Cigna modified MM 0287 covering cell-based therapy for cardiac and peripheral arterial disease, effective September 26, 2025. Every procedure in this policy — CPT 33999, 38206, 38232, 93799, and HCPCS C9782 and S2150 — is classified as experimental, investigational, or unproven. Here's what billing teams need to do.
Cigna Healthcare updated its cell-based therapy coverage policy under MM 0287 in September 2025. The policy covers proposed treatments for heart damage and peripheral arterial disease using several cell types, including autologous myoblasts, hematopoietic progenitor cells, and bone marrow-derived stem cells. The result is a blanket non-coverage position: no reimbursement for any of the six codes in this policy, regardless of clinical presentation.
Quick-Reference Table
| Field | Detail |
|---|---|
| Payer | Cigna Healthcare |
| Policy | Cell-Based Therapy for Cardiac and Peripheral Arterial Disease |
| Policy Code | MM 0287 |
| Change Type | Modified |
| Effective Date | September 26, 2025 |
| Impact Level | High |
| Specialties Affected | Cardiology, Cardiac Surgery, Vascular Surgery, Hematology/Oncology (when billing for harvest procedures in this context) |
| Key Action | Flag CPT 33999, 38206, 38232, 93799 and HCPCS C9782, S2150 as non-covered for cardiac and PAD indications in your charge capture and denial workflows before September 26, 2025 |
Cigna Cell-Based Therapy Coverage Criteria and Medical Necessity Requirements 2025
The direct answer here: Cigna does not consider cell-based therapy for cardiac disease or peripheral arterial disease (PAD) to meet medical necessity. Full stop.
Under MM 0287 in the Cigna Healthcare system, procedures in this category do not have a covered pathway. There are no qualifying criteria that unlock reimbursement. The policy does not describe a clinical scenario where these treatments become covered services.
That matters for your prior authorization workflow. Some teams burn time submitting prior auth requests for procedures that a payer has already categorized as experimental. For any Cigna member presenting for cell-based cardiac or PAD therapy, the coverage policy answer is the same regardless of diagnosis code, provider specialty, or site of service. Don't request prior authorization expecting a different result — the experimental designation is the position, not a default you can appeal around with additional documentation.
The procedures addressed in this policy use several cell types as a proposed method to treat heart damage or peripheral arterial disease. The specific cell types include autologous myoblasts (skeletal muscle cells), blood-derived hematopoietic progenitor cells, and bone marrow-derived stem cells. All of them fall under the same non-coverage determination.
Cigna Cell-Based Therapy Exclusions and Non-Covered Indications
This is where the substance of MM 0287 lives. Every code in this policy carries the same classification: experimental, investigational, or unproven.
That classification matters beyond just this specific denial. Experimental and investigational designations typically mean Cigna will not cover the service even if the member has a serious, documented diagnosis. It also affects how you handle claim denial responses. An E/I/U denial is not a medical necessity denial — the appeal pathway is different, and the supporting documentation required is different.
If your clinical team is pushing back on denials for these procedures, make sure your appeals team understands the distinction. You're not arguing clinical appropriateness against a coverage criterion. You're arguing that the technology or procedure meets the standard for coverage under Cigna's definition — a much harder bar and a different argument entirely.
The real risk here is for practices exploring newer cardiac regenerative therapies or participating in studies where billing occurs. If your organization is involved in any program that touches these cell types for cardiac or PAD indications and bills Cigna, audit those claims now.
