procedure.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 1999-2000 → 2001-2002

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Apply CDC/NCHS comparability or calibration guidance where available. If equivalence is not established, preserve separate method periods or perform sensitivity analyses rather than naively pooling raw values.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • Total calcium (mmol/L)1999-2000 · 2001-2002
Cycle-by-cycle release history
  • 1999-2000: l18_2_00 — Total calcium (mmol/L) — Standard Biochemistry Profile & Hormones, Second Exam (Laboratory) — Note: RDC Only
  • 2001-2002: L40_2_B — Total calcium (mmol/L) — Standard Biochemistry Profile, Follicle Stimulating Hormone & Luteinizing Hormone, Second Exam (Laboratory)
LB2SCHAdjustment required

Cholesterol (mg/dL)

Observed years
20002002
Release records
2
Datasets
2
Components
Laboratory
Qualified Praxis harmonization assessment

Adjustment required · high confidence

A methodological discontinuity falls inside the selected cycle span. Naive pooling of raw values across the flagged boundary is not recommended unless CDC/NCHS provides a defensible calibration or comparability procedure.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 1999-2000 → 2001-2002

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Apply CDC/NCHS comparability or calibration guidance where available. If equivalence is not established, preserve separate method periods or perform sensitivity analyses rather than naively pooling raw values.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • Cholesterol (mg/dL)1999-2000 · 2001-2002
Cycle-by-cycle release history
  • 1999-2000: l18_2_00 — Cholesterol (mg/dL) — Standard Biochemistry Profile & Hormones, Second Exam (Laboratory) — Note: RDC Only
  • 2001-2002: L40_2_B — Cholesterol (mg/dL) — Standard Biochemistry Profile, Follicle Stimulating Hormone & Luteinizing Hormone, Second Exam (Laboratory)
LB2SCHSIAdjustment required

Cholesterol (mmol/L)

Observed years
20002002
Release records
2
Datasets
2
Components
Laboratory
Qualified Praxis harmonization assessment

Adjustment required · high confidence

A methodological discontinuity falls inside the selected cycle span. Naive pooling of raw values across the flagged boundary is not recommended unless CDC/NCHS provides a defensible calibration or comparability procedure.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 1999-2000 → 2001-2002

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Apply CDC/NCHS comparability or calibration guidance where available. If equivalence is not established, preserve separate method periods or perform sensitivity analyses rather than naively pooling raw values.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • Cholesterol (mmol/L)1999-2000 · 2001-2002
Cycle-by-cycle release history
  • 1999-2000: l18_2_00 — Cholesterol (mmol/L) — Standard Biochemistry Profile & Hormones, Second Exam (Laboratory) — Note: RDC Only
  • 2001-2002: L40_2_B — Cholesterol (mmol/L) — Standard Biochemistry Profile, Follicle Stimulating Hormone & Luteinizing Hormone, Second Exam (Laboratory)
LB2SCLSIAdjustment required

Chloride (mmol/L)

Observed years
20002002
Release records
2
Datasets
2
Components
Laboratory
Qualified Praxis harmonization assessment

Adjustment required · high confidence

A methodological discontinuity falls inside the selected cycle span. Naive pooling of raw values across the flagged boundary is not recommended unless CDC/NCHS provides a defensible calibration or comparability procedure.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 1999-2000 → 2001-2002

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Apply CDC/NCHS comparability or calibration guidance where available. If equivalence is not established, preserve separate method periods or perform sensitivity analyses rather than naively pooling raw values.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • Chloride (mmol/L)1999-2000 · 2001-2002
Cycle-by-cycle release history
  • 1999-2000: l18_2_00 — Chloride (mmol/L) — Standard Biochemistry Profile & Hormones, Second Exam (Laboratory) — Note: RDC Only
  • 2001-2002: L40_2_B — Chloride (mmol/L) — Standard Biochemistry Profile, Follicle Stimulating Hormone & Luteinizing Hormone, Second Exam (Laboratory)
LB2SCRAdjustment required

Creatinine (mg/dL)

Observed years
20002002
Release records
2
Datasets
2
Components
Laboratory
Qualified Praxis harmonization assessment

Adjustment required · high confidence

A methodological discontinuity falls inside the selected cycle span. Naive pooling of raw values across the flagged boundary is not recommended unless CDC/NCHS provides a defensible calibration or comparability procedure.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 1999-2000 → 2001-2002

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Apply CDC/NCHS comparability or calibration guidance where available. If equivalence is not established, preserve separate method periods or perform sensitivity analyses rather than naively pooling raw values.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • Creatinine (mg/dL)1999-2000 · 2001-2002
Cycle-by-cycle release history
  • 1999-2000: l18_2_00 — Creatinine (mg/dL) — Standard Biochemistry Profile & Hormones, Second Exam (Laboratory) — Note: RDC Only
  • 2001-2002: L40_2_B — Creatinine (mg/dL) — Standard Biochemistry Profile, Follicle Stimulating Hormone & Luteinizing Hormone, Second Exam (Laboratory)
LB2SCRSIAdjustment required

Creatinine (umol/L)

Observed years
20002002
Release records
2
Datasets
2
Components
Laboratory
Qualified Praxis harmonization assessment

Adjustment required · high confidence

A methodological discontinuity falls inside the selected cycle span. Naive pooling of raw values across the flagged boundary is not recommended unless CDC/NCHS provides a defensible calibration or comparability procedure.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 1999-2000 → 2001-2002

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Apply CDC/NCHS comparability or calibration guidance where available. If equivalence is not established, preserve separate method periods or perform sensitivity analyses rather than naively pooling raw values.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • Creatinine (umol/L)1999-2000 · 2001-2002
Cycle-by-cycle release history
  • 1999-2000: l18_2_00 — Creatinine (umol/L) — Standard Biochemistry Profile & Hormones, Second Exam (Laboratory) — Note: RDC Only
  • 2001-2002: L40_2_B — Creatinine (umol/L) — Standard Biochemistry Profile, Follicle Stimulating Hormone & Luteinizing Hormone, Second Exam (Laboratory)
LB2SGLAdjustment required

Glucose (mg/dL)

Observed years
20002002
Release records
2
Datasets
2
Components
Laboratory
Qualified Praxis harmonization assessment

Adjustment required · high confidence

A methodological discontinuity falls inside the selected cycle span. Naive pooling of raw values across the flagged boundary is not recommended unless CDC/NCHS provides a defensible calibration or comparability procedure.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 1999-2000 → 2001-2002

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Apply CDC/NCHS comparability or calibration guidance where available. If equivalence is not established, preserve separate method periods or perform sensitivity analyses rather than naively pooling raw values.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • Glucose (mg/dL)1999-2000 · 2001-2002
Cycle-by-cycle release history
  • 1999-2000: l18_2_00 — Glucose (mg/dL) — Standard Biochemistry Profile & Hormones, Second Exam (Laboratory) — Note: RDC Only
  • 2001-2002: L40_2_B — Glucose (mg/dL) — Standard Biochemistry Profile, Follicle Stimulating Hormone & Luteinizing Hormone, Second Exam (Laboratory)
LB2SGLSIAdjustment required

Glucose, serum (mmol/L)

Observed years
20002002
Release records
2
Datasets
2
Components
Laboratory
Qualified Praxis harmonization assessment

Adjustment required · high confidence

A methodological discontinuity falls inside the selected cycle span. Naive pooling of raw values across the flagged boundary is not recommended unless CDC/NCHS provides a defensible calibration or comparability procedure.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 1999-2000 → 2001-2002

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Apply CDC/NCHS comparability or calibration guidance where available. If equivalence is not established, preserve separate method periods or perform sensitivity analyses rather than naively pooling raw values.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • Glucose, serum (mmol/L)1999-2000 · 2001-2002
Cycle-by-cycle release history
  • 1999-2000: l18_2_00 — Glucose, serum (mmol/L) — Standard Biochemistry Profile & Hormones, Second Exam (Laboratory) — Note: RDC Only
  • 2001-2002: L40_2_B — Glucose, serum (mmol/L) — Standard Biochemistry Profile, Follicle Stimulating Hormone & Luteinizing Hormone, Second Exam (Laboratory)
LB2SGTSIAdjustment required

Gamma glutamyltransferase

Observed years
20002002
Release records
2
Datasets
2
Components
Laboratory
Qualified Praxis harmonization assessment

Adjustment required · high confidence

A methodological discontinuity falls inside the selected cycle span. Naive pooling of raw values across the flagged boundary is not recommended unless CDC/NCHS provides a defensible calibration or comparability procedure.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 1999-2000 → 2001-2002

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Apply CDC/NCHS comparability or calibration guidance where available. If equivalence is not established, preserve separate method periods or perform sensitivity analyses rather than naively pooling raw values.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • Gamma glutamyltransferase1999-2000 · 2001-2002
Cycle-by-cycle release history
  • 1999-2000: l18_2_00 — Gamma glutamyltransferase — Standard Biochemistry Profile & Hormones, Second Exam (Laboratory) — Note: RDC Only
  • 2001-2002: L40_2_B — Gamma glutamyltransferase — Standard Biochemistry Profile, Follicle Stimulating Hormone & Luteinizing Hormone, Second Exam (Laboratory)
LB2SIRAdjustment required

Iron (ug/dL)

Observed years
20002002
Release records
2
Datasets
2
Components
Laboratory
Qualified Praxis harmonization assessment

Adjustment required · high confidence

A methodological discontinuity falls inside the selected cycle span. Naive pooling of raw values across the flagged boundary is not recommended unless CDC/NCHS provides a defensible calibration or comparability procedure.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 1999-2000 → 2001-2002

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Apply CDC/NCHS comparability or calibration guidance where available. If equivalence is not established, preserve separate method periods or perform sensitivity analyses rather than naively pooling raw values.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • Iron (ug/dL)1999-2000 · 2001-2002
Cycle-by-cycle release history
  • 1999-2000: l18_2_00 — Iron (ug/dL) — Standard Biochemistry Profile & Hormones, Second Exam (Laboratory) — Note: RDC Only
  • 2001-2002: L40_2_B — Iron (ug/dL) — Standard Biochemistry Profile, Follicle Stimulating Hormone & Luteinizing Hormone, Second Exam (Laboratory)
LB2SIRSIAdjustment required

Iron (umol/L)

Observed years
20002002
Release records
2
Datasets
2
Components
Laboratory
Qualified Praxis harmonization assessment

Adjustment required · high confidence

A methodological discontinuity falls inside the selected cycle span. Naive pooling of raw values across the flagged boundary is not recommended unless CDC/NCHS provides a defensible calibration or comparability procedure.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 1999-2000 → 2001-2002

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Apply CDC/NCHS comparability or calibration guidance where available. If equivalence is not established, preserve separate method periods or perform sensitivity analyses rather than naively pooling raw values.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • Iron (umol/L)1999-2000 · 2001-2002
Cycle-by-cycle release history
  • 1999-2000: l18_2_00 — Iron (umol/L) — Standard Biochemistry Profile & Hormones, Second Exam (Laboratory) — Note: RDC Only
  • 2001-2002: L40_2_B — Iron (umol/L) — Standard Biochemistry Profile, Follicle Stimulating Hormone & Luteinizing Hormone, Second Exam (Laboratory)
LB2SKSIAdjustment required

