Musculoskeletal Diseases Flashcards

1
Q

What is the pathophys of myasthenia gravis?

A
  • acetylcholine receptors are blocked by antibodies
  • there is normal ACh production
  • skeletal muscle weakness becomes worse later in the day or develops with exercise
  • thymectomy brings symptom relief
  • pregnancy makes it worse - crosses the placenta and may cause weakness in neonates for up to 4-6 wks
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

What is the treatment for myasthenia gravis?

A
  • oral pyridostigmine = first line tx
  • corticosteroids, cyclosporine, azathioprine, mycophenolate
  • thymectomy - via median sternotomy or transcervical approach
  • plasmapheresis
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

Does myasthenia graves cause an increased sensitivity or resistance to depolarizing and non-depolarizing NMB?

A
  • Non-depolarizing NMB: inc. sensitivity

- Depolarizing NMB: dec. sensitivity

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

How is Myasthenia Gravis diagnosed?

A
  • Tension test (with edrophoium)
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

What are the characteristics of Eaton-Lambert Syndrome?

A
  • destruction of presynaptic voltage-gated calcium channel at the presynaptic nerve terminal
  • post synaptic nicotinic receptor is present in normal quantity and functions normally
  • proximal muscles are most affected
  • is worse in the morning and gets better throughout the day
  • associated w/small cell carcinoma of the lung
  • pts are sensitive to succs and nondepolarizers
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

What is the pathophysiology of Guillian-Barre?

A
  • an acute idiopathic polyneuritis characterized by an immunologic assault on myelin in the peripheral nerves
  • action potential can’t be conducted, so the motor endplate never receives the signal
  • usually persists for 2 wks with full recovery in 4 wks
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

What is the clinical presentation of Guillian-Barre?

A
  • flu-like symptoms followed by ascending paralysis
  • common culprits = campylobacter jejune bacteria, epstein-barr virus, cytomegalovirus,
  • other causes = vaccinations, surgery, lymphomatous disease
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

What are anesthetic considerations for Guillian-Barre?

A
  • avoid succs d/t risk of hyperkalemia
  • inc. sensitivity to nondepolarizers
  • facial and pharyngeal weakness causes difficulty swallowing
  • pts w/autonomic dysfunction are at risk for hemodynamic instability
  • exaggerated response to indirect acting sympathomimetics
  • steroids do NOT help
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

What is safe to give in both hyper- and hypokalemic periodic paralysis?

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

What co-existing diseases is MH linked to?

A
  • King-Denborough Syndrome
  • Central Core Disease
  • Multiminicore Disease
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

What are the most common causes of drug-induced SLE?

A
  • isoniasid

- hydralazine

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

What is a medication given for SLE that increases the duration of Succs?

A
  • cyclophosphamide (inhibits plasma cholinesterase)
How well did you know this?
1
Not at all
2
3
4
5
Perfectly