The Office of Inspector General (OIG) released a report (June 2018) regarding replacement Positive Airway Pressure (PAP) supplies and denied claims. According to their report, most Medicare claims that DME suppliers submitted for replacement PAP device supplies did not comply with Medicare Local Coverage Determination (LCD) requirements. A statistical sample of Medicare claims for replacement PAP device supplies paid in 2014 and 2015 was completed. A total of 110 claims were reviewed with 24 claims complying with Medicare requirements and 86 claims being noncompliant.
Claims that did not comply with Medicare requirements included the following errors:
- Physicians’ orders were not in accordance with LCD requirements - Fifty-three claims had invalid orders due to missing required elements, lack of a detailed written order prior to billing, missing supplies that were billed, or lack of a new order after change in supplier.
- Replacement supplies were not reasonable and necessary. Fifty claims did not have a proper request for replacement supplies. Twenty-two claims did not have the proper documentation to support that the beneficiary continued to need PAP therapy and replacement of supplies. Only one claim was found where supplies dispensed were then allowed.
- Thirty-six claims had no Proof of Delivery (POD) documentation.
- Three claims had no response to their documentation request.