Highmark Medical Policy Bulletin

Section: Durable Medical Equipment
Number: E-35
Topic: Ultrasound Osteogenic Stimulator
Effective Date: April 30, 2001
Issued Date: April 30, 2001
Date Last Reviewed:

General Policy Guidelines

Low-intensity pulsed ultrasound has been investigated as a treatment of fracture nonunions. Low-intensity ultrasound can be delivered noninvasively with the use of a transducer applied to the skin surface overlying the fracture site and can be self-administered once daily for 20 minutes and continuing until the fracture has healed.

Devices used in this treatment (E0760) must be approved by the Food and Drug Administration (FDA). The Exogen 2000, also known as the Sonic Accelerated Fracture Healing System (SAFHS), has been approved for ultrasonic treatment of established nonunions, excluding the skull and vertebra. A nonunion fracture is defined as a fracture that has not united within a minimum of 3 months of the original fracture.

Therefore, low-intensity pulsed ultrasound treatment administered via an approved device, e.g., SAFHS, is considered medically necessary as a treatment of fracture nonunions of bones (733.82) excluding the skull and vertebra.

However, low-intensity ultrasound treatment used as an adjunct to conventional management (i.e., closed reduction and cast immobilization) for the treatment of fresh, closed fractures is considered not medically necessary. As such, it is noncovered and nonbillable by a participating/preferred provider.

Other applications of low-intensity ultrasound treatment are investigational, including but not limited to treatment of delayed unions or congenital pseudarthroses. Delayed unions are defined as a decelerating healing process as determined by serial X-rays.

Although ultrasound treatment is applied by the patient in the home setting, there may be physician involvement with this device. Eligible physician's services (20979) include assistance in positioning the device over an existing cast and instruction to the patient in the use of the device.


NOTE:

See Medical Policy Bulletin S-89 for information on Electrical Osteogenesis Bone Stimulation.

Procedure Codes

20979E0760    

Traditional (UCR/Fee Schedule) Guidelines

Refer to General Policy Guidelines

FEP Guidelines

Refer to General Policy Guidelines

Comprehensive/Wraparound/PPO Guidelines

Refer to General Policy Guidelines

Managed Care (HMO/POS) Guidelines

Refer to General Policy Guidelines

Publications

References

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Medical policies do not constitute medical advice, nor are they intended to govern the practice of medicine. They are intended to reflect Highmark's reimbursement and coverage guidelines. Coverage for services may vary for individual members, based on the terms of the benefit contract.

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