Last Modified: 7/4/2023
Location: FL, PR, USVI
Business: Part B
The following is a quick reference guide for physicians and non-physician practitioners concerning Medicare’s coverage of oxygen and oxygen equipment.
Claims for oxygen must be supported by medical documentation in the patient’s record.
• A condition requiring home use of oxygen,
• The oxygen flow rate; and,
• An estimate of the frequency, duration of use (e.g., 2 liters per minute, 10 minutes per hour, 12 hours per day), and duration of need (e.g., 6 months or lifetime); and,
• Any concerns for variations in oxygen measurements that may result from such factors as the patient's age, the patient’s skin pigmentation, the altitude level, or a decrease in oxygen carrying capacity (when applicable)
The type of oxygen delivery system to be used must be specified (e.g., stationary concentrator and portable gaseous tanks). If a portable system is ordered, there are specific requirements that must be included in the medical record, including that the patient is mobile within the home and that the qualifying blood gas study was performed either at rest or while exercising, but not while asleep.
In addition, for scenarios where the beneficiary has different daytime and nighttime oxygen flow requirements, these values must be documented in the patient's medical record. This information is used by the DME supplier to determine the appropriate billing information for Medicare.
Medicare can make payment for home oxygen only when the patient's medical record shows that the beneficiary has a condition expected to improve with home oxygen therapy, and meets medical documentation, test results, and health conditions required for coverage.
The Comprehensive Error Rate Testing (CERT) contractor has identified multiple errors in claims received for oxygen equipment and supplies. These errors include:
• Missing documentation of oxygen orders prior claim submission
• No documentation to support continued need for home oxygen therapy.
For continued coverage of oxygen, documentation must be included in the medical record supporting continued medical need. If oxygen is initially prescribed for short term use, an evaluation of a repeat test is required as well as a new order.
DMEPOS suppliers are your partners in caring for your patient. They will not receive payment from Medicare for the items that are ordered if you do not provide information from your medical records when it is requested. Furthermore, not providing this information may result in your patients having to pay for the item themselves. To help patients, the DME suppliers, and the Medicare program, be sure to verify that the medical documentation supports the oxygen ordered as this allows Medicare to pay claims appropriately and efficiently.
For additional information and resources on Medicare's coverage of oxygen and oxygen equipment, visit the DME MAC contractor websites.
Jurisdiction A (CT, DE, MA, ME, MD, NH, NH, NY, PA, RI, VT, District of Columbia) Jurisdiction C (AL, AR, CO, FL, GA, LA, MS, NM, NC, OK, SC, TN, TX, VA, WV, Puerto Rico, U.S. Virgin Islands) Physician’s Corner Jurisdiction D (AK, AZ, CA, HI, ID, IA, KS, MO, MT, NE, NV, ND, OR, SD, UT, WA, WY, American Samoa, Guam, Northern Mariana Islands)
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