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Official Description

Fetal congenital abnormalities, biochemical assays of two proteins (PAPP-A, hCG [any form]), utilizing maternal serum, algorithm reported as a risk score

© Copyright 2025 American Medical Association. All rights reserved.

Common Language Description

The CPT® Code 81508 refers to a specific laboratory test that assesses the risk of fetal congenital abnormalities through biochemical assays of two proteins found in maternal serum. This test measures the levels of pregnancy-associated plasma protein A (PAPP-A) and human chorionic gonadotropin (hCG) in the blood of pregnant individuals. The primary purpose of this test is to evaluate the risk for certain chromosomal abnormalities, notably trisomy 18 and trisomy 21, which is commonly known as Down syndrome. The test is most effective when conducted during a specific window of gestation, particularly between 10 weeks and 3 days to 13 weeks and 6 days. During this period, the sensitivity of the test results is maximized, allowing for a more accurate risk assessment. The blood sample required for this test is obtained through a procedure known as venipuncture, which is separately reportable. The serum collected is then analyzed using a quantitative chemiluminescent immunoassay, a sophisticated laboratory technique that quantifies the proteins in the sample to generate a risk score. This score is crucial for healthcare providers in making informed decisions regarding further diagnostic testing or monitoring during the pregnancy.

© Copyright 2025 Coding Ahead. All rights reserved.

1. Indications

The CPT® Code 81508 is indicated for use in the following scenarios:

  • Risk Assessment for Chromosomal Abnormalities This test is performed to evaluate the risk of fetal congenital abnormalities, specifically trisomy 18 and trisomy 21 (Down syndrome), based on the levels of specific proteins in maternal serum.

2. Procedure

The procedure for CPT® Code 81508 involves several key steps that ensure accurate measurement of the proteins in maternal serum:

  • Step 1: Patient Preparation The patient is informed about the test and the importance of timing, as the blood sample should be drawn within the optimal gestational window of 10 weeks and 3 days to 13 weeks and 6 days. Proper scheduling is essential to ensure the accuracy of the results.
  • Step 2: Venipuncture A trained healthcare professional performs a venipuncture to obtain a blood sample from the patient. This procedure involves inserting a needle into a vein, typically in the arm, to collect the necessary serum for testing. The venipuncture is a separately reportable procedure.
  • Step 3: Serum Preparation Once the blood sample is collected, it is processed to separate the serum from the cellular components. This serum is crucial for the subsequent analysis of the proteins.
  • Step 4: Quantitative Chemiluminescent Immunoassay The prepared serum is then subjected to a quantitative chemiluminescent immunoassay. This advanced laboratory technique measures the concentrations of PAPP-A and hCG in the serum, providing quantitative results that are essential for risk assessment.
  • Step 5: Risk Score Calculation After the assay is completed, the results are analyzed to generate a risk score. This score reflects the likelihood of the fetus having congenital abnormalities based on the measured protein levels.

3. Post-Procedure

After the procedure associated with CPT® Code 81508, patients may be advised to follow up with their healthcare provider to discuss the results of the test. Depending on the risk score obtained, further diagnostic testing may be recommended to confirm or rule out any potential abnormalities. Patients should also be informed about any signs or symptoms to monitor during their pregnancy and encouraged to maintain regular prenatal care appointments for ongoing assessment and support.

Short Descr FTL CGEN ABNOR TWO PROTEINS
Medium Descr FETAL CONGENITAL ABNOR ASSAY TWO PROTEINS
Long Descr Fetal congenital abnormalities, biochemical assays of two proteins (PAPP-A, hCG [any form]), utilizing maternal serum, algorithm reported as a risk score
Status Code Statutory Exclusion (from MPFS, may be paid under other methodologies)
Global Days XXX - Global Concept Does Not Apply
PC/TC Indicator (26, TC) 9 - Not Applicable
Multiple Procedures (51) 9 - Concept does not apply.
Bilateral Surgery (50) 9 - Concept does not apply.
Physician Supervisions 09 - Concept does not apply.
Assistant Surgeon (80, 82) 9 - Concept does not apply.
Co-Surgeons (62) 9 - Concept does not apply.
Team Surgery (66) 9 - Concept does not apply.
Diagnostic Imaging Family 99 - Concept Does Not Apply
CLIA Waived (QW) No
APC Status Indicator Conditionally packaged laboratory tests
Type of Service (TOS) 5 - Diagnostic Laboratory
Berenson-Eggers TOS (BETOS) T1H - Lab tests - other (non-Medicare fee schedule)
MUE 1
CCS Clinical Classification 234 - Pathology
XU Unusual non-overlapping service, the use of a service that is distinct because it does not overlap usual components of the main service
90 Reference (outside) laboratory: when laboratory procedures are performed by a party other than the treating or reporting physician or other qualified health care professional, the procedure may be identified by adding modifier 90 to the usual procedure number.
GW Service not related to the hospice patient's terminal condition
Date
Action
Notes
2013-01-01 Added Added
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