Additional Neuromuscular conditions Flashcards

1
Q

HEALTH CONDITION and BSF IMPAIRMENTS (Bells Palsy)

A
  • Affects CN VII due to infection
  • Motor loss is more marked than sensory loss
  • Peripheral nerve damaged
  • Full or near full recovery expected
  • Not progressive
  • Results in hemifacial paralysis
  • Presents unilaterally
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2
Q

Medications (Bell’s Palsy)

A
  • Steroids
  • Anti-virals
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3
Q

HEALTH CONDITION and BSF IMPAIRMENTS (Trigeminal Neuralgia)

A
  • Brief intense bursts of pain within a distribution of the nerve (typically V2)
  • Affects CN V
  • Sensory affected only
  • Peripheral nerve damaged
  • Not progressive
  • Full or near full recovery expected
  • Results in severe hemifacial pain
  • Pain control needed
  • Presents unilaterally
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4
Q

Medications (Trigeminal Neuralgia)

A
  • Neuropathic pain meds are used (Gabapentin)
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5
Q

HEALTH CONDITION and BSF IMPAIRMENTS (Diabetic Neuropathy)

A
  • The most common metabolic neuropathy
  • Peripheral nerve is damaged
  • Progressive disorder from distal to proximal
  • Symmetrical sensory and motor loss
  • LEs affected more than UEs
  • May develop a “Charcot foot” described as severe pes cavus, clawed toes and potential bony collapse
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6
Q

Pathogenesis of Diabetic Neuropathy

A
  • Vascular changes affect peripheral nerves
  • Chronic metabolic disturbances affect neurons and Schwann cells
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7
Q

Medications (Diabetic Neuropathy)

A
  • Glucose control
  • Insulin if needed
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8
Q

Interventions (Diabetic Neuropathy)

A
  • Prevent foot deformity and skin breakdown
  • Fall prevention
  • Remediate strength and balance
  • Pre-exercise considerations:
    • blood glucose, blood pressure, physician clearance
  • Proper footwear for support
  • Joint mobs and stretching - 1st toe and ankle
  • Footdrop:
    • Gait and balance training
  • Compensate with orthotics and gait aids
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9
Q

HEALTH CONDITION and BSF IMPAIRMENTS (Guillain-Barre Syndrome)

A
  • Typically presents weeks after viral infection
  • Immune-mediated disorder
  • Peripheral nerve damage (includes myelin sheath and possibly axon)
  • First symptom is often paresthesia in toes, followed within hours or days by weakness distally in the legs
  • May cause paralysis of respiratory muscles
  • Distal to proximal, symmetrical progression
  • Progresses initially (ascending phase) but then recovers (descending phase)
  • Full or near full recovery expected
  • Symmetrical motor loss more than sensory loss
  • Schwann cells are the primary targets of attack
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10
Q

Diagnosis of Guillain-Barre Syndrome

A
  • Lumbar puncture for CSF analysis - elevated albumin, mononuclear leukocyte count
  • Electrophysiologic studies - Slowed NCVs indicate damaged myelin
  • Fibrilations indicate damaged axons
  • May have tachycardia, cardiac arrhythmias, and labile blood pressure
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11
Q

Medications (Guillain-Barre Syndrome)

A
  • IV immunoglobulins
  • Plasmaheresis
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12
Q

Interventions (Guillain-Barre Syndrome)

A
  • Possible acute rehab
  • Prevention and compensation in ascending phase
  • Remediation in descending phase
  • Progression of more independent mobility
  • Recovery takes weeks or months
  • Prepared to protect airway if needed
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13
Q

SPECIAL CONSIDERATIONS and BONUS QUESTIONS (Guillain-Barre Syndrome)

A

CIDP: Chronic Inflammatory Demyelinating Polyneuropathy

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14
Q

HEALTH CONDITION and BSF IMPAIRMENTS (HEREDITARY MOTOR AND SENSORY NEUROPATHY (HMSN)

A
  • Hereditary disorder of the PNS
  • Peripheral nerve damage
  • Progressive disorder symmetrical distal to proximal
  • LEs affected more than UEs
  • Begins with a peroneal nerve disorder progressing to the foot and leg - ankle DF and EV affected
  • Progresses to weakness and wasting of intrinsic hand muscles then forearms
  • Significant disability results
  • Sensory and motor loss
  • May develop a “Charcot foot” describes as severe pes cavus, clawed toes and potential bony collapse
  • Abnormal DTRs
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15
Q

Interventions (HEREDITARY MOTOR AND SENSORY NEUROPATHY (HMSN)

A
  • Prevent foot deformity and skin breakdown, falls, contractures
  • Remediate strength and balance
  • Strengthen at 40-60% 1RM
  • Aerobic training at 70-90% HRMax with intervals
  • Muscle flexibility
  • Maximize QOL
  • Reduce pain
  • Supportive footwear
  • Compensate with orthotics, gait aids, splinting, wheelchair
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16
Q

Another name for Guillain-Barre Syndrome

A

Acute Inflammatory Demyelinating Polyneuropathy (AIDP)

17
Q

Another name for Charcot Marie Tooth

A

Hereditary Motor and Sensory Neuropathy (HMSN)

18
Q

HEALTH CONDITION and BSF IMPAIRMENTS (Poliomyelitis)

A
  • Infectious disease of the anterior horn cell in the spinal cord
  • Initial symptoms are fever, fatigue, headache, vomiting, stiffness of the neck and pain in limbs
  • Distal to proximal
  • May cause paralysis of respiratory muscles
  • Affects the whole LMN
  • Motor loss only
  • Significant disability results
  • Asymmetrical weakness
  • LEs affected more than UEs
19
Q

Interventions (Poliomyelitis)

A
  • Prevent deformity, contractures, falls, skin breakdown, deconditioning
  • Remediate aerobic conditioning, functional strengthening at submaximal intensity and avoid fatigue
  • Compensate with orthotics, gait aids, wheelchair, energy conservation
20
Q

HEALTH CONDITION and BSF IMPAIRMENTS (Postpolio Syndome)

A
  • Caused by a loss of motor units that became too large and metabolically taxing after initial recovery from an infectious disease
  • New neuromuscular weakness decades after initial infection
  • Anterior horn cell initially damaged, affecting the whole LMN
    not technically progressive, but occurs with age
  • Significant disability results
21
Q

Interventions (Postpolio syndrome)

A
  • Prevent deformity, contractures, falls, skin breakdown, deconditioning
  • Remediate aerobic conditioning, functional strengthening at submaximal intensity and avoid fatigue
  • Compensate with orthotics, gait aids, wheelchair, energy conservation
22
Q

HEALTH CONDITION and BSF IMPAIRMENTS (Myasthenia Gravis)

A
  • Chronic peripheral autoimmune disease of the neuromuscular junction
  • Fatigue major limiting factor
  • Skeletal muscle weakness that worsens after periods of activity
  • Number of Acetylcholine receptors is decreased and those present are flattened and less efficient
  • Typically mild disability results
  • Causes skeletal muscle weakness with intact DTRs and intact sensation
23
Q

Medications (Myasthenia Gravis)

A

AChE inhibitors
Plasmapheresis

24
Q

Interventions (Myasthenia Gravis)

A
  • Aerobic exercise in intervals
  • Strengthening
  • Monitor vital signs with exercise
25
Q

SPECIAL CONSIDERATIONS and BONUS QUESTIONS (Myasthenia Gravis)

A
  • Fatigue is common
  • Classically presents with ptosis
  • Myasthenic crisis possible - medical emergency requiring ventilation