Guillain-Barre syndrome Flashcards

1
Q

What is Guillain-Barre syndrome?

A

An acute paralytic polyneuropathy that affects the peripheral nervous system.

It causes acute, symmetrical, ascending weakness and can also cause sensory symptoms.

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2
Q

What is Guillain-Barre syndrome usually triggered by?

A

Usually triggered by an infection and is particularly associated with Campylobacter jejuni, cytomegalovirus (CMV) and Epstein-Barr virus (EBV).

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3
Q

Pathophysiology of Guillain-Barre syndrome?

A

A process called molecular mimicry. The B cells of the immune system create antibodies against the antigens on the triggering pathogen.

These antibodies also match proteins on the peripheral neurones. They may target proteins on the myelin sheath or the nerve axon itself.

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4
Q

Typical presentation of Guillain-Barre syndrome?

A

Symptoms usually start within four weeks of the triggering infection.

They begin in the feet and progress upward. Symptoms peak within 2-4 weeks. Then, there is a recovery period that can last months to years.

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5
Q

2 main characteristic features of Guillain-Barre syndrome?

A

Symmetrical ascending weakness

Reduced reflexes

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6
Q

2 methods for diagnosis of Guillain-Barre syndrome?

A

Nerve conduction studies (showing reduced signal through the nerves)

Lumbar puncture for cerebrospinal fluid (showing raised protein with a normal cell count and glucose)

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7
Q

Management of Guillain-Barre syndrome?

A

Supportive care

VTE prophylaxis (pulmonary embolism is a leading cause of death)

IV immunoglobulins (IVIG) first-line

Plasmapheresis is an alternative to IVIG

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8
Q

What is GBS?

A

Ascending inflammatory demyelinating polyneuropathy characterised by an acute onset of bilateral and roughly symmetric limb weakness

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9
Q

Typical aetiology of GBS?

A

Typically occurs 1-3 weeks following an infection with common causes being campylobacter, mycoplasma and EBV

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10
Q

Clinical features of GBS?

A

Progressive ascending symmetrical limb weakness (usually starting with lower limbs)

Potential respiratory muscle involvement in severe cases

Potential cranial nerve involvement leading to diplopia, facial droop

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11
Q

Investigations for GBS?

A

Monitoring of forced vital capacity for respiratory muscle involvement

Serological tests:anti-ganglioside antibodies

Lumbar puncture: combination of elevated protein levels and normal white blood cell count

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12
Q

Management of GBS?

A

Mostly supportive management:

VTE prophylaxis: LMWH
Analgesias: NSAIDs or opiates for rediculopathy related back pain
Regular monitoring of FVC

Specific medical management includes:

IV immunoglobulin over 5 day course
Plasmapheresis

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