Neurodegenerative Diseases Flashcards

1
Q

Identify interventions that address the motor, sensory, and social/emotional issues associated with Guillain-Barre Syndrome.

A

GUILLAIN-BARRE SYNDROME [gee-on bahray]

  • MAJOR SYMPTOMS- adaptive equipment
  • Flaccid motor paralysis
  • Loss of sensation below level of inflammation
  • Pain in proximal muscles
  • Pain during PROM or muscle palpation

SECONDARY SYMPTOMS- must range them

  • MOTOR PARALYSIS
  • Skin breakdown
  • Contractures
  • Loss of respiration
  • Fatigue
  • Dysphagia- if hits CNs
  • Dependent ADLs- for 1-2 yrs
  • Unable to work
  • ABSENT SENSATION
    • Loss of proprioception
    • Skin breakdown
  • COGNITION, PERCEPTION
    • No problems
  • SOCIAL/EMOTIONAL
    • Fear & anxiety
    • Frustration
    • Helplessness

MOTOR INTERVENTION

  • ROM, splinting, positioning to prevent contractures
  • Positioning to prevent skin breakdown
  • Adaptive equipment to allow maximum function
  • Coordination exercises during recovery

MOTOR INTERVENTION

  • Increase strength
  • Gentle non-resistive activity until nerves fully recovered
  • F+ muscle grade or higher may begin gently resistance
  • Endurance training
  • Avoid overfatigue- lots of breaks/rest
  • Energy conservation

SENSORY INTERVENTION

  • Sensory stimulation during recovery-
  • Patient education on skin protection until full sensory return
  • Proprioceptive & vestibular stimulation during recovery

SOCIAL/EMOTIONAL INTERVENTION

  • Patient/family education
  • Psychosocial OT for coping skills
  • Provide successful activities to increase feelings of control and life satisfaction
  • Modifications of home & work environment
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2
Q

Identify interventions that address motor, sensory, and social/emotional issues at each stage of Amyotrophic Lateral Sclerosis

A

Amyotrophic Lateral Sclerosis- prognosis 3-5yrs

  • MOTOR PRIMARY SYMPTOMS- strictly motor upper and lower and sometimes CNs
  • Ascending weakness progressing to atrophy
  • Muscle spasticity
  • Muscle cramping
  • Muscle fasciculations
  • Dysarthria
  • Dysphagia
  • Decreased ROM
  • Fatigue

SECONDARY SYMPTOMS

  • MOTOR
  • Contractures
  • Skin breakdown
  • Loss of mobility
  • Decreasing ADL function
  • Loss of ability to work
  • SOCIAL/EMOTIONAL
  • Fear, anxiety
  • Depression
  • Dependency

Stage I (Phase 1 – Independent)

  • Prevent disuse atrophy and depression
  • Energy Conservation Techniques
  • Provide psychosocial support and patient voices concerns
  • ROM program
  • Strengthening program of gentle resistance
  • Use caution to prevent overwork fatigue
  • Coping skills for client and family

Stage II (Phase 1 – Independent)

  • Adapt ADL, work, and leisure
  • Balance of roles; Include significant other
  • Use of adaptive equipment
  • Integrate use of hand orthotic into daily activities
  • Baseline dysphagia evaluation
  • Stretching to avoid contractures
  • Strengthening of muscles with MMT grade above F+ (3+)
  • Orthotic support

Stage III (Phase 1 – Independent)

  • Manual or power wheelchair
  • Prioritize activities and work simplification
  • Reassess for adaptive equipment needs
  • Assess and adapt communication devices

Stage III

  • Encourage physical independence
  • Explore alternative activities if there is loss of employment
  • Begin home modifications
  • Education regarding types of bathroom equipment for ECT’s and safety
  • Deep breathing exercises, chest stretching, postural draining

Stage IV (Phase II – Partially Independent)

  • Evaluate the need for slings, MAS, overhead slings, arm troughs, lap trays, splints for resting and positioning

Stage IV

  • Pain and spasm management: Heat, massage, anti-edema measures, AROM, PROM, and isometric exercises to tolerance
  • Power wheelchair with adaptable controls
  • Assistive technology

Stage IV

  • Role negotiation and psychosocial issues of loss
  • Home modifications
  • Closure activities
  • Coping skills for client and family ​

Stage V (Phase II – Partially Independent)

