A diagnosis of sleep apnea rarely changes or improves to the point CPAP would not be indicated. There is no mandate for re-testing when a replacement machine is acquired and the patient has been under the care of a physician, regularly discussed their CPAP therapy and indicated it is beneficial. The choice of a device to treat apnea is between the doctor and his patient and can be supported by a titration if the doctor deems it necessary, however; titration exams are never a requirement to obtain a PAP device. Medicare rules are typical. A patient qualifies for CPAP after an in-person clinical evaluation and a positive sleep test using PSG or type II, III or IV home sleep test. While the criteria for a positive sleep test is defined as greater than or equal to 15 events per hour, or 5 or more events per hour with documented symptoms of excessive daytime sleepiness, impaired cognition, mood disorders or insomnia, or documented hypertension, ischemic heart disease, or history of stroke.
https://www.cms.gov/medicare-coverage-da...?ncdid=226
Once that examination and testing has been satisfied, there is no requirement for a patient to be re-tested, including when obtaining a replacement CPAP. Patients entering Medicare that have been tested before obtaining Medicare coverage will continue to qualify for supplies and equipment provided they have previously met the diagnostic criteria, and have continued to be under the care of a treating physician and demonstrate continued benefits of the use of CPAP. Patients can be considered for
bilevel therapy if the treating physician (your doctor) makes the determinations described on this Medicare Policy summary by Resmed:
https://document.resmed.com/en-us/docume...er_eng.pdf
Treating physician documented that both of the following issues were addressed prior to changing a patient from an E0601 to an E0470 device due to ineffective therapy:
a. An appropriate interface has been properly fitted and the beneficiary is using it without difficulty. The properly fitted interface will be used with the E0470 device; and
b. The current pressure setting of the E0601 prevents the beneficiary from tolerating the therapy, and lower pressure settings of the E0601 were tried but failed to:
1. Adequately control the symptoms of OSA; or
2. Improve sleep quality; or
3. Reduce the AHI/RDI to acceptable levels.
In your case, your doctor needs to make these findings using your feedback on the efficacy of your treatment, where CPAP has failed to adequately improve symptoms of OSA, or improve sleep quality, or reduce AHI/RDI. Your Oscar data, qualitative feedback and other information can be used to make these determinations. There is NO REQUIREMENT for a test. For your husband, the use of
bilevel is not contingent upon a particular level of AHI in a diagnostic sleep test. The use of
bilevel is indicated by his need for two-channel pressure to resolve sleep quality, RDI and the factors listed above. His prescription for
bilevel can be made by his treating physician, which can overrule the "Recommendation" or conclusions of the sleep doctor. If you want discussion points for your treating physician, just have your husband try CPAP one night, and get his qualitative feedback. Why was he prescribed
bilevel previously? How does a one-night sleep test overrule the basis for his original
bilevel prescription? What are his current settings? Is he using pressure support?
Surround yourselves with a supportive medical team. Stay away from sleep specialists and clinics and DMEs who give you false information that you need more tests. Keep your original sleep tests and records and don't let anyone tell you to take another test. The purpose of a test is to extract money from you and your insurance and to make you a dependent on a quackery specialty. Stay with your treating physician and understand he has all the skill and power needed to support your sleep disordered breathing needs.