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[Dysphagia] PEG to oral
- Subject: [Dysphagia] PEG to oral
- From: kgoertz at paphr.sk.ca (Clarke-Goertz, Kim (PAPHR))
- Date: Tue Oct 5 08:08:36 2004
How do docs manage patients with epilepsy in regards to preventing
pneumonitis?
Kim
-----Original Message-----
From: Irene Campbell-Taylor [mailto:eripley@yahoo.com]
Sent: Tuesday, October 05, 2004 06:36
To: Harmony; dysphagia@b9.com
Subject: Re: [Dysphagia] PEG to oral
Respiratory problems associated with epilepsy are usually pneumonitis, not
pneumonia due to the inhalation of vomitus during the attack. That being the
case, there would appear to be no reason not to return him to the diet he
enjoyed before the pneumonitis.
Irene.
Harmony <harmony@bmlug.org> wrote:
I have a client (with developmental disability) who was recently in
hospital for 7 weeks, lost 9kg and then given a PEG since he was NBM
for the duration of his stay. I am looking into trialling him on oral
foods but I need some info about what foods/fluids to start with. He
was previously on a puree diet and honey thick fluids which he ate
quite well. He was admitted for status epilepticus and developed
pneumonia after 3 visits to ICU and intubated a number of times. He is
now stable and back 'home' and doing quite ok so far with the PEG
feeding. The dietitians are monitoring him closely as well.
Does anyone have any input on the initial foods/fluids that I can trial
him on?
Thanks,
Harmony
Speech Pathologist
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Dr I Campbell-Taylor
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