Aetna modified CPB 0996 for aducanumab-avwa (Aduhelm), effective December 10, 2025. Here's what billing teams need to know before submitting claims.
Aetna, a CVS Health company, updated its Aduhelm coverage policy under CPB 0996, tightening medical necessity criteria and exclusion rules for commercial plan members. The policy covers J0172 (injection, aducanumab-avwa, 2 mg) and ties coverage to a specific diagnostic workup — including PET imaging (CPT 78811, 78814) and lumbar puncture (CPT 62270). If your practice bills for anti-amyloid therapy in Alzheimer's disease patients, this update changes what documentation you need before submitting a claim.
Quick-Reference Table
| Field | Detail |
|---|---|
| Payer | Aetna |
| Policy | Aducanumab-avwa (Aduhelm) — CPB 0996 |
| Policy Code | CPB 0996 |
| Change Type | Modified |
| Effective Date | December 10, 2025 |
| Impact Level | High |
| Specialties Affected | Neurology, Geriatrics, Psychiatry, Neuropsychiatry |
| Key Action | Verify full documentation — amyloid confirmation, cognitive scoring, MRI safety clearance — before submitting J0172 claims |
Aetna Aduhelm Coverage Criteria and Medical Necessity Requirements 2025
Aetna's Aduhelm coverage policy under CPB 0996 requires prior authorization for every member on every applicable commercial plan. Call (866) 752-7021 or fax (866) 267-3277 to precertify. Submit a Statement of Medical Necessity (SMN) form through Aetna's Specialty Pharmacy Precertification portal.
The policy also applies Aetna's Site of Care Utilization Management Policy for specialty drug infusions. That means your billing team needs to confirm the infusion site meets Aetna's requirements before you administer or bill — reimbursement can be denied solely on site-of-service grounds, even if clinical criteria are met.
Who Qualifies: Age and Diagnosis
To meet medical necessity, the member must be 50 years of age or older. Members under 50 qualify only with a documented genetic mutation in APP (CPT 81406), PSEN1 (CPT 81405), or PSEN2, or other clinical documentation supporting early-onset AD.
The diagnosis must be mild cognitive impairment due to Alzheimer's disease or mild AD dementia. Moderate or severe AD does not qualify. Code G31.84 (mild cognitive impairment of uncertain or unknown etiology, mapped here to AD) is the key ICD-10 anchor alongside G30.x Alzheimer's disease codes.
Cognitive Scoring Requirements
The member must show objective evidence of cognitive impairment at baseline and score within specific ranges on at least one of the following tools:
| # | Covered Indication |
|---|---|
| 1 | CDR-Global Score of 0.5 or 1 |
| 2 | MMSE score of 21–30 |
| 3 | MoCA score of ≥16 |
Document the specific score and the specific tool used. Aetna will not accept a general reference to "cognitive testing." The score must be in the record and tied to a named assessment.
Amyloid Confirmation: PET or CSF
This is where a lot of claims will fall apart. The member must have amyloid pathology confirmed by either a PET scan or a lumbar puncture with CSF analysis.
For PET, bill CPT 78811 (limited area PET) or 78814 (PET/CT). Radiopharmaceuticals A9586 (florbetapir F-18) and Q9982 (flutemetamol F-18) are in the policy. For CSF confirmation via lumbar puncture (CPT 62270), Aetna accepts any of these findings:
| # | Covered Indication |
|---|---|
| 1 | Elevated phosphorylated tau (P-tau) and/or total tau (T-tau) with reduced Aβ42 |
| 2 | Low Aβ42/Aβ40 ratio |
| 3 | Elevated P-tau/Aβ42 ratio |
| 4 | Elevated T-tau/Aβ42 ratio |
CPT 0445U covers the ECLIA-based beta-amyloid and P-tau181 assay. If your lab uses this code, confirm results meet one of the CSF criteria above before treating it as confirmatory documentation.
MRI Safety Check
Per the full policy text, the member must have a recent MRI of the brain before treatment starts. CPT 70551 (without contrast), 70552 (with contrast), or 70553 (without then with contrast) covers this procedure. Because the available policy summary is truncated, verify the complete MRI requirement language in the untruncated CPB 0996 document before relying on this criterion — and confirm exactly what documentation Aetna requires in the prior authorization package.
