Cardiac Devices and Procedures for Occlusion of the Left Atrial Appendage (CPB 0791, reviewed 2026-06-25)
Summary
Aetna's Clinical Policy Bulletin 0791 covers percutaneous left atrial appendage closure (LAAC) for non-valvular atrial fibrillation only when the device has FDA premarket approval for its FDA-approved indication, the member meets the listed criteria, and LAAC is used as second-line therapy after oral anticoagulants. Surgical left atrial appendage ligation is covered for members with atrial fibrillation and a CHADS2 or CHA2DS2-VASc score of at least 2 who are undergoing open heart surgery and will continue long-term anticoagulation after surgery. Exclusion of the appendage alone during open heart surgery, the AtriClip device, and percutaneous closure with any device other than the Amplatzer Amulet and Watchman are listed as experimental, investigational, or unproven.
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