Guillan-Barre Syndrome
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Guillain–Barré syndrome (GBS) is potentially fatal, immune-mediated acute-onset ascending sensorimotor neuropathy usually triggered by infections. Timely recognition, diagnosis, and prompt referral to a centre equipped to provide ventilatory support is essential to improve mortality and minimize long term morbidity.
Clinical presentation
- Rapid ascending bilateral lower limb weakness
- Little or no sensory deficits
- Evolving respiratory distress
Investigations
- FBP, serum electrolytes
- CSF analysis-albuminocytologic dissociation (↑ protein without pleocytosis) Emergency MRI to exclude acute spina cord inflammation or compression
Pharmacological management
Admit to ICU and provide ventilatory support to all patients with evolving respiratory distress or severe autonomic cardiovascular dysfunction
S: human immunoglobulin G (IV) 0.4g/kg 24hourly for 5days (started within 2weeks of disease onset)
For severe cases, consider
S: plasma exchange 200-250ml plasma/kg body weight for 5sessions (started within 4weeks of disease onset)
Monitor respiratory function-patient is deemed at risk of respiratory failure if the vital capacity is <20ml/kg, the maximum inspiratory pressure is <30cmH2O or the maximum expiratory pressure is <40cmH2O
Non-pharmacological management
- Provide rehabilitation-exercises to assist ambulation
- Assisted ambulation devices—e.g., high back wheelchairs