Mountain State Medical Policy Bulletin

Section: Durable Medical Equipment
Number: E-7
Topic: Pneumatic Compression Devices
Effective Date: April 2, 2007
Issued Date: September 10, 2007
Date Last Reviewed:

General Policy Guidelines

Indications and Limitations of Coverage

Lymphedema Pump and Appliances (E0650-E0673)
Pneumatic compression devices are covered for the treatment of lymphedema (457.0, 457.1, 757.0) or for the treatment of chronic venous insufficiency with venous stasis ulcers (459.81).

NOTE:
Pneumatic compression devices used for the treatment of arterial insufficiency (E0675) are considered experimental/investigational, and are not eligible for reimbursement. Despite the fact that these devices have received FDA approval, there is a lack of long-term studies demonstrating the efficacy of these devices. A participating, preferred, or network provider can bill the member for the denied device.

Date Last Reviewed:  01/2006

Lymphedema
When prescribed by a physician, the rental or purchase of an intermittent compression unit (segmental, non-segmental) for home use is warranted when lymphedema of the arm or leg exists.

Chronic Venous Insufficiency (CVI)
When prescribed by a physician, pneumatic compression devices are covered in the home setting for the treatment of CVI of the lower extremities only if the patient has one or more venous stasis ulcer(s) that have failed to heal after a six-month trial of conservative therapy directed by the treating physician. The trial of conservative therapy must include a compression bandage system or compression garment, appropriate dressings for the wound, exercise, and elevation of the limb.

General Coverage Criteria
Pneumatic intermittent compression units/lymphedema pumps and appliances may be covered as durable medical equipment (DME) only as a prescription item with appropriate physician oversight (i.e., physician evaluation of the patient's condition to determine medical necessity of the device, suitable instruction in the operation of the machine as to the pressure to be used and the frequency and duration of use, and ongoing monitoring of use and response to treatment).

When pneumatic compression devices are provided for conditions other than those listed, they will be denied as not medically necessary. A participating, preferred or network provider cannot bill the member for the denied service.

Syncardon Therapy
Syncardon therapy (97139) has not been proven to be medically efficacious in the treatment of lymphedema of the extremities. Therefore, Syncardon therapy should be denied as not medically necessary. The rental or purchase of a Syncardon unit (E1399) for home use should also be denied in the same manner. A participating, preferred, or network provider cannot bill the member for the denied service.

Coverage for outpatient physical medicine and/or 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

Lymphedema Pump and Appliances
A pneumatic intermittent compression unit/lymphedema pump, (e.g., Jobst pneumatic compressor) consists of an inflatable garment for the arm or leg and an electrical pneumatic pump that fills the garment with compressed air. The garment is intermittently inflated and deflated with cycle times and pressures that vary between devices.

Lymphedema
Lymphedema is the swelling of subcutaneous tissues due to the accumulation of excessive lymph fluid. The accumulation of lymph fluid results from impairment to the normal clearing function of the lymphatic system and/or from an excessive production of lymph. Lymphedema is divided into two broad classes according to etiology. Primary lymphedema is a relatively uncommon, chronic condition which may be due to such causes as Milroy's Disease or congenital anomalies. Secondary lymphedema, which is much more common, results from the destruction of or damage to formerly functioning lymphatic channels, such as radical surgical procedures with removal of regional groups of lymph nodes (for example, after radical mastectomy), post-radiation fibrosis, and spread of malignant tumors to regional lymph nodes with lymphatic obstruction, among other causes.

Chronic Venous Insufficiency (CVI)
Chronic venous insufficiency (CVI) of the lower extremities is a condition caused by abnormalities of the venous wall and valves, leading to obstruction or reflux of blood flow in the veins. Signs of CVI include hyperpigmentation, stasis dermatitis, chronic edema, and venous ulcers.


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

97139E0650E0651E0652E0655E0660
E0665E0666E0667E0668E0669E0671
E0672E0673E0675E1399  

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

References

Guideline for Management of Wounds in Patients with Lower-Extremity Arterial Disease, Wound, Ostomy, and Continence Nurses Society - Professional Assoc., June 2002

Rapid Foot and Calf Compression Increases Walking Distance in Patients with Intermittent Claudication; Results of a Randomized Study, J Vasc Surg, May 1, 2005; 41(5): 794-801

Hemodynamic Effects of Intermittent Pneumatic Compression in Patients with Critical Limb Ischemia, J Vasc Surg, October 1, 2005; 42(4): 710-716

NCD for Pneumatic Compression Devices (280.6)

LCD for Pneumatic Compression Devices (L11503)

View Previous Versions

[Version 005 of E-7]
[Version 004 of E-7]
[Version 003 of E-7]
[Version 002 of E-7]
[Version 001 of E-7]

Table Attachment

Text Attachment

Procedure Code Attachment


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 Mountain State Blue Cross Blue Shield 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.

Mountain State Blue Cross Blue Shield (MSBCBS) retains the right to review and update its medical policy guidelines at its sole discretion. These guidelines are the proprietary information of MSBCBS. Any sale, copying or dissemination of the medical policies is prohibited; however, limited copying of medical policies is permitted for individual use.