Immediate Treatment for Guillain-Barré Syndrome (GBS)
The immediate treatment for Guillain-Barré Syndrome is intravenous immunoglobulin (IVIG) at a dose of 0.4 g/kg body weight daily for 5 consecutive days (total dose of 2 g/kg), which should be initiated within 2 weeks of symptom onset. 1
First-Line Treatment Options
IVIG Therapy
- IVIG is recommended as the first-line treatment by the American College of Physicians with high-strength evidence 1
- Standard dosing: 0.4 g/kg/day for 5 days (total 2 g/kg)
- Should be initiated as soon as diagnosis is suspected, even before confirmation 2
- Advantages: easier administration, fewer complications, and better tolerability compared to plasma exchange 1, 3
Plasma Exchange (Alternative First-Line)
- Equally effective as IVIG in improving clinical outcomes 1, 3
- Typically 4-6 exchanges over 1-2 weeks
- Should continue until anti-GBM antibodies are no longer detectable 2
- Requires specialized equipment and has higher complication rates 1, 4
- Continuous flow plasma exchange may be superior to intermittent flow 5
Treatment Algorithm
Immediate intervention: Start treatment without delay if GBS is suspected, even before diagnosis confirmation 2
First-line treatment decision:
- IVIG (preferred): 0.4 g/kg/day for 5 days
- Plasma exchange (if IVIG unavailable/contraindicated): 4 sessions for moderate GBS, 2 for mild GBS 5
Do NOT use:
Supportive Care and Monitoring
Respiratory monitoring: Use the "20/30/40" rule 1:
- Vital Capacity < 20 ml/kg
- Maximum Inspiratory Pressure < 30 cmH₂O
- Maximum Expiratory Pressure < 40 cmH₂O
ICU admission criteria: Consider for patients with 1:
- Evolving respiratory difficulty
- Severe autonomic dysfunction
- Swallowing difficulties
- Rapidly progressive weakness
Pain management: Use gabapentinoids, tricyclic antidepressants, or carbamazepine for neuropathic pain 1
Managing Complications
Treatment-Related Fluctuations (TRFs): Occur in 6-10% of patients within 2 months following initial improvement 2
- Consider repeating full course of IVIG or plasma exchange, although evidence is limited 2
Progression to CIDP: About 5% of GBS patients develop acute-onset Chronic Inflammatory Demyelinating Polyneuropathy 2
- Characterized by ≥3 TRFs and/or clinical deterioration ≥8 weeks after onset
Common complications requiring management 2:
- Deep vein thrombosis prophylaxis
- Swallowing assessment for bulbar palsy
- Eye care for facial palsy
- Prevention of limb contractures
- Management of pain, hallucinations, anxiety, and depression
Prognosis
- Despite treatment, GBS remains serious with 3-10% mortality 2, 1
- About 80% of patients regain walking ability within 6 months 2
- Long-term residual complaints are common (pain, weakness, fatigue) 2, 1
- Recovery may continue for >5 years after disease onset 1
Important Caveats
- Treatment should begin immediately upon suspicion of GBS, as early intervention improves outcomes 2
- Patients with mild GBS (still able to walk) may benefit from treatment, but evidence is limited 6
- Regular monitoring of respiratory function is crucial as respiratory failure can develop rapidly 1
- Pain management should be proactive as pain is often underrecognized but significantly impacts quality of life 2