Myasthenia Gravis Flashcards

1
Q

what occurs in myasthenia gravis

A

autoimmune disease

  • antibodies block/destroy nicotinic acetylcholine receptors at the NMJ
  • prevents nerve impulses from triggering muscle contractions
  • FATIGUABLE
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2
Q

what are the types of MG

A

main:

  • ocular (eye only)
  • bulbar (pharynx/larynx/lowerCN)
  • generalised

others:
congenital myasthenia syndrome (genetic, paeds)

Lambert-eaton myasthenia syndrome (para-neoplastic syndrome that presents as MG)

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3
Q

what are common signs/symptoms of ocular MG

A

ptosis (drooping - levator palebrae superioris weakness)

diplopia (double vision - extraocular weakness

general eye muscle weakness (above + orbicularis oculi)

dryness (not being able to close eyes properly due to weakness)

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4
Q

what are common signs/symptoms of bulbar MG

A

difficulty swallowing (dysphagia)

motor of speech (dysarthria - muscle problem, slow/slurred)

weak muscles of mastication (hanging jaw sign)

weakness of the tongue (can flop back easily when lying down)

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5
Q

what are common signs/symptoms fo generalised MG

A

all of ocular and bulbar as well as

  • proximal weakness
  • head and neck weakness
  • SOB from weakness in muscles controlling breathing/diaphragm - ask if improved when sitting instead of lying down
  • early morning headaches - from hypoventilation during the night not blowing off enough CO2
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6
Q

what is a myasthenic crisis

A

paralysis of the respiratory muscles, needs assisted ventilation

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7
Q

what can trigger a myasthenic crisis

A

infection, fever, adverse drug reaction, emotional stress, starting high dose steroids

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8
Q

what can be found on neuro exam in MG

A

tone - usually normal but can be slightly lowered

reflexes - normal

power - can be reduced after fatiguing

coordination - normal - if seems uncoordinated make sure its not just from weakness

sensation - normal

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9
Q

what investigations can be done for MG

A

EMG
blood tests - antibodies
CXR - look for thymoma!
vitalograph

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10
Q

what antibodies are involved in MG

A

most common = anti acetylcholine receptor antibodies

more rare, affects face only = anti MUSK antibodies

Lambert - Eaton = anti voltage gated calcium channel antibodies

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11
Q

what is a vitalograph and how can it help with monitoring

A

measures patients vital capacity

as soon as a downward trend begins = respiratory muscles are being affected by MG - may need resp support/ventilation/intubation

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12
Q

what is the first line management of MG

A

steroids - VERY LOW DOSE then build up

acetylcholinesterase inhibitors eg pyridostigmine

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13
Q

what are the side affects of the first line drugs

A

steroids - if dose too high can trigger a myasthenic crisis as when starting on steroids patients get worse before they get better

pyristigmine - works by stimulating muscle contractions so can cause severe stomach cramping and diarrhoea

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14
Q

what is the second line management of MG

A

if patients condition worsens

Immunoglobulins - IV

plasmapheresis - removes ab from blood

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15
Q

what is the best longterm management for MG

A

steroid sparing drugs eg
azathioprine
rituximab

still immunosuppressive but without all the side effects of steroids

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16
Q

what are some side effects of steroids

A
increased risk of infection
diabetes (need BG monitored)
cushingoid syndrome
glaucoma, cataracts (need eye check ups)
osteoporosis (need dexa scans)
17
Q

who should be involved in the treatment of a patient with MG

A

MDT:

PT, OT, doctors, nurses, speech+language therapist, dietician

18
Q

how do you check for fatiguability in an examination

A

eyes - check eye movements/power of eyelids then ask them to look up for ~30 seconds then check again

upper limb - do 15 “chicken wings” on one arm then check power between both arms

lower limb - test power the ask them to walk around for a bit - check again and should be reduced