Aetna · Identified Aug 17, 2026Medium impact
Leadless Cardiac Pacemaker (CPB 0893, reviewed 2025-12-22)
Aetna considers FDA-approved leadless cardiac pacemakers, such as the Micra and Aveir systems, medically necessary when the member has symptomatic paroxysmal or permanent high-grade atrioventricular block, symptomatic bradycardia-tachycardia syndrome, or sinus node dysfunction (sinus bradycardia or sinus pauses), and also has a significant contraindication that precludes placement of conventional single chamber ventricular pacemaker leads. The listed contraindications are a history of an endovascular or cardiovascular implantable electronic device (CIED) infection or high risk for infection, limited access for trans-venous pacing, and the presence of a bio-prosthetic tricuspid valve. Aetna considers leadless pacemakers experimental, investigational, or unproven for all other indications, and considers a leadless pacemaker combined with cardiac resynchronization therapy, or with a subcutaneous implantable cardioverter-defibrillator for prevention of sudden cardiac death, experimental, investigational, or unproven.