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Interrogation device evaluation (in person) with analysis, review and report by a physician or other qualified health care professional, includes connection, recording and disconnection per patient encounter; wearable defibrillator system

CPT4 code

Name of the Procedure:

Interrogation Device Evaluation (in person) with Analysis, Review, and Report by a Physician or Other Qualified Health Care Professional; Wearable Defibrillator System

Summary

This procedure involves an in-person evaluation of a wearable defibrillator system. A healthcare provider connects the device to specialized equipment, records necessary data, analyzes the device's performance, reviews the findings, and prepares a detailed report.

Purpose

The procedure is performed to ensure the wearable defibrillator system is functioning correctly and effectively detecting and treating potentially life-threatening cardiac arrhythmias. The goal is to verify that the device provides adequate protection to the patient against sudden cardiac arrest.

Indications

  • Patients with a high risk of sudden cardiac arrest.
  • Individuals who have experienced a recent heart attack or have newly diagnosed heart failure.
  • Patients awaiting implantable defibrillator surgery or those who are temporarily unable to receive one.

Preparation

  • Patients are usually advised to wear the defibrillator as prescribed continuously.
  • No specific pre-procedure instructions such as fasting are typically required.
  • Patients should bring any relevant medical records or device usage logs to the appointment.

Procedure Description

  1. Connection: The healthcare provider attaches the wearable defibrillator system to a specialized diagnostic device.
  2. Recording: Data from the defibrillator is recorded, including any arrhythmic events or shocks delivered by the device.
  3. Analysis: The physician reviews the recorded data to assess the device's performance and check for any malfunction or necessary adjustments.
  4. Review: The findings are discussed with the patient.
  5. Report: A comprehensive report is prepared outlining the device's performance and any recommendations for adjustments or further action.

Duration

The procedure typically takes about 30 to 60 minutes.

Setting

The procedure is usually performed in a hospital or outpatient clinic.

Personnel

  • Cardiologist or cardiac electrophysiologist
  • Trained nurses or medical technicians

Risks and Complications

  • Minimal risk as this is a non-invasive procedure.
  • Potential discomfort from electrode attachment or skin irritation.
  • Rarely, inaccurate readings could occur if the device is not properly connected.

Benefits

  • Ensures the wearable defibrillator system is functioning correctly.
  • Provides peace of mind to patients and their families.
  • Early detection of device malfunction can prevent life-threatening events.

Recovery

  • No specific recovery period; normal activities can typically be resumed immediately after the evaluation.
  • Patients might need follow-up appointments based on the findings.

Alternatives

  • Implanted Cardioverter Defibrillator (ICD) if the patient is eligible.
  • Manual external defibrillators in less critical cases.
  • Pros and cons depend significantly on the individual's medical condition and risk profile.

Patient Experience

  • During the procedure, patients may feel minor discomfort from the attachment of the device electrodes but generally not pain.
  • After the procedure, they might feel reassured knowing their device is functioning properly.

Medical Policies and Guidelines for Interrogation device evaluation (in person) with analysis, review and report by a physician or other qualified health care professional, includes connection, recording and disconnection per patient encounter; wearable defibrillator system

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