Aetna modified CPB 0282 for noninvasive Down syndrome and fetal aneuploidy screening, effective September 26, 2025. Here's what billing teams need to act on now.
Aetna, a CVS Health company, updated CPB 0282 to clarify when first-trimester nuchal translucency ultrasound and serum analyte screening are — and aren't — covered. The change has direct implications for CPT codes 76813 and 76814 in particular. If your practice bills prenatal screening for Aetna members, this coverage policy affects your charge capture, your claim denial exposure, and your medical necessity documentation.
Quick-Reference: Aetna CPB 0282 Noninvasive Down Syndrome Screening (2025)
| Field | Detail |
|---|---|
| Payer | Aetna, a CVS Health company |
| Policy | Noninvasive Down Syndrome Screening |
| Policy Code | CPB 0282 |
| Change Type | Modified |
| Effective Date | September 26, 2025 |
| Impact Level | High |
| Specialties Affected | OB/GYN, Maternal-Fetal Medicine, Laboratory, Radiology |
| Key Action | Stop billing CPT 76813/76814 for NT measurement when the patient already has negative cfDNA/NIPT results in the current pregnancy |
Aetna Noninvasive Fetal Aneuploidy Screening Coverage Criteria and Medical Necessity Requirements 2025
The Aetna Down syndrome screening coverage policy recognizes six pathways to medical necessity for fetal aneuploidy screening. Each is distinct. Billing the wrong pathway — or stacking tests that fall outside one pathway — will get your claim denied.
Here's what Aetna covers under CPB 0282 in the CPB 0282 Aetna system:
Pathway 1: First-trimester NT alone (multiple gestations). Aetna covers nuchal translucency ultrasound — billed as CPT 76813 for the primary fetus and add-on code 76814 for each additional gestation — without serum analytes when the patient is carrying multiples.
Pathway 2: First-trimester combined screen. NT measurement (76813/76814) plus serum analytes — pregnancy-associated plasma protein A (PAPP-A, billed as CPT 84163) and beta-hCG (CPT 84702 or 84704 depending on method). Aetna treats free beta subunit of hCG, total hCG, and hyperglycosylated hCG (invasive trophoblast antigen) as interchangeable for this policy.
Pathway 3: Integrated, sequential, or contingent screening. This is the most code-intensive pathway. It combines first-trimester triple test (NT plus PAPP-A plus hCG) with a second-trimester quadruple screen — maternal serum alpha-fetoprotein (MSAFP, CPT 82105), unconjugated estriol (CPT 82677), inhibin A (CPT 86336), and hCG. Panel codes 81509 through 81512 apply here depending on which analytes are ordered. Reimbursement for this pathway requires documentation supporting the sequential or contingent screening decision.
Pathway 4: Second-trimester serum analyte screening only. Aetna defers to CPB 0464 for the full criteria here.
Pathway 5: Serum integrated screening (when NT is unavailable). If NT measurement can't be obtained — provider not available, patient can't tolerate the exam, gestational age outside the window — Aetna covers first-trimester PAPP-A plus hCG combined with second-trimester quad screening. Document why NT was unobtainable. Without that documentation, expect a medical necessity denial.
Pathway 6: Cell-free fetal DNA (cfDNA/NIPT). Covered when criteria in CPB 0464 are met. This is billed under CPT 81420 or 81507 depending on the test type.
The prior authorization requirements for these pathways follow Aetna's standard prenatal screening rules. Check current plan-level requirements before assuming routine screening is exempt from prior auth.
Aetna Noninvasive Down Syndrome Screening Exclusions and Non-Covered Indications
This is where the September 26, 2025 update has the most teeth.
No stacking with NIPT/cfDNA. Aetna considers all the screening pathways listed above — NT ultrasound, serum analytes, integrated screens, the whole list — not medically necessary if the patient has already had or is currently having microarray or NIPT with cell-free DNA in the same pregnancy. One or the other. Not both.
NT ultrasound after negative cfDNA results. This is the sharpest new edge in this coverage policy. Aetna states directly: if a patient already has reassuring negative cfDNA results, a follow-up ultrasound at 10–14 weeks solely to measure nuchal translucency is not recommended and is not medically necessary. CPT 76813 and 76814 should not be billed in that scenario — even if the NT measurement is physically obtained during the visit.
That last clause is the one to flag for your billing team. The measurement can happen. The bill should not. This distinction is a common source of claim denial because the encounter looks billable on its face.
Circular RNA (circRNA) testing. CPT 83520 appears in this policy under the label "Maternal fetal-derived circular RNA (circRNAs), measurement." This test is not included in the covered pathways. Treat it as non-covered unless Aetna updates the policy.
Cross-reference this policy with CPB 0464 (Serum and Urine Marker Screening for Fetal Aneuploidy) and CPB 0787 (Comparative Genomic Hybridization) before billing any cell-free DNA or microarray codes on an Aetna prenatal claim.
