1.24 Myasthenia Gravis Flashcards

1
Q

Define Myasthenia Gravis

A

Autoimmune disease
Younger women + Older Men

IgG abod attack AChR
@ Post synaptic membrane of NMJ

Prevent binding of ACh to rec
↑ rate AChR degradation
Stimulate complement related damage
to Post synaptic membrane

Margin of safety lost in NM transmission

Assoc thymus hyperplasia in majority patients

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2
Q

Signs and Symptoms

A

Demonstrable weakness skeletal muscle

  • worse post exercise + evening
  • improves w/ rest
  • Prox > Distal

Partial + Unilateral ptosis
diplopia
blurred vision -
solitary signs in 15% ocular myasthenia gravis

Bulbar involvement

Resp muscle involvement
20-30%
especially intercost / diaphragm

Sparing sensory and reflex abnormality

Effects of LT steroids
Cushingoid

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3
Q

Anaesthetic Mx

Preop

A

Assess bulbar and resp fxn
Serial FVC
- poor <2.9L (indicative need post op ventilation)

PreOp physio

Optimisation anticholinesterase +
Immunosuppression therapy
Consider PLEX / IV IgG if poor control

Omit anticholesterase on morning srugery
ensure steroid cover @ induction if approp

Premed in patients w/ good reserve

Aware other autoimmune disease
- thyroid DM Rheumatoid

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4
Q

Intraop

A

Intubation advisable
- high risk aspiration (bulbar)

Avoid Sux
relative resistance (↓AChR)
Prolong action and propensity phase 2 block
NDMB
quicker onset + prolong action
- consider ETT without NDMB 
- Reduce dose trac prob safest - 
metab and avoidance of reversal agents

Intubation facilitated exacerbated
NMB properties of volatile agents

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5
Q

Post op

A

Extubate if uncomplicated

Low threshold CCM postop

If ↓preop FVC/Bulbar involvement / co existing resp disedase
- elective post op IPPV in ICU
- Restart antichol tx and titrate to effect
↓requirements in 48h post op

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