  • Family education in ADL, transfers, and positioning
  • Family training on use of mechanical lift

Stage V

  • Adapt and select environmental control devices
  • X-ten technology
  • Adapt wheelchair for respiratory unit; Assess wheelchair cushion
  • Family education in skin inspection, use of electric hospital bed, and anti-pressure device

Stage VI (Phase III – Dependent)

  • Evaluate dysphagia
  • Evaluate for suction machine
  • Augmentative speech devices
  • PROM in all joints
  • Sensory stimulation with massage and skin care ​ ​
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3
Q

Identify interventions that address cognition, motor, fatigue, and social/emotional issues associated with Huntington’s Disease.

A

•EARLY SYMPTOMS

  • Personality changes
  • Irritability, anger, depression
  • Cognitive decline
  • Decision making, new learning, memory
  • Physical
  • Mild balance problems, clumsiness, involuntary facial movements

LATER SYMPTOMS

  • Chorea—sudden jerky movements
  • Rigidity
  • Severe balance & coordination problems
  • Shifting gaze
  • Hesitant, halting, or slurred speech
  • Dysphagia
  • Dementia
  • Seizures

Cognition: Early Stages

  • Daily Routine
  • Checklists
  • Task Analysis
  • Environmental Modification for Impaired Cognition
  • Quiet workplace
  • Organizers
  • Kitchen timer
  • Watch with a beeper
  • Visual cues for sequencing tasks

Fine Motor

  • Modifications to diminish chorea and fine motor incoordination
  • Clothing modification
  • ECU’s – Late Stage

Gross Motor

  • Decreased balance
  • Perform activities in sitting
  • Use of a wheelchair or rollator walker ​

Wheelchair Positioning

  • Padding on armrests
  • Move wheelchair with feet
  • Firm seat and back
  • Positioning - Final Stages
  • Splints to prevent contractures

Home Modifications

  • Cooking and eating utensils with built-up handles
  • Unbreakable dishes ​
  • Shower bench or seat with tub safety bars
  • Sturdy chairs with high backs and armrests
  • Remove throw rugs
  • Remove clutter ​

Fatigue: Middle Stage

  • Frequent rest breaks
  • Scheduled breaks ​

Adapted Clothing

  • Clothing with few or no fasteners

Adapted Equipment

  • Shower mitts
  • Electric razor
  • Covered mugs
  • Non-slip placemat
  • Bed with railing and padding ​
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4
Q

What are the areas for evaluation and assessments used for an individual with Multiple Sclerosis?

A

Primary Symptoms

  • Fatigue, weakness
  • Intention tremor
  • Double vision, optic neuritis
  • Paresthesia, neuralgia, spasticity
  • Ataxia, unsteady gait
  • Pain
  • Decreased cognition
  • Dysarthria, Dysphagia
  • Evaluation
  • Reevaluation
  • Evaluation over a period of time
  • Daily activity patterns
  • Habits and Routines
  • Home Assessment
  • Modified Fatigue Impact Scale (MFIS)
  • MS Quality of Life Inventory
  • Symptom Management
  • Spasticity
    • Medication
  • Bladder
    • Incontinence Pads or Catheters
    • Prevention of UTI’s
  • Pain and Fatigue
    • Nutrition
    • Prevent overfatigue with ECT’s
    • Regular exercise
    • Routines for rest and sleep
    • Control stress

MOTOR

  • Intermittent muscle weakness or paralysis
  • Intermittent intention tremor
  • Possible spasticity
  • Low endurance
  • Cerebellar ataxia

MOTOR INTERVENTION ​

  • Strength, endurance, ROM, coordination
  • Energy conservation
  • Adaptive equipment and environment

SENSORY

  • Impaired or Absent vibratory, temperature, pain, touch, proprioception, kinesthesia
  • Vertigo
  • Visual problems***
  • Diplopia
  • Nystagamus
  • Color discrimination
  • Decreased acuity
  • Acute pain
  • Electric like shocks–Lhermitte’s sign

SENSORY INTERVENTION

  • Visual acuity, tracking, and scanning
  • Adaptive equipment and techniques
  • Patient education for safety

COGNITIVE ​

  • Short attention span
  • Short term memory loss
  • Difficulty learning
  • Decreased problem-solving