Coverage Indications at a Glance
| Indication | Status | Relevant Codes | Notes |
|---|---|---|---|
| NT ultrasound alone — multiple gestations | Covered | 76813, 76814 | No serum analytes required for multiples |
| First-trimester combined screen (NT + PAPP-A + hCG) | Covered | 76813, 76814, 84163, 84702/84704 | Document trimester and analytes ordered |
| Integrated/sequential/contingent screening | Covered | 76813, 76814, 81509–81512, 82105, 82677, 86336, 84163, 84702/84704 | Both first- and second-trimester components required |
| Second-trimester serum analyte screening | Covered | 81510, 81511, 82105, 82677, 86336, 84702 | See CPB 0464 for full criteria |
| Serum integrated screening (NT unavailable) | Covered | 84163, 84702/84704, 81511, 82105, 82677, 86336 | Document why NT could not be obtained |
| Cell-free fetal DNA / NIPT | Covered (criteria apply) | 81420, 81507 | See CPB 0464 for patient selection criteria |
| NT ultrasound after negative cfDNA result | Not Covered | 76813, 76814 | Do not bill even if NT is measured |
| Any serum/NT screen when cfDNA/NIPT already done in same pregnancy | Not Covered | All pathway codes above | NIPT and traditional screens are mutually exclusive under this policy |
| Microarray (CGH) | See CPB 0787 | 59015 (related) | Not covered under CPB 0282; governed by CPB 0787 |
| Maternal fetal-derived circRNA measurement | Not Covered | 83520 | Not part of any covered pathway |
| Amniocentesis, chorionic villus sampling | Related/Diagnostic | 59000, 59015 | Diagnostic — not screening; governed by separate criteria |
Aetna Fetal Aneuploidy Screening Billing Guidelines and Action Items 2025
The effective date is September 26, 2025. If you haven't already reviewed your charge capture for prenatal screening, do it now.
| # | Action Item |
|---|---|
| 1 | Audit your 76813/76814 charge triggers. Pull claims from the past 90 days where 76813 or 76814 was billed alongside or after an NIPT/cfDNA order. Flag any where cfDNA results were available before the NT ultrasound took place. Those encounters represent your highest claim denial risk going forward. |
| 2 | Update your order workflow to check for prior cfDNA. Before billing NT ultrasound, your intake or clinical workflow should confirm whether the patient had NIPT or cell-free DNA in the current pregnancy. Build this as a checkpoint — not a manual lookup that depends on someone remembering. |
| 3 | Document NT-unavailable encounters before billing Pathway 5. If you're billing serum integrated screening because NT couldn't be obtained, document the reason in the chart before the claim goes out. "NT measurement not available" as a bare assertion won't hold up. Note provider availability, gestational age issues, or patient-specific factors. |
| 4 | Map your panel codes correctly. CPT 81509 (three proteins: PAPP-A, hCG, DIA), 81510 (AFP, uE3, hCG), 81511 (AFP, uE3, hCG, DIA — quad), and 81512 (five analytes including hyperglycosylated hCG) each map to different screening pathways. Billing the wrong panel code for the pathway ordered is a denial waiting to happen. Match the code to the analytes actually tested. |
| 5 | Remove 83520 from your prenatal screening charge master. If CPT 83520 (circRNA measurement) is active in your charge capture for prenatal encounters, remove it or flag it as non-covered under this Aetna Down syndrome screening billing policy. It has no covered pathway under CPB 0282. |
| 6 | Cross-check ICD-10 codes. Claims should carry Z36.0–Z36.9 (antenatal screening encounter) codes appropriate to the indication. For patients with identified chromosomal findings, Q90.0–Q99.9 applies. Make sure your coders aren't defaulting to a single Z36.0 across all prenatal screening — the specific Z36 sub-codes matter for documentation alignment. |
| 7 | If your practice handles high-volume prenatal screening for Aetna members, loop in your compliance officer. The NIPT/cfDNA mutual exclusivity rule is straightforward in text but complex in practice — especially for patients who start cfDNA at one provider and come to you for NT measurement. The liability for a not-medically-necessary determination lands on the billing provider. |
| Previous Version | Current Version |
|---|---|
| Coverage is considered experimental and investigational for all indications | Coverage is considered medically necessary when specific criteria are met |
| Prior authorization is not required | Prior authorization is required for initial treatment |
| Documentation must include clinical history | Documentation must include clinical history |
| Re-review every 24 months | Re-review every 12 months with updated clinical documentation |
CPT, HCPCS, and ICD-10 Codes for Noninvasive Down Syndrome Screening Under CPB 0282
Covered CPT Codes (When Selection Criteria Are Met)
| Code | Type | Description |
|---|---|---|
| 76813 | CPT | Ultrasound, pregnant uterus, real time with image documentation, first trimester fetal nuchal translucency measurement |
| +76814 | CPT | Each additional gestation (add-on to 76813) |
| 81509 | CPT | Fetal congenital abnormalities, biochemical assays of three proteins (PAPP-A, hCG [any form], DIA) |
| 81510 | CPT | Fetal congenital abnormalities, biochemical assays of three analytes (AFP, uE3, hCG [any form]) |
| 81511 | CPT | Fetal congenital abnormalities, biochemical assays of four analytes (AFP, uE3, hCG [any form], DIA) |
| 81512 | CPT | Fetal congenital abnormalities, biochemical assays of five analytes (AFP, uE3, total hCG, hyperglycosylated hCG, and DIA) |
| 84704 | CPT | Gonadotropin, chorionic (hCG); free beta chain |
Not Covered / Non-Standard Codes Under This Policy
| Code | Type | Description | Reason |
|---|---|---|---|
| 83520 | CPT | Immunoassay, analyte quantitative; not otherwise specified [maternal fetal-derived circRNA measurement] | Not part of any covered screening pathway under CPB 0282 |
Key ICD-10-CM Diagnosis Codes
| Code | Description |
|---|---|
| Q90.0–Q99.9 | Chromosomal anomalies |
| Z36.0 | Encounter for antenatal screening of mother |
| Z36.1 | Encounter for antenatal screening of mother |
| Z36.2 | Encounter for antenatal screening of mother |
| Z36.3 | Encounter for antenatal screening of mother |
| Z36.4 | Encounter for antenatal screening of mother |
| Z36.82 | Encounter for antenatal screening of mother |
| Z36.89–Z36.9 | Encounter for antenatal screening of mother |
| Z36.8A | Encounter for antenatal screening of mother |
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