Guillain-Barré Syndrome (GBS) Flashcards

1
Q

What is Guillain-Barré Syndrome (GBS)?

A

GBS is an acute, immune-mediated polyneuropathy causing muscle weakness and sensory loss, often triggered by infection.

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2
Q

What are the typical symptoms of GBS?

A

Progressive symmetrical weakness, areflexia, paraesthesia, and sometimes autonomic dysfunction.

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3
Q

What is the usual pattern of weakness in GBS?

A

Weakness typically starts in the lower limbs and ascends proximally (ascending paralysis).

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4
Q

What is the most common trigger for GBS?

A

Infections such as Campylobacter jejuni, cytomegalovirus (CMV), Epstein-Barr virus (EBV), and influenza.

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5
Q

What is the pathophysiology of GBS?

A

It involves immune-mediated damage to peripheral nerves and myelin sheaths, often through molecular mimicry.

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6
Q

What are the subtypes of GBS?

A

Acute inflammatory demyelinating polyneuropathy (AIDP), Miller Fisher syndrome, and acute motor axonal neuropathy (AMAN).

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7
Q

What is the prevalence of GBS?

A

GBS occurs in approximately 1–2 cases per 100,000 people annually.

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8
Q

What are the risk factors for GBS?

A

Recent infections (especially Campylobacter), recent vaccination, and certain autoimmune conditions.

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9
Q

What is the clinical course of GBS?

A

Symptoms typically progress over days to weeks, plateau, and then gradually resolve over weeks to months.

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10
Q

What autonomic symptoms can occur in GBS?

A

Tachycardia, bradycardia, hypotension, hypertension, and urinary retention.

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11
Q

What are the hallmark clinical examination findings in GBS?

A

Symmetrical flaccid weakness, absent or reduced reflexes, and sensory abnormalities.

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12
Q

What is the role of lumbar puncture in GBS diagnosis?

A

It typically shows raised protein with normal white cell count (albuminocytological dissociation).

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13
Q

What is the role of nerve conduction studies in GBS?

A

They confirm peripheral nerve dysfunction and help differentiate between demyelinating and axonal subtypes.

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14
Q

What are the differential diagnoses for GBS?

A

Chronic inflammatory demyelinating polyneuropathy (CIDP), myasthenia gravis, botulism, and transverse myelitis.

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15
Q

What is the first-line treatment for GBS?

A

Intravenous immunoglobulin (IVIG) or plasma exchange.

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16
Q

When is ventilatory support required in GBS?

A

In cases of respiratory muscle weakness or bulbar dysfunction leading to respiratory failure.

17
Q

What supportive care is important in GBS management?

A

Regular physiotherapy, pain management, prevention of venous thromboembolism, and monitoring for autonomic instability.

18
Q

What is the prognosis of GBS?

A

Most patients recover fully, though some may experience residual weakness or fatigue.

19
Q

What percentage of GBS patients require intensive care?

A

Approximately 25% of GBS patients require ventilatory support in an ICU.

20
Q

What is Miller Fisher syndrome?

A

A variant of GBS characterised by ophthalmoplegia, ataxia, and areflexia.

21
Q

What is the association between GBS and vaccines?

A

A very small risk of GBS has been associated with certain vaccines, such as the influenza vaccine.

22
Q

What role does physiotherapy play in GBS management?

A

Physiotherapy helps maintain muscle strength, prevent contractures, and promote functional recovery.

23
Q

What is the mortality rate of GBS?

A

Mortality is approximately 3–7%, often due to complications such as respiratory failure or autonomic instability.

24
Q

What is albuminocytological dissociation?

A

It refers to elevated protein levels in cerebrospinal fluid (CSF) without an increase in white blood cells, a hallmark of GBS.

25
Q

What long-term complications can result from GBS?

A

Chronic fatigue, residual weakness, pain, and psychological effects such as depression or anxiety.