Neurodegenerative Flashcards

1
Q

Akinesia

A

impairment in voluntary movement and initiation that causes “freezing” especially during gait activities

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2
Q

Bradykinesia

A

slowed motor movement

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3
Q

Dysmetria

A

decreased coordination of movement

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4
Q

Fasciculation

A

observed as a muscle twitch; involuntary muscle contraction and relaxaiton

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5
Q

Festinating gait

A

small rapid steps that result in forward tilted head an trunk

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6
Q

Multiple Sclerosis (MS)

A

demyelinating disease, own body attacks myelin sheath of brain and spinal cord

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7
Q

Motor symptoms of MS

A

ataxia, paralysis, weakness, fatigue, tremors, dysphagia

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8
Q

Sensory symptoms of MS

A

paresthesia, vertigo, pain

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9
Q

Visual symptoms of MS

A

diplopia, optic neuritis (sudden loss of vision), blurred vision

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10
Q

Communication symptoms of MS

A

dysarthria, scanning speech

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11
Q

Bladder/Bowel symptoms of MS

A

incontinence, urgency/frequency

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12
Q

Cognitive symptoms of MS

A

ST memory, attention, decreased processing, executive functioning, visuospatial ability

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13
Q

OT eval for MS

A

pain, medication review, ask questions about dizziness, sensaiton, fine motor skills, fatigue, balance, sleep, etc

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14
Q

Standardized eval tools for MS

A
  • COPM
  • mod fatigue impact scale
  • beck depression
  • 9 hole peg/purdue pegboard
  • semmes weinstein
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15
Q

PAMs for MS

A

focal heat to trigger points

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16
Q

Fatigue management for MS

A
  • diary card to monitor activity level
  • reduce standing
  • cooling techniques (cooling vest, ice packs)
  • energy conservation techniques
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17
Q

Ataxia management for MS

A
  • proximal stabilization to improve distal movement
  • hand over hand techniques (using non-affected UE over hand with tremor when dialing phone)
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18
Q

T/F: maintaining hip flexion for MS reduces extensor spasms

A

TRUE
- you can provide stools to reach during LB dressing or bathing

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19
Q

Parkinson’s Disease

A

affects production of dopamine, influences speed and accuracy of movement, psoture, cognition, affect, and expression

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20
Q

Stage 1 PD

A

unilateral symptoms, no/minimal loss of function

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21
Q

Stage 2 PD

A

BL symptoms, balance not affected

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22
Q

Stage 3 PD

A

impaired balance/posture, mild-mod ADL impairment

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23
Q

Stage 4 PD

A

needs assistance with ADLs

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24
Q

Stage 5 PD

A

total dependence for ADLs/mobility

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25
What type of cues should be used with a pt with PD?
single auditory cues - produce quicker and smoother movement - rhythm also helps
26
ALS
destroys motor neurons in the brain, spinal cord, and PNS
27
Initial signs of ALS
weakness of small muscles of the hand or foot drop causing tripping/stumbling
28
LMN symptoms
muscle atrophy, cramping, twitching
29
T/F: cognition, sensation, vision, and bladder/bowel are affected with ALS
FALSE
30
How many stages of ALS are there?
6
31
Stage IV ALS
requires WC, some assistance with ADL
32
Stage V ALS
WC, dependent in ADL
33
Stage VI ALS
confined to bed, dependent in ADL
34
Stage I ALS
some weakness, independent in ADLs
35
Stage II ALS
can walk, moderate weakness
36
Stage II ALS
can walk, severe weakness
37
Life expectancy for ALS
1-5 years
38
OT treatment for ALS
- compensatory - keeping person active and independent for as long as possible
39
Ideal WC for ALS
high back, recliner, lightweight - power WC as ALS advances
40
Guillain Barre Syndrome (GBS)
demyelination of axons in peripheral nerves
41
What phase of GBS is most disabling?
Plateau phase - little or no change in days/weeks
42
What phase of GBS indicates a significant, if not complete, return to function?
Progressive recovery
43
T/F: individuals with GBS may experience postural hypotension?
True
44
Sensory deficits in GBS
hands and legs "glove and stocking" distribution
45
What is the most frequently reported symptom of GBS?
fatigue
46
OT role in plateau phase of GBS
- TEMPORARY modifications ex) communication tools, hands-free telephone, positioning
47
OT role in recovery phase of GBS
resumption of occupations and roles ex) safe mobility, dynamic splinting for ROM, modified techniques for self-care, energy conservation/fatigue management, home assessments
48
Huntington's Disease (HD)
severe physical and mental disabilities characterized by loss of nerve cells in the brain
49
HD involuntary movement pattersn
Chorea (rapid, involuntary), akathisia (restlessness), dystonia (abnormal posturing)
50
HD voluntary movement patterns
Bradykinesia, akinesia (delayed initiation), incoordination
51
T/F: HD causes difficulty with smaller movements and hand-eye coordination
TRUE
52
T/F: At the later stages of HD, pt's are unable to talk, walk, and perform BADLs
TRUE
53
OT Eval tool for HD
Unified HD Rating Scale, assesses motor, cognitive function and functional capacity
54
OT intervention for early stage of HD
- address memory and concentration (checklists, routines, use of open ended questions) - work sit evals - home mods/safety (reminders to turn off appliances, unbreakable dinner-wear, covered mugs for hot liquid) - support groups
55
OT intervention in middle stage of HD
- engagement in leisure activity - pt/family education (use simple written cues/words for self care completion, positioning, adaptive equipment) - fatigue management - oral-motor exercises
56
OT intervention in final stages of HD
- positioning - environmental controls - consistent schedules/routines - smooth transition to tube feeding
57
Procedural memory
info on how to perform a task (e.g., how to ride a bike) - stays intact with Alzheimer's/Dementia
58
Topographic orientation
orientation to self within the environment, gets lost easily
59
Cognitive assistance level: ACL 1 (automatic actions)
totalA
60
Cognitive assistance level: ACL 2 (postural actions)
maxA
61
Cognitive assistance level: ACL 3 (manual actions)
modA
62
Cognitive assistance level: ACL 4 (goal-directed)
minA
63
Cognitive assistance level: ACL 5 (exploratory actions)
stand-byA
64
Cognitive assistance level: ACL 6 (planned actions)
independent
65
At what ACL does a patient: wander, pace, eat finger foods, performs one-step motor patterns, and requires 24hr supervision?
ACL 2 (postural reactions)
66
At what ACL does a patient: require tactile cues, cannot learn new behaviors, and should perform activities that reinforce predictable tactile effects on the environment (e.g., walking, washing/drying dishes, wiping countertops)
ACL 3 (manual actions)
67
At what ACL does a patient: no longer problem solve, participate in simple, concrete activities, require visual/tactile cues?
ACL 4 (goal-directed)
68
At what ACL does a patient: participate in self-initiated motor actions, have difficulty with judgement, reasoning, and planning, and use trial-error learning?
ACL 5 (exploratory actions)