Week 8 Myasthenia Gravis Flashcards

1
Q

what is MG

A

grave muscle weakness

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

what is MG characterized by

A

varying degrees of weakness, which increases with activity and improves with rest

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

what muscles are affected first

A

repetitive muscles, high contracting muscles, like the eyelids, facial expression and respiratory muscles

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

what kind of disease is this and what does that mean

A

a chronic autoimmune neuromuscular disease, that produces antibodies against ACh receptors. affects the peripheral nerve system

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

how many people per year, what gender, and life expectancy

inherited?

A

3 in 100,000
women
normal
not directly inherited

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

what is the most common complaint of people with MG

A

fatigue

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

what muscles are affected

A

voluntary, mostly muscles that control eye and eyelid movements, facial expressions and swallowing

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

what are generally the first signs

A

eyes, speech and swallowing

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

how does severity range

A

from ocular (eye muscles only) to generalized form (everything)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

what are some other symptoms and signs

A

diplopia, unstable or waddling gait, SOB, weak arms, hands, fingers, legs and back

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

what do people with MG develop, what is it

A

thymomas (tumors of the thalamus gland) usually benign .results in autoimmunity, and the production of ACh receptor antibodies

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

what is the dysfunction for diagnosis

A

motor dysfunction without sensation, cognitive, autonomic symptoms

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

what kinds of tests pick it up and treat it

A
blood test (for ACh antibodies)
IV edrophonium chloride (blocks breakdown of ACh and increases it at junction)
EMG to fatigue the nerves
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

what is myasthenic crisis

A

occurs when muscles that control breathing are weakened, and you need artificial ventilation
already weak, triggered by infection, fever or reactions.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

what are the three classes of MG medications

A

Antocholinesterase agents,
immunsupressive
IV (transfusions or injections?)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

what is a surgical consideration for MG

A

thymectomy (especially with thymoma). rebalances the immune system

17
Q

what is the prognosis of MG

A

stable or slow progressive, and medical treatment means over 90% survival.

long lasting with thyroidectomy is about 50%

some go into remission, or their weakness disappears altogether

respiratory failure with severe MG, medical emergency

18
Q

what are some exercise considerations for MG

A

functional training, no set exercise guidelines, but endurance exercises hinger and we do not want inflammatory effects of overworking,

also, avoid fatigue, more of a concern then muscle damage.