Printer Friendly Version

Section: Durable Medical Equipment
Number: E-25
Topic: Pulse Oximetry Device
Effective Date: August 22, 2011
Issued Date: August 22, 2011
Date Last Reviewed: 01/2011

General Policy Guidelines

Indications and Limitations of Coverage

A pulse oximeter for home use is considered medically necessary durable medical equipment (DME) when one of the following indications is met:

  • To determine appropriate home oxygen liter flow for ambulation, exercise, or sleep; or
  • To monitor individuals on a ventilator at home; or
  • When a change in the member's physical condition requires an adjustment in the liter flow of their home oxygen needs; or
  • When weaning the member from home oxygen.

When used for indications other than those listed above including, but not limited to, asthma management or when used alone as a screening/testing technique for suspected obstructive sleep apnea (OSA), a pulse oximeter for home use is considered not medically necessary. 

Services that do not meet the medical necessity criteria on this policy will be considered not medically necessary. A participating, preferred, or network provider cannot bill the member for the denied service unless the provider has given advance written notice, informing the member that the service may be deemed not medically necessary and providing an estimate of the cost. The member must agree in writing to assume financial responsibility, in advance of receiving the service. The signed agreement should be maintained in the provider's records.

The pulse oximeter may also be used in a physician's office during non-invasive ear or pulse oximetry testing to determine oxygen saturation levels. When used in this setting, the device is not eligible for reimbursement. A participating, preferred, or network provider cannot bill the member for the denied service. For information on pulse oximetry testing, see Medical Policy Bulletin V-31, Medical Visits and Associated Services.

Coverage for durable medical equipment (DME) is determined according to individual or group customer benefits.

NOTE:
Total payments for a rental item may not exceed its allowable purchase price, except for those items identified as life sustaining DME. For information on continuous rental of life sustaining DME, see Medical Policy Bulletin E-38, Continuous Rental of Life Sustaining Durable Medical Equipment (DME).

Description

The pulse oximeter (E0445) is a device used to measure arterial (blood) oxygen saturation. A small clamp is placed on a patient's finger, toe or earlobe. A light beam from within the clamp is then passed from one side of the clamp to the other. The oximeter then interprets the information gathered and determines the saturation of oxygen in the blood. The data obtained from the device is then interpreted by a health care professional who uses the data to determine appropriate treatment of the patient.

The device, in addition to monitoring the oxygen level of the blood, can be equipped with an alarm which sounds when the oxygen level falls below a certain threshold. This alarm permits immediate definitive action to be performed. The definitive action may be as little as reattaching a dislodged clamp, to administering medical care in response to the condition which caused the oxygen level to fall below the specified threshold.

NOTE:
This policy is designed to address medical guidelines that are appropriate for the majority of individuals with a particular disease, illness, or condition. Each person's unique clinical circumstances may warrant individual consideration, based on review of applicable medical records.

Procedure Codes

A4606E0445    

Traditional Guidelines

Refer to General Policy Guidelines

FEP Guidelines

This medical policy may not apply to FEP.  Medical policy is not an authorization, certification, explanation of benefits, or a contract. Benefits are determined by the Federal Employee Program.

PPO Guidelines

Refer to General Policy Guidelines

Managed Care POS Guidelines

Refer to General Policy Guidelines

Publications

Provider News

04/2011, Guidelines change for pulse oximeters used in the home

References

American Association for Respiratory Care (AARC). AARC Clinical Practice Guideline. Pulse Oximetry. Respir Care. 1991;36(12):1406-1409.

American Association for Respiratory Care (AARC). AARC Clinical Practice Guideline. Oxygen Therapy in the Home or Extended Care Facility. Respir Care. 1992;37(8):918-922.

American Association for Respiratory Care (AARC). AARC Clinical Practice Guideline. Long-Term Invasive Mechanical Ventilation in the Home. Respir Care. 1995;40(12):1313–1320.

Gay PC. Chronic obstructive pulmonary disease and sleep. Respir Care. 2004;49(1):39-51; discussion 51-52.

Ingram G. The use (or otherwise) of pulse oximetry in general practice. Br J Gen Pract. 2005 July 1;55(516):501–502.

Ramsey R, Mehra R, Strohl KP. Variations in Physician Interpretation of Overnight Pulse Oximetry Monitoring. Chest. 2007 September;132(3):852–859.

View Previous Versions

[Version 004 of E-25]
[Version 003 of E-25]
[Version 002 of E-25]
[Version 001 of E-25]

Table Attachment

Text Attachment

Procedure Code Attachments

Diagnosis Codes

ICD-9 Diagnosis Codes

ICD-10 Diagnosis Codes

Glossary





This policy is designed to address medical guidelines that are appropriate for the majority of individuals with a particular disease, illness, or condition. Each person's unique clinical circumstances may warrant individual consideration, based on review of applicable medical records.

Medical policies are designed to supplement the terms of a member's contract. The member's contract defines the benefits available; therefore, medical policies should not be construed as overriding specific contract language. In the event of conflict, the contract shall govern.

Medical policies do not constitute medical advice, nor the practice of medicine. Rather, such policies are intended only to establish general guidelines for coverage and reimbursement under Highmark West Virginia plans. Application of a medical policy to determine coverage in an individual instance is not intended and shall not be construed to supercede the professional judgment of a treating provider. In all situations, the treating provider must use his/her professional judgment to provide care he/she believes to be in the best interest of the patient, and the provider and patient remain responsible for all treatment decisions.

Highmark West Virginia retains the right to review and update its medical policy guidelines at its sole discretion. These guidelines are the proprietary information of Highmark West Virginia. Any sale, copying or dissemination of the medical policies is prohibited; however, limited copying of medical policies is permitted for individual use.



back to top