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Percutaneous Transluminal Septal Myocardial Ablation (PTSMA)
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This policy governs the medical necessity and coverage criteria for alcohol-induced percutaneous transluminal septal myocardial ablation (PTSMA) for hypertrophic obstructive cardiomyopathy (HOCM) in adults, and identifies indications considered experimental/investigational.
No material clinical or coverage changes in this revision.
Coverage and Medical Necessity Criteria
Medical Necessity — Covered when ALL of the following are met
Covered when ALL of the following are met
Aetna considers percutaneous transluminal septal myocardial ablation (PTSMA) by alcohol-induced septal branch occlusion medically necessary only for adult patients with hypertrophic obstructive cardiomyopathy (HOCM) who meet all of the specified medical necessity criteria. These criteria require: severe symptoms for at least 6 months despite optimal drug therapy, dual-chamber pacing and/or prior ineffective myotomy/myectomy; NYHA class III or IV; classical asymmetric subaortic HOCM on echocardiography (excluding mid-ventricular, concealed membranous subaortic stenosis, and supravalvular forms); echocardiographic left ventricular wall thickness > 13 mm in adults (or > 15 mm in an athlete); systolic anterior motion of the mitral valve; and a left ventricular outflow tract (LVOT) gradient of > 30 mm Hg resting or > 60 mm Hg stressed (alternative thresholds for less severe symptoms: > 50 mm Hg resting or > 100 mm Hg stressed), with no coronary artery disease that would preclude the procedure.
Any use of PTSMA for indications other than the adult HOCM presentation that meets the policy’s listed criteria is considered experimental and investigational because of insufficient evidence of safety and effectiveness, and therefore is not covered.
Codes and Clinical Thresholds
| 93583 | Percutaneous transcatheter septal reduction therapy (eg, alcohol septal ablation) including temporary pacemaker insertion when performed. |
| C1886 | Catheter, extravascular tissue ablation, any modality (insertable). |
| I42.1 | Obstructive hypertrophic cardiomyopathy |
Provider Requirements and Authorization
Prior Authorization
Prior authorization not specified in the provided excerpt. The policy text does not state any operational prior authorization procedures or explicit authorization/denial triggers for CPT 93583 or related codes.
- No prior authorization procedure described in excerpt
- No operational authorization/denial triggers present
Documentation Requirements
Documentation must demonstrate that all medical necessity criteria are met. Records should support symptom duration, NYHA class, echocardiographic findings (including LV wall thickness, systolic anterior motion, LVOT gradients), prior optimal medical therapy, and absence of coronary disease that would preclude the procedure.
- Symptom duration ≥ 6 months despite optimal drug therapy and other measures
- NYHA class III or IV documented
- Echocardiography: asymmetric subaortic HOCM, LV wall thickness (>13 mm adults; 15 mm for athletes), systolic anterior motion, LVOT gradient values
- Documentation of prior therapies/trials (beta-blockers, calcium-antagonists, DDD pacing, prior myotomy/myectomy) and their outcomes
- Absence of coronary artery disease that would preclude procedure
Prior Therapies Required
Patients should have had optimal medical therapy and consideration/trial of device therapy where applicable prior to PTSMA. The excerpt specifies at least 6 months of severe symptoms despite optimal drug therapy (e.g., beta-blockers, calcium-antagonists), dual-chamber pacing therapy and/or ineffective previous surgical myotomy/myectomy. Allow sufficient time to assess effects of chronic DDD pacing when used.
- Optimal drug therapy: beta-blockers, calcium-antagonists
- Consideration/trial of DDD (dual‑chamber) pacing where applicable
- Previous surgical myotomy/myectomy documented as ineffective when applicable
- Allow adequate follow-up time to assess DDD pacing benefits
Step Therapy
No step therapy requirements are described in the provided portion of the document.
- Excerpt contains no step therapy or quantity-limit constraints
Policy History / Disclaimer
The document portion includes policy history and a disclaimer. The policy history shows last review dates and effective/next review dates; the bulletin includes the standard Aetna disclaimer about the policy being informational and subject to change.
- Effective date: 08/14/2001
- Last review: 07/27/2023
- Next review: 06/13/2024
- Policy disclaimer: bulletin not a contract; subject to change
Coverage Limitations
Procedures for indications other than adult hypertrophic obstructive cardiomyopathy (HOCM) meeting the stated criteria are considered experimental/investigational and are not eligible for coverage per the excerpt.
- PTSMA considered experimental/investigational for all other indications
Clinical Background
Hypertrophic obstructive cardiomyopathy (HOCM) is characterized by asymmetric interventricular septal hypertrophy that can produce a dynamic left ventricular outflow tract (LVOT) gradient. Systolic anterior motion (SAM) of the mitral valve frequently contributes to obstruction and symptoms such as dyspnea, angina, presyncope or syncope. Echocardiography is the primary diagnostic modality used to document asymmetric septal thickening, SAM, and to quantify the resting and provoked LVOT gradients that guide therapy.
Definitions and Classifications
Policy History and References
Policy became effective.
Policy was last reviewed.
Next scheduled policy review date.
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