Potassium (mmol/L)

Observed years
20002002
Release records
2
Datasets
2
Components
Laboratory
Qualified Praxis harmonization assessment

Adjustment required · high confidence

A methodological discontinuity falls inside the selected cycle span. Naive pooling of raw values across the flagged boundary is not recommended unless CDC/NCHS provides a defensible calibration or comparability procedure.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 1999-2000 → 2001-2002

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Apply CDC/NCHS comparability or calibration guidance where available. If equivalence is not established, preserve separate method periods or perform sensitivity analyses rather than naively pooling raw values.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • Potassium (mmol/L)1999-2000 · 2001-2002
Cycle-by-cycle release history
  • 1999-2000: l18_2_00 — Potassium (mmol/L) — Standard Biochemistry Profile & Hormones, Second Exam (Laboratory) — Note: RDC Only
  • 2001-2002: L40_2_B — Potassium (mmol/L) — Standard Biochemistry Profile, Follicle Stimulating Hormone & Luteinizing Hormone, Second Exam (Laboratory)
LB2SLDSIAdjustment required

Lactate dehydrogenase (U/L)

Observed years
20002002
Release records
2
Datasets
2
Components
Laboratory
Qualified Praxis harmonization assessment

Adjustment required · high confidence

A methodological discontinuity falls inside the selected cycle span. Naive pooling of raw values across the flagged boundary is not recommended unless CDC/NCHS provides a defensible calibration or comparability procedure.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 1999-2000 → 2001-2002

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Apply CDC/NCHS comparability or calibration guidance where available. If equivalence is not established, preserve separate method periods or perform sensitivity analyses rather than naively pooling raw values.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • Lactate dehydrogenase (U/L)1999-2000 · 2001-2002
Cycle-by-cycle release history
  • 1999-2000: l18_2_00 — Lactate dehydrogenase (U/L) — Standard Biochemistry Profile & Hormones, Second Exam (Laboratory) — Note: RDC Only
  • 2001-2002: L40_2_B — Lactate dehydrogenase (U/L) — Standard Biochemistry Profile, Follicle Stimulating Hormone & Luteinizing Hormone, Second Exam (Laboratory)
LB2SNASIAdjustment required

Sodium (mmol/L)

Observed years
20002002
Release records
2
Datasets
2
Components
Laboratory
Qualified Praxis harmonization assessment

Adjustment required · high confidence

A methodological discontinuity falls inside the selected cycle span. Naive pooling of raw values across the flagged boundary is not recommended unless CDC/NCHS provides a defensible calibration or comparability procedure.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 1999-2000 → 2001-2002

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Apply CDC/NCHS comparability or calibration guidance where available. If equivalence is not established, preserve separate method periods or perform sensitivity analyses rather than naively pooling raw values.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • Sodium (mmol/L)1999-2000 · 2001-2002
Cycle-by-cycle release history
  • 1999-2000: l18_2_00 — Sodium (mmol/L) — Standard Biochemistry Profile & Hormones, Second Exam (Laboratory) — Note: RDC Only
  • 2001-2002: L40_2_B — Sodium (mmol/L) — Standard Biochemistry Profile, Follicle Stimulating Hormone & Luteinizing Hormone, Second Exam (Laboratory)
LB2SPHAdjustment required

Phosphorus (mg/dL)

Observed years
20002002
Release records
2
Datasets
2
Components
Laboratory
Qualified Praxis harmonization assessment

Adjustment required · high confidence

A methodological discontinuity falls inside the selected cycle span. Naive pooling of raw values across the flagged boundary is not recommended unless CDC/NCHS provides a defensible calibration or comparability procedure.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 1999-2000 → 2001-2002

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Apply CDC/NCHS comparability or calibration guidance where available. If equivalence is not established, preserve separate method periods or perform sensitivity analyses rather than naively pooling raw values.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • Phosphorus (mg/dL)1999-2000 · 2001-2002
Cycle-by-cycle release history
  • 1999-2000: l18_2_00 — Phosphorus (mg/dL) — Standard Biochemistry Profile & Hormones, Second Exam (Laboratory) — Note: RDC Only
  • 2001-2002: L40_2_B — Phosphorus (mg/dL) — Standard Biochemistry Profile, Follicle Stimulating Hormone & Luteinizing Hormone, Second Exam (Laboratory)
LB2SPHSIAdjustment required

Phosphorus (mmol/L)

Observed years
20002002
Release records
2
Datasets
2
Components
Laboratory
Qualified Praxis harmonization assessment

Adjustment required · high confidence

A methodological discontinuity falls inside the selected cycle span. Naive pooling of raw values across the flagged boundary is not recommended unless CDC/NCHS provides a defensible calibration or comparability procedure.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 1999-2000 → 2001-2002

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Apply CDC/NCHS comparability or calibration guidance where available. If equivalence is not established, preserve separate method periods or perform sensitivity analyses rather than naively pooling raw values.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • Phosphorus (mmol/L)1999-2000 · 2001-2002
Cycle-by-cycle release history
  • 1999-2000: l18_2_00 — Phosphorus (mmol/L) — Standard Biochemistry Profile & Hormones, Second Exam (Laboratory) — Note: RDC Only
  • 2001-2002: L40_2_B — Phosphorus (mmol/L) — Standard Biochemistry Profile, Follicle Stimulating Hormone & Luteinizing Hormone, Second Exam (Laboratory)
LB2STBAdjustment required

Bilirubin, total (mg/dL)

Observed years
20002002
Release records
2
Datasets
2
Components
Laboratory
Qualified Praxis harmonization assessment

Adjustment required · high confidence

A methodological discontinuity falls inside the selected cycle span. Naive pooling of raw values across the flagged boundary is not recommended unless CDC/NCHS provides a defensible calibration or comparability procedure.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 1999-2000 → 2001-2002

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Apply CDC/NCHS comparability or calibration guidance where available. If equivalence is not established, preserve separate method periods or perform sensitivity analyses rather than naively pooling raw values.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • Bilirubin, total (mg/dL)1999-2000 · 2001-2002
Cycle-by-cycle release history
  • 1999-2000: l18_2_00 — Bilirubin, total (mg/dL) — Standard Biochemistry Profile & Hormones, Second Exam (Laboratory) — Note: RDC Only
  • 2001-2002: L40_2_B — Bilirubin, total (mg/dL) — Standard Biochemistry Profile, Follicle Stimulating Hormone & Luteinizing Hormone, Second Exam (Laboratory)
LB2STBSIAdjustment required

Bilirubin, total (umol/L)

Observed years
20002002
Release records
2
Datasets
2
Components
Laboratory
Qualified Praxis harmonization assessment

Adjustment required · high confidence

A methodological discontinuity falls inside the selected cycle span. Naive pooling of raw values across the flagged boundary is not recommended unless CDC/NCHS provides a defensible calibration or comparability procedure.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 1999-2000 → 2001-2002

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Apply CDC/NCHS comparability or calibration guidance where available. If equivalence is not established, preserve separate method periods or perform sensitivity analyses rather than naively pooling raw values.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • Bilirubin, total (umol/L)1999-2000 · 2001-2002
Cycle-by-cycle release history
  • 1999-2000: l18_2_00 — Bilirubin, total (umol/L) — Standard Biochemistry Profile & Hormones, Second Exam (Laboratory) — Note: RDC Only
  • 2001-2002: L40_2_B — Bilirubin, total (umol/L) — Standard Biochemistry Profile, Follicle Stimulating Hormone & Luteinizing Hormone, Second Exam (Laboratory)
LB2STPAdjustment required

Protein, total (g/dL)

Observed years
20002002
Release records
2
Datasets
2
Components
Laboratory
Qualified Praxis harmonization assessment

Adjustment required · high confidence

A methodological discontinuity falls inside the selected cycle span. Naive pooling of raw values across the flagged boundary is not recommended unless CDC/NCHS provides a defensible calibration or comparability procedure.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 1999-2000 → 2001-2002

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Apply CDC/NCHS comparability or calibration guidance where available. If equivalence is not established, preserve separate method periods or perform sensitivity analyses rather than naively pooling raw values.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • Protein, total (g/dL)1999-2000 · 2001-2002
Cycle-by-cycle release history
  • 1999-2000: l18_2_00 — Protein, total (g/dL) — Standard Biochemistry Profile & Hormones, Second Exam (Laboratory) — Note: RDC Only
  • 2001-2002: L40_2_B — Protein, total (g/dL) — Standard Biochemistry Profile, Follicle Stimulating Hormone & Luteinizing Hormone, Second Exam (Laboratory)
LB2STPSIAdjustment required

Total protein (g/L)

Observed years
20002002
Release records
2
Datasets
2
Components
Laboratory
Qualified Praxis harmonization assessment

Adjustment required · high confidence

A methodological discontinuity falls inside the selected cycle span. Naive pooling of raw values across the flagged boundary is not recommended unless CDC/NCHS provides a defensible calibration or comparability procedure.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 1999-2000 → 2001-2002

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Apply CDC/NCHS comparability or calibration guidance where available. If equivalence is not established, preserve separate method periods or perform sensitivity analyses rather than naively pooling raw values.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • Total protein (g/L)1999-2000 · 2001-2002
Cycle-by-cycle release history
  • 1999-2000: l18_2_00 — Total protein (g/L) — Standard Biochemistry Profile & Hormones, Second Exam (Laboratory) — Note: RDC Only
  • 2001-2002: L40_2_B — Total protein (g/L) — Standard Biochemistry Profile, Follicle Stimulating Hormone & Luteinizing Hormone, Second Exam (Laboratory)
LB2STRAdjustment required

Triglycerides (mg/dL)

Observed years
20002002
Release records
2
Datasets
2
Components
Laboratory
Qualified Praxis harmonization assessment

Adjustment required · high confidence

A methodological discontinuity falls inside the selected cycle span. Naive pooling of raw values across the flagged boundary is not recommended unless CDC/NCHS provides a defensible calibration or comparability procedure.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 1999-2000 → 2001-2002

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Apply CDC/NCHS comparability or calibration guidance where available. If equivalence is not established, preserve separate method periods or perform sensitivity analyses rather than naively pooling raw values.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • Triglycerides (mg/dL)1999-2000 · 2001-2002
Cycle-by-cycle release history
  • 1999-2000: l18_2_00 — Triglycerides (mg/dL) — Standard Biochemistry Profile & Hormones, Second Exam (Laboratory) — Note: RDC Only
  • 2001-2002: L40_2_B — Triglycerides (mg/dL) — Standard Biochemistry Profile, Follicle Stimulating Hormone & Luteinizing Hormone, Second Exam (Laboratory)
LB2STRSIAdjustment required

Triglycerides (mmol/L)

Observed years
20002002
Release records
2
Datasets
2
Components
Laboratory
Qualified Praxis harmonization assessment

Adjustment required · high confidence

A methodological discontinuity falls inside the selected cycle span. Naive pooling of raw values across the flagged boundary is not recommended unless CDC/NCHS provides a defensible calibration or comparability procedure.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 1999-2000 → 2001-2002

