Peg tube : Did anyone have a peg tube placed and... - ICUsteps

ICUsteps

7,509 members2,408 posts

Peg tube

jld85 profile image
6 Replies

Did anyone have a peg tube placed and your NG tube removed? They’re going to put a peg tube in Monday on my dad. They said there is still inflammation in his throat bc of the ventilator, so they want the NG tube out. I’m just worried about the procedure but I know it’s necessary and will help his throat heal more.

Written by
jld85 profile image
jld85
To view profiles and participate in discussions please or .
6 Replies
FamilyHistorian profile image
FamilyHistorian

I know people who have had one and manage it well at home.

I was offered one before going home but declined. My wife didn’t think she would be able to manage it especially as all my drugs were crushed and fed through the tube. The hospital had enough problems with the tube blocking as some of the tabs don’t grind into a powder. And my wife was involved because I have arthritis with useless 🤔 fingers with fused wrists.

As it happens the day I went home the tube was removed and of course previously I had had a trachy

jld85 profile image
jld85 in reply to FamilyHistorian

Yea, they think his NG Tune is not allowing the throat to heal like it should, so ENT doctor wants it out. I just hope he’s alright being so weak and tired and then having to be put back under for 30 min. They said it’s a very short lived procedure.

Jaycamb profile image
Jaycamb

I had an NG tube for 10 months then had it replaced with a peg in September. It is so much more manageable and is hidden! I was sore for a couple of days as mine had to be be done under a general anaesthetics due to lots of abdominal scar tissue. It is so easy to maintain and I have had no problems with medication through it. In fact, I used to get lots of blockages with my NG but (touchwood) have not had any with my peg. Good luck to your dad, it should be so much better for him x

jld85 profile image
jld85 in reply to Jaycamb

Oh great, this helps a lot! Thank you for your reply!!

Ren2985 profile image
Ren2985

My dad did. The peg was much easier to manage. After the procedure he was in a lot of pain for maybe a day. After that he was good and much more comfortable. After about a month, he did a swallowing test and the peg was removed and he could eat all foods. That was a great day!

jld85 profile image
jld85 in reply to Ren2985

I’m sure it was! I’m glad to know it’s better! I can’t wait for the he swallows for sure! Was your dad still pretty weak when he had the procedure done?

You may also like...

Feeding tube leak? Is this common?

We were informed on Monday, that dad's feeding tube was leaking in his lungs, he has now developed...

Dad is trying to take his tubes out Is this common?

today when I call they tell me my dad has been trying to pull his tubes out has anyone dealt with...

Without Trach procedure on ventilator tube from mouth

news from hospital today that Mom procedure wouldn’t be perform as it’s not in their hospital...

One stiff arm - is it caused by icu tubes?

the drip lines etc. going into one arm and ventilator tubes keeping it immobile. Does anyone else...

Pressure from doctors to for feeding tube or trachea

friend is still on a ventilator. The doctor is saying no more Covid, no more pneumonia. His parents...