Week 4 - Neurological and Peripheral Nerve problems Flashcards

1
Q

What is multiple sclerosis

A

-Autoimmune disorder that affects nerve cells in brain and spinal cord
-Demyelination of nerve fibers of brain and spinal cord

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2
Q

Initial symptoms of MS

A

-Blurred/double vision (usually first symptom)
-Red-green color distribution
-Blindness in one eye

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3
Q

Motor manifestations of MS

A

-Spasticity of muscles
-Tremors
-Scanning speech
Weakness/paralysis of:
Head, trunk, lumbs

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4
Q

Sensory Manisfestations of MS

A

-Numbness (Paresthesia)
-Pain
- Decrease hearing
-Vertigo and tinnitus
-Lhermitte’s sign
-Chronic neuropathic pain

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5
Q

Cerebellar manisfesation of MS

A

Nystagmus
Ataxia - lack of muscle control
Dysarthria - speech disorder
Dysphagia - difficulty swallowing
Severe fatigue caused by heat and medications

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6
Q

Diagnostic Studies for MS

A

-No definitive diagnostic test
-Primarily based on:
1) MRI of brain and spinal cord (plaques, inflammation, atrophy, tissue breakdown)
2) Cerebral spinal fluid analysis (increase immunoglobin G)

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7
Q

Drug Therapy for MS

A

-Corticosteroids (methylprednisolone, prednisone)
-immunomodulators
(interferon B-1a - Avonex, Rebif)
(Interferon B-1b - Betaseron)

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8
Q

AST levels

A

0 - 35

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9
Q

ALT ranges

A

4 - 36

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10
Q

Billirubin

A

0.1 - 1.0

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11
Q

Albumin

A

3.5 - 5

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12
Q

What is Guillain-Barre Syndrome?

A

Acute destruction of the myelin sheath of peripheral nerves

GBS is acute illness, MS is chronic

autoimmune disorder

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13
Q

Diagnostic studies for GBS

A
  • Progressive weakness of more than one limb
  • Absent/diminished reflexes
  • CSF
  • EMG/Nerve conduction
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14
Q

Clinical manisfestations of GBS

A
  • Ascending muscle weakness
  • Respiratory compromise
  • Muscle flaccidity –> muscle atrophy
  • Paresthesia
  • Double vision, facial weakness, dysarthria, dysphagia
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15
Q

GBS management

A
  • Plasmapheresis: removes antibodies
  • High-dose IV IG: interferes with antigen presentation
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16
Q

What is myasthenia gravis?

A

-Autoimmune disease affecting neuromuscular junction (antibodies attack ACH receptors)
-Causes fluctuating muscle weakness that increase with muscle use

17
Q

Clinical manifestations of myasthenia gravis?

A

-THINK FACIAL
-Fluctuating weakness of skeletal muscles
-Facial immobility
-Bilateral ptosis (drooping of upper eyelid) and diplopia (double vision)
-Dysarthria (speech), dysphagia(swallow), chewing
-Difficulty w/speech, chewing, swalling

18
Q

Diagnostic studies for Myasthenia Gravis

A

-EMG
-Labs: 90% of pts have anti-AchR antibodies
-Tensilon test

19
Q

What is Bell’s Palsy

A

-Inflammation of cranial nerve 7, unilateral
-Unilateral facial drooping

20
Q

Manifestations of Bell’s Palsy (think stroke)

A

-Unilateral
-Affects ears, eyes and mouth
-Pain around ears
-Drooping, drooling on affected side
-Inability to smile, frown, whistle
-Excessive tearing

21
Q

Diagnostics for BP

A

No definitive test
MRI and CT to rule out stroke

22
Q

What is Amyotrophic Lateral Sclerosis

A

-Degeneration of motor neurons
-Progressive paralysis –> respiratory paralysis and death

23
Q

Manifestations of amyotrophic lateral sclerosis

A

-Muscle weakness
-Muscle atrophy
-Dysarthria, dysphagie
-Twitching/cramping muscles –> pain

24
Q

Nursing management for ALS

A

Reduce risk of aspiration
Assess respiratory
Pain control due to twitching muscles

25
Q

What is Parkinson’s Disease

A

Slowness in initiation/execution of movement
-Decreased dopamine, excessive acetylcholine

26
Q

Clinical Manifestations for Parkinson’s: TRAP

A

Tremor
Rigidity
Akinesia (loss/impairment of voluntary movement)
Postural Instability