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Apnea monitor, with recording feature

HCPCS code

Name of the Procedure:

Apnea Monitor with Recording Feature (E0619)

Summary

An apnea monitor with a recording feature is a medical device used to track and record breathing patterns in individuals who are susceptible to sleep apnea. This device helps monitor and detect episodes of apnea (a temporary cessation of breathing) and records data for further analysis by healthcare professionals.

Purpose

The apnea monitor addresses medical conditions such as sleep apnea. The primary goals are to:

  • Detect and record instances of apnea and hypopnea episodes during sleep.
  • Provide data to help diagnose sleep-related breathing disorders.
  • Assist in determining the effectiveness of treatments for sleep disorders.

Indications

The apnea monitor is indicated for individuals who:

  • Experience symptoms of sleep apnea, such as excessive daytime sleepiness, loud snoring, or observed episodes of stopped breathing during sleep.
  • Have been diagnosed with sleep apnea.
  • Require monitoring due to conditions like chronic obstructive pulmonary disease (COPD) or heart failure.

Preparation

  • No specific preparation, such as fasting or medication adjustments, is generally needed.
  • A brief consultation to discuss how to use the device properly.
  • Patients may undergo a polysomnography to confirm sleep apnea diagnosis before the use of the monitor.

Procedure Description

  1. Device Setup: The apnea monitor is set up by healthcare professionals, ensuring proper placement and functionality.
  2. Attachment: The patient attaches sensors to their body, usually around the chest and abdomen, and sometimes on a finger or near the nose.
  3. Operation: As the patient sleeps, the monitor tracks their breathing, heart rate, and oxygen levels.
  4. Data Recording: The device records data continuously throughout the night.
  5. Data Review: After the monitoring period, the collected data is reviewed by healthcare professionals to assess breathing patterns and identify apnea episodes.

Duration

The monitoring is conducted overnight, typically for 6-8 hours.

Setting

The procedure is performed at the patient's home, often after initial setup and instruction at a hospital or outpatient clinic.

Personnel

  • Respiratory therapists or sleep specialists set up and provide instructions.
  • Sleep technologists and physicians review and interpret the recorded data.

Risks and Complications

  • Mild skin irritation from sensor attachment points.
  • Discomfort or inconvenience during sleep due to the equipment.
  • Rarely, false negative or positive results that may necessitate further testing.

Benefits

  • Early detection and accurate diagnosis of sleep apnea and other sleep disorders.
  • Improved treatment plans leading to better quality of life.
  • Collection of comprehensive data that supports ongoing healthcare management.

Recovery

  • Minimal recovery is needed. The patient can resume normal activities immediately after the monitoring period.
  • Follow-up appointments may be scheduled to review results and discuss treatment plans.

Alternatives

  • Polysomnography: A comprehensive sleep study conducted in a specialized lab. It's more detailed but less convenient.
  • Home Sleep Apnea Test (HSAT): Similar to an apnea monitor, but often less comprehensive.
  • Clinical Observation and Questionnaires: Less objective but useful for initial assessments.

Patient Experience

  • The patient may feel self-conscious or experience mild discomfort due to wearing monitoring equipment.
  • Usually, there's no pain, but sleep patterns might temporarily be disturbed.
  • Clear instructions and minimal invasiveness ensure a generally straightforward experience.

Pain management is usually unnecessary as the procedure is non-invasive and primarily involves monitoring.

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