Chapter 50: nursing care of patients with peripheral nervous system disorders Flashcards
multiple sclerosis: pathophysiology
- degeneration of myelin sheath
- inflamed nerves
- slowed or blocked nerve impulses
multiple sclerosis: etiology
- unknown
- a possible autoimmune response
- possible viral infection
- heredity
signs and symptoms of MS
- muscle weakness
- numbness
- fatigue
- slurred speech
- vision disturbances
- vertigo
- ataxia
- dysphagia
- bowel/bladder problems
- sexual dysfunction
- mood alterations
disease progression
- relapsing remitting
- secondary progressive
- primary progressive
relapsing remitting (RRMS)
relapses that resolve
secondary progressive (SPMS)
patients may progress to symptoms not completely resolving after relapse
primary progressive (PPMS)
patients have progressive worsening of neurological condition throughout course of the disease
additional manifestations of MS
- remissions
- exacerbations: due to stress or illness
- immobility
- death usually from infection
diagnostic tests for MS
- history and physical
- CSF analysis
- MRI
therapeutic interventions for MS
- steroids
- interferon therapy
- immunosuppressant gents
- anticonvulsants
- muscle relaxants
- plasmapheresis
- physical, occupational, speech therapies
myasthenia gravis: pathophysiology
- antibodies destroy acetylcholine receptors
- Ach cannot stimulate muscle contraction
- loss of voluntary muscle strength results
etiology of myasthenia gravis
- unknown
- autoimmune
- thymus disorders
- possible viral origin
signs and symptoms of myasthenia gravis
- progressive muscle weakness
- fatigue w/ activity
- ptosis
- difficulty chewing, swallowing
- difficulty breathing
- remissions
- exacerbations: stress
complications for myasthenia gravis
- aspiration
- respiratory infection and failure
- myasthenic crisis
- cholinergic crisis: sludge
diagnostic tests for myasthenia gravis
- history and physical
- Tensilon test
- anti ach receptor antibodies
- electrop,&myography
therapeutic interventions for myasthenia gravis
- thymectomy
- anticholinesterase agents
- steroids
- plasmapheresis
nursing process of myasthenia gravis: activity intolerance
- teach methods to conserve energy
- teach avoidance of infection
- teach signs and symptoms of crisis
- teach medications to avoid
pathophysiology of Amyotrophic lateral sclerosis (ALS)
- also called Lou Gehrig’s disease
- motor neurons degenerate
- nerve impulse transmission blocked
- muscle weakness and atrophy
etiology of ALS
- unknown
- possible genetic predisposition
ALS signs and symptoms
- progressive muscle weakness and atrophy
- decreased coordination
- muscle spasm
- difficulty chewing and swallowing
- emotional lability
- speech difficulty
- pulmonary compromise
- death due to pulmonary complications
diagnostic tests for ALS
- history and phycal
- lumbar puncture w/ CSF analysis
- electroencephalogram
- nerve biopsy
- EMG
therapeutic interventions for ALS
- muscle relaxants
- Riluzole (Rilutek)
- physical, occupational, speech therapies
- pain control
- enteral feedings
- prevention of infection
- augmentative alternative communication