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Apply CDC/NCHS comparability or calibration guidance where available. If equivalence is not established, preserve separate method periods or perform sensitivity analyses rather than naively pooling raw values.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • Triglycerides (mmol/L)1999-2000 · 2001-2002
Cycle-by-cycle release history
  • 1999-2000: l18_2_00 — Triglycerides (mmol/L) — Standard Biochemistry Profile & Hormones, Second Exam (Laboratory) — Note: RDC Only
  • 2001-2002: L40_2_B — Triglycerides (mmol/L) — Standard Biochemistry Profile, Follicle Stimulating Hormone & Luteinizing Hormone, Second Exam (Laboratory)
LB2SUAAdjustment required

Uric acid (mg/dL)

Observed years
20002002
Release records
2
Datasets
2
Components
Laboratory
Qualified Praxis harmonization assessment

Adjustment required · high confidence

A methodological discontinuity falls inside the selected cycle span. Naive pooling of raw values across the flagged boundary is not recommended unless CDC/NCHS provides a defensible calibration or comparability procedure.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 1999-2000 → 2001-2002

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Apply CDC/NCHS comparability or calibration guidance where available. If equivalence is not established, preserve separate method periods or perform sensitivity analyses rather than naively pooling raw values.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • Uric acid (mg/dL)1999-2000 · 2001-2002
Cycle-by-cycle release history
  • 1999-2000: l18_2_00 — Uric acid (mg/dL) — Standard Biochemistry Profile & Hormones, Second Exam (Laboratory) — Note: RDC Only
  • 2001-2002: L40_2_B — Uric acid (mg/dL) — Standard Biochemistry Profile, Follicle Stimulating Hormone & Luteinizing Hormone, Second Exam (Laboratory)
LB2SUASIAdjustment required

Uric acid (umol/L)

Observed years
20002002
Release records
2
Datasets
2
Components
Laboratory
Qualified Praxis harmonization assessment

Adjustment required · high confidence

A methodological discontinuity falls inside the selected cycle span. Naive pooling of raw values across the flagged boundary is not recommended unless CDC/NCHS provides a defensible calibration or comparability procedure.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 1999-2000 → 2001-2002

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Apply CDC/NCHS comparability or calibration guidance where available. If equivalence is not established, preserve separate method periods or perform sensitivity analyses rather than naively pooling raw values.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • Uric acid (umol/L)1999-2000 · 2001-2002
Cycle-by-cycle release history
  • 1999-2000: l18_2_00 — Uric acid (umol/L) — Standard Biochemistry Profile & Hormones, Second Exam (Laboratory) — Note: RDC Only
  • 2001-2002: L40_2_B — Uric acid (umol/L) — Standard Biochemistry Profile, Follicle Stimulating Hormone & Luteinizing Hormone, Second Exam (Laboratory)
LB2TCAdjustment required

Total cholesterol (mg/dL)

Observed years
20002002
Release records
2
Datasets
2
Components
Laboratory
Qualified Praxis harmonization assessment

Adjustment required · high confidence

A methodological discontinuity falls inside the selected cycle span. Naive pooling of raw values across the flagged boundary is not recommended unless CDC/NCHS provides a defensible calibration or comparability procedure.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 1999-2000 → 2001-2002

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Apply CDC/NCHS comparability or calibration guidance where available. If equivalence is not established, preserve separate method periods or perform sensitivity analyses rather than naively pooling raw values.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • Total cholesterol (mg/dL)1999-2000 · 2001-2002
Cycle-by-cycle release history
  • 1999-2000: l13_2_r — Total cholesterol (mg/dL) — Cholesterol - Total, HDL, LDL & Triglycerides, Second Exam (Laboratory) — Note: RDC Only
  • 2001-2002: l13_2_b — Total cholesterol (mg/dL) — Cholesterol - Total, HDL, LDL & Triglycerides, Second Exam (Laboratory)
LB2TCSIAdjustment required

Total cholesterol (mmol/L)

Observed years
20002002
Release records
2
Datasets
2
Components
Laboratory
Qualified Praxis harmonization assessment

Adjustment required · high confidence

A methodological discontinuity falls inside the selected cycle span. Naive pooling of raw values across the flagged boundary is not recommended unless CDC/NCHS provides a defensible calibration or comparability procedure.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 1999-2000 → 2001-2002

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Apply CDC/NCHS comparability or calibration guidance where available. If equivalence is not established, preserve separate method periods or perform sensitivity analyses rather than naively pooling raw values.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • Total cholesterol (mmol/L)1999-2000 · 2001-2002
Cycle-by-cycle release history
  • 1999-2000: l13_2_r — Total cholesterol (mmol/L) — Cholesterol - Total, HDL, LDL & Triglycerides, Second Exam (Laboratory) — Note: RDC Only
  • 2001-2002: l13_2_b — Total cholesterol (mmol/L) — Cholesterol - Total, HDL, LDL & Triglycerides, Second Exam (Laboratory)
LB2THGEvidence developing

Mercury, total (ug/L)

Observed years
20012002
Release records
1
Datasets
1
Components
Laboratory
Qualified Praxis harmonization assessment

Evidence developing · low confidence

No normalized longitudinal change evidence is available for this variable. Absence of events must not be interpreted as proof of cross-cycle equivalence.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Variable names / labels over time
  • Mercury, total (ug/L)2001-2002
Cycle-by-cycle release history
  • 2001-2002: L06_2_B — Mercury, total (ug/L) — Cadmium, Lead, Total Mercury, Ferritin, Serum Folate, RBC Folate, Vitamin B12, Homocysteine, Methylmalonic acid, Cotinine - Blood, Second Exam (Laboratory)
LB2THGSIEvidence developing

Mercury, total (umol/L)

Observed years
20012002
Release records
1
Datasets
1
Components
Laboratory
Qualified Praxis harmonization assessment

Evidence developing · low confidence

No normalized longitudinal change evidence is available for this variable. Absence of events must not be interpreted as proof of cross-cycle equivalence.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Variable names / labels over time
  • Mercury, total (umol/L)2001-2002
Cycle-by-cycle release history
  • 2001-2002: L06_2_B — Mercury, total (umol/L) — Cadmium, Lead, Total Mercury, Ferritin, Serum Folate, RBC Folate, Vitamin B12, Homocysteine, Methylmalonic acid, Cotinine - Blood, Second Exam (Laboratory)
LB2TIBEvidence developing

TIBC (ug/dL)

Observed years
20002000
Release records
1
Datasets
1
Components
Laboratory
Qualified Praxis harmonization assessment

Evidence developing · low confidence

No normalized longitudinal change evidence is available for this variable. Absence of events must not be interpreted as proof of cross-cycle equivalence.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Variable names / labels over time
  • TIBC (ug/dL)1999-2000
Cycle-by-cycle release history
  • 1999-2000: L06_2_00 — TIBC (ug/dL) — Cadmium, Lead, Ferritin, Serum Folate, RBC Folate, Vitamin B12, Homocysteine, Methylmalonic acid, Cotinine & Other Selected Nutritional Biochemistries - Blood, Second Exam (Laboratory) — Note: RDC Only
LB2TIBSIEvidence developing

TIBC (umol/L)

Observed years
20002000
Release records
1
Datasets
1
Components
Laboratory
Qualified Praxis harmonization assessment

Evidence developing · low confidence

No normalized longitudinal change evidence is available for this variable. Absence of events must not be interpreted as proof of cross-cycle equivalence.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Variable names / labels over time
  • TIBC (umol/L)1999-2000
Cycle-by-cycle release history
  • 1999-2000: L06_2_00 — TIBC (umol/L) — Cadmium, Lead, Ferritin, Serum Folate, RBC Folate, Vitamin B12, Homocysteine, Methylmalonic acid, Cotinine & Other Selected Nutritional Biochemistries - Blood, Second Exam (Laboratory) — Note: RDC Only
LB2TRAdjustment required

Triglyceride (mg/dL)

Observed years
20002002
Release records
2
Datasets
2
Components
Laboratory
Qualified Praxis harmonization assessment

Adjustment required · high confidence

A methodological discontinuity falls inside the selected cycle span. Naive pooling of raw values across the flagged boundary is not recommended unless CDC/NCHS provides a defensible calibration or comparability procedure.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 1999-2000 → 2001-2002

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Apply CDC/NCHS comparability or calibration guidance where available. If equivalence is not established, preserve separate method periods or perform sensitivity analyses rather than naively pooling raw values.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • Triglyceride (mg/dL)1999-2000 · 2001-2002
Cycle-by-cycle release history
  • 1999-2000: l13_2_r — Triglyceride (mg/dL) — Cholesterol - Total, HDL, LDL & Triglycerides, Second Exam (Laboratory) — Note: RDC Only
  • 2001-2002: l13_2_b — Triglyceride (mg/dL) — Cholesterol - Total, HDL, LDL & Triglycerides, Second Exam (Laboratory)
LB2TRSIAdjustment required

Triglyceride (mmol/L)

Observed years
20002002
Release records
2
Datasets
2
Components
Laboratory
Qualified Praxis harmonization assessment

Adjustment required · high confidence

A methodological discontinuity falls inside the selected cycle span. Naive pooling of raw values across the flagged boundary is not recommended unless CDC/NCHS provides a defensible calibration or comparability procedure.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 1999-2000 → 2001-2002

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Apply CDC/NCHS comparability or calibration guidance where available. If equivalence is not established, preserve separate method periods or perform sensitivity analyses rather than naively pooling raw values.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • Triglyceride (mmol/L)1999-2000 · 2001-2002
Cycle-by-cycle release history
  • 1999-2000: l13_2_r — Triglyceride (mmol/L) — Cholesterol - Total, HDL, LDL & Triglycerides, Second Exam (Laboratory) — Note: RDC Only
  • 2001-2002: l13_2_b — Triglyceride (mmol/L) — Cholesterol - Total, HDL, LDL & Triglycerides, Second Exam (Laboratory)
LB2VARCompatible with harmonization

Varicella

Observed years
20002002
Release records
2
Datasets
2
Components
Laboratory
Qualified Praxis harmonization assessment

Compatible with harmonization · moderate confidence

No blocking method discontinuity is identified inside the selected cycle span, but one or more longitudinal changes require explicit harmonization conditions before pooling.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 1999-2000 → 2001-2002

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • Varicella1999-2000 · 2001-2002
Cycle-by-cycle release history
  • 1999-2000: L19_2_R — Varicella — Measles, Rubella, & Varicella, Second Exam (Laboratory) — Note: RDC Only
  • 2001-2002: L19_2_B — Varicella — Measles, Rubella, & Varicella, Second Exam (Laboratory)
LB2VIACompatible with harmonization

Vitamin A (ug/dL)

Observed years
20002002
Release records
3
Datasets
3
Components
Laboratory
Qualified Praxis harmonization assessment

Compatible with harmonization · moderate confidence

No blocking method discontinuity is identified inside the selected cycle span, but one or more longitudinal changes require explicit harmonization conditions before pooling.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 1999-2000 → 2001-2002

