Stepwise, Part 2 (NY)

Stepwise, Part 2 (NY)

Test Code

16466
81511
16466
81511
This test is not available in all locations. Please provide SERVICE AREA INFORMATION to confirm Test Code for the lab that services your account or to find available tests you can order.
In-home collection is not available in your area through Quest Mobile.

Clinical Significance

Stepwise, Part 2 (NY)

Test Resources

None found for this test
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Test Details

Includes

  • AFP
    Unconjugated Estriol
    hCG
    Inhibin A, Dimeric
    PAPP-A (Pregnancy-associated Plasma Protein-A) and hCG from Stepwise, Part 1
    Interpretation

Methodology

Chemiluminescence (CL) • Immunoassay (IA)

Assay Category

PAPP-A: This test was performed using a kit that has not been cleared or approved by the FDA. The analytical performance characteristics of this test have been determined by Quest Diagnostics. This test should not be used for diagnosis without confirmation by other medically established means.

This test code is for New York patient testing. For non-New York patient testing, use test code 16465.

Reference Range(s)

See Laboratory Report

LOINC® Codes, Performing Laboratory

AFP
Unconjugated Estriol
hCG
Inhibin A, Dimeric
PAPP-A (Pregnancy-associated Plasma Protein-A) and hCG from Stepwise, Part 1
Interpretation

Methodology

Chemiluminescence (CL) • Immunoassay (IA)
PAPP-A: This test was performed using a kit that has not been cleared or approved by the FDA. The analytical performance characteristics of this test have been determined by Quest Diagnostics. This test should not be used for diagnosis without confirmation by other medically established means.

This test code is for New York patient testing. For non-New York patient testing, use test code 16465.

Reference Range(s)

See Laboratory Report

Preferred Specimen(s)

3 mL serum

Minimum Volume

1 mL

Collection Instructions

Collect between 14.0 weeks to 22.9 weeks.
Mother's date of birth (mm/dd/yy), Estimated Date of Delivery by US/LMP/PE, weight, race, insulin-dependent diabetes status, repeat sample (Y/N), number of fetuses, and neural tube defect history must be provided for interpretation of results.
Must complete all patient demographic information using the appropriate questions from the entry fields in the regular requisition.

Transport Container

Transport tube

Transport Temperature

Room temperature

Specimen Stability

  • Room temperature: 14 days
  • Refrigerated: 14 days
  • Frozen: 28 days

Reject Criteria

Gross hemolysis • Grossly lipemic

Setup Schedule

3 mL serum
1 mL
Collect between 14.0 weeks to 22.9 weeks.
Mother's date of birth (mm/dd/yy), Estimated Date of Delivery by US/LMP/PE, weight, race, insulin-dependent diabetes status, repeat sample (Y/N), number of fetuses, and neural tube defect history must be provided for interpretation of results.
Must complete all patient demographic information using the appropriate questions from the entry fields in the regular requisition.
Transport tube

Room temperature

Room temperature: 14 days
Refrigerated: 14 days
Frozen: 28 days
Gross hemolysis • Grossly lipemic
This test is not available in all locations. Please provide ACCOUNT INFORMATION NEEDED to confirm Test Code for the lab that services your account or to find available tests you can order.
In-home collection is not available in your area through Quest Mobile.
Test Details

Clinical Significance

Test Resources

Reference ranges are provided as general guidance only. To interpret test results use the reference range in the laboratory report.

The CPT codes provided are based on AMA guidance and are for informational purposes only. CPT coding is the sole responsibility of the billing party. Please direct any questions regarding coding to the payer being billed.

This material contains content from LOINC® (http://loinc.org). The LOINC Table, LOINC Table Core are copyright © 1995-2019, Regenstrief Institute, Inc. and the Logical Observation Identifiers Names and Codes (LOINC) Committee and is available at no cost under the license at http://loinc.org/license.

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