Week 4 - Neurological and Peripheral Nerve problems Flashcards
What is multiple sclerosis
-Autoimmune disorder that affects nerve cells in brain and spinal cord
-Demyelination of nerve fibers of brain and spinal cord
Initial symptoms of MS
-Blurred/double vision (usually first symptom)
-Red-green color distribution
-Blindness in one eye
Motor manifestations of MS
-Spasticity of muscles
-Tremors
-Scanning speech
Weakness/paralysis of:
Head, trunk, lumbs
Sensory Manisfestations of MS
-Numbness (Paresthesia)
-Pain
- Decrease hearing
-Vertigo and tinnitus
-Lhermitte’s sign
-Chronic neuropathic pain
Cerebellar manisfesation of MS
Nystagmus
Ataxia - lack of muscle control
Dysarthria - speech disorder
Dysphagia - difficulty swallowing
Severe fatigue caused by heat and medications
Diagnostic Studies for MS
-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)
Drug Therapy for MS
-Corticosteroids (methylprednisolone, prednisone)
-immunomodulators
(interferon B-1a - Avonex, Rebif)
(Interferon B-1b - Betaseron)
AST levels
0 - 35
ALT ranges
4 - 36
Billirubin
0.1 - 1.0
Albumin
3.5 - 5
What is Guillain-Barre Syndrome?
Acute destruction of the myelin sheath of peripheral nerves
GBS is acute illness, MS is chronic
autoimmune disorder
Diagnostic studies for GBS
- Progressive weakness of more than one limb
- Absent/diminished reflexes
- CSF
- EMG/Nerve conduction
Clinical manisfestations of GBS
- Ascending muscle weakness
- Respiratory compromise
- Muscle flaccidity –> muscle atrophy
- Paresthesia
- Double vision, facial weakness, dysarthria, dysphagia
GBS management
- Plasmapheresis: removes antibodies
- High-dose IV IG: interferes with antigen presentation
What is myasthenia gravis?
-Autoimmune disease affecting neuromuscular junction (antibodies attack ACH receptors)
-Causes fluctuating muscle weakness that increase with muscle use
Clinical manifestations of myasthenia gravis?
-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
Diagnostic studies for Myasthenia Gravis
-EMG
-Labs: 90% of pts have anti-AchR antibodies
-Tensilon test
What is Bell’s Palsy
-Inflammation of cranial nerve 7, unilateral
-Unilateral facial drooping
Manifestations of Bell’s Palsy (think stroke)
-Unilateral
-Affects ears, eyes and mouth
-Pain around ears
-Drooping, drooling on affected side
-Inability to smile, frown, whistle
-Excessive tearing
Diagnostics for BP
No definitive test
MRI and CT to rule out stroke
What is Amyotrophic Lateral Sclerosis
-Degeneration of motor neurons
-Progressive paralysis –> respiratory paralysis and death
Manifestations of amyotrophic lateral sclerosis
-Muscle weakness
-Muscle atrophy
-Dysarthria, dysphagie
-Twitching/cramping muscles –> pain
Nursing management for ALS
Reduce risk of aspiration
Assess respiratory
Pain control due to twitching muscles