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • Vitamin A (ug/dL)1999-2000
  • Retinol(ug/dL)1999-2000 · 2001-2002
Cycle-by-cycle release history
  • 1999-2000: L06_2_00 — Vitamin A (ug/dL) — Cadmium, Lead, Ferritin, Serum Folate, RBC Folate, Vitamin B12, Homocysteine, Methylmalonic acid, Cotinine & Other Selected Nutritional Biochemistries - Blood, Second Exam (Laboratory) — Note: RDC Only
  • 1999-2000: VIT_2_R — Retinol(ug/dL) — Vitamin A & Vitamin E, Second Exam (Laboratory) — Note: RDC Only
  • 2001-2002: VIT_2_B — Retinol(ug/dL) — Vitamin A, Vitamin E, & Carotenoids, Second Exam (Laboratory)
LB2VIASICompatible with harmonization

Vitamin A (umol/L)

Observed years
20002002
Release records
3
Datasets
3
Components
Laboratory
Qualified Praxis harmonization assessment

Compatible with harmonization · moderate confidence

No blocking method discontinuity is identified inside the selected cycle span, but one or more longitudinal changes require explicit harmonization conditions before pooling.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 1999-2000 → 2001-2002

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • Vitamin A (umol/L)1999-2000
  • Retinol(umol/L)1999-2000 · 2001-2002
Cycle-by-cycle release history
  • 1999-2000: L06_2_00 — Vitamin A (umol/L) — Cadmium, Lead, Ferritin, Serum Folate, RBC Folate, Vitamin B12, Homocysteine, Methylmalonic acid, Cotinine & Other Selected Nutritional Biochemistries - Blood, Second Exam (Laboratory) — Note: RDC Only
  • 1999-2000: VIT_2_R — Retinol(umol/L) — Vitamin A & Vitamin E, Second Exam (Laboratory) — Note: RDC Only
  • 2001-2002: VIT_2_B — Retinol(umol/L) — Vitamin A, Vitamin E, & Carotenoids, Second Exam (Laboratory)
LB2VIDCompatible with harmonization

Vitamin D (ng/mL)

Observed years
20002002
Release records
2
Datasets
2
Components
Laboratory
Qualified Praxis harmonization assessment

Compatible with harmonization · moderate confidence

No blocking method discontinuity is identified inside the selected cycle span, but one or more longitudinal changes require explicit harmonization conditions before pooling.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 1999-2000 → 2001-2002

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Review the adjacent codebooks/methods. Keep this boundary as documentation variation unless source evidence confirms a substantive method or instrument change.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • Vitamin D (ng/mL)1999-2000 · 2001-2002
Cycle-by-cycle release history
LB2VIECompatible with harmonization

Vitamin E (ug/dL)

Observed years
20002002
Release records
3
Datasets
3
Components
Laboratory
Qualified Praxis harmonization assessment

Compatible with harmonization · moderate confidence

No blocking method discontinuity is identified inside the selected cycle span, but one or more longitudinal changes require explicit harmonization conditions before pooling.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 1999-2000 → 2001-2002

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • Vitamin E (ug/dL)1999-2000
  • alpha-tocopherol(ug/dL)1999-2000 · 2001-2002
Cycle-by-cycle release history
  • 1999-2000: L06_2_00 — Vitamin E (ug/dL) — Cadmium, Lead, Ferritin, Serum Folate, RBC Folate, Vitamin B12, Homocysteine, Methylmalonic acid, Cotinine & Other Selected Nutritional Biochemistries - Blood, Second Exam (Laboratory) — Note: RDC Only
  • 1999-2000: VIT_2_R — alpha-tocopherol(ug/dL) — Vitamin A & Vitamin E, Second Exam (Laboratory) — Note: RDC Only
  • 2001-2002: VIT_2_B — alpha-tocopherol(ug/dL) — Vitamin A, Vitamin E, & Carotenoids, Second Exam (Laboratory)
LB2VIESICompatible with harmonization

Vitamin E (umol/L)

Observed years
20002002
Release records
3
Datasets
3
Components
Laboratory
Qualified Praxis harmonization assessment

Compatible with harmonization · moderate confidence

No blocking method discontinuity is identified inside the selected cycle span, but one or more longitudinal changes require explicit harmonization conditions before pooling.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 1999-2000 → 2001-2002

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • Vitamin E (umol/L)1999-2000
  • alpha-tocopherol(umol/L)1999-2000 · 2001-2002
Cycle-by-cycle release history
  • 1999-2000: L06_2_00 — Vitamin E (umol/L) — Cadmium, Lead, Ferritin, Serum Folate, RBC Folate, Vitamin B12, Homocysteine, Methylmalonic acid, Cotinine & Other Selected Nutritional Biochemistries - Blood, Second Exam (Laboratory) — Note: RDC Only
  • 1999-2000: VIT_2_R — alpha-tocopherol(umol/L) — Vitamin A & Vitamin E, Second Exam (Laboratory) — Note: RDC Only
  • 2001-2002: VIT_2_B — alpha-tocopherol(umol/L) — Vitamin A, Vitamin E, & Carotenoids, Second Exam (Laboratory)
LB2WBCSICompatible with harmonization

White blood cell count (1000 cells/uL)

Observed years
20002002
Release records
2
Datasets
2
Components
Laboratory
Qualified Praxis harmonization assessment

Compatible with harmonization · moderate confidence

No blocking method discontinuity is identified inside the selected cycle span, but one or more longitudinal changes require explicit harmonization conditions before pooling.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 1999-2000 → 2001-2002

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • White blood cell count (1000 cells/uL)1999-2000 · 2001-2002
Cycle-by-cycle release history
  • 1999-2000: l25_2_r — White blood cell count (1000 cells/uL) — Complete Blood Count with 5-part Differential - Whole Blood, Second Exam (Laboratory) — Note: RDC Only
  • 2001-2002: l25_2_b — White blood cell count (1000 cells/uL) — Complete Blood Count with 5-part Differential - Whole Blood, Second Exam (Laboratory)
LBAMMT1Compatible with harmonization

Molecular Type 1

Observed years
20012004
Release records
2
Datasets
2
Components
Laboratory
Qualified Praxis harmonization assessment

Compatible with harmonization · moderate confidence

No blocking method discontinuity is identified inside the selected cycle span, but one or more longitudinal changes require explicit harmonization conditions before pooling.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 2001-2002 → 2003-2004

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Review the adjacent codebooks/methods. Keep this boundary as documentation variation unless source evidence confirms a substantive method or instrument change.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • Molecular Type 12001-2002 · 2003-2004
Cycle-by-cycle release history
  • 2001-2002: L35_B — Molecular Type 1 — Methicillin - Resistant Staphylococcus aureus (MRSA) (Laboratory)
  • 2003-2004: L35_C — Molecular Type 1 — Methicillin - Resistant Staphylococcus aureus (MRSA) (Laboratory)
LBAMMT2Compatible with harmonization

Molecular type 2

Observed years
20012004
Release records
2
Datasets
2
Components
Laboratory
Qualified Praxis harmonization assessment

Compatible with harmonization · moderate confidence

No blocking method discontinuity is identified inside the selected cycle span, but one or more longitudinal changes require explicit harmonization conditions before pooling.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 2001-2002 → 2003-2004

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Review the adjacent codebooks/methods. Keep this boundary as documentation variation unless source evidence confirms a substantive method or instrument change.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • Molecular type 22001-2002 · 2003-2004
Cycle-by-cycle release history
  • 2001-2002: L35_B — Molecular type 2 — Methicillin - Resistant Staphylococcus aureus (MRSA) (Laboratory)
  • 2003-2004: L35_C — Molecular type 2 — Methicillin - Resistant Staphylococcus aureus (MRSA) (Laboratory)
LBAVOCSDEvidence developing

The time (in minutes) between start time of wearing the badge and stop time of wearing the badge.

Observed years
19992000
Release records
1
Datasets
1
Components
Laboratory
Qualified Praxis harmonization assessment

Evidence developing · low confidence

No normalized longitudinal change evidence is available for this variable. Absence of events must not be interpreted as proof of cross-cycle equivalence.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Variable names / labels over time
  • The time (in minutes) between start time of wearing the badge and stop time of wearing the badge.1999-2000
Cycle-by-cycle release history
  • 1999-2000: LAB21 — The time (in minutes) between start time of wearing the badge and stop time of wearing the badge. — Volatile Organic Compounds (VOC) - Personal Exposure Badge (Laboratory)
LBC028Compatible with harmonization

PCB 28 (ng/g)

Observed years
20052016
Release records
6
Datasets
6
Components
Laboratory
Qualified Praxis harmonization assessment

Compatible with harmonization · moderate confidence

No blocking method discontinuity is identified inside the selected cycle span, but one or more longitudinal changes require explicit harmonization conditions before pooling.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 2005-2006 → 2007-2008 · 2007-2008 → 2009-2010 · 2009-2010 → 2011-2012 · 2011-2012 → 2013-2014 · 2013-2014 → 2015-2016

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Review the adjacent codebooks/methods. Keep this boundary as documentation variation unless source evidence confirms a substantive method or instrument change.
  • Confirm that the construct and coding are unchanged before pooling or recoding.
  • Select the weight appropriate to each cycle and subsample; when pooling cycles, construct the combined weight according to NHANES guidance rather than reusing a single-cycle weight unchanged.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • PCB 28 (ng/g)2005-2006 · 2007-2008
  • 2,4,4’-Trichlorobiphenyl (pg/g)2009-2010
  • 2,4,4'-Trichlorobiphenyl (pg/g)2011-2012 · 2013-2014 · 2015-2016
Cycle-by-cycle release history
  • 2005-2006: PCBPOL_D — PCB 28 (ng/g) — Non-dioxin-like Polychlorinated Biphenyls & Mono-ortho-substituted Polychlorinated Biphenyls - Pooled Samples (Laboratory)
  • 2007-2008: PCBPOL_E — PCB 28 (ng/g) — Non-dioxin-like Polychlorinated Biphenyls & Mono-ortho-substituted Polychlorinated Biphenyls - Pooled Samples (Laboratory)
  • 2009-2010: PCBPOL_F — 2,4,4’-Trichlorobiphenyl (pg/g) — Non-dioxin-like Polychlorinated Biphenyls & Mono-ortho-substituted Polychlorinated Biphenyls - Pooled Samples (Laboratory)
  • 2011-2012: PCBPOL_G — 2,4,4'-Trichlorobiphenyl (pg/g) — Non-dioxin-like Polychlorinated Biphenyls & Mono-ortho-substituted Polychlorinated Biphenyls - Pooled Samples (Laboratory)
  • 2013-2014: PCBPOL_H — 2,4,4'-Trichlorobiphenyl (pg/g) — Non-dioxin-like Polychlorinated Biphenyls & Mono-ortho-substituted Polychlorinated Biphenyls - Serum - Pooled Samples (Laboratory)
  • 2015-2016: PCBPOL_I — 2,4,4'-Trichlorobiphenyl (pg/g) — Non-dioxin-like Polychlorinated Biphenyls & Mono-ortho-substituted Polychlorinated Biphenyls - Pooled Samples (Laboratory)
LBC028LACompatible with harmonization

PCB 28 Lipid Adj (ng/g)

Observed years
20052016
Release records
6
Datasets
6
Components
Laboratory
Qualified Praxis harmonization assessment

