eMedicine Specialties > Emergency Medicine > Neurology
Guillain-Barre Syndrome: Follow-up
Updated: Jul 1, 2009
Follow-up
Further Inpatient Care
- Admission to the ICU should be considered for all patients with labile dysautonomia, an FVC of less than 20 mL/kg, or severe bulbar palsy.42
- Any patients exhibiting clinical signs of respiratory compromise, in any degree, also should be admitted to an ICU.42
- The risk of sepsis and infection can be decreased by use of minimal sedation, frequent physiotherapy, and mechanical ventilation with positive end expiratory pressure where appropriate.42
- The risk of DVT and pulmonary embolus may be minimized by administration of heparin or a low molecular weight heparin and intermittent pneumatic compression devices.42
- The use of cardiac telemetry and pacing in the case of severe bradycardia may help to reduce the risk of cardiac morbidity and mortality.42
- Pain may be symptomatically improved by frequent passive limb movements, gentle massage, frequent position changes, and use of carbamazepine and gabapentin.43,42
- Narcotics should be used judiciously because patients may already be at risk for ileus.42
Further Outpatient Care
- Physical therapy and occupational therapy may be beneficial in helping patients with Guillain-Barré syndrome to regain their baseline functional status.10,42
Transfer
- Transfer may be appropriate if a facility does not have the proper resources to care for patients who may require prolonged intubation or prolonged intensive care.
Complications
- With modern methods of respiratory management, most complications result from long-term paralysis. Possible complications include the following:
- Persistent paralysis
- Respiratory failure, mechanical ventilation
- Hypotension or hypertension
- Thromboembolism, pneumonia, skin breakdown
- Cardiac arrhythmia
- Ileus
- Aspiration
- Urinary retention
- Psychiatric problems such as depression and anxiety
- Nephropathy reported in pediatric patients44
Prognosis
- Poor prognosis for patients with Guillain-Barré syndrome is associated with rapid progression of symptoms, advanced age, prolonged ventilation (>1 mo), and severe reduction of action potentials on neuromuscular testing.
- Published reports indicate full recovery may be expected in 50-95% of patients with Guillain-Barré syndrome.
- Long-term follow-up studies show nearly 50% of patients exhibit histological and clinical residual neuropathies years after the initial syndrome. Patients may have residual motor and sensory dysfunction.45
- Increased CSF levels of neurone-specific enolase and S-100b protein are associated with longer duration of illness.1
- A longer-lasting increase in IgM anti-GM1 predicts slow recovery.1
- Neurologic sequelae
- Reported incidence of permanent neurologic sequelae ranges from 10-40%.
- The worst-case scenario is tetraplegia within 24 hours with incomplete recovery after 18 months or longer.
- The best-case scenario is mild difficulty walking, with recovery within weeks.
- The usual scenario is peak weakness in 10-14 days with recovery in weeks to months. Average time on a ventilator (without treatment) is 50 days.
- Recent studies report that patients with Guillain-Barré syndrome may exhibit long-term differences in pain intensity, fatigability, and functional impairment compared with healthy controls.46
- Mortality
Patient Education
- For excellent patient education resources, visit eMedicine's Brain and Nervous System Center. Also, see eMedicine's patient education article Guillain-Barré Syndrome.
Miscellaneous
Medicolegal Pitfalls
- Failure to anticipate dysrhythmias and autonomic instability
- Failure to anticipate progressive respiratory failure
- Failure to correctly diagnose Guillain-Barré syndrome in patients with a variant form of the disease or in those with a normal CSF protein
- Failure to provide adequate DVT prophylaxis in a patient that develops a DVT and/or pulmonary embolism
Special Concerns
- The leading cause of death in elderly patients with Guillain-Barré syndrome is arrhythmia.
- Recurrence of Guillain-Barré syndrome is rare but has been reported in 2-5% of patients.50
- Variants of Guillain-Barré syndrome may present with pure motor dysfunction or acute dysautonomia.
- The Miller-Fisher syndrome is a variant of Guillain-Barré syndrome in which the initial symptoms include ataxia, ophthalmoplegia, and areflexia.
More on Guillain-Barre Syndrome |
| Overview: Guillain-Barre Syndrome |
| Differential Diagnoses & Workup: Guillain-Barre Syndrome |
| Treatment & Medication: Guillain-Barre Syndrome |
Follow-up: Guillain-Barre Syndrome |
| References |
| « Previous Page |
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Further Reading
Keywords
Guillain-Barre syndrome, Guillain-Barré syndrome, GBS, nervous system, myelin sheath, neuropathy, nerves, causes, symptoms, treatment, viral infection, weakness, autoimmune disease, acute inflammatory demyelinating polyneuropathy, AIDP, acute motor axonal neuropathy, AMAN, acute motor-sensory axonal neuropathy, AMSAN, Miller-Fisher syndrome, MFS, acute panautonomic neuropathy, pharyngeal-brachial-cervical variant, pure sensory variant, Campylobacter jejuni, IVIG, plasmapheresis, acute flaccid paralysis
Follow-up: Guillain-Barre Syndrome