Questions about the Use of a Trelegy Machine
Hello Everyone, Pt diagnosed with COPD and congestive heart failure this time last year. Has been readmitted 1/19/18 to 1/31/18 out for about 2 weeks and admitted again for 4 days for shortness of breath and slight fever. Went to the PCP Tues. for follow-up and there was talk of placing her on a triolgy machine. She currently uses an oxygen cannula during the day and a Bipap at night.
My questions are;
1)...Is this almost the same as a Bipap?
2)...How is it different?
3)...Do they prescribe this for end stage COPD?
4)...Does the use of a Triolgy machine mean permanent use?
5)...What are the pros and cons of use?
6)...How do patients feel about use it?
7)...Any questions to ask the pulmonary Dr next Friday?
Any help is greatly appreciated.
Interested in more discussions like this? Go to the COPD: Chronic obstructive pulmonary disease Support Group.
One other suggestion to you all....use the SoClean nightly. And. I had trouble setting it up correctly and understanding. YouTube has several good instructional videos that helped me so much. Worth a try! ess77
Hello, @stewie, @cepheid815 and others. Well, it happened again. I just a half hour ago sent you a message. It's disappeared. I'll never get used to losing all that thought and work.....
I use a BiPap nightly. It is saving my life. This has been quite a journey getting to this place of loving my breathing machine!
Had a cpap several years ago, quit using for various reasons. Then things changed after I started going to Mayo doctors. A night hooked-up to all the tests and seeing the results, I made a decision to make this work. I have severe obstructive apnea,- 46 events per minute, with multiple events over 60 sec w/o breathing, asthma and CHF, Sarcoid lung, not active presently. Chronic bronchitis which I haven't had since using this machine every night!!!! So, this is how it works for me.
This new machine is excellent. It's really quiet. Much smaller. Easier to use and set up. I did something very important.....bought a SoClean machine on sale from the company I got the BiPAP machine. Very important to my proper, nightly usage since I have have difficulty cleaning the things due to arthritis and other issues. I put the headgear, nasal pillow inside the machine, attached to the hose and the BiPAP machine so it cleans it all, including the water container. I use a heated hose, very important to me as I keep a cool room and the warm air is comfortable to breath.
Also, something which may help you with comfort.....I use the small nasal pillow. Experts tried to get me to use medium or small medium, but they leaked and were not comfortable, had to adjust all night. So, it's small size for me. It fits just right under my nose, not over it nor inside, and requires little adjusting at all. I have almost no leaking. No noise. I can not have anything over my nose or mouth, face at all. AND, the hose is connected to the top of my headgear. Not at the nose or face. It's much more comfortable for me and easy to manipulate during the night when I turn over. I do move a lot, as I must sleep on my sides, can't breath on my back, I have RLS, severe, and take iron +C and Requip for that. What a difference they make.
So, there you go. While I don't use Trilogy now, I depend entirely on the BiPAP for my health and survival. And, it's keeping me much healthier as I haven't had any bronchitis or lung infections since using it regularly. Sinus infection is down as well. There are times I want to use it during the day, as sometimes I can't get my breaths easily, but hope that will ease up as allergies and mold issues are gone!
Blessings to you on your breathing journey. I hope some of my information and experiences may help you.
Elizabeth
suggestion: once you find the right mask or nasal couch or pillow, and do keep trying until you are really comfortable.....the machine provider will work with you to find the best for you. Same with headgear, hose in front of face or on top of your head. I prefer on top of the head with a 6' hose so I can move around more easily. Also, change your mask or nasal pillow often to keep it fitting well, therefore no leaks. I have very few leaks now that I've come to this procedure. Trial and error, work frequently with the experts with the machine. You can get this to work for you. ess77
Thanks so for the information I will try that thanks again
I use a nasal pillow with my CPAP. The strap was recently redesigned and works close to perfect. All the system is Phillips and the redesigned headgear has a thin rigid strap halfway between the hose and the nose pillow. Very little noise so far.
Air gets under my mask and makes a horrible noise halfway through the night. It is very tight when I put it on. Does anyone else have this problem, Thanks so much
I have a few questions about the use of the T Machine, I have been using it since January very pleased with how it makes me feel but have questions. Is it ok to ask about them
i have never had any insomnia and the last 2 nights I have slept 3 1/2 hrs. Doctor yesterday took blood to test for 'low blood sugar'. I wake up mentally sharp and physically well rested however a bit lightheaded. My mom and one sister had that condition and would occasionally faint.
Absolutely I will.I I hope that anything I provide will help others.
Hello @vincejames and welcome to Mayo Clinic Connect. Thank you for sharing your experience with your Trilogy. The fact that you are feeling fresh sounds really promising, and as you mentioned, perhaps your sleep schedule is still regulating from your stay in the ICU.
Will you come back and update us when you have had some more time to see if your sleep pattern regulates and give another update?
I have been using the Trilogy for 10 nights now . I got used to the mask with the memory foam immediately. Here is my only concern. I cannot seem to sleep more than about 3 hours. I feel very fresh as I'm getting what I need into my lungs which in turn will help my heart function. I think it works fabulously but I get up for awhile and after about an hour I try again and sleep for 2 hours more. I was in I.C.U. for 10 days so maybe my body is still adjusting? But at least I know this 'mouth breather' isn't depriving the heart of the proper oxygen anymore. Best wishes to all of you.