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Excellus BlueCross BlueShieldCommercial · Coverage · Heart & Blood Vessels (Cardiovascular) · NY · Cardiology, Cardiothoracic SurgeryMedium impact

Left Atrial Appendage Closure Devices 7.01.92

Effective date
Sep 17, 2026
Identified
Jun 20, 2026

Summary

Percutaneous left atrial appendage occlusion devices, such as WATCHMAN and Amplatzer Amulet, are considered medically appropriate when the device is FDA approved, the patient has nonvalvular atrial fibrillation with a CHA2DS2-VASc score of 2 or greater, systemic anticoagulation is recommended, and long-term anticoagulation risks outweigh the risks of implantation. Surgical LAA exclusion during cardiac surgery is considered medically appropriate when the patient plans long-term anticoagulation after surgery, the goal is to reduce stroke risk, and the patient has atrial fibrillation with a CHA2DS2-VASc score of 2 or greater or equivalent stroke risk. Surgical LAA exclusion devices, including AtriClip, are considered investigational for stroke prevention in atrial fibrillation as a stand-alone procedure or during a thoracoscopic cardiac procedure, and the current effective date is September 17, 2026.

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What to do

Action · 6 steps
01Already effective September 17, 2026: Billing team, before billing percutaneous LAA closure (CPT 33340), confirm the device is FDA approved and the record documents nonvalvular atrial fibrillation with a CHA2DS2-VASc score of 2 or greater.
02Confirm the record shows systemic anticoagulation is recommended and that long-term anticoagulation risks outweigh device implantation risks, decided with an evidence-based decision tool that takes the patient's demonstrated bleeding episodes into account.
03If the patient can take short-term but not long-term oral anticoagulation, confirm this is documented in the medical record and decided through shared decision-making between the patient and the non-implanting physician (primary care physician and/or primary cardiologist).
04For surgical LAA exclusion during cardiac surgery, confirm the patient plans to continue long-term anticoagulation after surgery, the goal is reducing stroke risk, and the patient has atrial fibrillation (ICD-10 codes I48.0 through I48.21 or I48.91).
05CPT 33267 and 33269 are listed as (E/I) experimental/investigational in the code table.
06Codes may not be covered under all circumstances.

Codes mentioned

33267332683326933340I48.91

Original notice

Left Atrial Appendage Closure Devices 7.01.92
excellusbcbs.com · Always check the source before changing claims.
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