GBS
MS
PAIN
NEUROMUSCULAR DISORDERS
ALS
NEURO DEGENERATIVE ILLNESS
COGNITIVE AND PERCEPTION
DELIRIUM
DEMENTIA
100

what are the signs and symptoms of GBS

symmetrical ascending paralysis from feet

pain

absence of deep tendon reflexes

glove and stocking distribution of mild sensory loss

cranial nerve problems

postural hypertension and tachycardia

paralysis of respiratory muscles

urinary dysfunction

100

explain the four types of MS

Clinically isolated syndrome

relapsing-remitting (lesions on the brain)

secondary progressive 

primary progressive (lesions on the spinal cord)

100

what are the 3 categories of pain?

nociceptive- actual or threatened damage to non-neural tissue

neuropathic- pain caused by a lesion or disease of the somatosensory nervous system

nociplastic pain- no clear evidence of actual or threatened tissue damage causing the activation of peripheral nociceptors

100

What are the 4 most common Neuromuscular disorders? What are their signs?

Spinal Muscular Atrophy- progressive muscle loss and atrophy

Charcot-Marie-Tooth-Disease- distal muscle weakness and wasting; sensory loss

Myasthenia Gravis- weakness with voluntary muscle activity and fatigue

Muscular Dystrophies

100

What intervention would you give someone with ALS

primary focus- adaptation and prevention of secondary complications while maintaining max I and positive QoL

Early tx- address symptoms that inhibit occupational performance to maintain highest level of independence as long as possible

Later tx- focus on individual functional needs and physical/social environment (caregiver training and home modifications)

movement programs (ROM, strengthening, endurance, breathing programs)

assistive technology and DME

Dysphagia interventions

100

what are the similarities and differences between Huntington's and Parkinson's Disease?

Similarities: Neurodegenerative Illness, bradykinesia,

Differences:

Parkinson's- asymmetric onset, officially diagnosed with a DATSCAN, does not have proper amount of dopamine, tremors, bradykinesia, smaller amplitude of movement


Huntington's- hereditary, involuntary movement disorders, voluntary movement disorders (delayed initiation of mvmt, bradykinesia, incoordination, visual changes, posture)

100

treatments for MCI

Aerobic exercise or resistance training, mental activity/physical activity

use word association, story, mnemonics visual inputs, learning activities, concrete examples, provide feedback, active learning, etc

100

define delirium

disturbance in attention and awareness

a sudden onset of confusion

100

dementia diagnosis

Major Neurocognitive Disorder

Deficits in memory and significant cognitive decline in 1+ cognitive domains

independence in daily activities is affected (min requiring assistance with IALDS)

200

Madison is a 19 year that stepped on a nail but did not feel anything. She also is experiencing midline back pain. What phase of GBS is she in? What intervention would the OT do during this stage?

phase 1: acute inflammatory progressive phase

position for pain management, stability, prevention of secondary complications and function

environmental control- access to nurse call light, TV, lights, phone, etc

communication- picture boards, voice activated devices

range of motion- avoid overwork of denervated muscles

mental wellness- coping with anxiety or depression

swallowing and respiratory care if issues are present

200

what is the neurophysiologic change?

lesions/plaques in the gray and white matter 

spinal cord, optic nerve, brainstem/cerebellum, periventricular white mater, inflammation, demyelination, axonal injury, and cell death

200

what makes up the Loeser's model of pain?

nociception- tissue damage/irritation

psychological- your unique experience with pain

social- feelings about pain

behavioral- behaviors because of pain

200

Liam’s parents report that he:

Frequently falls when running, has difficulty climbing stairs, uses furniture or his legs to push himself upright after sitting on the floor, shows increased fatigue after short play periods, has gained weight and appears “clumsy” compared to peers.

what neuromuscular disease does liam have?

Duchenne muscular distrophy

200

Which one is not tested on the ALDFRS scale?

handwriting, balance, salivation, breathing

balance

200

How do on and off periods of Parkinson's impact treatment

heavier symptoms return after medications wear off- important for us to know if we are doing treatment because if someone is off, they will have a poor response and less carry over

200
What are typical aging changes?

changes in memory retrieval

slower rate of acquisition

poor processing speed

less divided attention

200

role of OT an delirium in ICU (evidence based)

OT decreases the incidence and duration of delirium in ICU and improved function outcomes

200

What are the 3 stages of Alzheimer's Disease?

Pre-clinical Dementia: Brain changes observable on tests no no challenges with memory

Mild Cognitive Impairment due to Alzheimer's Disease: Evidence of Alzheimer's-related biomarker + challenges with cognition compared to peers, problems with memory and thinking that are beyond that of peers but generally able to complete ADL/IADL without assistance

Dementia due to Alzheimer's disease: challenges with memory, tests show evidence of disease, challenges to other areas of thinking that lead to occupational dysfunction

300

what intervention would you do in the recovery phase?

do not overwork partially innervated muscles, monitor for OH

splinting, increase occupational engagement, safe transferring training, desensitization program, adaptations/modifications, energy conservation, fine motor activity, home assessment

300

What are the 2 instruments used to measure MS?