Compatible with harmonization · moderate confidence

No blocking method discontinuity is identified inside the selected cycle span, but one or more longitudinal changes require explicit harmonization conditions before pooling.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 2005-2006 → 2007-2008 · 2007-2008 → 2009-2010 · 2009-2010 → 2011-2012 · 2011-2012 → 2013-2014 · 2013-2014 → 2015-2016

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Review the adjacent codebooks/methods. Keep this boundary as documentation variation unless source evidence confirms a substantive method or instrument change.
  • Select the weight appropriate to each cycle and subsample; when pooling cycles, construct the combined weight according to NHANES guidance rather than reusing a single-cycle weight unchanged.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • PCB 28 Lipid Adj (ng/g)2005-2006 · 2007-2008
  • 2,4,4’-Trichlorobiphenyl Lipid Adjusted2009-2010
  • 2,4,4'-Trichlorobiphenyl Lipid Adjusted2011-2012 · 2013-2014 · 2015-2016
Cycle-by-cycle release history
  • 2005-2006: PCBPOL_D — PCB 28 Lipid Adj (ng/g) — Non-dioxin-like Polychlorinated Biphenyls & Mono-ortho-substituted Polychlorinated Biphenyls - Pooled Samples (Laboratory)
  • 2007-2008: PCBPOL_E — PCB 28 Lipid Adj (ng/g) — Non-dioxin-like Polychlorinated Biphenyls & Mono-ortho-substituted Polychlorinated Biphenyls - Pooled Samples (Laboratory)
  • 2009-2010: PCBPOL_F — 2,4,4’-Trichlorobiphenyl Lipid Adjusted — Non-dioxin-like Polychlorinated Biphenyls & Mono-ortho-substituted Polychlorinated Biphenyls - Pooled Samples (Laboratory)
  • 2011-2012: PCBPOL_G — 2,4,4'-Trichlorobiphenyl Lipid Adjusted — Non-dioxin-like Polychlorinated Biphenyls & Mono-ortho-substituted Polychlorinated Biphenyls - Pooled Samples (Laboratory)
  • 2013-2014: PCBPOL_H — 2,4,4'-Trichlorobiphenyl Lipid Adjusted — Non-dioxin-like Polychlorinated Biphenyls & Mono-ortho-substituted Polychlorinated Biphenyls - Serum - Pooled Samples (Laboratory)
  • 2015-2016: PCBPOL_I — 2,4,4'-Trichlorobiphenyl Lipid Adjusted — Non-dioxin-like Polychlorinated Biphenyls & Mono-ortho-substituted Polychlorinated Biphenyls - Pooled Samples (Laboratory)
LBC044Compatible with harmonization

PCB 44 (ng/g)

Observed years
20052008
Release records
2
Datasets
2
Components
Laboratory
Qualified Praxis harmonization assessment

Compatible with harmonization · moderate confidence

No blocking method discontinuity is identified inside the selected cycle span, but one or more longitudinal changes require explicit harmonization conditions before pooling.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 2005-2006 → 2007-2008

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Review the adjacent codebooks/methods. Keep this boundary as documentation variation unless source evidence confirms a substantive method or instrument change.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • PCB 44 (ng/g)2005-2006 · 2007-2008
Cycle-by-cycle release history
  • 2005-2006: PCBPOL_D — PCB 44 (ng/g) — Non-dioxin-like Polychlorinated Biphenyls & Mono-ortho-substituted Polychlorinated Biphenyls - Pooled Samples (Laboratory)
  • 2007-2008: PCBPOL_E — PCB 44 (ng/g) — Non-dioxin-like Polychlorinated Biphenyls & Mono-ortho-substituted Polychlorinated Biphenyls - Pooled Samples (Laboratory)
LBC044LACompatible with harmonization

PCB 44 Lipid Adj (ng/g)

Observed years
20052008
Release records
2
Datasets
2
Components
Laboratory
Qualified Praxis harmonization assessment

Compatible with harmonization · moderate confidence

No blocking method discontinuity is identified inside the selected cycle span, but one or more longitudinal changes require explicit harmonization conditions before pooling.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 2005-2006 → 2007-2008

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Review the adjacent codebooks/methods. Keep this boundary as documentation variation unless source evidence confirms a substantive method or instrument change.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • PCB 44 Lipid Adj (ng/g)2005-2006 · 2007-2008
Cycle-by-cycle release history
  • 2005-2006: PCBPOL_D — PCB 44 Lipid Adj (ng/g) — Non-dioxin-like Polychlorinated Biphenyls & Mono-ortho-substituted Polychlorinated Biphenyls - Pooled Samples (Laboratory)
  • 2007-2008: PCBPOL_E — PCB 44 Lipid Adj (ng/g) — Non-dioxin-like Polychlorinated Biphenyls & Mono-ortho-substituted Polychlorinated Biphenyls - Pooled Samples (Laboratory)
LBC049Compatible with harmonization

PCB 49 (ng/g)

Observed years
20052008
Release records
2
Datasets
2
Components
Laboratory
Qualified Praxis harmonization assessment

Compatible with harmonization · moderate confidence

No blocking method discontinuity is identified inside the selected cycle span, but one or more longitudinal changes require explicit harmonization conditions before pooling.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 2005-2006 → 2007-2008

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Review the adjacent codebooks/methods. Keep this boundary as documentation variation unless source evidence confirms a substantive method or instrument change.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • PCB 49 (ng/g)2005-2006 · 2007-2008
Cycle-by-cycle release history
  • 2005-2006: PCBPOL_D — PCB 49 (ng/g) — Non-dioxin-like Polychlorinated Biphenyls & Mono-ortho-substituted Polychlorinated Biphenyls - Pooled Samples (Laboratory)
  • 2007-2008: PCBPOL_E — PCB 49 (ng/g) — Non-dioxin-like Polychlorinated Biphenyls & Mono-ortho-substituted Polychlorinated Biphenyls - Pooled Samples (Laboratory)
LBC049LACompatible with harmonization

PCB 49 Lipid Adj (ng/g)

Observed years
20052008
Release records
2
Datasets
2
Components
Laboratory
Qualified Praxis harmonization assessment

Compatible with harmonization · moderate confidence

No blocking method discontinuity is identified inside the selected cycle span, but one or more longitudinal changes require explicit harmonization conditions before pooling.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 2005-2006 → 2007-2008

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Review the adjacent codebooks/methods. Keep this boundary as documentation variation unless source evidence confirms a substantive method or instrument change.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • PCB 49 Lipid Adj (ng/g)2005-2006 · 2007-2008
Cycle-by-cycle release history
  • 2005-2006: PCBPOL_D — PCB 49 Lipid Adj (ng/g) — Non-dioxin-like Polychlorinated Biphenyls & Mono-ortho-substituted Polychlorinated Biphenyls - Pooled Samples (Laboratory)
  • 2007-2008: PCBPOL_E — PCB 49 Lipid Adj (ng/g) — Non-dioxin-like Polychlorinated Biphenyls & Mono-ortho-substituted Polychlorinated Biphenyls - Pooled Samples (Laboratory)
LBC052Compatible with harmonization

PCB 52 (ng/g)

Observed years
20052008
Release records
2
Datasets
2
Components
Laboratory
Qualified Praxis harmonization assessment

Compatible with harmonization · moderate confidence

No blocking method discontinuity is identified inside the selected cycle span, but one or more longitudinal changes require explicit harmonization conditions before pooling.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 2005-2006 → 2007-2008

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Review the adjacent codebooks/methods. Keep this boundary as documentation variation unless source evidence confirms a substantive method or instrument change.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • PCB 52 (ng/g)2005-2006 · 2007-2008
Cycle-by-cycle release history
  • 2005-2006: PCBPOL_D — PCB 52 (ng/g) — Non-dioxin-like Polychlorinated Biphenyls & Mono-ortho-substituted Polychlorinated Biphenyls - Pooled Samples (Laboratory)
  • 2007-2008: PCBPOL_E — PCB 52 (ng/g) — Non-dioxin-like Polychlorinated Biphenyls & Mono-ortho-substituted Polychlorinated Biphenyls - Pooled Samples (Laboratory)
LBC052LACompatible with harmonization

PCB 52 Lipid Adj (ng/g)

Observed years
20052008
Release records
2
Datasets
2
Components
Laboratory
Qualified Praxis harmonization assessment

Compatible with harmonization · moderate confidence

No blocking method discontinuity is identified inside the selected cycle span, but one or more longitudinal changes require explicit harmonization conditions before pooling.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 2005-2006 → 2007-2008

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Review the adjacent codebooks/methods. Keep this boundary as documentation variation unless source evidence confirms a substantive method or instrument change.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • PCB 52 Lipid Adj (ng/g)2005-2006 · 2007-2008
Cycle-by-cycle release history
  • 2005-2006: PCBPOL_D — PCB 52 Lipid Adj (ng/g) — Non-dioxin-like Polychlorinated Biphenyls & Mono-ortho-substituted Polychlorinated Biphenyls - Pooled Samples (Laboratory)
  • 2007-2008: PCBPOL_E — PCB 52 Lipid Adj (ng/g) — Non-dioxin-like Polychlorinated Biphenyls & Mono-ortho-substituted Polychlorinated Biphenyls - Pooled Samples (Laboratory)
LBC066Compatible with harmonization

PCB 66 (ng/g)

Observed years
20052016
Release records
6
Datasets
6
Components
Laboratory
Qualified Praxis harmonization assessment

Compatible with harmonization · moderate confidence

No blocking method discontinuity is identified inside the selected cycle span, but one or more longitudinal changes require explicit harmonization conditions before pooling.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 2005-2006 → 2007-2008 · 2007-2008 → 2009-2010 · 2009-2010 → 2011-2012 · 2011-2012 → 2013-2014 · 2013-2014 → 2015-2016

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Review the adjacent codebooks/methods. Keep this boundary as documentation variation unless source evidence confirms a substantive method or instrument change.
  • Confirm that the construct and coding are unchanged before pooling or recoding.
  • Select the weight appropriate to each cycle and subsample; when pooling cycles, construct the combined weight according to NHANES guidance rather than reusing a single-cycle weight unchanged.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • PCB 66 (ng/g)2005-2006 · 2007-2008
  • 2,3’,4,4’-Tetrachlorobiphenyl (pg/g)2009-2010
  • 2,3',4,4'-Tetrachlorobiphenyl (pg/g)2011-2012 · 2013-2014 · 2015-2016
Cycle-by-cycle release history
  • 2005-2006: PCBPOL_D — PCB 66 (ng/g) — Non-dioxin-like Polychlorinated Biphenyls & Mono-ortho-substituted Polychlorinated Biphenyls - Pooled Samples (Laboratory)
  • 2007-2008: PCBPOL_E — PCB 66 (ng/g) — Non-dioxin-like Polychlorinated Biphenyls & Mono-ortho-substituted Polychlorinated Biphenyls - Pooled Samples (Laboratory)
  • 2009-2010: PCBPOL_F — 2,3’,4,4’-Tetrachlorobiphenyl (pg/g) — Non-dioxin-like Polychlorinated Biphenyls & Mono-ortho-substituted Polychlorinated Biphenyls - Pooled Samples (Laboratory)
  • 2011-2012: PCBPOL_G — 2,3',4,4'-Tetrachlorobiphenyl (pg/g) — Non-dioxin-like Polychlorinated Biphenyls & Mono-ortho-substituted Polychlorinated Biphenyls - Pooled Samples (Laboratory)
  • 2013-2014: PCBPOL_H — 2,3',4,4'-Tetrachlorobiphenyl (pg/g) — Non-dioxin-like Polychlorinated Biphenyls & Mono-ortho-substituted Polychlorinated Biphenyls - Serum - Pooled Samples (Laboratory)
  • 2015-2016: PCBPOL_I — 2,3',4,4'-Tetrachlorobiphenyl (pg/g) — Non-dioxin-like Polychlorinated Biphenyls & Mono-ortho-substituted Polychlorinated Biphenyls - Pooled Samples (Laboratory)
LBC066LACompatible with harmonization

