Ch 44 Outline Neurologic Disorders 4

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Created by:

jbake74  on April 22, 2012

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Nuring Class#5

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Ch 44 Outline Neurologic Disorders 4

Myasthenia Gravis Incidence greater in men
Manifestations manifest generally >50, Chronic, Autoimmune, Neuromuscular disorder, Periods of remission/exacerbation
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Myasthenia Gravis Incidence greater in men Manifestations manifest generally >50, Chronic, Autoimmune, Neuromuscular disorder, Periods of remission/exacerbation
Myasthenia Gravis Pathophysiology Antibodies destroy or block neuromuscular junction receptor sites, Decrease number of acetylcholine receptors, Results in decreased ability of muscle to contract
Myasthenia Gravis Manifestations Diplopia or ptosis, Difficulty chewing food, Dysarthria, Dysphagia, Weak facial and speech muscles, Spreads as disease progresses
Myasthenia Gravis Complications Myasthenic crisis Sudden exacerbation of motor weakness caused by undermedication
Myasthenia Gravis Diagnosis Anticholinesterase test, Nerve stimulation studies, Analysis of anti-acetylcholine receptor antibodies
Myasthenia Gravis Meds Anticholinesterases, Glucocorticoids
Myasthenia Gravis cholinergic crisis result of overdosage with the cholinergic medications; severe muscle weakness, vertigo, and respiratory distress are signs
Anticholinesterases allow acetycholine to gather at receptor sites which promotes muscle contraction
Pyridostigmine Mestinon; most common used acetycholinesterase inhibitor
Glucocorticoids improves muscle strength by immunosuppression
Thymectomy For patients under 60 Two surgical approaches Transcervical approach, Transternal approach
Rhizotomy Surgical severing of a nerve root
Percutaneous rhizotomy Partially destroys trigeminal nerve
Plasmapheresis Procedure used to separate blood cells from plasma, Used for treatment of MG and GB

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