cpap titration treatment

I have been utilizing my CPAP treatment since my diagnosis and until this year, when I moved and began seeing a new doctor, I have had my machine on automatic titration. My new doctor said that this was not a good thing and I went through a titration study. My machine is now set to a setting of 9. Previously, when my machine was on automatic, my machine was exerting pressures to 22 at certain points in time throughout the night.

with sleep apnea. Did you do a follow-up sleep test (polysomnography with titration)? Or, did they actually put a CPAP mask on you during your test(s) at the laboratory? If not, you may need to see your sleep physician again and have a PSGT (Polysomnography with titration). If your problem is not "simple" obstructive sleep apnea, CPAP/BiPAP/AutoPAP, etc. may not meet your needs.

Hi Bob How long have you had your machine mate, how often do you change the silicone face mask, how often do you clean the whole apparatus, how many hours on average per night or week do you use the CPAP machine , do you use a humidifier on the CPAP , have you had any trouble with the CPAP. I have had my CPAP machine just over 12 months I have used it for approx 1850 Hrs and used two face masks ( silicone ) I have my humidifier set at 2 no more.

Yes, there can be a link. Every time you stop breathing, you create a vacuum effect that can suck up your stomach juices into your throat (causing your voice box inflammation which can lead to hoarseness, cough, lump sensation and post-nasal drip). It's been shown that stomach contents can then either go into your lungs or into your ears or sinuses. Consider that it's not just acid, but bile, digestive enzymes, and bacteria that's coming up.

Been on the CPAP for the last year. three months ago I had a septoplasty...All went well. Two weeks ago I had UPPP surgery and ever since the first night as soon as I fall asleep I start choking. Seems like even when I'm awake i can take a deep breath through my nose and feel my tonge/throat closing off. I"ve video taped myself sleeping the last few nights and it's happening about every 5 to 10 minutes. I'm choking on the inhale...

My original polysomnography showed 1 obstructive apnea, 1 central apnea, 2 hypopneas and 148 respiratory effort-related arousals in 6 hours of sleep, with greatly increased stage 1 and significantly decreased stage 3 and REM sleep, so I think UARS fits. However, the 2 titration studies I had seemed to have been focused on apnea; the CPAP pressure used only reduced my RERAS to 12/hr hour, and the sleep fragmentation was worse than my diagnostic study.

I had a home sleep study done and it came out that I had apnea and they ordered a CPAP titration. I also had some other bloodwork done and i was wondering if this could have anything to do with my symptoms and apnea. B12 --231 (reference range 211-911) Folic Acid --- 20.9 (says supposed to be below 5.4) I know that folic acid can mask B12 deficiency and was wondering if this could be my problem.

First of all, you are placing yourself at risk taking sedating meds and not using your CPAP. Secondly, you will not be able to fix your sleep while you have untreated sleep apnea, unless you take enough meds to knock out a horse, and then you'd really be in danger. My nonprofessional opinion is that you should focus your efforts on making CPAP work. Maybe your pressure needed adjusting or you needed a different mask.

i wont go to bed till i know that i can sleep..im on disabilty so i dont have any times to be any place..so i go to bed at 3:00am..i put the mask on and mess with it so it wont leak..once i get it taken car of,..i fall asleep within 15 min or less..if ur apnea then you know that the 1st 90 min is ( rem) sleep..then within 2-3 hrs you get to level 3 stage..then stage 4.. well i never seem to get to stage 4..i never did on my sleep study..about 30 min there..

I was diagnosed with OSA about 2 years. For all this time I am struggling with the cpap machine/mask. I got over the embarrsement/discomfort but still having problems that make me not use it. I have a good machine with humidfyer. But I get so bone dry in the mouth-tongue that it wakes me up.(no moisture to even swallow) I have tried different things but guess I am still mouth breathing with mask on. I have a full faced Mirage Quattro mask.