PCB 66 Lipid Adj (ng/g)

Observed years
20052016
Release records
6
Datasets
6
Components
Laboratory
Qualified Praxis harmonization assessment

Compatible with harmonization · moderate confidence

No blocking method discontinuity is identified inside the selected cycle span, but one or more longitudinal changes require explicit harmonization conditions before pooling.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 2005-2006 → 2007-2008 · 2007-2008 → 2009-2010 · 2009-2010 → 2011-2012 · 2011-2012 → 2013-2014 · 2013-2014 → 2015-2016

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Review the adjacent codebooks/methods. Keep this boundary as documentation variation unless source evidence confirms a substantive method or instrument change.
  • Select the weight appropriate to each cycle and subsample; when pooling cycles, construct the combined weight according to NHANES guidance rather than reusing a single-cycle weight unchanged.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • PCB 66 Lipid Adj (ng/g)2005-2006 · 2007-2008
  • 2,3’,4,4’-Tetrachlorobiphenyl Lipid Adjusted (ng/g)2009-2010
  • 2,3',4,4'-Tetrachlorobiphenyl Lipid Adjusted (ng/g)2011-2012 · 2013-2014 · 2015-2016
Cycle-by-cycle release history
  • 2005-2006: PCBPOL_D — PCB 66 Lipid Adj (ng/g) — Non-dioxin-like Polychlorinated Biphenyls & Mono-ortho-substituted Polychlorinated Biphenyls - Pooled Samples (Laboratory)
  • 2007-2008: PCBPOL_E — PCB 66 Lipid Adj (ng/g) — Non-dioxin-like Polychlorinated Biphenyls & Mono-ortho-substituted Polychlorinated Biphenyls - Pooled Samples (Laboratory)
  • 2009-2010: PCBPOL_F — 2,3’,4,4’-Tetrachlorobiphenyl Lipid Adjusted (ng/g) — Non-dioxin-like Polychlorinated Biphenyls & Mono-ortho-substituted Polychlorinated Biphenyls - Pooled Samples (Laboratory)
  • 2011-2012: PCBPOL_G — 2,3',4,4'-Tetrachlorobiphenyl Lipid Adjusted (ng/g) — Non-dioxin-like Polychlorinated Biphenyls & Mono-ortho-substituted Polychlorinated Biphenyls - Pooled Samples (Laboratory)
  • 2013-2014: PCBPOL_H — 2,3',4,4'-Tetrachlorobiphenyl Lipid Adjusted (ng/g) — Non-dioxin-like Polychlorinated Biphenyls & Mono-ortho-substituted Polychlorinated Biphenyls - Serum - Pooled Samples (Laboratory)
  • 2015-2016: PCBPOL_I — 2,3',4,4'-Tetrachlorobiphenyl Lipid Adjusted (ng/g) — Non-dioxin-like Polychlorinated Biphenyls & Mono-ortho-substituted Polychlorinated Biphenyls - Pooled Samples (Laboratory)
LBC074Compatible with harmonization

PCB 74 (ng/g)

Observed years
20052016
Release records
6
Datasets
6
Components
Laboratory
Qualified Praxis harmonization assessment

Compatible with harmonization · moderate confidence

No blocking method discontinuity is identified inside the selected cycle span, but one or more longitudinal changes require explicit harmonization conditions before pooling.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 2005-2006 → 2007-2008 · 2007-2008 → 2009-2010 · 2009-2010 → 2011-2012 · 2011-2012 → 2013-2014 · 2013-2014 → 2015-2016

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Review the adjacent codebooks/methods. Keep this boundary as documentation variation unless source evidence confirms a substantive method or instrument change.
  • Confirm that the construct and coding are unchanged before pooling or recoding.
  • Select the weight appropriate to each cycle and subsample; when pooling cycles, construct the combined weight according to NHANES guidance rather than reusing a single-cycle weight unchanged.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • PCB 74 (ng/g)2005-2006 · 2007-2008
  • 2,4,4’,5-Tetrachlorobiphenyl (pg/g)2009-2010
  • 2,4,4',5-Tetrachlorobiphenyl (pg/g)2011-2012 · 2013-2014 · 2015-2016
Cycle-by-cycle release history
  • 2005-2006: PCBPOL_D — PCB 74 (ng/g) — Non-dioxin-like Polychlorinated Biphenyls & Mono-ortho-substituted Polychlorinated Biphenyls - Pooled Samples (Laboratory)
  • 2007-2008: PCBPOL_E — PCB 74 (ng/g) — Non-dioxin-like Polychlorinated Biphenyls & Mono-ortho-substituted Polychlorinated Biphenyls - Pooled Samples (Laboratory)
  • 2009-2010: PCBPOL_F — 2,4,4’,5-Tetrachlorobiphenyl (pg/g) — Non-dioxin-like Polychlorinated Biphenyls & Mono-ortho-substituted Polychlorinated Biphenyls - Pooled Samples (Laboratory)
  • 2011-2012: PCBPOL_G — 2,4,4',5-Tetrachlorobiphenyl (pg/g) — Non-dioxin-like Polychlorinated Biphenyls & Mono-ortho-substituted Polychlorinated Biphenyls - Pooled Samples (Laboratory)
  • 2013-2014: PCBPOL_H — 2,4,4',5-Tetrachlorobiphenyl (pg/g) — Non-dioxin-like Polychlorinated Biphenyls & Mono-ortho-substituted Polychlorinated Biphenyls - Serum - Pooled Samples (Laboratory)
  • 2015-2016: PCBPOL_I — 2,4,4',5-Tetrachlorobiphenyl (pg/g) — Non-dioxin-like Polychlorinated Biphenyls & Mono-ortho-substituted Polychlorinated Biphenyls - Pooled Samples (Laboratory)
LBC074LACompatible with harmonization

PCB 74 Lipid Adj (ng/g)

Observed years
20052016
Release records
6
Datasets
6
Components
Laboratory
Qualified Praxis harmonization assessment

Compatible with harmonization · moderate confidence

No blocking method discontinuity is identified inside the selected cycle span, but one or more longitudinal changes require explicit harmonization conditions before pooling.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 2005-2006 → 2007-2008 · 2007-2008 → 2009-2010 · 2009-2010 → 2011-2012 · 2011-2012 → 2013-2014 · 2013-2014 → 2015-2016

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Review the adjacent codebooks/methods. Keep this boundary as documentation variation unless source evidence confirms a substantive method or instrument change.
  • Select the weight appropriate to each cycle and subsample; when pooling cycles, construct the combined weight according to NHANES guidance rather than reusing a single-cycle weight unchanged.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • PCB 74 Lipid Adj (ng/g)2005-2006 · 2007-2008
  • 2,4,4’,5-Tetrachlorobiphenyl Lipid Adjusted (ng/g)2009-2010
  • 2,4,4',5-Tetrachlorobiphenyl Lipid Adjusted (ng/g)2011-2012 · 2013-2014 · 2015-2016
Cycle-by-cycle release history
  • 2005-2006: PCBPOL_D — PCB 74 Lipid Adj (ng/g) — Non-dioxin-like Polychlorinated Biphenyls & Mono-ortho-substituted Polychlorinated Biphenyls - Pooled Samples (Laboratory)
  • 2007-2008: PCBPOL_E — PCB 74 Lipid Adj (ng/g) — Non-dioxin-like Polychlorinated Biphenyls & Mono-ortho-substituted Polychlorinated Biphenyls - Pooled Samples (Laboratory)
  • 2009-2010: PCBPOL_F — 2,4,4’,5-Tetrachlorobiphenyl Lipid Adjusted (ng/g) — Non-dioxin-like Polychlorinated Biphenyls & Mono-ortho-substituted Polychlorinated Biphenyls - Pooled Samples (Laboratory)
  • 2011-2012: PCBPOL_G — 2,4,4',5-Tetrachlorobiphenyl Lipid Adjusted (ng/g) — Non-dioxin-like Polychlorinated Biphenyls & Mono-ortho-substituted Polychlorinated Biphenyls - Pooled Samples (Laboratory)
  • 2013-2014: PCBPOL_H — 2,4,4',5-Tetrachlorobiphenyl Lipid Adjusted (ng/g) — Non-dioxin-like Polychlorinated Biphenyls & Mono-ortho-substituted Polychlorinated Biphenyls - Serum - Pooled Samples (Laboratory)
  • 2015-2016: PCBPOL_I — 2,4,4',5-Tetrachlorobiphenyl Lipid Adjusted (ng/g) — Non-dioxin-like Polychlorinated Biphenyls & Mono-ortho-substituted Polychlorinated Biphenyls - Pooled Samples (Laboratory)
LBC087Compatible with harmonization

PCB 87 (ng/g)

Observed years
20052008
Release records
2
Datasets
2
Components
Laboratory
Qualified Praxis harmonization assessment

Compatible with harmonization · moderate confidence

No blocking method discontinuity is identified inside the selected cycle span, but one or more longitudinal changes require explicit harmonization conditions before pooling.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 2005-2006 → 2007-2008

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Review the adjacent codebooks/methods. Keep this boundary as documentation variation unless source evidence confirms a substantive method or instrument change.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • PCB 87 (ng/g)2005-2006 · 2007-2008
Cycle-by-cycle release history
  • 2005-2006: PCBPOL_D — PCB 87 (ng/g) — Non-dioxin-like Polychlorinated Biphenyls & Mono-ortho-substituted Polychlorinated Biphenyls - Pooled Samples (Laboratory)
  • 2007-2008: PCBPOL_E — PCB 87 (ng/g) — Non-dioxin-like Polychlorinated Biphenyls & Mono-ortho-substituted Polychlorinated Biphenyls - Pooled Samples (Laboratory)
LBC087LACompatible with harmonization

PCB 87 Lipid Adj (ng/g)

Observed years
20052008
Release records
2
Datasets
2
Components
Laboratory
Qualified Praxis harmonization assessment

Compatible with harmonization · moderate confidence

No blocking method discontinuity is identified inside the selected cycle span, but one or more longitudinal changes require explicit harmonization conditions before pooling.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 2005-2006 → 2007-2008

