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Official Description

Alpha-fetoprotein (AFP); amniotic fluid

© Copyright 2026 American Medical Association. All rights reserved.

Common Language Description

Alpha-fetoprotein (AFP) is a crucial biomarker measured in both serum and amniotic fluid during pregnancy. The measurement of AFP in amniotic fluid, designated by CPT® Code 82106, is particularly significant for screening various fetal conditions. AFP is a protein that is initially produced by the yolk sac of the developing fetus during early gestation and subsequently by the liver and gastrointestinal tract as the pregnancy progresses. The assessment of AFP levels is instrumental in identifying potential neural tube defects, such as spina bifida and anencephaly, as well as chromosomal abnormalities, including Down syndrome (trisomy 21) and Edwards syndrome (trisomy 18). Additionally, elevated AFP levels can indicate the presence of omphalocele, a congenital defect. The procedure for obtaining the amniotic fluid involves a separately reportable amniocentesis, which is performed to collect the fluid for analysis. This testing is typically conducted between 14 and 22 weeks of gestation, aligning with the critical window for effective screening and diagnosis of these conditions.

© Copyright 2026 Coding Ahead. All rights reserved.

1. Indications

Alpha-fetoprotein (AFP) testing in amniotic fluid is indicated for the following conditions:

  • Neural Tube Defects - Screening for conditions such as spina bifida and anencephaly.
  • Chromosomal Abnormalities - Detection of abnormalities including Down syndrome (trisomy 21) and Edwards syndrome (trisomy 18).
  • Omphalocele - Assessment for this congenital defect associated with abdominal wall malformations.

2. Procedure

The procedure for measuring alpha-fetoprotein (AFP) in amniotic fluid involves several critical steps:

  • Step 1: Amniocentesis - The first step in the procedure is the performance of amniocentesis, a medical procedure in which a thin needle is inserted through the abdominal wall into the uterus to collect a sample of amniotic fluid. This is typically done under ultrasound guidance to ensure the safety of both the mother and the fetus. The procedure is usually performed between 14 and 22 weeks of gestation, which is the optimal time frame for obtaining accurate results.
  • Step 2: Sample Collection - Once the needle is correctly positioned, a small amount of amniotic fluid is withdrawn. This fluid contains fetal cells and various substances, including alpha-fetoprotein, which are crucial for the subsequent analysis. The amount of fluid collected is generally sufficient for testing while minimizing any risk to the fetus.
  • Step 3: Laboratory Analysis - After the amniotic fluid sample is obtained, it is sent to a laboratory for analysis. The laboratory will measure the level of AFP present in the fluid. Elevated or decreased levels of AFP can provide important information regarding the risk of neural tube defects and chromosomal abnormalities in the fetus.

3. Post-Procedure

Following the amniocentesis procedure, patients are typically monitored for any immediate complications, such as cramping or bleeding. It is common for healthcare providers to advise patients to rest and avoid strenuous activities for a short period after the procedure. Results from the AFP testing may take several days to process, and patients will be informed of the findings during a follow-up appointment. If abnormal levels of AFP are detected, further diagnostic testing or counseling may be recommended to assess the health of the fetus and discuss potential next steps.

Short Descr ALPHA-FETOPROTEIN AMNIOTIC
Medium Descr ALPHA-FETOPROTEIN AMNIOTIC FLUID
Long Descr Alpha-fetoprotein (AFP); amniotic fluid
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 2
CCS Clinical Classification 233 - Laboratory - Chemistry and Hematology
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.
Date
Action
Notes
2011-01-01 Changed Short description changed.
2007-01-01 Changed Code description changed.
1993-01-01 Added First appearance in code book in 1993.
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