I was doing quite well with my therapy for a long time, but this has been a rough year for me, medically. Among other things, my data went a little awry (and I felt it) a few months ago. Told my PCP about it, as I haven’t had a sleep doc in years, and she insisted that I have another sleep study. As it’d been four years since my last, I acquiesced and said okay. My data had not indicated (to my eyes, anyway) that I needed to change my settings. But why my data suddenly indicated more activity was a mystery to me, and I figured they get more detailed info during a study. So I had the sleep study done in July, hoping they'd find something I had missed. They recommended that I change my settings to accommodate higher pressures, which I did, and my therapy’s been good again since then.
Fast-forward to now. One of my medical maladies required surgery just over two weeks ago. My therapy’s been off since, and I’m having to nap frequently. I’m sleeping about the same amount as I usually do (some nights more), so it’s not for lack of sleep that I'm experiencing daytime sleepiness. My usual (good therapy) data shows a normal AHI of under 2 every night, no periodic breathing, and almost 100% patient-triggered breaths. Since my surgery, my AHI can be anywhere under 10, there's lots more PB, and my patient-triggered breaths are down.
If you asked me how I’m sleeping and I had no data to review, I’d think I was sleeping pretty well for what I’ve gone through recently. As far as I know, the pain isn’t keeping me awake or making me restless. But the data shows how many more events I’m having (mostly hypopneas, but also CAs and OAs and periodic breathing), and the % of patient-triggered breaths has declined. The leaks are good, so I know it’s not that. I also don't seem to be hitting the ceiling on my IPAP pressure, so I don't think an adjustment is warranted. (But that's what I thought before my recent sleep study, too; I never saw data indicating that I approached the previous IPAP ceiling, either, but my data indicated that I was back to normal sleep with the new higher settings.) I’m waking often in the morning with dry mouth, but I'm still wearing the Hybrid, so I’m not losing therapy air via mouth-breathing; I’m just uncomfortably dry.
I’m not sure what, if anything, I can/should do to improve my sleep while I recover from the surgery. My new settings (EPAP 10-17, IPAP 10-25, PS 0-15) seem to be adequate, but maybe more oxygen would be a benefit? I use an O2 concentrator with my ASV at 1L per minute (prescribed a years ago). I don’t know if upping the setting (it can go from 1-5 LPM) would help alleviate the sudden uptick in events and/or the frequency in my periodic breathing. If I don’t change the settings or the amount of O2 I’m getting, what else might I change?
Perhaps I should leave everything alone, nap as needed, and just wait until my body has recovered more from the surgery? I don’t like having to nap, but I can when I need to, so it’s not imperative that I do something to solve the current problem. I just hate being tired during the day and seeing this awful data. Napping has been a luxury for me, and now it’s a necessity. I hope it’s only temporary.
I’m putting this out there to see what others think. Here's the data from a couple of typical nights lately:


Opinions/thoughts/ideas? TIA