The clinical rationale is clear regardless: Aduhelm carries risk of amyloid-related imaging abnormalities (ARIA), and pre-treatment MRI is standard practice for this drug class. Talk to your compliance officer if you have questions about how to document this requirement under the current policy language.
Aetna Aduhelm Exclusions and Non-Covered Indications
Aetna's coverage policy is explicit: five categories result in automatic denial. Train your prior auth team on all of them.
Excluded conditions:
| # | Excluded Procedure |
|---|---|
| 1 | Suspected non-AD neurodegeneration — frontotemporal lobar degeneration (FTLD) or Lewy body disease (possible or probable DLB per consensus criteria). ICD-10 codes in the G23.x and G31.x ranges appear in the policy's code set, and Aetna is watching for these on claims. |
| 2 | Requirement for therapeutic anticoagulation. Aspirin at prophylaxis dose (≤325mg/day) is the only exception. Any other anticoagulant or antiplatelet agent triggers exclusion. |
| 3 | History of TIA, stroke, or seizures within the past 12 months. |
| 4 | Uncontrolled bleeding disorder — defined as platelet count below 50,000 or INR above 1.5. |
| 5 | Combination use with any other amyloid beta-directed antibody — specifically J0174 (lecanemab-irmb) or J0175 (donanemab-azbt). You cannot bill J0172 alongside either of these codes for the same member. |
The combination-use exclusion is a billing team issue, not just a clinical one. If a member switches therapies, document the stop date of the prior agent before prior authorization for Aduhelm goes through. A claim denial on this basis is hard to overturn without clear transition records.
Coverage Indications at a Glance
| Indication | Status | Relevant Codes | Notes |
|---|---|---|---|
| Mild cognitive impairment due to AD (age ≥50) | Covered | J0172, G31.84, G30.x | Prior auth required; CDR/MMSE/MoCA score required |
| Mild AD dementia (age ≥50) | Covered | J0172, G30.x | Amyloid confirmation via PET or CSF required |
| Early-onset AD with APP/PSEN1/PSEN2 mutation (age <50) | Covered | J0172, CPT 81405, 81406 | Genetic documentation required |
| Moderate or severe AD | Not Covered | — | Policy limited to mild stage only |
| Non-AD neurodegeneration (FTLD, Lewy body) | Not Covered | G23.x, G31.x | Explicit exclusion |
| Combination with lecanemab or donanemab | Not Covered | J0174, J0175 | Cannot bill J0172 with these codes for same member |
| Members on therapeutic anticoagulation | Not Covered | — | Aspirin ≤325mg/day only exception |
| Members with TIA/stroke/seizure in past 12 months | Not Covered | — | Applies to history within preceding 12 months |
| Uncontrolled bleeding disorder (platelets <50K, INR >1.5) | Not Covered | D69.x | Hard exclusion |
Aetna Aduhelm Billing Guidelines and Action Items 2025
The effective date is December 10, 2025. If you bill J0172 for Aduhelm under commercial Aetna plans, act on these steps now.
