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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.
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Alpha-fetoprotein (AFP) testing in amniotic fluid is indicated for the following conditions:
The procedure for measuring alpha-fetoprotein (AFP) in amniotic fluid involves several critical steps:
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. |
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| 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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