Jerry69 wrote:Been on CPAP for a little over a month. Currently using the Remstar Pro II with integrated heated humidifier that my DME set me up with. But, I've not been heating the humidifier. I put water in it, but that's all. So, only the water that will evaporate at room temperature, 70 degrees, gets added to the air.
My question: why bother with the humidifier. Can't be doing that much.
Indeed a humidifier is an added feature to deal with a xPAP emergent symptom. Another “band-aid” to cover a “band-aid” compliments of our “modern medicine”.
Jerry69 wrote: And my DME left instructions to '...empty the reservoir and clean every day. Allow to dry before use.' Does that make any sense?
I suppose it does if your goal is to be sure that there are the fewest microbia involved in the system – and of course the DME might be found responsible for anything the microbia did...
Jerry69 wrote: And, I use distilled water in it, which is rapidly consumed with the above maintenance regimen.
Modern medicine is not known for economy.
Jerry69 wrote:Further, the logic of the humidifier escapes me. I've been breathing room air when I sleep for my entire life. Never used a room humidifier. Once lived in a house with very humid air in the summer (No AC) and very dry air in the winter. "But, we always cracked a window to combat the dryness.) Now, we use AC for most of the summer here in florida and a little heat in the winter. We still crack the window in the winter.
Apparently the use of CPAP changes things for many people but not so much for you.
Jerry69 wrote:Why should CPAP require humidification?
Indeed in terms of it's intended purpose the fact that it does tend to foster the need for added humidification (and how it does it) is contrary to it's intended purpose.
Jerry69 wrote: ( I tried heating the humidifier one night, but found it to be 'unnatural'. I couldn't feel the 'normal' cool air entering my nose.)
Your system has been processing cool air for a long time. It would not like the change I suppose.
Jerry69 wrote: I suppose the inclination is to say, 'But, you are increasing the air flow." I don't think that is the case. I think our flow is the same, i.e., whatever is required by the lungs to oxygenate the blood.
You are so right!!! With good chemoreflexes even adding a bit of pressure should be a small matter to compensate for. The air use should be the same as the metabolic issues have not changed. You are at rest and in bed so should use little air. You should use only the air you need to keep the body going (and apparently you do) - - but...
Jerry69 wrote: Granted, if we are in apnea or hypopnea a lot, we are not getting as much air flow, but that is the purpose of CPAP, isn't it: to reduce the apneas and hypopneas to 'normal.'
Well now there are indeed obstructive apnea and hypopnea true enough. But what about the “other kind” of apnea and hypopnea?
Indeed there are those poor souls who might well have an obstructive apnea but then follow it with a hypocapneic central apnea. The only thing that CPAP can help us with is preventing the closure of the airway by not letting the pressure fall below the “critical closing pressure”. But the pressure of CPAP, I do believe and as many in this thread have already attested, works toward increasing the amount of air used and so also works toward causing hypocapnic central apnea and hypopnea.
Jerry69 wrote:BTW, when I post, I don't use a lot of 'IMO's', because since I'm the poster, it is obviously 'IMO'.
Any thoughts?
Jerry
I am not a mouth breather. Yet sometimes while using CPAP I wake up with a dry mouth.
Consistently this clears as I bring my air use down to those levels more appropriate for being at rest and in bed.
While I do agree with those who have mentioned that there is increased air use and so more water would be moved away from the airway walls I think the bigger problem is a lack of circulation in those airway walls which limits the production and distribution of saliva and mucous along with the frustration of metabolism in the tissues of the airway. I believe that this is caused by less carbon dioxide in the blood (carbon dioxide washed out by the increased air use) and so vascular constriction and limited oxygen transport (Bohr effect) - - along with higher stress hormone levels from any events the CPAP either failed to prevent or caused.
Oh that we all were like you whose chemoreflexes seem to be good enough to well adapt to CPAP pressure. And I am glad that I can now use less pressure and so now no longer need and do not use a humidifier. But for many this “band-aid added to a band-aid” is likely helpful.