Summary & Overview
HCPCS C1823: Implantable Non-Rechargeable Neurostimulator with Transvenous Leads
HCPCS Level II code C1823 identifies an implantable, non-rechargeable neurostimulator generator paired with transvenous sensing and stimulation leads. This code covers devices used to provide targeted neural stimulation via transvenous access for therapeutic neuromodulation. Nationally, such devices are significant for management of select neurologic and cardiac-related conditions where transvenous lead placement is indicated.
Key payers covered in typical coverage analyses include Aetna, Blue Cross Blue Shield, Cigna Health, UnitedHealthcare, and Medicare. Readers will find a concise overview of the clinical context for C1823, typical sites of service, and the kinds of benchmarks and policy considerations that influence coverage and billing for implantable neurostimulator systems. The publication summarizes reimbursement benchmarks, common billing modifiers and claim-line practices, and policy updates that affect coding and payment for transvenous neurostimulation systems. It also outlines clinical considerations relevant to billing, such as device type (non-rechargeable generator) and lead configuration (transvenous sensing and stimulation leads).
Data not available in the input: associated taxonomies, ICD-10 diagnoses, related CPT/HCPCS crosswalks, and specific payer policy details. The content supports national audiences seeking a clear coding and clinical snapshot for HCPCS Level II code C1823.
Billing Code Overview
HCPCS Level II code C1823 describes an implantable, non-rechargeable neurostimulator generator with transvenous sensing and stimulation leads. This device is used to deliver electrical stimulation via leads placed through the venous system to targeted neural structures.
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Service type: Implantation and management of an implanted neurostimulation system with transvenous leads
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Typical site of service: Hospital operating room or ambulatory surgical center for implantation; subsequent programming and follow-up may occur in outpatient specialty clinics or device clinics
Clinical & Coding Specifications
Clinical Context
A 62-year-old patient with drug-refractory, symptomatic bradyarrhythmia and documented episodes of syncope is evaluated by a cardiac electrophysiologist. After noninvasive testing and invasive electrophysiology study, the team determines that an implantable, non-rechargeable neurostimulator with transvenous sensing and stimulation leads (C1823) is indicated to provide chronic pacing and sensing therapy via transvenous leads. The typical workflow includes pre-procedure evaluation (history, medication review, informed consent, device and lead selection), perioperative antibiotic prophylaxis, implantation in an electrophysiology lab or hybrid operating room under conscious sedation or monitored anesthesia care, transvenous lead placement via subclavian or cephalic approach, creation of a subcutaneous generator pocket (usually left or right subclavian), intraoperative device interrogation and programming, wound closure, and immediate post-operative device and wound checks. Typical site of service is an ambulatory surgical center or hospital outpatient department; inpatient admission occurs if medical comorbidities require observation or if complications arise. Typical patient scenario modifiers that may apply include AS for anesthesia services, UE for an item furnished by the hospital to its outpatient, and NU for a new device. Postoperative care includes device interrogation at discharge and scheduled follow-up in device clinic for programming and remote monitoring enrollment.
Coding Specifications
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