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Please help: Day 9 with CPAP and AHI still over 7 (Oscar data included)
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09-21-2021, 01:42 PM
RE: Please help: Day 9 with CPAP and AHI still over 7 (Oscar data included)
I'm not sure my other message came through, but as I stated, I've already told my sleep clinic how I feel about my treatment. I told them I don't feel an effect from the treatment and their response was to encourage me to stop using CPAP and move on, since they don't think an AHI this low can cause my symptoms of fatigue. They said that I can continue to use it if I really insisted but they don't feel it's necessary. Thus my subjective feeling of treatment isn't even an argument, since their position is that the subjective feeling comes from something not sleep related.
09-21-2021, 03:20 PM
RE: Please help: Day 9 with CPAP and AHI still over 7 (Oscar data included)
And of course we know then that they don't want to credit Central Apnea as the cause. They can't and won't be of any help. In this case, I'd say appealing to your doctor would be a real time waste. Feel free to quote me. Your doctor is a quack.
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01-20-2022, 05:38 AM
RE: Please help: Day 9 with CPAP and AHI still over 7 (Oscar data included)
Update: Fate has solved my issue for me. My nose in such a bad state that I'm no longer allowed to use CPAP (and can't since it causes pain). I need to get me teeth taken care of, and after that I will get a MAD device. I should've just went with MAD from the beginning and saved myself all this trouble, considering my super low AHI.
02-15-2022, 11:37 PM
RE: Please help: Day 9 with CPAP and AHI still over 7 (Oscar data included)
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(03-12-2021, 06:19 AM)ashwa Wrote: Hello. Hi! I can not speak to your CPAP results but I can speak to the problems associated with poor sinus drainage and a deviated septum. From the time I started using and benefits from a CPAP, I was less fatigued and was blessed with and extremely lower AHI. However, during the past two to three years sinus issues have affected my ability to sleep well and in some cases I could not use the device at all. This prompted me to see an ENT who says surgery in my case is not elective but medically necessary. The doctor could not use a 4mm scope to look into the nasal passage. He has assured me that surgery will open my left airwave and breathing will improve greatly. So I think it is reasonable to assume you too will benefit from surgery. Some other thoughts to consider. Are you using a comfortable mask? Do you have a good mask fit 90 to 100 percent of the time? Are you mouth breathing? Have you sought council with the DME who fitted you for the CPAP? Is this the device prescribed by your Doctor? Is the CPAP properly set per your Doctor's instructions? Have you talked to you Doctor about your concerns? I am sure there are others here who can add to my thoughts. Words of encouragement: My Doctor's initial impressions from the polysomnogprahy study included the following: severe central sleep apnea with 70% of the events being central apneas; severe obstructive sleep apnea; nocturnal hypoxia with a lowest SpO2 of 82% and 177 minutes spent below 89%; moderate snoring. Total sleep time was 313 minutes. Total number of respiratory events was 397 (51 OAs, 279 CAs, 39 mixed and 28 Hypopneas). My AHI was 76. The total sleep time during the titration study was 341 minutes where the number of respiratory events was 37 (2 OAs, 25 CAs, 2 mixed and 8 Hypopneas). Benefit: 2.4 AHI. At the final ASV pressure there were significant improvements: total of 6 events( 0 OAs, 0 CAs, 1 mixed and 5 Hypopneas). The lowest SpO2 was 91% and no time below 89%. Finally, while my treatment results may not be the norm, I am sure that there are forum members here who struggled a while until they found relief, weeks later after initial use or even longer, and you too will find benefits to your treatment. Be patient. Make use of the terrific membership here and their wealth of experience. |
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