| # | Action Item |
|---|---|
| 1 | Update your prior authorization checklist before December 10, 2025. Every J0172 claim requires precertification. Build a checklist that includes: age documentation, cognitive score (CDR/MMSE/MoCA with numeric value), amyloid confirmation method (PET or CSF), recent MRI report, and prescriber specialty. Missing any one item will kill the authorization. |
| 2 | Confirm prescriber credentials before submitting. Aduhelm billing under CPB 0996 requires the prescribing physician to be a geriatrician, neurologist, psychiatrist, or neuropsychiatrist — or a documented consultation with one. A PCP-only prescribing record is a claim denial waiting to happen. |
| 3 | Review active Aduhelm patients for combination therapy conflicts. Pull any members currently authorized for J0172 and cross-check against active J0174 (lecanemab) or J0175 (donanemab) claims. Concurrent authorization violates the exclusion criteria and will trigger denial on both drugs. |
| 4 | Flag anticoagulation records in your pre-auth workflow. The exclusion for therapeutic anticoagulation is easy to miss if your team only reviews the neurology chart. Route a pharmacy review into the Aduhelm prior auth process to catch warfarin, DOAC, or antiplatelet use beyond aspirin ≤325mg. |
| 5 | Confirm site of care approval separately. Aetna's Site of Care UM Policy applies here. Infusion billing under CPT 96365–96368 can be denied on site-of-service grounds even if the clinical prior auth is approved. Confirm the approved site in writing before scheduling infusion. |
| 6 | Document MRI findings explicitly. CPT 70551, 70552, or 70553 must appear in the record with a report. Verify the complete MRI requirement language in the untruncated CPB 0996 before finalizing your documentation checklist — the available policy summary is truncated. Build MRI documentation into your intake workflow once you've confirmed the full requirement. |
| 7 | If your volume is significant, loop in your compliance officer. The combination-use restriction, the anticoagulation rules, and the amyloid confirmation requirements create several overlapping denial risks. If you treat more than a handful of Aduhelm patients under commercial Aetna plans, have your compliance officer review your documentation standards against the updated CPB 0996 criteria before the effective date. |
| 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 Aduhelm Under CPB 0996
Covered HCPCS Codes (When Selection Criteria Are Met)
| Code | Type | Description |
|---|---|---|
| J0172 | HCPCS | Injection, aducanumab-avwa, 2 mg |
Supporting CPT and HCPCS Codes Referenced in CPB 0996
These codes support the diagnostic workup, administration, and exclusion criteria. They are not independently covered under this CPB — coverage follows the procedures they describe.
| Code | Type | Description |
|---|---|---|
| 0445U | CPT | β-amyloid (Aβ42) and phospho tau (181P), electrochemiluminescent immunoassay (ECLIA) |
| 62270 | CPT | Spinal puncture, lumbar, diagnostic |
| 70551 | CPT | MRI brain without contrast |
| 70552 | CPT | MRI brain with contrast |
| 70553 | CPT | MRI brain without contrast, followed by contrast |
| 78608 | CPT | Brain PET imaging, metabolic evaluation |
| 78811 | CPT | PET imaging, limited area (e.g., head/neck) |
| 78814 | CPT | PET/CT for attenuation correction |
| 81401 | CPT | Molecular pathology procedure, Level 2 — APOE variants |
| 81405 | CPT | Molecular pathology procedure, Level 6 — PSEN1 full gene sequence |
| 81406 | CPT | Molecular pathology procedure, Level 7 — APP full gene sequence |
| 96365 | CPT | Intravenous infusion administration |
| 96366 | CPT | Intravenous infusion administration |
| 96367 | CPT | Intravenous infusion administration |
| 96368 | CPT | Intravenous infusion administration |
| A9586 | HCPCS | Florbetapir F-18, diagnostic, per study dose, up to 10 millicuries |
| A9598 | HCPCS | PET radiopharmaceutical, diagnostic, non-tumor, NOS |
| J0174 | HCPCS | Injection, lecanemab-irmb, 1 mg (combination use — excluded) |
| J0175 | HCPCS | Injection, donanemab-azbt, 2 mg (combination use — excluded) |
| Q9982 | HCPCS | Flutemetamol F-18, diagnostic, per study dose, up to 5 millicuries |
| S3852 | HCPCS | DNA analysis for APOE epsilon 4 allele for Alzheimer's susceptibility |
Key ICD-10-CM Diagnosis Codes
| Code | Description |
|---|---|
| G30.0–G30.9 | Alzheimer's disease (various manifestations) |
| G31.84 | Mild cognitive impairment of uncertain or unknown etiology (mapped to AD under this policy) |
| G31.1–G31.9 | Other degenerative diseases of nervous system (excluding G31.84 where noted) |
| G23.0–G23.9 | Other degenerative diseases of basal ganglia |
| G32.0–G32.24+ | Other degenerative disorders of nervous system in diseases classified elsewhere |
| D69.0–D69.9 | Purpura and other hemorrhagic conditions (bleeding disorder exclusion criteria) |
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