Summary & Overview
HCPCS C1740: Leadless Electrode and Battery for Left Ventricular Pacing
HCPCS Level II code C1740 denotes an implantable leadless electrode, transmitter and battery system used for sequential left ventricular pacing. The code represents a specialized cardiac implant designed to provide targeted pacing of the left ventricle, an important option in cardiac resynchronization and management of certain heart rhythm disorders. Nationally, such devices affect hospital and outpatient procedural billing, device supply chains, and cardiac device utilization patterns.
Key payers in this analysis include Aetna, Blue Cross Blue Shield, Cigna Health, UnitedHealthcare and Medicare. Readers will find a concise overview of the code’s clinical purpose and typical settings of implantation, an explanation of what benchmarks and coverage items are commonly examined for implantable cardiac devices, and context on coding relationships that influence reimbursement and facility billing. The publication outlines where C1740 fits within device-based cardiac care and what aspects of policy and billing readers should monitor.
The report covers: code definition and clinical context; typical sites of service and service type; payer coverage landscape and common contractual considerations; and areas for further review such as claims bundling, device supply reporting, and hospital outpatient payment impacts. Data not available in the input is noted where applicable.
Billing Code Overview
HCPCS Level II code C1740 describes a leadless electrode, transmitter, battery (all implantable), for sequential left ventricular pacing. This device is intended for implantation to provide sequential left ventricular pacing as part of cardiac rhythm management therapy.
Service type: Implantable cardiac device — left ventricular pacing system
Typical site of service: Inpatient or outpatient hospital setting or ambulatory surgical center where device implantation and generator placement for cardiac pacing are performed
Data not available in the input.
Clinical & Coding Specifications
Clinical Context
A 76-year-old patient with a history of ischemic cardiomyopathy and persistent symptomatic heart failure despite guideline-directed medical therapy is evaluated for device-based cardiac resynchronization. The patient has chronic atrial fibrillation with a slow ventricular response and prior infections at transvenous device sites, making a conventional transvenous left ventricular lead high risk. A multidisciplinary heart team (electrophysiology, cardiac anesthesia, and implant nursing) determines the patient is a candidate for implantation of a leadless electrode, transmitter, and battery system for sequential left ventricular pacing (C1740). The clinical workflow includes pre-procedure imaging (echocardiography, chest radiograph), device selection and consent, pre-op antibiotic prophylaxis, intraoperative device implantation in a cardiac catheterization or hybrid operating room under monitored anesthesia care or general anesthesia, device programming and interrogation, post-procedure monitoring for hemodynamic stability and device function, and discharge planning with outpatient device clinic follow-up for remote monitoring and longitudinal pacing optimization.
Coding Specifications
| Modifier | Description | When to Use |
|---|---|---|
51 | Multiple Procedures | When the leadless left ventricular pacing system implantation is one of multiple distinct procedures performed the same day and payer allows modifier . |