Expanded Disability Status Scale (EDSS) and MS Functional Composite. 

300

what does OPQRST stand for?

guide when asking about pain:

O: Origin & Onset- gradual, sudden?

P: Position & Pattern- location of pain? what makes pain better or worse?

Q: Quality- what does the pain feel like (mechanical, chemical, neural, vascular)

R: Radiation- does the pain spread to other areas?

S: Severity

T: Time- how long ago did it start?

300

What are the 3 types of SMA? How is the onset characterized?

Type 1- most severe; lowest life expectancy

Type 2- proximal muscle weakness, low muscle tone, spinal curvature, and lower limbs more than upper limbs

Type 3- least severe; foot deformities, scoliosis, and respiratory muscle weakness

Characterized by age, the earlier = type 1; later = type 3

300

How many stages of ALS are there?

Describe each one

1- ambulatory, ind in ADL

2- ambulatory, slightly dec ind

3- ambulatory, inc weakness, introduce adaptive equipment

4- wheel chair, can do ADL with fatigue, ind with PWC

5- dep for wc, inc dep in ADL

6- in bed, dep ADL/max a for mobility

300

Describe the differences between

Progressive Supra Nuclear Palsy

Multiple System Atrophy

Corticobasilar Degeneration

Lewy Body Dementia

Drug Induced Parkinsonism

Vascular Parkinsonism

PSP- symmetric symptoms, no tremors, vertical gaze palsy (leads to falls), early and sig cog impairments

MSA- multiple systems atrophying quickly, extreme OH, tremors, bradykinesia, rigidity, dec balance, arm swing

CBD- asymmetric motor involvement, apraxia (idea motor, ideation), alien limb syndrome, no cognitive impairment

LBD- cognitive impairments, behavioral symptoms, sig fluctuations in symptoms/functional level

DIP- caused by anti-psychotic drug, can be reversible

VP- multiple small strokes, abrupt onset

300

what are skills that remain stable with age?

recognition memory, temporal order memory, procedural memory

300

what intervention would you do with a person who has delirium

continual reassessment, orienting activities, sensory stimulation, modifying the environment to support memory, sleep hygiene, function, integrate family and friends, work in multidisciplinary team

300

Lisa is a 79 year old who is unable to remember what she ate for breakfast, has impairments in language, wanders around at night, needs help with BADL/IADL, and withdraws socially.

is she in the early, middle, or late stage of dementia?

middle 

400

what intervention would you do in the plateau phase?

continued monitoring and symptoms management

400

Which type of MS experiences muscle paralysis

Primary Progressive PPMS

400

Jordan reports:

  • Pain in the left shoulder when lifting items overhead at work.

  • Describes pain as “sharp and tight” on elevation and “pulling” on lowering.

  • Intermittent numbness and tingling along dorsal forearm and thumb when turning his head to the right.

  • Fatigue and weakness when gripping tools at work.

No recent trauma, but symptoms have worsened over the past month.

is it a joint issue, muscular issue, arthritic issue, or neural issue?

muscular issue and neural issue

400

what are the 4 categories of CMD?

type 1- hypotonia, generalized muscle weakness, contractures, but no severe intellectual disability

type 2- affects the muscle and brain

type 3/4- affects the muscle, brain, and eye

400

What stage of ALS should a wheelchair be prescribed

Stage 3, in preparation for Stage 4 (Non Ambulatory)

400

define chorea, akathisia, and dystonia

are these symptoms found in Parkinson's or Huntington's?

explain how these symptoms impair function

Huntington's

chorea- involuntary jerking/twitching movements

akathisia- motor restlessness

dystonia- sustained abnormal rigidity causing changes in posture 

unable to hold onto a walker, unable to stay seated in a wheelchair, contractures, tendons shortening, ADLS, IADLS

400

What are the 6 neurocognitive domains

1. language

2. learning and memory

3, social cognition

4. complex attention

5. executive function

6. perceptual-motor function

400

general approaches to treat dementia

enhance occupational performance and quality of life

maintenance, restoration, improvement of capabilities

adaptation of tasks and environment

compensation for declining function

promotion of respite care and support groups for family

education/provision of resources on handling behavioral disturbances and mood liability

(task simplification, environmental modification, remediation, compensation, caregiver training)

500

Maria reports a 3-month history of persistent fatigue that is “constant,” “not relieved by sleep,” and “making daily tasks feel heavier.” She states that she can get through her workday but crashes immediately after arriving home. She has reduced social engagement and decreased exercise participation.

She denies fever, weight loss, joint pain, depression, anxiety, or night sweats. She has no difficulty initiating sleep and does not snore. She describes her fatigue as mental and physical exhaustion, distinct from sleepiness.

What type of fatigue is this?

primary fatigue