Coverage Indications at a Glance
| Indication | Status | Relevant Codes | Notes |
|---|---|---|---|
| Cell-based therapy for cardiac/heart damage using autologous myoblasts | Experimental/Investigational/Unproven | CPT 33999, 93799 | No covered pathway; prior auth will not override E/I/U status |
| Blood-derived hematopoietic progenitor cell harvesting for cardiac/PAD indication | Experimental/Investigational/Unproven | CPT 38206, HCPCS S2150 | Harvest procedure itself is non-covered in this context |
| Bone marrow harvesting for cardiac/PAD indication | Experimental/Investigational/Unproven | CPT 38232, HCPCS S2150 | Non-covered regardless of autologous vs. allogeneic source |
| NYHA Class II or III heart failure cell therapy (blinded procedure) | Experimental/Investigational/Unproven | HCPCS C9782 | Includes Canadian Cardiovascular Society angina classification — no coverage |
| Cell-based therapy for peripheral arterial disease | Experimental/Investigational/Unproven | CPT 33999, 93799, HCPCS S2150 | PAD explicitly included in scope of policy |
Cigna Cell-Based Therapy Billing Guidelines and Action Items 2025
| # | Action Item |
|---|---|
| 1 | Update your charge capture before September 26, 2025. Flag CPT 33999, 38206, 38232, and 93799 — and HCPCS C9782 and S2150 — as non-covered for cardiac and PAD indications in your billing system. Any claim hitting Cigna on or after the effective date will deny under this policy if the indication is cardiac repair or peripheral arterial disease. |
| 2 | Stop routing prior authorization requests for these procedures. An E/I/U classification under the Cigna coverage policy is not a prior auth denial — it's a coverage position. Submitting prior auth for an experimental procedure adds cost and delay for no clinical or financial benefit. Your authorization team should know this before September 26. |
| 3 | Audit open claims and pending encounters now. Pull any Cigna claims from the past 90 to 180 days where CPT 38206, 38232, or 33999 was billed alongside a cardiac or PAD diagnosis. If those claims haven't been worked, understand what you're facing under the updated policy. |
| 4 | Review your appeals workflow for E/I/U denials specifically. Cell-based therapy billing denials under this policy require a different appeal argument than standard medical necessity denials. If your team defaults to clinical documentation appeals, they'll be arguing the wrong point. The challenge is the experimental classification itself — that requires evidence the technology meets Cigna's coverage threshold, not just that the patient needed it. |
| 5 | Address any research or study billing carefully. HCPCS C9782 specifically references blinded procedures for heart failure. If your facility participates in cardiac cell therapy research and bills Cigna, talk to your compliance officer before the September 26 effective date. Research billing and commercial insurance coverage intersect in ways that can create real exposure — don't assume research context changes the coverage position. |
| 6 | Inform your cardiology and vascular surgery teams. This isn't a billing team problem in isolation. If physicians are proposing cell-based therapies for Cigna-covered patients, they need to know patients will bear the full financial burden. Patient financial counseling should be in place before any procedure, not after the claim denies. |
| 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 Cell-Based Therapy Under MM 0287
The policy data for MM 0287 contains no covered codes. All six codes in this policy carry an experimental, investigational, or unproven designation. There are no ICD-10 diagnosis codes listed in the policy data.
Experimental / Investigational / Unproven CPT Codes
| Code | Type | Description | Status |
|---|---|---|---|
| 33999 | CPT | Unlisted procedure, cardiac surgery | Experimental/Investigational/Unproven when used for cell-based cardiac therapy |
| 38206 | CPT | Blood-derived hematopoietic progenitor cell harvesting for transplantation, per collection; autologous | Experimental/Investigational/Unproven when used for cardiac/PAD indication |
| 38232 | CPT | Bone marrow harvesting for transplantation; autologous | Experimental/Investigational/Unproven when used for cardiac/PAD indication |
| 93799 | CPT | Unlisted cardiovascular service or procedure | Experimental/Investigational/Unproven when used for cell-based cardiac therapy |
Experimental / Investigational / Unproven HCPCS Codes
| Code | Type | Description | Status |
|---|---|---|---|
| C9782 | HCPCS | Blinded procedure for New York Heart Association (NYHA) Class II or III heart failure, or Canadian Cardiovascular Society angina classification | Experimental/Investigational/Unproven |
| S2150 | HCPCS | Bone marrow or blood-derived stem cells (peripheral or umbilical), allogeneic or autologous, harvesting, transplantation, and related complications | Experimental/Investigational/Unproven when used for cardiac/PAD indication |
One note on the unlisted codes — CPT 33999 and 93799 are catch-all unlisted procedure codes. Their use for cell-based therapy is specifically called out as non-covered here, but these codes appear across many cardiac and cardiovascular procedures. The E/I/U status applies when used in the context of cell-based therapy for cardiac repair or PAD. Your billing team should not interpret this as a blanket non-coverage of all 33999 or 93799 submissions.
Similarly, CPT 38206 and 38232 and HCPCS S2150 are used in bone marrow transplant and stem cell harvest contexts that may be covered under entirely different policies. The non-coverage designation under MM 0287 is specific to cell-based therapy for cardiac and peripheral arterial disease. If you bill these codes for oncology or transplant indications, this policy does not govern that.
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