Summary & Overview
CPT 0927T: Implantable Cardiac Contractility Modulation–Defibrillator Interrogation Evaluation
CPT code 0927T represents an in‑person interrogation and evaluation of an implantable cardiac contractility modulation–defibrillation system. This procedural code documents the hands‑on connection to the implanted device, capture and analysis of device data, clinical review of findings, and preparation of a report. The code is relevant nationally as the use of advanced cardiac implantable devices grows and payers standardize coverage and billing practices for device management services.
Key payers covered in this summary include Aetna, Blue Cross Blue Shield, Cigna Health, UnitedHealthcare, and Medicare. Readers will find a concise overview of the clinical context for the service, common billing modifiers associated with device services, typical sites of service, and the primary operational components of the encounter. The publication also outlines what to expect in benchmarking and policy discussions: how payers approach coverage for device interrogation services, documentation elements that support medical necessity, and typical reporting elements that accompany device evaluations.
This national‑level summary is intended for clinicians, billing professionals, and policy analysts who need a clear account of what CPT code 0927T captures, why it matters in care delivery and reimbursement workflows, and the areas where payers and providers commonly focus when recording and adjudicating device evaluation services. Data not available in the input.
Billing Code Overview
CPT code 0927T describes an in-person interrogation device evaluation for an implantable cardiac contractility modulation–defibrillation system. The service includes connecting to the implanted device, recording device data, analyzing the information, reviewing the results with clinical interpretation, and preparing a report for the patient’s medical record.
Service Type: Device interrogation and evaluation
Typical Site of Service: Hospital outpatient department or specialized cardiac device clinic (in-person)
Clinical & Coding Specifications
Clinical Context
A 68-year-old patient with symptomatic heart failure and reduced ejection fraction, previously implanted with an implantable cardiac contractility modulation–defibrillation (CCM‑D) system, presents for a scheduled in‑person device interrogation. The clinical workflow begins with patient check‑in and device history review, including indication, implantation date, and recent events. The provider performs connection to the device programmer and interrogates stored telemetry and diagnostics, including sensing thresholds, lead integrity, battery status, therapy delivery logs, and arrhythmia records. Recorded data are analyzed for therapy efficacy, arrhythmia detection/appropriate shocks, and device performance issues. The provider reviews findings with the patient and documents clinical interpretation and recommended follow‑up. A formal written report is prepared and placed in the medical record. Typical site of service is an outpatient cardiology clinic or device clinic; occasional evaluations occur in the hospital setting for inpatients with device‑related concerns. Common clinical scenarios include routine scheduled follow‑up, post‑procedure baseline checks, evaluation after syncope or palpitations, and assessment following device alerts or shocks.
Coding Specifications
| Modifier | Description | When to Use |
|---|---|---|
22 | Increased procedural service | Use when work required is substantially greater than typically required for 0927T, documented and justified in the record. |