PAP Device Program

Highmark has implemented the DMEPOS Quality Program for PAP devices and accessories in an effort to ensure that high quality services are provided to our members with the goal of helping to improve medical outcomes.

To learn more about the program, including participation requirements, criteria for compliance, and reimbursement levels, please review the DMEPOS Quality Program Administrative Requirements below.

NOTE: The period from July 1, 2018, through June 30, 2019 will be the final period in which DMEPOS providers will be required to submit compliance measurement data.

Completed patient compliance data may be submitted as early as July 1, 2019. All final compliance data must be received by Highmark no later than Oct. 1, 2019.

Effective July 1, 2019, DMEPOS providers will no longer be required to perform compliance measurement activity.

Review Special eBulletin dated May 7, 2019 for additional information.

Last updated on 5/7/2019

 

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