[Dysphagia] Dry mouth

[Jennie.Morgan at cddah.nhs.uk (Morgan Jennie (RXP) Speech & Language Therapy)]

Tricia,

I've used an artificial saliva spray in the past but this only lasts for a limited time. The best I've come across is 'Oramoist' (it was provided by a dentist) but I also use 'Glandosane' as it comes in several flavours (original, mint and lemon). Unfortunately it's not an ideal solution, especially in severe dysphagia.

Jennie

Jennie Morgan (Mrs)
Specialist Speech and Language Therapist
 
Department of Speech and Language Therapy
University Hospital of North Durham
North Road
Durham
DH1 5TW
Tel/Fax: 0191 3332608
Email: jennie.morgan@cddah.nhs.uk


-----Original Message-----
From: dysphagia-bounces@b9.com [mailto:dysphagia-bounces@b9.com]On
Behalf Of Tricia Clark
Sent: 10 June 2005 07:05
To: dysphagia@b9.com
Subject: [Dysphagia] Dry mouth


Hello everyone
 
Just wondering if someone may be able to assist me.  I have a client who
is PEG fed and is NBM due to severe dysphagia.  She has had her PEG
since approx. 1999.  It has been raised by staff that she often gets a
very dry mouth (and throat).
 
I know that research has suggested ice chips in the past, do you know if
this is still considered a 'safe' thing to do considering she has severe
dysphagia .  Could someone provide any other suggestions.  I have tried
wetting lips, however staff report that this doesn't satisfy the 'dry'
throat (obviously).
 
Any suggestions would be appreciated.
 
Trish
 

Tricia Clark

Speech Pathologist

Cootharinga Society of North Queensland

Ph: 07 4759 2018

Fax: 07 4779 9443
Email: Tricia.Clark@cootharinga.org.au
Web: www.cootharinga.org.au <http://www.cootharinga.org.au/> 

<blocked::http://www.cootharinga.org.au/> 

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