COPD & Emphysema Support Group
COPD is a progressive disease characterized by airflow obstruction or limitation. Emphysema is characterized by loss of elasticity of the lung tissue, destruction of structures supporting the alveoli and of capillaries feeding the alveoli. Both have symptoms that include shortness of breath, among other respiratory troubles. If you are a COPD or Emphysema sufferer, join...
Theres two types of ventalation support used- invasive and non invasive.
Invasive includes ventilation via trach or via endo tracheal tube- a tube thats inserted down your throat. Generally they give you some sedation for this and because the tube passes through the vocal cords you can't talk. ( as if we wanted to when we're in such distress!)
Non invasive ventilation is becoming more of a first line for us COPDers.. using a BiPap mask. Its like this big face mask . Its kinda hard to talk with it on since it feels like your talking against this big air push.Sometimes ( rarer) they use CPAP- a nasal prong type ventilation.
Vent settings are adjusted to what your needing.. some just need the pressure and O2 to get air in, others need a combination of pressure to get O2 in and exhalation pressure to remove Co2.
Invasive ventilation tends to be a bit harder for us COPDers to get off of in some cases but if BiPap fails its our last choice for help . Personally I much prefer BiPap as its more comfortable and less invasive... plus I hate stuff down my throat! You also in many facilities can be in a step down unit instead of ICU on BiPap.. another plus IMO.
Hugs, Sue
But one good thing is I went in on 3L of 02 and came out on 1L sometimes with activity I use 1.5L
have a great day !!!!
Roe
I personally think had they left me on the vent longer right after the surgey instead of trying to push me like they did a healthier person I might not have had to go back on the vent.
My decision to go ahead with the surgery was a big gamble but I was not able to do anything due to the SOB I was having from the defective valve in heart.So I just prepared my children and myself for the worse and with by the Grace of God he carried me through.
Happy Easter
The first time, I'd been on for a few days, woke up and the nurses were very good to explain what was going on and giving me something to write with so I could ask questions. The 2nd time, I must have been much weaker, because I remember little between the a drugstore we stopped at enroute to the church and 5 days later, when I left ICU for stepdown. It was at a hospital I'd been at back in 2004 and 2005, so the same doc was assigned to me. He said "you know, you coded in the parking lot, don't you?" He was the same one who when found I knew the Lord told me how the medical symbol got it's start.
Essentially, they will sedate you so you don't get anxious and try to pull out the tubes. When they took me off sedation then put me back on, and I didn't respond as they wanted, they thought I'd had a stroke, so did a bunch of tests...negative all of 'em - except the MRI did find a brain! . I think that I just react differently to medication and sedation.
I am going to write down that I will take a ventilator------but not if I have to stay on it extended period-----I want to pass unhooked from machines. My Dad signed a DO NOT RESUSITATE (DNR) and the hospital my step sisters had him sent to; sent him back home. That IS what my Dad stated he wanted repeatedly---he wanted to die in his own bed, at home. Fortunately, he went into a coma and died later that day. I did not think he suffered. He died from Emphysema.