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Arpan - Overview of Guillain-Barré Syndrome (GBS)

Apr 1, 2025

Lecture Notes: Guillain-Barré Syndrome (GBS)

Introduction

  • Recent outbreak in India, particularly in Pune.
  • One of the largest outbreaks as per WHO.
  • Out of 140 affected patients, 18 on ventilators.

What is Guillain-Barré Syndrome?

  • Also known as Acute Inflammatory Demyelinating Polyneuropathy.
  • An autoimmune disease affecting the peripheral nervous system.
  • Body's immune system attacks the myelin sheath of nerves.

Pathophysiology

  • Myelin sheath damage leads to poor nerve impulse conduction.
  • Affects several body functions:
    • Breathing Rhythm
    • Motor functions (movement of limbs)
  • Visible symptoms:
    • Numbness in extremities (fingertips, toe tips)
    • Muscle Weakness
    • Tingling Sensations
    • Swallowing Difficulty
    • Shortness of Breath

Clinical Presentation

  • Progressive onset of pain in a "stocking pattern".
  • Paresthesia: Numbness and tingling in extremities.
  • Loss of Reflexes (Areflexia): Fine-tuned reflexes are hampered.
  • Autonomic Dysfunction:
    • Irregular heartbeat, blood pressure instability.
  • Respiratory Involvement:
    • Phrenic nerve and intercostal muscle weakness.
    • Possible aspiration pneumonia due to bulbar dysfunction.

Risk Factors

  • Bacterial Infections: Campylobacter jejuni.
  • Viral Infections: Epstein-Barr virus, cytomegalovirus.
  • Influenza Vaccine (rare cases).
  • Molecular Mimicry: Antibodies mistakenly attack myelin due to bacterial antigen resemblance.

Subtypes of GBS

  • AIDP (Acute Inflammatory Demyelinating Polyneuropathy): Most common in the US and Europe.
  • Acute Motor Axonal Neuropathy: Often linked to Campylobacter jejuni infection.
  • Acute Motor Sensory Axonal Neuropathy: Severe, affects both sensory and motor systems.
  • Miller Fisher Syndrome: Characterized by ataxia and areflexia.

Diagnosis

  • Electromyography Test: Checks nerve conduction velocity.
  • CSF Examination:
    • Increased protein concentration (>55 mg/dL).
    • Little or no pleomorphic cells.

Treatment

  • First-line Treatments: Plasmapheresis and IVIG.
  • Corticosteroids: Generally not indicated.
  • Monitoring:
    • Frequent respiratory function checks.
    • ICU admission may be required.
  • Rehabilitation: Aggressive physical therapy.
  • Recovery could take up to 1 year.

Summary

  • GBS is an auto-immune condition with progressive paralysis and autonomic dysfunction.
  • Clinical hallmark includes increased protein in CSF.
  • For a detailed follow-up, monitoring and early treatment are crucial to manage the condition effectively.

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