LyleHaze wrote:So there's an interesting point for this discussion. How many people have OSA and want to treat it, but are not willing to be officially diagnosed?
If it were your brother or sister, would you help them?
Lyle,
Most definitely I would help them. I would be willing to help anyone I know to get them using the equipment if the symptoms are there but there were some reason blocking them from seeking treatment.
As for OTC xPAPs, I agree that most of us here are here because we want to be informed patients and in charge of our health. There are too many sheeple out there who just follow the doc's orders and don't push back, research, question, etc.
Yeah, I go to WebMD, but more to confirm a diagnosis than to find a "disease of the week." I was the silly person who looked up the symptoms of appendicitis (actually I was looking for the side symptoms were prevalent on) prior to calling the doctor at 3:00 a.m. because I didn't want to bother them if it wasn't anything serious. Then when she told me to go to the ER, I said "well couldn't it just be a pulled muscle - I was weeding a lot today..." She replied that she couldn't diagnose a pulled muscle over the phone and I should go to the ER. I did. Appendix came out.
When the doc first prescribed a sleep study, when I backpedaled after he first tried to push Provigil at me, that's when I went on the Internet and collected all the information I could about sleep disorders. I figured out that I really wasn't a candidate for Narcolepsy but I sure had all the symptoms of OA and had had them for a long time.
I knew before the study that I had OA, RLS and PLMD. It was just a confirmation for me. I found out some interesting things that needed addressing in addition to just Apnea (high leg movements with arousal, RLS medication not correct, lack of Delta sleep, etc.) But the main issue was SDB and treated with xpap.
I was so frustrated in the amount of time it took between getting the order for the study and actually getting my equipment. That was almost 4 months! If machines were available OTC, I doubt I would have purchased one prior to the study even knowing I most likely had OA. Too cost prohibitive. But, if my doc had prescribed an APAP with data capabilities to check and titrate me and insurance covered it, I would have done so.
It does irk me that we need a prescription to get equipment. It also ticks me off that we don't always get the equipment we want without a fight. Every time I see how much insurance is charged vs. what they pay out (contracted rates) I flip. There is so much seriously wrong with the medical/insurance community today I don't even know where to begin. If I'm Joe Blow (no pun intended) walking in off the street without insurance I would have paid about 30k for my sinus surgery. With insurance writeoffs, etc. they were paid about 5. I think that's so backwards.
I don't think anyone off the street should be able to just go get an xPAP, but with a note (not a script per se) from their doc, they should have access to whatever they want to buy. I would probably prefer to see standards of care instituted instead where the mask fitting would have to be done in a setting where the patient could lay down, possibly even nap, try all kinds of positions, masks, etc. with a trained person fitting them and showing them how to use the mask properly. I would also like to see it SOP to have follup calls and visits, with data reviews for those with data capable machines, to ensure that treatment is effective. If I were getting this type of service from my DME I wouldn't complain at the amount insurance is paying them. But it's more like "here's your equipment, good luck and see you in 6 months for new hoses and masks." Now THAT should be illegal!