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Arpan - Overview of Guillain-Barré Syndrome (GBS)
Apr 1, 2025
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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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