I
did some research on palatal lifts for our clinic a few months ago.
We got a list of dental prosthodontists from another SLP who works with the
head & neck cancer population. However, we have not actually had
any PALS actually go through with the process. Part of that is
because there are few PALS who seem to be appropriate for them (see list of
recommended patient attributes below), and part of it is because of the
cost. When I contacted the local prosthodontists, they said that
Medicare will cover it, but that Medicare
reimbursement is less than what it costs the prosthodontist to make the
prosthesis. That means that none of our local prosthodontists will
bother billing Medicare, and the patient cannot get reimbursed if they pay
out of pocket. Our state’s version of Medicaid won’t
cover palatal lifts, and private insurance coverage varies widely, as
usual. The cost is $3000-5000. If anyone’s interested, I found this
list of patient attributes favorable for benefiting
from a palatal lift in Motor Speech Disorders by Joseph
Duffy: ·
Slow rate of
progression ·
Adequate respiratory function and
articulation ·
Resonance change with
occlusion ·
Evidence of lateral pharyngeal wall
movement during speech ·
Pressure sounds less adequate than
others ·
No hyperactive gag
reflex ·
No significant
spasticity ·
Adequate swallowing & saliva
management ·
Adequate dentition ·
Able to insert and remove prosthesis
without assistance I would be very interested to hear the
experiences of anyone who has experience working with PALS and palatal
lifts. If you recommend them at your clinic or practice, how do you
determine which PALS should get them? Are your criteria similar to
those listed above? How are PALS getting funding for these
prostheses? What kind of feedback do you get from PALS that have
them? Thanks! Betts Peters, MA, CCC-SLP Assistive Technology Services
Coordinator The ALS Association Oregon and SW
Washington Chapter 700 NE Multnomah St, Suite
870 Portland, OR 97232 503-238-5559 800-681-9851 Fax: 503-296-5590 Website: www.alsa-or.org Find our chapter on
Facebook!
Register
TODAY to join the Walk to Defeat ALS®.
Participate because YOU CAN! From:
xxxxxx@xxxxxxxxxxxxxxxxxxxx
[mailto:xxxxxx@xxxxxxxxxxxxxxxxxxxx] On Behalf Of Tara
Klucker I
have had someone recently ask me about a lift, also. I have asked our
local SLP, and got a resource in St. Louis, but looking for someone much
closer to the Bloomington area. Does anyone know how to go about
finding someone that can do this? This is a first for
me. Tara Klucker, MA, CRC, LPC From:
xxxxxx@xxxxxxxxxxxxxxxxxxxx
[mailto:xxxxxx@xxxxxxxxxxxxxxxxxxxx] On Behalf Of Erin
Singleton Thanks
Tami Do
other SLP’s regularly suggest lifts for ALS patient’s? I have
been trying to find someone in my area that does them in the event that
it’s appropriate. Erin From: xxxxxx@xxxxxxxxxxxxxxxxxxxx
[mailto:xxxxxx@xxxxxxxxxxxxxxxxxxxx]
On Behalf Of Tami Brancamp They could be
assessed for a palatal lift. Tami Tami Brancamp, PhD Assistant
Professor Speech
Pathology & Audiology University
of Nevada School of Medicine 775.784.4887 775.682.7020
(office) On Aug 9,
2011, at 11:33 AM, Erin Singleton wrote: Hey
everyone, I realize we
typically focus on augmentative communication on this list serve so it may
not be the most appropriate forum for this
question. I have had two
ALS patient’s ask me this week about what they should do for nasal
regurgitation when swallowing liquids. I don’t get asked this a lot
so I don’t feel as though I have the best suggestions for them. The
two men that asked are brothers and oddly enough have almost no pharyngeal
dysphagia. Their most frustrating symptom is nasal regurgitation. It
surprises me that it’s happening so often for them because their
speech is only slightly nasal. If anyone has suggestions for me I’d
love the advice! If it’s
easier to answer off the listserv my email is xxxxxx@xxxxxxxxxxxxxxxxxxxx Thanks so
much. Erin Singleton
M.A., CCC-SLP ________________________________ ------------------------------------------------------- |