Parkinsons and huntingtons Flashcards
with insufficient dopamine, which pathway is dominant?
“no go pathway”
hypokinesia
Movement symptoms of Parkinson’s
Bradykinesia
Tremor
Rigidity
Postural instability
Drooling
Micrographia
Festination
Freezing
Soft speech
Masked face
Non-movement symptoms of Parkinson’s
apathy
Anxiety
Breathing difficulty
Anosmia
Constipation and nausea
Cognitive changes
Depression
Fatigue
Hallucinations
Pain
Sleep disorders
Bone health
prognosis of Parkinson’s
Shift from unilateral to bilateral involvement
Increasing rigidity and postural flexion
Increasingly limited mobility and increasing need for assistance
Eventually, wheelchair and or bedbound
Cause of death, usually pneumonia
no cure
stage 1 and 1.5 of Parkinson’s
1- unilateral movement only
1.5- unilateral and axial involvement
stage 2, 2.5, 3 Parkinson’s disease staging
2- bilateral involvement without impairment of balance
2.5- mild bilateral disease with recovery on pull test
3- mild to moderate bilateral disease, some postural instability, physically independent
stage 4, 5 Parkinson’s disease staging
4- severe disability, still able to walk or stand unassisted
5- wheelchair bound or bedridden, unless aided
problem with the modified hoehn and yahr staging
It only takes into account the motor aspect of the symptoms of Parkinson’s
based on mobility, not the mental or behavioral symptoms, not ADLs
not based on dominant or nondominant side
unified Parkinson’s disease rating scale
Meditation behavior and mood
Activities of daily living
Motor
Modified hoen and yahr scale
schwab and england adl scale
Score of zero equals no disability
max 199 points
Huntingtons disease
degeneration of caudate nucleus
decreases output signals from the basal ganglia leads to disinhibition
then there is Excessive output from the motor cortex
Hyperkinesia
Psychiatric effects of Huntington’s disease
depression, irritability, anxiety, apathy
Aggressive, outburst, impulsivity, social withdrawal, suicidal ideation
Depressive symptoms associated with the rapid declining functional abilities
cognitive impairments of Huntington’s disease
Slowed thinking, impaired ability to manipulate information, poor attention, impaired memory
Difficulty switching from one task to the other
can lead to difficulty with ADLs
sensorimotor involuntary deficits of Huntington’s
chorea
dystonia (up to 95%) muscle spasms
-Prevalent; shoulder internal rotation, fist clenching, excessive knee flexion, foot inversion
-increase with disease, severity, and associated decline in functional capacity
sensorimotor voluntary movements deficits HD
Slow and hypometric saccadic eye movements
dysphasia and dysarthria
Slow and uncoordinated arm and hand movements
Abnormal control of posture, balance, and gait
Highly correlated with disease severity, and functional disability
What do you want to assess with Huntington’s disease?
balance
Mobility
berg balance scale BBS
higher score the better
Increase risk of falls if the score is less than equal to 40/56
timed up and go TUG
Stand up walk 10 feet turn around and come back and sit down
Increased the risk of falls if the score is greater than equal to 14 seconds
activities specific balance confidence scale, ABC scale
patient reported scale
confidence with keeping balance
100% Is best score
Less than 50% with recurrent fallers
tinettis mobility test
correlated with UHRS
1.8 more likely to fall if the score is less than equal to 21/28