cpap titration trial

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.

What type? What are your thoughts regarding automatic titration vs. setting the titration to a constant setting? Do some people require oral devices in conjunction with CPAP treatment? Thank you for your opinion.

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.

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...

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..

Hi there, i recently had a trial of cpap , but the mask covered my nose and mouth , i found it very difficult to wear. I only had a 5 day trial, my doc says not enough evidence from the results so i have to have further indepth tests done, awaiting a date for this. It was thought that i had osa ( obstructive sleep apnoae ) . I felt tired in the mornings cos it would take me a long time to get any sleep with the machine on .

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.

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.

I know that they are going to put me on a cpap machine. I know I would do okay with the mask that is just the two little prongs that go in your nose. However in the past when I have had surgery I have gone crazy when they have put the mask over my mouth and nose. I have always had very bad allergies and can not stand to have anything touching my nose and mouth. So I was wondering how do they determine what is the best mask for you to have?

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.

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.

Hi everyone. I was dizgnosed with sleep apnea a few years ago... I used my CPAP machine for a while in the beginning and thaqt seemed to have helped. Latelly, Due to several factors such as stress, withdrawing from seroquel, withdrawing from xanax, and such, I have had to ask for sleep meds prescription. I take restoril which helps, however I stay in bed for 12 hours at a time... I decided to try cutting the capsule in half, to see if that would help with the amount of time I spend in bed...

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).

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.

ventricular function significantly improved after 3 months, associated with a relative 81% risk reduction for mortality or cardiac transplantation. Recently, in a randomized trial in 55 patients, CPAP therapy for 3 months improved ventricular function and reduced sympathetic activity in patients with heart failure and obstructive sleep apnea (OSA).

s been prescribed for you, but I do recommend a slow titration of the dose. I remember starting out and getting pretty nauseous on 75mg. The reduced me to 37.5mg and then slowly raised it to the 112.5mg I've been on for a few years now.

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.

Some patients need SLOW titration upward of thyroid meds. Would increase gradually in conjunction with your doctor -- for example, we might recommend 25mcg 1 tab on odd days, 1.5 tablets on even days for a few weeks, then increase, etc....the key is slow titration. Occassionally some people do better with one brand over another, so a change to levoxyl for a trial would not be unreasonable.

One time when I had a dataless CPAP, my doctor ordered a 2 week trial on an auto to redetermine my pressure needs. That's one route you can take, short of another study. Check the exact name of your machine in case it has data in it that can be retrieved. Is your doctor aware you are having nighttime headaches? It's one thing to not do another study when a patient is symptom free and all is well, but the development of new symptoms merits further investigation.

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..

hi my daughter has OSA,she is 18 just turned,she was supposed to do a CPAP trial and she refused it once we got home as she was too frightened of the mask,as she sleeps with her mouth open she needs the full mask,but she point blank refused,.im now searching for alternative options..my daughter has learning difficulties,and although she is as bright as a button..she didnt like the CPAP an as much as i was heartbroken,i cant force her to have it..

Cpap titration trial

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