Summary & Overview
CPT 33264: Implantable Defibrillator Pulse Generator Removal and Replacement
CPT code 33264 captures the surgical removal and replacement of an implantable defibrillator pulse generator in patients with leads to at least three cardiac chambers. This procedure is clinically important for maintaining or restoring device function when a pulse generator fails, reaches end of service life, or is implicated in device-related infection. Nationally, device replacement procedures carry implications for acute care resource use, perioperative management, and device registry reporting.
Key payers in this analysis include Aetna, Blue Cross Blue Shield, Cigna Health, UnitedHealthcare, and Medicare. The publication outlines coverage and billing benchmarks, common modifier usage, and clinical context relevant to electrophysiology and cardiac surgery service lines. Readers will find a concise explanation of the service description and typical sites of care, a summary of payer coverage considerations, and pointers to related service coding where available.
This overview is intended for revenue cycle professionals, coding and compliance teams, and clinicians involved in device management. It focuses on the code definition, clinical scenario, and where the service is commonly performed, providing a foundation for coding, billing, and administrative workflows. Data not available in the input is noted where applicable.
Billing Code Overview
CPT code 33264 describes the removal of a previously implanted defibrillator pulse generator and replacement with a new pulse generator for a patient with leads to at least three chambers of the heart. This procedure involves explanting the existing implantable cardioverter-defibrillator (ICD) pulse generator and inserting a replacement device while the transvenous leads for three-chamber therapy remain in place.
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Service type: Surgical device revision/replacement of an implantable defibrillator pulse generator
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Typical site of service: Hospital inpatient or outpatient surgical setting (electrophysiology lab or operating room)
Clinical & Coding Specifications
Clinical Context
A 68-year-old man with ischemic cardiomyopathy and prior implantation of a CRT‑D (cardiac resynchronization therapy defibrillator) presents with progressive device malfunction characterized by recurrent inappropriate shocks and non‑functioning pulse generator diagnostics. He has transvenous leads coursing to the right atrium, right ventricle and a left ventricular coronary sinus branch (three‑chamber system). The electrophysiology team schedules replacement of the implantable cardioverter‑defibrillator pulse generator under monitored anesthesia care in the cardiac catheterization/EP lab. The clinical workflow includes preoperative device interrogation, informed consent, antibiotic prophylaxis, sterile preparation, incision over the device pocket, removal of the old generator from the header, connection and testing of the existing leads to the new pulse generator, intraoperative sensing/threshold testing and defibrillation threshold testing as indicated, pocket closure, postoperative device interrogation and programming, and discharge with device follow‑up arranged. ICD‑10 diagnoses that commonly justify the procedure include lead or generator malfunction, device infection, and generator depletion requiring replacement.
Coding Specifications
| Modifier | Description | When to Use |
|---|---|---|
00 | Invalid or not in use in current CMS modifier set | Data not available in the input |