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NSG 232 Exam #3 Part 2-Questions with Correct Answers/ Verified/ Latest Update

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Myasthenia gravis (MG) - a chronic autoimmune neuromuscular disease; a lack of nerve impulses and muscle responses at the myoneural junction, causes fatigue and muscular weakness of the respiratory system, facial muscles, and extremities Because of cranial nerve involvement, what often occurs wi...

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MikeHarris
NSG 232 Exam #3 Part 2-Questions with Correct Answers/
Verified/ Latest Update

Myasthenia gravis (MG) - ✔✔a chronic autoimmune neuromuscular disease; a lack of nerve
impulses and muscle responses at the myoneural junction, causes fatigue and muscular
weakness of the respiratory system, facial muscles, and extremities


Because of cranial nerve involvement, what often occurs with Myasthenia gravic? -
✔✔ptosis (drooping eyelid) and difficulty chewing and swallowing



The symptoms of MG are caused by: - ✔✔inadequate secretion of acetylcholine (ACh) or a
loss of ACh because of an increase in the enzyme acetylcholinesterase



Multpile sclerosis is - ✔✔an autoimmune neuromuscular disorder that attacks the myelin
sheath of nerve fibers in the brain and spinal cord, causing lesions known as plaques



Muscle spasms have various causes including - ✔✔injury or motor neuron disorders that
lead to conditions such as cerebral palsy, MS, spinal cord injuries, cerebral vascular accident,
or hemiplegia



Spasticity of muscles can be reduced with the use of - ✔✔skeletal muscle relaxants



MG is not a genetic disorder, but - ✔✔there can be familial tendency



MG results from - ✔✔lack of ACh at receptor sites because the body's immune system has
an antibody response against an alpha subunit of the ACh receptor sites, meaning
antibodies attack the sites making it to where ACh cannot bind to the site



AChR means - ✔✔acetylcholine receptor



What happens when ACh cannot bind to the muscle receptor sites? - ✔✔ineffective muscle
contraction and muscle weakness

,About 90% of clients with MG have _____ that can be detected through serum testing -
✔✔anti-acetylcholine antibodies


The thymus gland is involved in systemic immunity that is active during infancy and early
childhood, but it normally - ✔✔shrinks during adulthood



Approximately 60% of MG clients have - ✔✔thymic hyperplasia



Myasthenia gravis is characterized primiarily by - ✔✔weakness and fatigue of the skeletal
muscles



Early symptoms of MG are - ✔✔ptosis (drooping eyelid) and diplopia (double vision)



The group of drugs used to control MG is - ✔✔AChE inhibitors



AChE inhibitors inhibit the action of - ✔✔cholinesterase


What may occur when muscular weakness of a client with MG becomes generalized? -
✔✔myasthenia crisis



What can relieve myasthenia crisis? - ✔✔Neostigmine (a fast -acting AChE inhibitor)



Overdosing with AChE inhibitors might cause another crisis called - ✔✔cholinergic crisis



Cholinergic crisis is - ✔✔an acute exacerbation of symptoms of MG



Accompanying symptoms of cholinergic crisis include: - ✔✔miosis (abnormal pupil
constriction), pallor, sweating, vertigo, excess salivation, nausea, vomiting, abdominal craps,
diarrhea, bradycardia, and fasciculations (involuntary muscle twitching)

,Neostigmine (Prostigmine) is - ✔✔a short-acting AChE inhibitor with a half life of 0.5 to 1
hour, given for MG


What is usually given to a client with MG who does not respond to neostigmine or
pyridostigmine? - ✔✔Ambenonium chloride (Mytelase)



Because of its short half life, pyridostigmine must be given - ✔✔several times a day



What can be given for pyridostigmine overdose? - ✔✔atropine sulfate



What may clients who do not respond to AChE inhibitors require? - ✔✔prednisone or
immunosuppressive drugs


Overdosing and underdosing of AChE inhibitors have similar symptoms which include: -
✔✔muscle weakness, dyspnea, and dysphagia



Underdosing may result in myasthenia crisis, and overdosing may result in - ✔✔cholinergic
crisis


What is a short-acting AChE inhibitor that may be used to distinguish between myashenia
crisis and cholinergic crisis? - ✔✔Edrophonium chloride


After administering Edrophonium chloride to a patient how can you tell if the cause of the
symptoms was from myasthenia crisis? - ✔✔if symptoms were alleviated because of an
increase of ACh


After administering Edrophonium chloride to a patient how can you tell if the cause of the
symptoms was from cholinergic crisis? - ✔✔if muscle weakness becomes more severe

, Why can Edrophonium be used to diagnose MG? - ✔✔because its ultra-short duration of 5-
20 minutes increases muscle strength immediately; if ptosis is immediately corrected, the
Dx is most likely MG



Available laboratory tests that may suggest MS include: - ✔✔eleveated immunoglobulin G
(IgG) in cerebrospinal fluid, increased IgG/albumin ratio, and multiple lesions observable
through MRI



What are the goals for treatment strategies of MS? - ✔✔to decrease the inflammatory
process of nerve fibers and improve conduction of demyelinated axons



Clients with MS should avoid the following drugs: - ✔✔histamine (H2) blockers such as
cimetidine and ranitidine, indomethacin (an NSAID), and beta blockers



Name the drugs that are given for Myasthenia gravis: - ✔✔ambenonium (Mytelase),
edrophonium Cl (Tensilon), neostigmine bromide (Prostigmin), pyridostigmine bromide
(Mestinon)


What are the common characteristics associated with the acute attack phase of MS? -
✔✔fatigue; motor weakness; optic neuritis


What are the common characteristics associated with the remission-exacerbation phase of
MS? - ✔✔recurrence of clinical MS symptoms; spasticity


What are the common characteristics associated with the chronic progressive phase of MS?
- ✔✔progressive MS symptoms (wheelchair bound)



What are the treatment strategies for the acute attack phase of MS? - ✔✔tapering course
of glucocorticoids (prednisone); ACTH stimulares the adrenal cortex to secrete cortisol


What are the treatment strategies for the remission-exacerbation phase of MS? -
✔✔biologic immune response modifiers (BRMs), immunosuppressant drugs (e.g. Imuran),
interferons

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