Morbius wrote: ↑Fri Feb 04, 2022 4:25 am
Well I'll toss in a couple things!
Pugsy wrote: ↑Thu Feb 03, 2022 11:15 pm
Which was just how critical is that medical profession line in the sand of 5.0 AHI????
IMO the "medical profession" as a whole, NEVER drew lines in the sand re: treatment for anything. Certainly, a good clinician wouldn't allow himself to be boxed in by insurance-driven criteria.
AHI has ALWAYS been under critical review. Even more so recently:
https://onlinelibrary.wiley.com/doi/ful ... /jsr.13066
That said, I'd really like to see some of these cases with <5.0 AHI with complete turnarounds in their lives. Were they HSTs? Self-diagnose and treat? "I feel great since starting CPAP, lowering my AHI from 3.1 to 2.5 and oh BTW stopped downing a bottle of Stoli every day!" Placebo?
I guess using the term "medical profession" probably wasn't the best but I can't think of any other term for the system that relies on the AHI marker for classification. I am also including the insurance system here which relies on a line in the sand before they will pay for anything. Doctors would be happy to treat whatever/however but insurance doesn't always want to pay for said treatment so that's where the line in the sand grows in importance.
My doc would be happy to prescribe a hot tub for my back problems but my insurance still won't pay for that hot tub I might want.

There's no doubt that a hot tub would help my general unwanted symptoms but not everyone has the funds to say screw the insurance I will just buy one on my own. Same thing applies to cpap therapy.
I did read that article you linked to and it does affirm what a lot of us have always said....we need to look at the big picture more and rely less on one set of numbers. Clinical correlation is still important.
This statement particularly hit home with me.
In summary, to have OSA is not necessarily the same as to suffer from OSA.
And I would also like to see some studies where someone has a nice low "normal" sub 5.0 diagnostic AHI but substantial clinical symptoms get resolved by going on cpap.
Subjective feelings are always difficult to measure though. I get that reality every time someone wants me to rate my pain levels from 1 to 10. It's not always so easy.
Then there's the "bad sleep from other factors" thing muddying up the waters and people want to put all their eggs in the OSA basket and expect cpap to fix them when cpap can't fix them.
You know the person who takes a medication that messes with sleep and makes them feel like crap during the day who starts cpap and doesn't see any improvement yet it's cpap failure because cpap didn't alleviate the problem when they expected cpap to fix a problem that it was never designed to fix but it's cpaps fault.
I guess all I can do is work with what we have currently though and perhaps at some point in the future we will have a different standard to work with when trying to help people sort through all these varying issues.
I am still of the opinion that cpap is worth at least trying for those that "suffer from OSA symptoms" and we can't blame those symptoms on anything else. Might get lucky and have success and even though a remote chance...a chance nonetheless. Expensive experiment though and with insurance not helping out due to their line in the sand it's an experiment that not everyone will be able to do.
Nothing is ever simple no matter how much we might want it to be.
I may have to RISE but I refuse to SHINE.