198. Myasthenia Gravis Flashcards

1
Q

What is myasthenia gravis?

A

The most common disorder of the neuromuscular junction, a chronic autoimmune disease resulting in antibody-mediated functional decrease in acetylcholine receptors.

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2
Q

What are the pathognomonic symptoms of myasthenia gravis?

A

Fluctuating skeletal muscle weakness exacerbated by activity and improving with rest.

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3
Q

What is the gender distribution pattern of myasthenia gravis?

A

Women are often affected in their third or fourth decade of life, while men are typically diagnosed in their sixth decade.

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4
Q

What antibodies are involved in myasthenia gravis?

A

Antibodies directed against the α-subunit of nicotinic acetylcholine receptors.

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5
Q

What is the typical age of onset for myasthenia gravis in women?

A

Third or fourth decade of life.

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6
Q

What is the typical age of onset for myasthenia gravis in men?

A

Sixth decade of life.

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7
Q

What is the initial diagnostic test for myasthenia gravis?

A

Short-acting anticholinesterase test, typically using edrophonium (Tensilon test).

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8
Q

True or False: In myasthenia gravis, deep tendon reflexes are typically absent or reduced.

A

False. Deep tendon reflexes are present.

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9
Q

What comorbidities are associated with myasthenia gravis?

A

Thymoma and small cell lung cancer.

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10
Q

What first-line treatment is commonly used for myasthenia gravis?

A

Acetylcholinesterase inhibitors, with pyridostigmine being the most commonly used.

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11
Q

Fill in the blank: Myasthenia gravis is characterized by a decrease in functional receptors by _______.

A

70%–80%.

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12
Q

What role does the thymus gland play in myasthenia gravis?

A

It is thought to be the origin of the autoimmune antibodies.

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13
Q

What is the effect of plasmapheresis in myasthenia gravis treatment?

A

It removes circulating antibodies from the bloodstream.

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14
Q

What should be avoided preoperatively in patients with myasthenia gravis?

A

Routine administration of sedatives, including barbiturates and opioids, to avoid respiratory depression.

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15
Q

What is the risk factor for ventilator dependence associated with myasthenia gravis?

A

Duration of illness > 72 months, daily pyridostigmine dose > 750 mg, vital capacity < 2.9 L, concomitant respiratory disease.

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16
Q

What is the recommended approach for neuromuscular blockade in myasthenia gravis?

A

Reduce dosing to 0.1–0.2 times the effective dose in 95% of the population (ED95).

17
Q

True or False: Patients with myasthenia gravis are resistant to depolarizing neuromuscular blockade.

A

True.

18
Q

What is the effect of volatile anesthetics on neuromuscular transmission?

A

They decrease neuromuscular transmission.

19
Q

What is a significant complication of brachial plexus blocks in myasthenia gravis patients?

A

Ipsilateral diaphragmatic paralysis.

20
Q

What should be monitored postoperatively in myasthenia gravis patients?

A

Adequate respiratory function and potential need for mechanical ventilation.

21
Q

What is the treatment for severe symptoms in myasthenia gravis?

A

Plasmapheresis and intravenous immunoglobulin.