However, I know that there is more to it than that, because prior to CPAP therapy I did not experience this, and with the increase in CPAP pressure to 12 cm H20 following titration, the swelling is quite severe. More telling is the fact that when I suspended CPAP therapy for almost a week (due to difficulties with the DME provider), the swelling went down (and night time visits to the bathroom to urinate returned).

I stopped breathing 15 times an hour and my Blood O2 got to 82%.. I dont know, are those results bad or mid range?? I had a CPAP titration last night and slept great. It took a while to get used to the mask but i felt really good today. I hope over time i will be back to 100%. The only thing is that the machine pumped my stomach full of air.. Makes an unpleasant morning!! I will be set up on a machine by the end of the week..

The problem started for me one fine day when there was absolutely no stress in my life. I have been using CPAP after the titration study, but the sleep pattern hasn't changed. This leads me to believe something else as the cause of this fragmented sleep pattern. Any ideas?

I was told that you correct it with a CPAP or variant of. I understand this, but what is causing this to happen. I had two sleep obstructions, four nuero, two mixed, and 29 hypopneas. I never went into Deep sleep NR3 or NR4. It recorded I had zero leg movements, but I kept popping off the leads on my legs from moving them. Venting aside, what is the path I must follow to get the underlying cause answered? Since childhood I have many symptoms of Narcolepsy and other sleep Disorders.

Welcome to the club. CPAP made a tremendous difference for me in terms of the quality of my sleep. I think it's been two years or so. I do have OSA. I've never really understood the difference between hypopnea and obstructive sleep apnea. I think I understand central sleep apnea, and to be honest, I'm surprised more MS patients don't mention that. I'm sure our friend Dr. Park could add some clarification here, if he reads this forum regularly.

• With use of a CPAP or bilevel, they show a pattern of central apneas and hypopneas that meets the Centers for Medicare Services (CMS) definition of CSA Patients with CompSA may be seen as those who cannot tolerate conventional CPAP or bilevel therapy both during lab titration and at home. Neither CPAP nor bilevel therapy seems to alleviate their sleep disorders.

Could you include CPAP as a treatment? CPAP is so commonly used that it deserves a place. Thanks. Dave.

As important is to start treatment immediately. Even if another course may be chosen down the line, CPAP treatment can be used until then, and who knows, one may decide to just continue with it. I've used it for a few years and while there was an adjustment phase, I now find it quite comfortable and very effective. It would be hard to say if SA is for forever with you. As with most things in life, we do what we've gotta do till we don't have to do it any longer.

The most common treatment and arguably the most consistently effective treatment for sleep apnea is the use of a continuous positive airway pressure (CPAP) device. In addition to CPAP, a dentist specializing in sleep disorders can prescribe Oral Appliance Therapy (OAT). So please contact your doctor if you have not done it before so that treatment can be started. Regards and God bless.

I am not sleeping as I keep taking off the CPAP to blow my nose or to cough. Could I be allergic to the CPAP, or the dirt or germs in the tubing, or to the air that is sucked in thru the CPAP? No matter how good I feel in the day.....I get worse at night? Help Please.

I am Garth Howell, live in the UK and am a OSA sufferer and am on CPAP treatment. Becoming aware of how under diagnosed sleep apnea is and how dangerous the condition is I decided to write a book about and have published it as an Amazon Kindle book and a paperback via Amazon Createspace and it is titled All you need to know.... about Sleep Apnea by Garth Howell and can be viewed on Amazon by going to the Kindle store and selecting Garth Howell.

I had to discontinue using my cpap, due to chronic lung infections. Changing the tubing, keeping it spotless, did not help prevent infection for me. Stopping the cpap treatment, is the only thing that prevented the chronic lung infections...and I always used the humitifer, which never helped prevent any infection... I regret ever having the sleep study and I regret what all the money and time it cost me, and the suffering of 3 years of lung infections...I am so done using the cpap treatment!

If so, are you certain your treatment is effective? Some machines record treatment data that reports how well the treatment is working for your apnea. Also, if you are on CPAP, some masks have straps that are too tight around the lower back of the head and hurt the muscles of the neck that connect the head and shoulders.

Cpap titration treatment

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