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Review the adjacent codebooks/methods. Keep this boundary as documentation variation unless source evidence confirms a substantive method or instrument change.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • PCB 87 Lipid Adj (ng/g)2005-2006 · 2007-2008
Cycle-by-cycle release history
  • 2005-2006: PCBPOL_D — PCB 87 Lipid Adj (ng/g) — Non-dioxin-like Polychlorinated Biphenyls & Mono-ortho-substituted Polychlorinated Biphenyls - Pooled Samples (Laboratory)
  • 2007-2008: PCBPOL_E — PCB 87 Lipid Adj (ng/g) — Non-dioxin-like Polychlorinated Biphenyls & Mono-ortho-substituted Polychlorinated Biphenyls - Pooled Samples (Laboratory)
LBC099Compatible with harmonization

PCB 99 (ng/g)

Observed years
20052016
Release records
6
Datasets
6
Components
Laboratory
Qualified Praxis harmonization assessment

Compatible with harmonization · moderate confidence

No blocking method discontinuity is identified inside the selected cycle span, but one or more longitudinal changes require explicit harmonization conditions before pooling.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 2005-2006 → 2007-2008 · 2007-2008 → 2009-2010 · 2009-2010 → 2011-2012 · 2011-2012 → 2013-2014 · 2013-2014 → 2015-2016

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Review the adjacent codebooks/methods. Keep this boundary as documentation variation unless source evidence confirms a substantive method or instrument change.
  • Confirm that the construct and coding are unchanged before pooling or recoding.
  • Select the weight appropriate to each cycle and subsample; when pooling cycles, construct the combined weight according to NHANES guidance rather than reusing a single-cycle weight unchanged.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • PCB 99 (ng/g)2005-2006 · 2007-2008
  • 2,2’,4,4’,5-Pentachlorobiphenyl (pg/g)2009-2010
  • 2,2',4,4',5-Pentachlorobiphenyl (pg/g)2011-2012 · 2013-2014 · 2015-2016
Cycle-by-cycle release history
  • 2005-2006: PCBPOL_D — PCB 99 (ng/g) — Non-dioxin-like Polychlorinated Biphenyls & Mono-ortho-substituted Polychlorinated Biphenyls - Pooled Samples (Laboratory)
  • 2007-2008: PCBPOL_E — PCB 99 (ng/g) — Non-dioxin-like Polychlorinated Biphenyls & Mono-ortho-substituted Polychlorinated Biphenyls - Pooled Samples (Laboratory)
  • 2009-2010: PCBPOL_F — 2,2’,4,4’,5-Pentachlorobiphenyl (pg/g) — Non-dioxin-like Polychlorinated Biphenyls & Mono-ortho-substituted Polychlorinated Biphenyls - Pooled Samples (Laboratory)
  • 2011-2012: PCBPOL_G — 2,2',4,4',5-Pentachlorobiphenyl (pg/g) — Non-dioxin-like Polychlorinated Biphenyls & Mono-ortho-substituted Polychlorinated Biphenyls - Pooled Samples (Laboratory)
  • 2013-2014: PCBPOL_H — 2,2',4,4',5-Pentachlorobiphenyl (pg/g) — Non-dioxin-like Polychlorinated Biphenyls & Mono-ortho-substituted Polychlorinated Biphenyls - Serum - Pooled Samples (Laboratory)
  • 2015-2016: PCBPOL_I — 2,2',4,4',5-Pentachlorobiphenyl (pg/g) — Non-dioxin-like Polychlorinated Biphenyls & Mono-ortho-substituted Polychlorinated Biphenyls - Pooled Samples (Laboratory)
LBC099LACompatible with harmonization

PCB 99 Lipid Adj (ng/g)

Observed years
20052016
Release records
6
Datasets
6
Components
Laboratory
Qualified Praxis harmonization assessment

Compatible with harmonization · moderate confidence

No blocking method discontinuity is identified inside the selected cycle span, but one or more longitudinal changes require explicit harmonization conditions before pooling.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 2005-2006 → 2007-2008 · 2007-2008 → 2009-2010 · 2009-2010 → 2011-2012 · 2011-2012 → 2013-2014 · 2013-2014 → 2015-2016

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Review the adjacent codebooks/methods. Keep this boundary as documentation variation unless source evidence confirms a substantive method or instrument change.
  • Select the weight appropriate to each cycle and subsample; when pooling cycles, construct the combined weight according to NHANES guidance rather than reusing a single-cycle weight unchanged.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • PCB 99 Lipid Adj (ng/g)2005-2006 · 2007-2008
  • 2,2’,4,4’,5-Pentachlorobiphenyl Lipid Adjusted(ng/g)2009-2010
  • 2,2',4,4',5-Pentachlorobiphenyl Lipid Adjusted(ng/g)2011-2012 · 2013-2014 · 2015-2016
Cycle-by-cycle release history
  • 2005-2006: PCBPOL_D — PCB 99 Lipid Adj (ng/g) — Non-dioxin-like Polychlorinated Biphenyls & Mono-ortho-substituted Polychlorinated Biphenyls - Pooled Samples (Laboratory)
  • 2007-2008: PCBPOL_E — PCB 99 Lipid Adj (ng/g) — Non-dioxin-like Polychlorinated Biphenyls & Mono-ortho-substituted Polychlorinated Biphenyls - Pooled Samples (Laboratory)
  • 2009-2010: PCBPOL_F — 2,2’,4,4’,5-Pentachlorobiphenyl Lipid Adjusted(ng/g) — Non-dioxin-like Polychlorinated Biphenyls & Mono-ortho-substituted Polychlorinated Biphenyls - Pooled Samples (Laboratory)
  • 2011-2012: PCBPOL_G — 2,2',4,4',5-Pentachlorobiphenyl Lipid Adjusted(ng/g) — Non-dioxin-like Polychlorinated Biphenyls & Mono-ortho-substituted Polychlorinated Biphenyls - Pooled Samples (Laboratory)
  • 2013-2014: PCBPOL_H — 2,2',4,4',5-Pentachlorobiphenyl Lipid Adjusted(ng/g) — Non-dioxin-like Polychlorinated Biphenyls & Mono-ortho-substituted Polychlorinated Biphenyls - Serum - Pooled Samples (Laboratory)
  • 2015-2016: PCBPOL_I — 2,2',4,4',5-Pentachlorobiphenyl Lipid Adjusted(ng/g) — Non-dioxin-like Polychlorinated Biphenyls & Mono-ortho-substituted Polychlorinated Biphenyls - Pooled Samples (Laboratory)
LBC101Compatible with harmonization

PCB 101 (ng/g)

Observed years
20052008
Release records
2
Datasets
2
Components
Laboratory
Qualified Praxis harmonization assessment

Compatible with harmonization · moderate confidence

No blocking method discontinuity is identified inside the selected cycle span, but one or more longitudinal changes require explicit harmonization conditions before pooling.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 2005-2006 → 2007-2008

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Review the adjacent codebooks/methods. Keep this boundary as documentation variation unless source evidence confirms a substantive method or instrument change.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • PCB 101 (ng/g)2005-2006 · 2007-2008
Cycle-by-cycle release history
  • 2005-2006: PCBPOL_D — PCB 101 (ng/g) — Non-dioxin-like Polychlorinated Biphenyls & Mono-ortho-substituted Polychlorinated Biphenyls - Pooled Samples (Laboratory)
  • 2007-2008: PCBPOL_E — PCB 101 (ng/g) — Non-dioxin-like Polychlorinated Biphenyls & Mono-ortho-substituted Polychlorinated Biphenyls - Pooled Samples (Laboratory)
LBC101LACompatible with harmonization

PCB 101 Lipid Adj (ng/g)

Observed years
20052008
Release records
2
Datasets
2
Components
Laboratory
Qualified Praxis harmonization assessment

Compatible with harmonization · moderate confidence

No blocking method discontinuity is identified inside the selected cycle span, but one or more longitudinal changes require explicit harmonization conditions before pooling.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 2005-2006 → 2007-2008

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Review the adjacent codebooks/methods. Keep this boundary as documentation variation unless source evidence confirms a substantive method or instrument change.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • PCB 101 Lipid Adj (ng/g)2005-2006 · 2007-2008
Cycle-by-cycle release history
  • 2005-2006: PCBPOL_D — PCB 101 Lipid Adj (ng/g) — Non-dioxin-like Polychlorinated Biphenyls & Mono-ortho-substituted Polychlorinated Biphenyls - Pooled Samples (Laboratory)
  • 2007-2008: PCBPOL_E — PCB 101 Lipid Adj (ng/g) — Non-dioxin-like Polychlorinated Biphenyls & Mono-ortho-substituted Polychlorinated Biphenyls - Pooled Samples (Laboratory)
LBC105Compatible with harmonization

PCB 105 (ng/g)

Observed years
20052016
Release records
6
Datasets
6
Components
Laboratory
Qualified Praxis harmonization assessment

Compatible with harmonization · moderate confidence

No blocking method discontinuity is identified inside the selected cycle span, but one or more longitudinal changes require explicit harmonization conditions before pooling.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 2005-2006 → 2007-2008 · 2007-2008 → 2009-2010 · 2009-2010 → 2011-2012 · 2011-2012 → 2013-2014 · 2013-2014 → 2015-2016

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Review the adjacent codebooks/methods. Keep this boundary as documentation variation unless source evidence confirms a substantive method or instrument change.
  • Confirm that the construct and coding are unchanged before pooling or recoding.
  • Select the weight appropriate to each cycle and subsample; when pooling cycles, construct the combined weight according to NHANES guidance rather than reusing a single-cycle weight unchanged.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • PCB 105 (ng/g)2005-2006 · 2007-2008
  • 2,3,3’,4,4’-Pentachlorobiphenyl (pg/g)2009-2010
  • 2,3,3',4,4'-Pentachlorobiphenyl (pg/g)2011-2012 · 2013-2014 · 2015-2016
Cycle-by-cycle release history
  • 2005-2006: PCBPOL_D — PCB 105 (ng/g) — Non-dioxin-like Polychlorinated Biphenyls & Mono-ortho-substituted Polychlorinated Biphenyls - Pooled Samples (Laboratory)
  • 2007-2008: PCBPOL_E — PCB 105 (ng/g) — Non-dioxin-like Polychlorinated Biphenyls & Mono-ortho-substituted Polychlorinated Biphenyls - Pooled Samples (Laboratory)
  • 2009-2010: PCBPOL_F — 2,3,3’,4,4’-Pentachlorobiphenyl (pg/g) — Non-dioxin-like Polychlorinated Biphenyls & Mono-ortho-substituted Polychlorinated Biphenyls - Pooled Samples (Laboratory)
  • 2011-2012: PCBPOL_G — 2,3,3',4,4'-Pentachlorobiphenyl (pg/g) — Non-dioxin-like Polychlorinated Biphenyls & Mono-ortho-substituted Polychlorinated Biphenyls - Pooled Samples (Laboratory)
  • 2013-2014: PCBPOL_H — 2,3,3',4,4'-Pentachlorobiphenyl (pg/g) — Non-dioxin-like Polychlorinated Biphenyls & Mono-ortho-substituted Polychlorinated Biphenyls - Serum - Pooled Samples (Laboratory)
  • 2015-2016: PCBPOL_I — 2,3,3',4,4'-Pentachlorobiphenyl (pg/g) — Non-dioxin-like Polychlorinated Biphenyls & Mono-ortho-substituted Polychlorinated Biphenyls - Pooled Samples (Laboratory)
LBC105LACompatible with harmonization