COGNITION EVAL & INTERVENTION

  • Executive Function Performance Test
  • Memory aids
  • Patient/family education
  • Level of supervision
  • Problem-Solving Compensatory Strategies
  • Time Management
  • PERCEPTUAL EVAL & INTERVENTION ​

SOCIAL/EMOTIONAL/BEHAVIORAL

  • Indifference
  • Emotional lability
  • Decreased ability to work or do ADLs
  • Cognitive Deficits + Denial of progressive nature of disease = Behavior that puts client at risk****
  • Client and family education to understand and recognize behavioral problems and fluctuating nature of disease
  • Examples: Depressed, labile, poor memory, refuses assistance from others, poor judgment and safety with medication and transfers

SOCIAL/EMOTIONAL/BEHAVIORAL INTERVENTION

  • Stress management , coping strategies
  • Family, caregiver education
  • Activity adaptation ​

SECONDARY SYMPTOMS

  • Contractures
  • Urinary tract infections
  • Decubitus ulcers
  • Pain
  • Cognitive impairments

Goal Setting

  • Client’s need to adapt as the disability progresses
  • Family and client need to negotiate role changes ​

Role Delegation

  • Eliminate
  • Modify
  • Delegate ​
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5
Q

Identify the interventions that address the motor, fatigue, cognitive, dysphagia, and social/emotional issues that are present for an individual with Parkinson’s Disease.

A

Parkinson’s disease- (Becky Farley)

PRIMARY SYMPTOMS

  • Resting tremor
  • Bradykinesia
  • Rigidity
  • Impaired postural reflexes

SECONDARY SYMPTOMS

  • Autonomic dysfunction
  • Excess sweating
  • Greasy skin
  • Flushed skin
  • Bladder problems
  • Cardiopulmonary problems
  • Nutritional issues
  • Impotence
  • Shallow breathing

SECONDARY SYMPTOMS

  • Muscle atrophy
  • Decreased flexibility & contracture
    • Kyphosis
    • Scoliosis
  • Akathisia—restless feeling
  • Decreased coordination
  • Low, monotone voice
  • Sensory changes – Numbness, Tingling
  • Visual perceptual difficulties

Postural abnormalities

  • Flexed, stooped
  • Head forward
  • Flexion at knees and hips

Balance

  • Reactions compromised
  • Righting and equilibrium reactions decreased
  • Leads to increased falls ​

Daily Exercise Routine

  • Full ROM
  • Short exercise program 5-10 minutes daily
  • Postural flexibility exercises, especially trunk extension
  • Relaxation techniques and controlled breathing
  • Rhythmic auditory stimulation with accentuated first beat
  • Dancing
  • Rocking motion to initiate movements ​

Daily Activities

  • Time with medication
  • On-off periods ​

ADL

  • Tremors
  • Compensation for postural instability
  • Clothing Management
    • -Slip-on Shoes
    • -Velcro Closures
  • Time and energy required for task

Environment and Task Modification ​

  • Decrease impact of tremors
  • Built-up handles for eating and writing
  • Perform tasks that require handwriting after taking medication
  • ​Remove throw rugs
  • Place furniture close to wall
  • Chairs with armrests
  • Bath and toilet railings and elevated toilet seats
  • Environmental Control Units (ECU’s) in late stages that utilize switch plates for light touch

Fatigue

  • Energy Conservation Techniques•
  • Frequent Rest Breaks Throughout Day
  • Habits and Routines
  • Role Delegation

Cognition

  • Higher order cognitive deficits
  • Decreased shifting of attention among various stimuli
  • Easier to process simultaneous information with sequential processing ​

External Cues

  • Improve speed and sequential performance of novel motor tasks
  • Visual Cues
  • Verbal Prompts
  • Rehearsal of Movements
  • ​Time Management

Dysphagia

  • Drooling may cause social embarrassment
  • Oral motor exercises
  • Alter food consistencies

SECONDARY SYMPTOMS

  • Depression
  • Anxiety
  • Behavioral & personality changes ​

Client and Family Education

  • Disease process
  • Community Resources
  • Support Groups
  • Community Mobility ​
  • Disease process
  • Caregiver support groups
  • Respite care plans ​

Habits and routines

  • Typical Day
  • Planner
  • Role Delegation
  • Energy Conservation and Work Simplification Techniques

Adaptation

  • Home Assessment
  • Environmental Modification
  • Task Modification ​
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