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Physiological AdaptationAscending paralysis, watch breathing

Guillain-Barre SyndromeNCLEX cheat sheet

Guillain-Barre syndrome is an acute autoimmune disorder that attacks peripheral nerve myelin, causing rapid, progressive muscle weakness and paralysis.

20 key facts 3 practice questions Reviewed Oct 2026
The 1-minute sheetCinnaRN

Mechanism

  • Autoimmune demyelinates peripheral
  • Post-viral/GI infection trigger

Signs

  • Ascending symmetric weakness
  • Starts feet → moves up
  • Paresthesias, ↓ DTRs, autonomic

Report

  • Resp muscle paralysis = #1 risk
  • Monitor vital capacity, prep vent
  • BP/HR swings = autonomic instab.

Do

  • Plasmapheresis or IVIG
  • DVT prevention, recovery descends
Key takeaway

Weakness and paralysis are symmetric and typically ascend from the legs upward.

Before you read

Test yourself first: 3 questions

Question 1 of 3

A nurse cares for a client with Guillain-Barre syndrome who develops a rapid heart rate, then bradycardia, and labile blood pressure. The nurse recognizes these findings as evidence of which complication?

What is guillain-barre syndrome?

It classically begins in the lower extremities and ascends symmetrically upward, often following a recent respiratory or GI infection. The greatest danger is ascending paralysis reaching the respiratory muscles. Most patients recover, with weakness then resolving in descending order.

Guillain-Barre Syndrome illustrated

Guillain-Barré syndrome: patterns of ascending weakness
Guillain-Barré syndrome: patterns of ascending weakness. Illustration: Leonhard et al. via Wikimedia Commons, CC BY 4.0.

Key points to remember

  • Weakness and paralysis are symmetric and typically ascend from the legs upward.
  • Symptoms often appear 1 to 3 weeks after a viral respiratory or GI infection.
  • Diminished or absent deep tendon reflexes, paresthesias, and pain are common.
  • Ascending paralysis can reach the diaphragm and intercostal muscles, causing respiratory failure.
  • Autonomic dysfunction may cause labile blood pressure, tachycardia or bradycardia, and arrhythmias.

Signs & symptoms

  • Ascending symmetric weakness
  • Starts feet → moves up
  • Paresthesias, ↓ DTRs, autonomic

Nursing priorities

  1. Continuously monitor respiratory status (vital capacity, rate, depth) as respiratory failure is the leading cause of death.
  2. Keep intubation and mechanical ventilation equipment ready at the bedside.
  3. Administer plasmapheresis or IV immunoglobulin (IVIG) as prescribed to shorten the course.
  4. Monitor for autonomic instability: watch blood pressure and cardiac rhythm closely.
  5. Prevent complications of immobility with DVT prophylaxis, repositioning, and range-of-motion exercises.

Labs & values

Cerebrospinal fluid protein (elevated with normal cell count is characteristic)

Patient teaching

  • Recovery is usually gradual and may take weeks to months; most patients regain function.
  • Participate in physical and occupational therapy to rebuild strength and prevent contractures.
  • Report any returning weakness, breathing difficulty, or swallowing trouble immediately.

Red flags: report now

  • Declining vital capacity, shallow breathing, or difficulty clearing secretions signals impending respiratory failure, an emergency.
  • Wide swings in blood pressure or heart rate from autonomic dysfunction require immediate attention.
  • Difficulty swallowing or weakening cough indicates the paralysis is reaching cranial/bulbar muscles.

References

Clinical references for this topic

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