PCB 105 Lipid Adj (ng/g)

Observed years
20052016
Release records
6
Datasets
6
Components
Laboratory
Qualified Praxis harmonization assessment

Compatible with harmonization · moderate confidence

No blocking method discontinuity is identified inside the selected cycle span, but one or more longitudinal changes require explicit harmonization conditions before pooling.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 2005-2006 → 2007-2008 · 2007-2008 → 2009-2010 · 2009-2010 → 2011-2012 · 2011-2012 → 2013-2014 · 2013-2014 → 2015-2016

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Review the adjacent codebooks/methods. Keep this boundary as documentation variation unless source evidence confirms a substantive method or instrument change.
  • Select the weight appropriate to each cycle and subsample; when pooling cycles, construct the combined weight according to NHANES guidance rather than reusing a single-cycle weight unchanged.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • PCB 105 Lipid Adj (ng/g)2005-2006 · 2007-2008
  • 2,3,3’,4,4’-Pentachlorobiphenyl Lipid Adjusted (ng/g)2009-2010
  • 2,3,3',4,4'-Pentachlorobiphenyl Lipid Adjusted (ng/g)2011-2012 · 2013-2014 · 2015-2016
Cycle-by-cycle release history
  • 2005-2006: PCBPOL_D — PCB 105 Lipid Adj (ng/g) — Non-dioxin-like Polychlorinated Biphenyls & Mono-ortho-substituted Polychlorinated Biphenyls - Pooled Samples (Laboratory)
  • 2007-2008: PCBPOL_E — PCB 105 Lipid Adj (ng/g) — Non-dioxin-like Polychlorinated Biphenyls & Mono-ortho-substituted Polychlorinated Biphenyls - Pooled Samples (Laboratory)
  • 2009-2010: PCBPOL_F — 2,3,3’,4,4’-Pentachlorobiphenyl Lipid Adjusted (ng/g) — Non-dioxin-like Polychlorinated Biphenyls & Mono-ortho-substituted Polychlorinated Biphenyls - Pooled Samples (Laboratory)
  • 2011-2012: PCBPOL_G — 2,3,3',4,4'-Pentachlorobiphenyl Lipid Adjusted (ng/g) — Non-dioxin-like Polychlorinated Biphenyls & Mono-ortho-substituted Polychlorinated Biphenyls - Pooled Samples (Laboratory)
  • 2013-2014: PCBPOL_H — 2,3,3',4,4'-Pentachlorobiphenyl Lipid Adjusted (ng/g) — Non-dioxin-like Polychlorinated Biphenyls & Mono-ortho-substituted Polychlorinated Biphenyls - Serum - Pooled Samples (Laboratory)
  • 2015-2016: PCBPOL_I — 2,3,3',4,4'-Pentachlorobiphenyl Lipid Adjusted (ng/g) — Non-dioxin-like Polychlorinated Biphenyls & Mono-ortho-substituted Polychlorinated Biphenyls - Pooled Samples (Laboratory)
LBC110Compatible with harmonization

PCB 110 (ng/g)

Observed years
20052008
Release records
2
Datasets
2
Components
Laboratory
Qualified Praxis harmonization assessment

Compatible with harmonization · moderate confidence

No blocking method discontinuity is identified inside the selected cycle span, but one or more longitudinal changes require explicit harmonization conditions before pooling.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 2005-2006 → 2007-2008

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Review the adjacent codebooks/methods. Keep this boundary as documentation variation unless source evidence confirms a substantive method or instrument change.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • PCB 110 (ng/g)2005-2006 · 2007-2008
Cycle-by-cycle release history
  • 2005-2006: PCBPOL_D — PCB 110 (ng/g) — Non-dioxin-like Polychlorinated Biphenyls & Mono-ortho-substituted Polychlorinated Biphenyls - Pooled Samples (Laboratory)
  • 2007-2008: PCBPOL_E — PCB 110 (ng/g) — Non-dioxin-like Polychlorinated Biphenyls & Mono-ortho-substituted Polychlorinated Biphenyls - Pooled Samples (Laboratory)
LBC110LACompatible with harmonization

PCB 110 Lipid Adj (ng/g)

Observed years
20052008
Release records
2
Datasets
2
Components
Laboratory
Qualified Praxis harmonization assessment

Compatible with harmonization · moderate confidence

No blocking method discontinuity is identified inside the selected cycle span, but one or more longitudinal changes require explicit harmonization conditions before pooling.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 2005-2006 → 2007-2008

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Review the adjacent codebooks/methods. Keep this boundary as documentation variation unless source evidence confirms a substantive method or instrument change.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • PCB 110 Lipid Adj (ng/g)2005-2006 · 2007-2008
Cycle-by-cycle release history
  • 2005-2006: PCBPOL_D — PCB 110 Lipid Adj (ng/g) — Non-dioxin-like Polychlorinated Biphenyls & Mono-ortho-substituted Polychlorinated Biphenyls - Pooled Samples (Laboratory)
  • 2007-2008: PCBPOL_E — PCB 110 Lipid Adj (ng/g) — Non-dioxin-like Polychlorinated Biphenyls & Mono-ortho-substituted Polychlorinated Biphenyls - Pooled Samples (Laboratory)
LBC114Compatible with harmonization

PCB 114 (ng/g)

Observed years
20052016
Release records
6
Datasets
6
Components
Laboratory
Qualified Praxis harmonization assessment

Compatible with harmonization · moderate confidence

No blocking method discontinuity is identified inside the selected cycle span, but one or more longitudinal changes require explicit harmonization conditions before pooling.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 2005-2006 → 2007-2008 · 2007-2008 → 2009-2010 · 2009-2010 → 2011-2012 · 2011-2012 → 2013-2014 · 2013-2014 → 2015-2016

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Review the adjacent codebooks/methods. Keep this boundary as documentation variation unless source evidence confirms a substantive method or instrument change.
  • Confirm that the construct and coding are unchanged before pooling or recoding.
  • Select the weight appropriate to each cycle and subsample; when pooling cycles, construct the combined weight according to NHANES guidance rather than reusing a single-cycle weight unchanged.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • PCB 114 (ng/g)2005-2006 · 2007-2008
  • 2,3,4,4',5-Pentachlorobiphenyl (pg/g)2009-2010 · 2011-2012 · 2013-2014 · 2015-2016
Cycle-by-cycle release history
  • 2005-2006: PCBPOL_D — PCB 114 (ng/g) — Non-dioxin-like Polychlorinated Biphenyls & Mono-ortho-substituted Polychlorinated Biphenyls - Pooled Samples (Laboratory)
  • 2007-2008: PCBPOL_E — PCB 114 (ng/g) — Non-dioxin-like Polychlorinated Biphenyls & Mono-ortho-substituted Polychlorinated Biphenyls - Pooled Samples (Laboratory)
  • 2009-2010: PCBPOL_F — 2,3,4,4',5-Pentachlorobiphenyl (pg/g) — Non-dioxin-like Polychlorinated Biphenyls & Mono-ortho-substituted Polychlorinated Biphenyls - Pooled Samples (Laboratory)
  • 2011-2012: PCBPOL_G — 2,3,4,4',5-Pentachlorobiphenyl (pg/g) — Non-dioxin-like Polychlorinated Biphenyls & Mono-ortho-substituted Polychlorinated Biphenyls - Pooled Samples (Laboratory)
  • 2013-2014: PCBPOL_H — 2,3,4,4',5-Pentachlorobiphenyl (pg/g) — Non-dioxin-like Polychlorinated Biphenyls & Mono-ortho-substituted Polychlorinated Biphenyls - Serum - Pooled Samples (Laboratory)
  • 2015-2016: PCBPOL_I — 2,3,4,4',5-Pentachlorobiphenyl (pg/g) — Non-dioxin-like Polychlorinated Biphenyls & Mono-ortho-substituted Polychlorinated Biphenyls - Pooled Samples (Laboratory)
LBC114LACompatible with harmonization

PCB 114 Lipid Adj (ng/g)

Observed years
20052016
Release records
6
Datasets
6
Components
Laboratory
Qualified Praxis harmonization assessment

Compatible with harmonization · moderate confidence

No blocking method discontinuity is identified inside the selected cycle span, but one or more longitudinal changes require explicit harmonization conditions before pooling.

Evidence provenance: Praxis automated inference from indexed CDC/NCHS evidence

Relevant boundaries: 2005-2006 → 2007-2008 · 2007-2008 → 2009-2010 · 2009-2010 → 2011-2012 · 2011-2012 → 2013-2014 · 2013-2014 → 2015-2016

Praxis harmonization actions
  • Verify merge grain, companion variables, and component-specific analytic guidance for the new file context.
  • Review the adjacent codebooks/methods. Keep this boundary as documentation variation unless source evidence confirms a substantive method or instrument change.
  • Select the weight appropriate to each cycle and subsample; when pooling cycles, construct the combined weight according to NHANES guidance rather than reusing a single-cycle weight unchanged.
Supporting CDC/NCHS evidence
Variable names / labels over time
  • PCB 114 Lipid Adj (ng/g)2005-2006 · 2007-2008
  • 2,3,4,4',5-Pentachlorobiphenyl Lipid Adjusted (ng/g)2009-2010 · 2011-2012 · 2013-2014 · 2015-2016
Cycle-by-cycle release history
  • 2005-2006: PCBPOL_D — PCB 114 Lipid Adj (ng/g) — Non-dioxin-like Polychlorinated Biphenyls & Mono-ortho-substituted Polychlorinated Biphenyls - Pooled Samples (Laboratory)
  • 2007-2008: PCBPOL_E — PCB 114 Lipid Adj (ng/g) — Non-dioxin-like Polychlorinated Biphenyls & Mono-ortho-substituted Polychlorinated Biphenyls - Pooled Samples (Laboratory)
  • 2009-2010: PCBPOL_F — 2,3,4,4',5-Pentachlorobiphenyl Lipid Adjusted (ng/g) — Non-dioxin-like Polychlorinated Biphenyls & Mono-ortho-substituted Polychlorinated Biphenyls - Pooled Samples (Laboratory)
  • 2011-2012: PCBPOL_G — 2,3,4,4',5-Pentachlorobiphenyl Lipid Adjusted (ng/g) — Non-dioxin-like Polychlorinated Biphenyls & Mono-ortho-substituted Polychlorinated Biphenyls - Pooled Samples (Laboratory)
  • 2013-2014: PCBPOL_H — 2,3,4,4',5-Pentachlorobiphenyl Lipid Adjusted (ng/g) — Non-dioxin-like Polychlorinated Biphenyls & Mono-ortho-substituted Polychlorinated Biphenyls - Serum - Pooled Samples (Laboratory)
  • 2015-2016: PCBPOL_I — 2,3,4,4',5-Pentachlorobiphenyl Lipid Adjusted (ng/g) — Non-dioxin-like Polychlorinated Biphenyls & Mono-ortho-substituted Polychlorinated Biphenyls - Pooled Samples (Laboratory)