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29 Cards in this Set

  • Front
  • Back
ALS patho
overstimulation of glutamate leads to cell injury is the current theory
hallmark signs of ALS
weakess of upper extremities
dysarthria - difficulty w/ speech
dysphagia - difficulty w/ swallowing
deep tendon reflexes brisk/overactive
post op nursing for crainiotomy patients
monitor respiratory status q1hr
permissive hypercapnia may be necessary
assess for Cushing's Triad
monitor for hypothermia
management of cerebral edema - post op
IV Decadron
osmotic diuretics
Dilantin
avoid excessive stimulation
monitor these post op for crainiotomy
urine/serum osmolality daily
urine specific gravity q2h
standard fluids post op for crainiotomy
D5 1/2 NS @ 75 mL/hr
watch for SIADH
Migraine
results from vasodilation
tension headache
skeletal muscle tension
Tx for migraine & cluster headache
serotonin receptor antagonist
Imitrex
Stages of a seizure
prodromal - signs & activity preceding a seizure
aural - any sensory warning
ictal - full seizure
postictal - recovery
Partial seizure types
focal - one area or hemisphere
jacksonian - no loss of consciousness
complex partial - altered LOC
Generalized seizure types
tonic-clonic - grand mal
absence - petit mal; staring spells
myoclonic - "drop attack"
most common side effect of dilantin (anti-seizure med)
gingival hypertrophy
patho for Multiple Sclerosis
destruction of myelin sheath leading to poor nerve transmission
primary progressive MS
continual decline with development of quadreparesis, cognitive dysfunction & vision loss
S/S of Multiple Sclerosis
coordination problems - loss of balance
vision difficulties - diplopia, patchy or total blindness
bowel/bladder dysfunction
symptoms improve during pregnancy
med's for Multiple Sclerosis
ABC & R
Avonex, Betaseron, Copaxone, Rebif
nursing interventions for MS patients
mobility exercises
teach wide gait stance
don't raise body temp too much
ROM exercises
myasthenia gravis patho
autoimmune disorder of the myoneural junction; characterized by weakness of voluntary muscles
S/S of myasthenia gravis
diplopia & ptosis
weakness of facial, throat, ocular muscles
respiratory muscle effect - decreased vital capacity
purely motor - no affect on sensation or coordination
Tensilon Test
anticholinesterase test
facial muscle weakness resolves for about 5 min
positive test for MG
myasthenia gravis med's
pyridostimine bromide
prostigmin
plan meals around med admin time
med's that can worsen MG
antibiotics
CV med's (b-blockers)
antisezure med's
psychotropics
morphine
novacaine
S/S of myasthenia crisis
respiratory muscle fatigue
dysphagia
inadequate cough
impaired gag reflex
decreased vital capacity
S/S of cholinergic crisis
mimic myasthenic crisis
respiratory muscle fatigue
dysphagia
inadequate cough
decreased vital capacity & decreased inspiratory force
from overmedication; tx is to hold all med's and give atropine
used to control side effects of Tensilon
atropine
keep at bedside
interventions for myasthenia gravis
mobility:plan adequate rest during the day
time activity with peak med effects
conserve energy
Communication: allow pt time to speak, yes/no questions
Eye care: patch 1 eye if diplopia, sunglasses
secondary progressive pattern of MS
progresses between relapses
relapse-remission pattern of MS
periods of symptoms followed by periods of complete recovery