Guillain-Barré Syndrome (GBS): A Neurology Emergency Explained

Guillain-Barré Syndrome (GBS) is a rare but potentially life-threatening neurological condition in which the body’s immune system mistakenly attacks the peripheral nerves. It often follows a minor infection, such as a respiratory illness or diarrhea, and can result in rapid-onset muscle weakness, sensory disturbances, and even paralysis. This post explains GBS in detail, including its causes, pathophysiology, clinical features, subtypes, diagnosis, and treatment options.


🧬 What is Guillain-Barré Syndrome?

Guillain-Barré Syndrome is an acute immune-mediated polyneuropathy. The hallmark feature is ascending, symmetrical flaccid paralysis, often starting in the legs and progressing upwards.

How It Starts:

  • A person gets an infection (respiratory or GI).
  • The body forms antibodies to fight that infection.
  • These antibodies mistakenly attack the myelin sheath of peripheral nerves.
  • Resulting in slowed or blocked nerve conduction → motor weakness, sensory loss, and paralysis.

🦠 Common Triggers & Causative Pathogens

GBS is typically preceded by an infection within 2–4 weeks. Notable pathogens include:

PathogenTypical IllnessNotes
Campylobacter jejuniBloody diarrheaMost common trigger of GBS
CytomegalovirusFlu-like viral illnessCommon in immunocompromised individuals
SARS-CoV-2 (COVID-19)Viral respiratory illnessDocumented cases with post-COVID GBS

🧪 Pathophysiology: What Happens to the Nerves?

  • Antibody-mediated segmental demyelination of peripheral nerves.
  • Myelin sheath is damaged, reducing or halting nerve impulse transmission.
  • In some cases, axonal damage may also occur.
  • Affects motor, sensory, and autonomic fibers.

❗ Key Concept: Albuminocytologic dissociation in CSF – High protein, normal WBC count.


🧍‍♂️ Clinical Presentation

SymptomDescription
Muscle WeaknessSymmetrical, ascending (legs → arms → face)
Reflex LossDiminished or absent deep tendon reflexes
Sensory SymptomsParesthesia, numbness in stocking-glove distribution
Autonomic DysfunctionBP fluctuations, arrhythmias, urinary retention
Cranial Nerve InvolvementBilateral facial palsy, dysphagia, weak gag reflex
Respiratory Muscle InvolvementRisk of respiratory arrest due to diaphragmatic paralysis

🧬 GBS Subtypes (Variants)

1. Classic GBS (AIDP)

Ascending symmetric flaccid paralysis + areflexia.

2. Miller Fisher Syndrome

  • Triad: Ophthalmoplegia, Ataxia, Areflexia.
  • Often with facial nerve involvement.

3. AMAN (Acute Motor Axonal Neuropathy)

  • Motor paralysis only (no sensory loss).
  • Seen more commonly in Asia & Central America.

4. Multifocal Motor Neuropathy

  • Asymmetrical motor weakness.
  • Spares sensory fibers.

🧪 Diagnostic Workup

TestFindings
CSF AnalysisElevated protein with normal cell count (albuminocytologic dissociation)
Nerve Conduction StudiesSlowed or blocked conduction (demyelination)
EMGReduced transmission from nerves to muscles
ECG MonitoringArrhythmias, signs of autonomic instability

🛏️ ICU Admission Criteria

Admit to ICU if:

  • Respiratory distress (e.g., RR > 30, SpO₂ < 90%)
  • Cannot count to 15 in one breath
  • Autonomic instability (BP or heart rate fluctuations)
  • Bulbar dysfunction (gag/swallowing difficulty)
  • Rising CO₂ (hypercapnia on ABG)

💉 Treatment Overview

✅ Supportive Care

  • DVT prophylaxis: Low molecular weight heparin, compression stockings.
  • Pain management: Gabapentin, NSAIDs, opioids (if severe).
  • Ventilatory support if required.

✅ Immunomodulatory Therapy

TherapyDosage/ApproachNotes
IVIG0.4 g/kg/day × 5 daysFirst-line; easier to administer
Plasmapheresis4–6 exchanges over 8–10 daysEqual efficacy, but more invasive

🛑 Steroids are not effective in GBS.


⏳ Prognosis & Recovery

  • 70–80% recover fully within 6 months to 1 year.
  • Recovery often happens in reverse order: cranial nerves → arms → legs.
  • 3–7% mortality (usually due to respiratory failure or arrhythmias).
  • Key takeaway: Early detection + prompt immunotherapy = good prognosis.

🔍 Guillain-Barré vs Transverse Myelitis (Comparison)

FeatureGBSTransverse Myelitis
OnsetPost-infectionPost-infection
Sensory LevelAbsentPresent
Bowel/Bladder InvolvementRareCommon
PainMild/absentSevere (burning/stabbing)
ReflexesAbsentHyperreflexia possible

🧠 Summary Checklist for GBS Management

✅ Recent infection
✅ Symmetrical ascending weakness
✅ Areflexia
✅ Autonomic instability
✅ Respiratory monitoring
✅ CSF: ↑ protein, normal WBC
✅ Early IVIG or plasma exchange
✅ No steroids
✅ ICU care if breathing, arrhythmia or bulbar signs present

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