Dear LungLine Nurse,
Thanks for the opportunity to ask this question. I have severe
COPDChronic obstructive pulmonary disease
Copd (chronic obstructive pulmonary disorder)
Smoking and copd (chronic obstructive pulmonary disorder) & severe asthma & will be at National Jewish for my annual re-evaluation. While there, I need to use supplemental O2 for sleep & exertion (only at altitudes, like Denver). I have a VERY difficult time adjusting to using the cannula to sleep with and would appreciate ANY tips you have to help make sleeping with O2 more comfortable. I tried cutting off the
nasalAllergic rhinitis
Juvenile angiofibroma
Nasal
Nasal 12 hour
Nasal anatomy
Nasal biopsy
Nasal congestion
Nasal cpap
Nasal decongestant
Nasal decongestant tablet
Nasal decongestant-antihistamine prongs, but the cannula rolled & I ended up not getting much sleep or O2 last time.
I've read about the OxyArm, Softhose cannulas, Salter
ComfortComfort pac with cyclobenzaprine
Comfort pac with naproxen
Comfort tears HeadHead and face reconstruction
Head injury
Head lice
Indications of head injury
Radial head injury Cannula and putting the cannula in my mouth to sleep. I would GREATLY appreciate any suggestions and advice you have of
effectiveEffective strength cough syrup strategies folks have used to sleep comfortably with oxygen as it is my biggest challenge in using the oxygen I'm prescribed in Denver. The provider I use in Denver is Lincare via their Englewood branch.
Aloha,
Starion
I'm sorry to hear you're having a tough time sleeping with the nasal prongs. I do hear some complaints from my patients regarding this. Msotly about how the prongs themselves cause irritation in the inside of the nares. With this, I suggest using a different brand of cannula. Some companies carry nasal prongs that "flare" out at the tips. This is supposed to prevent sliding inside the nares and have a more "secure" fitting. Other are the plain ole' straight ones. Regardless, what I ussualy did with them was I would trim the prongs down about 1/2 way. Not completely off. This is why they were probably rolling off your face.
Nasal prongs are probably your best bet. Anything else is going to be too bulky or expensive for that matter. How much oxygen are you on anyways?
-Andy, RRT, CPFT
I'm on 2 liters/minute for exertion & sleep when at 5000 feet altitude. At sea level (where I live), I do NOT require any oxygen & generally maintain saturation rates of 94-97% 24/7.
Someone suggested a Salter Head Comfort Cannula with a padded headband as being especially comfortable, and Lincare is looking into getting that for me. Other suggestions are certainly welcome as well. Lincare says many folks have difficulty adjusting to sleeping with O2, so I guess that's somewhat comforting, knowing the problem isn't unique to me. Someone said pediatric cannulas are sometimes a bit more comfortable, but I've never tried those.
I just find it hard to adjust to having ANYTHING in my nose all night. During the day, I can put up with it, especially since I don't need to wear O2 while I'm just sitting, so I can give my nose a break.
Starion
We used these at the Dana-Farber CAncer Institute in Boston. It a mask like device that cups around the tip of your nose, yet still secures like regular nasal prongs. The mask itself has two small holes across from each other that directs the oxygen flow into the nares. We used these because the prongs not only irritated our patients noses, but the direct flow also dried out their nares and put them at risk of bleeding. (we dont like patients with low platlets counts to bleed!)
Here is a link of a photo of what ehy look like. They are relatively inexpensive. Give it a try!
-Andy, RRT, CPFT
http://trimed.freeservers.com/TM/adultbiflo1.jpg
http://trimed.freeservers.com/TM/biflomaskped.jpg
Aloha,
Starion
People tolerated the nasal mask just fine. You have to remember though that since this isn't direct flow into the nares like standard nasal prongs, oxygen can lost around the nose, lessening your inspired oxygen intake. I have found that some patients required an extra liter of oxygen to make up whats lost.
-Andy, RRT, CPFT
Starion
Be sure you check with your doctor before you change your oxygen literflow. also, let it be known that people with COPD don't typically have saturations of 96-97%. You're body isn't used to having higher oxygen levels, and has adjusted without it. In the hospital, we titrate patients oxygen levels to bve maintained between 88-92%. Anything higher is excessive and can cause respiratory depression.
Goodluck kiddo....and keep in touch!
Andy, RRT, CPFT
Just got off the phone from chatting again with the nice Lincare RRT & he says I've given him a LOT to think about & discuss with the Salter rep.
Aloha,
Starion
Thanks for all your suggestions and comments. I'll call Lincare again & see what they can provide. So far, they have offered the standard cannula and the salter Micro 1616. I'll call again on Monday & ask.
Aloha,
Starion