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[Dysphagia] PEG to oral
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
- References:
- [Dysphagia] New
- From: speechhearing_my at yahoo.com (Speech and Hearing Centres)
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