Think of a recent therapy session.
First two appointments with an 80 year old actress who's stutter had recently deteriorated.
Describe the experience
I had never worked on dysfluency with a patient. I asked the patient for a history of her dysfluency and a medical hstory. She had a diagnosis of Parkinson's but had had a stutter as a child and her dysfluency appeared to be due to a stutter rather than a dysarthria. I used the 'Overall assessment of the speaker's experience of stuttering' (OASES) to get a baseline for therapy. This assessment involved getting information on the patient's reactions to their stuttering, communication in daily situations and quality of life. I haden't quite been prepared enough for the way the questionnaire elicited personnal/ emotional reflections/ information.
How did this make you feel?
I felt empathetic torwards the patient and felt that it was the first time i had truely considered the emotional impact of having a stutter. I made a conscious effort to listen to the patient's experiences.
What would you change and why?
I would revise my counselling training materials and really consider how i could incorporate these skills into a therapy assessment session.
Sunday, 20 October 2013
Montreal Cognitive Assessment
I often get handovers from different therapists with MOCA scores. I thought i would further research what the MOCA assesses and what the diifferent scores mean.
Z.S. Nasreddine et al (2005) The Montreal cognitive assessment, MOCA: A brief screening tool for mild cognitive impairment, Journal of american geriatrics society, 53(4), p605-699
Introduction
- 1 page, 30 point test taking 10 minutes.
- 26 or above is considered normal.
- Apraxia of speech - reduced score due to repetition difficulties/ naming difficulties.
- Receptive aphasia - reduced score due to reduced ability to understand instructions.
- Expressive aphasia - reduced score due to naming impairments/ word generation difficulties
Why was the MOCA created?
- Very sensitive to mild Alzheimers disease (100% predictor in one study), and mild cognitive impairment (89%).
- Usefull for assessing mild stages of the cognitive impairment spectrum.
Assessment
|
Task
|
Visuospatial
abilities
Short term memory
recall
Attention
Working memory
Language
Orientation to time/
place
|
- Clock drawing/
cube copying
- reading ‘face,
velvet, church, daisy, red’ – recall after 5 minutes.
Tapping task – tap when
say ‘A’
Serial subtraction
task (taking 7 away from 100)
Confrontation naming
task (camel, lion, Rhinoceros).
Repetition of 2
syntactically complex sentences.
Word fluency task
(words beginning with F in one minute, norm = 11 words).
Date, month, year,
day, place, city
|
Sunday, 13 October 2013
Dysphagia Outcome Scales
In this current healthcare climate i've started to realise that i need to use more recognised/stardardised empirical measures and standardised outcome measures to proove the worth of my interventions. One area i feel i've neglected is dysphagia. I write detailed observations and goals but need a static scale or measure to clearly demonstrate change after intervention. I've chosen one impairment based scale and one functional scale. I've decided to try and incorporate the following scales into my practice:
The Dysphagia Outcome and Severity Scale , (DOSS) - a 7-point scale developed to systematically rate the functional severity of dysphagia based on objective assessment and make recommendations for diet level, independence level, and type of nutrition. (O'Neil, Purdy,Falk,Gallo,1999).
The Dysphagia Outcome and Severity Scale , (DOSS) - a 7-point scale developed to systematically rate the functional severity of dysphagia based on objective assessment and make recommendations for diet level, independence level, and type of nutrition. (O'Neil, Purdy,Falk,Gallo,1999).
Level 7: Normal in all situations |
Level 6: Within functional limits/ Modified idependance |
Level 5: Mild Dysphagia:Distant supervision. May need one diet consistency restricted |
Level 4: Mild Moderate Dysphagia .Intermittent supervision /cueing; One to two diet consistecies restricted |
Level 3: Moderate Dysphagia. Total assisstence , supervision or strategies;2 or more diet cosistencies restricted |
Level 2: Moderate Severe Dysphagia: Maximum assisstance or maximum use of strategies with partial PO only |
Level 1:Severe Dysphagia: NPO: Unable to tolerate any PO safely (National Dysphagia Diet Task force,American Dietetic Association,2002) |
The Functional Oral Intake Scale (FOIS)
Crary MA, Carnaby GD, Groger ME. (2005) Initial psychometric assessment of a functional oral intake scale for dysphagia in stroke patients. Archive of physical medicine and rehabilitation. 86, 1516-20.
TUBE DEPENDENT (levels 1-3)
1 No oral intake
2 Tube dependent with minimal/inconsistent oral intake
3 Tube supplements with consistent oral intake
TOTAL ORAL INTAKE (levels 4-7)
4 Total oral intake of a single consistency
5 Total oral intake of multiple consistencies requiring special
preparation
6 Total oral intake with no special preparation, but must avoid
specific foods or liquid items
7 Total oral intake with no restrictions
Sunday, 6 October 2013
Community SLT
Think of a recent therapy session or event.
I’ve just completed my
first month working in a community SLT service.
Describe the experience
I work between 3 teams
(neuro, stroke and community) managing my own caseload and screening referrals
for the stroke team. I average around three home visits a day, less sometimes
on days with meetings and more on other days. At times I have found it hard to
keep track of all of the admin I need to complete and sometimes forget to
record all correspondence/ time spent doing admin. Gathering client history information and contacting GP's/ hospital therapists for information has been surprisingly difficult.
How did this make you feel?
I have enjoyed being
out of my comfort zone. I feel that I am learning to become better at
communicating with other teams e.g. charities, GP consortiums, Hospital
therapists etc and with managing a complex caseload.
What has this taught you?
- To keep a weekly to do list with all of my patient’s on it.
- To upload any letters I send to GP’s/ write down on RIO when I try to contact other services e.g. by phone but do not get through.
- To make a careplan for new complex patients in which I record assessment results, goals and therapy activities/ desired outcomes.
- To timetable in time for admin (discharge reports etc.)
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