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Published on: November 9, 2017
Outcome in childhood Guillain-Barré syndrome
Veena Kalra1, Naveen Sankhyan, Suvasini Sharma
1Department of Pediatrics, All India Institute of Medical Science, New Delhi 110029, India.
Insights
Most children with Guillain-Barré syndrome (GBS) achieve good long-term recovery, even after severe acute phases. Early indicators like ventilation needs predict poorer short-term outcomes for pediatric GBS patients.
Area of Science:
- Pediatric Neurology
- Clinical Neuroscience
- Immunology
Background:
- Guillain-Barré syndrome (GBS) is a rare autoimmune disorder affecting the peripheral nervous system in children.
- Understanding long-term functional outcomes is crucial for managing pediatric GBS.
- Prognostic factors in children with GBS require further elucidation.
Purpose of the Study:
- To prospectively evaluate the long-term functional outcomes of children diagnosed with Guillain-Barré syndrome.
- To identify clinical and electrophysiological factors associated with good versus poor outcomes in pediatric GBS.
Main Methods:
- Prospective follow-up study of 52 children with GBS over a median of 25 months.
- Functional recovery assessed using the Hughes scale at 12 months and beyond.
- Comparison of clinical and electrophysiological variables between outcome groups.
Main Results:
- Mortality in the acute phase was 11.5%.
- At 1 year, 87.5% of survivors had full or minimal symptoms; this increased to 95% long-term.
- Need for ventilation, inexitable nerves, and delayed walking predicted poor outcomes.
Conclusions:
- Ventilator-dependent children face the worst short-term prognosis in GBS.
- Most children with GBS experience significant long-term functional recovery, regardless of initial severity.
Objective:
To prospectively assess the outcome of children diagnosed with Guillain-Barré syndrome (GBS), followed up for a median duration of 25 months.
Methods:
Tertiary center, prospective follow up of children with GBS enrolled between, Dec 2003 to Sep 2006. Functional recovery was determined at 12 months and later using Hughes scale (0-6). Clinical, electrophysiological variables were compared between the good outcome (grade 0/1) and bad outcome groups (died or functional grade >1).
Results:
Among 52 children with a median age of five yr there was male preponderance (75.4%). Mortality during acute phase was 11.5% (6/52). Among the survivors long term data was obtainable in 40 of the 46 children. At one year follow up 87.5% children had fully recovered or had minimal symptoms, beyond one year this rose to 95%. Only 2 among 40 had significant symptoms at last follow up (1 grade-2 and 1 grade-3). Factors significantly associated with poor outcome were: need for artificial ventilation, inexitable nerves on nerve conduction testing and delayed independent walking.
Conclusion:
Children needing ventilation have the worst short-term prognosis. However, irrespective of severity during acute phase, good long-term recovery can be expected in most children.
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