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15 Cards in this Set

  • Front
  • Back
Myasthenia Gravis
Sporadic, progressive neuromuscular disease characterized by a decrease in acetylcholine level at the receptor sites in the neuromuscular junction. Inadequate acetylcholine level results in a disturbance in nerve impulse transmission, causing progressive weakness in skeletal muscles.
Risk factors for myasthenia gravis.
Autoimmune disease
More common in women younger than 40 and men older than 60, but may occur at any age.
True or false, symptoms of myasthenia gravis are predominantly bilateral?
True.
Primary problem of MG
Primary problem is skeletal muscle fatigue with sustained muscle contraction.
Clinical manifestations of Myasthenia Gravis
Muscular fatigue increases with activity
Ptosis ( drooping of eyelids) and diplopia are frequently the first symptoms.
Impairment of facial mobility and expression
Impairment of chewing and swallowing
Speech impairment
No sensory deficit, loss of reflexes, or muscular atrophy
Poor bowel and bladder control
Myasthenic Crisis
an acute exacerbation of symptoms that may require intubation and mechanical ventilation to support respiratory effort.Caused by major muscular weakness and inability to maintain respiratory function.
Clinical Manifestations lse and blof Myasthenic crisis
Severe respiratory distress and crisis
Increased pulse and BP
Decreased or absent cough or swallow reflex
Cholinergic crisis
A toxic response to the anticholinesterase medications; anticholinesterase medications must be withheld-this response is rare with proper dosing of Mestinon.
Clinical Manifestations of Cholinergic Crisis
n/v, diarrhea
Weakness with difficulty in swallowing, chewing, and speaking.
Increased secretions and saliva
Muscle fasciculation ( twitching) and constricted pupils.
Electromyography:
Shows a decreasing response of muscles to stimuli.
Ice Pack Test
assess clients with ptosis; muscles improve with cold application; plack pack on closed lids for two minuets to see whether ptosis improves.
Tensilon Test
Used for diagnosing myasthenic crisis.
Used to differentiate cholingergic crisis from myasthenic crisis
IV injection of neostigmine or edrophonium causes immediate, altho-lived, relief of muscle weakness.
Treatment
Anticholinesterase medications
Neostigmine
Pyridostigmine
Corticosteriods
Plasma electrophoresis.
Immunosupressive therapy
Surgical removal of thymus.
Nursing Interventions.
Goal: To maintain respiratory function.

Asseses for increasing problems with difficulty breathing.
Measure forced vital capacity frequently to assess respiratory status.
Determine clients medication schedule. When was medication last taken?
Assess ability to swallow; prevent problems of aspiration.
Evalluate effectiveness of cough reflex
Be prepared to intubate or provide ventilatory assistance.
Administration of Tensilon
Myasthenic crisis: Clients condition will improve.

Cholinergic crisis: clients condition will temporarily worsen