Guillain-Barre syndrome

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Background

Clinical Features

  • Viral illness → ascending, symmetric weakness or paralysis and loss of DTRs
  • Little or no sensory involvement
  • May progress to diaphragm resulting in need for mechanical ventilation (33% of patients)
  • Autonomic dysfunction occurs in 50% of patients

Miller-Fisher Syndrome

  • Associated w/ campylobacter infection
  • More likely to be preceded by diarrhea than viral prodrome
  • Consists of ophthalmoplegia and ataxia
  • Weakness is less severe but DESCENDING; disease course milder than classic GBS
  • May present similarly to botulism, which is also descending paralysis

Differential Diagnosis

Weakness

Diagnosis

Required

  • Progressive weakness of more than one limb
  • Areflexia

Suggestive

Treatment

IVIG

  • Treat nonambulatory patients within 2 weeks of symptom onset

IVIG vs plasmapharesis

  • IVIG a/w thromboembolism and asceptic meningitis
  • Plasmapheresis a/w greater hemodynamic instability, lower rate of relapse
  • Combined IVIG and plasmapharesis no better than single therapy (IVIG or plasmapharesis)
  • IVIG preferred due to convenience and availability

Intubation indications

  • Vital capacity <15mL/kg
  • Negative Inspiratory Force < 30 cm H2O
  • PaO2 <70 mm Hg on room air
  • Bulbar dysfunction (difficulty with breathing, swallowing, or speech)
  • Aspiration

Disposition

Indications for admission to ICU

  • Autonomic dysfunction
  • Bulbar dysfunction
  • Initial vital capacity <20 mL/kg
  • Initial negative inspiratory force <–30 cm of water
  • Decrease of >30% of vital capacity or negative inspiratory force
  • Inability to ambulate
  • Treatment with plasmapheresis
  • Anticipated clinical course requiring mechanical ventilation

See Also

References

  1. 1.0 1.1 Bunney EB, Gallagher EJ: Peripheral Nerve Disorders, in Marx JA, Hockberger RS, Walls RM, et al (eds): Rosen’s Emergency Medicine: Concepts and Clinical Practice, ed 7. St. Louis, Mosby, Inc., 2010, (Ch) 105:p 1400-1401.