First Trimester Screen, Hyperglycosylated hCG (h-hCG)

First Trimester Screen, Hyperglycosylated hCG (h-hCG)

Test Code

16020
81508
16020
81508
Ordering Restrictions may apply. Please provide SERVICE AREA INFORMATION to find available tests you can order.
Not offered in Quest Diagnostics Nichols Institute (IFD) – San Juan Capistrano. Please provide SERVICE AREA INFORMATION to find available tests you can order.
In-home collection may be available in your area for purchase through Quest Mobile.

Clinical Significance

First Trimester Screen, Hyperglycosylated hCG (h-hCG) - To screen for Down syndrome and trisomy 18 at 9.0-13.9 weeks gestation.

Test Details

Includes

  • PAPP-A (Pregnancy-associated Plasma Protein), h-hCG (hyperglycosylated hCG), risk calculation which includes NT (Nuchal Translucency)

Methodology

Chemiluminescence (CL) • Immunoassay (IA)

Assay Category

h-hCG: This test was developed and its analytical performance characteristics have been determined by Quest Diagnostics. It has not been cleared or approved by FDA. This assay has been validated pursuant to the CLIA regulations and is used for clinical purposes.

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 non-New York patient testing. For New York patient testing, use test code 16969.
This test is not available for California patient testing.

Alternative Name(s)

Invasive Trophoblast Antigen (ITA),Nuchal Translucency (NT),Hyperglycosylated hCG (h-hCG),Pregnancy-associated Plasma Protein-A (PAPP-A),MSS, 1st Trimester,Down Syndrome and Trisomy 18 Screen

LOINC® Codes, Performing Laboratory

PAPP-A (Pregnancy-associated Plasma Protein), h-hCG (hyperglycosylated hCG), risk calculation which includes NT (Nuchal Translucency)

Methodology

Chemiluminescence (CL) • Immunoassay (IA)
h-hCG: This test was developed and its analytical performance characteristics have been determined by Quest Diagnostics. It has not been cleared or approved by FDA. This assay has been validated pursuant to the CLIA regulations and is used for clinical purposes.

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 non-New York patient testing. For New York patient testing, use test code 16969.
This test is not available for California patient testing.

Alternative Name(s)

Invasive Trophoblast Antigen (ITA),Nuchal Translucency (NT),Hyperglycosylated hCG (h-hCG),Pregnancy-associated Plasma Protein-A (PAPP-A),MSS, 1st Trimester,Down Syndrome and Trisomy 18 Screen

Preferred Specimen(s)

1.5 mL serum

Minimum Volume

0.8 mL

Transport Container

Transport tube

Transport Temperature

Room temperature

Specimen Stability

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

Reject Criteria

Moderate and gross hemolysis • Lipemia

Setup Schedule

1.5 mL serum
0.8 mL
Transport tube
Room temperature
Room temperature: 14 days
Refrigerated: 14 days
Frozen: 28 days
Moderate and gross hemolysis • Lipemia
Ordering Restrictions may apply. Please provide SERVICE AREA INFORMATION to find available tests you can order.
Not offered in Quest Diagnostics Nichols Institute (IFD) – San Juan Capistrano. Please provide SERVICE AREA INFORMATION to find available tests you can order.
In-home collection may be available in your area for purchase 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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