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Updated: Jul 4, 2026

Induction and Clinical Scoring of Chronic-Relapsing Experimental Autoimmune Encephalomyelitis
Published on: July 4, 2007
Acute disseminated encephalomyelitis in children: focus on relapsing patients
Agnese Suppiej1, Roberta Vittorini, Marta Fontanin
1Department of Pediatrics, University of Padua, Padua, Italy. suppiej@pediatria.unipd.it
Insights
Pediatric acute disseminated encephalomyelitis (ADEM) prognosis is uncertain. Early spinal fluid and visual-evoked potential findings may predict poor outcomes in children with ADEM.
Area of Science:
- Pediatric Neurology
- Neuroimmunology
- Clinical Neuroscience
Background:
- Pediatric acute disseminated encephalomyelitis (ADEM) is an immune-mediated demyelinating disease.
- Prognostic factors and diagnostic criteria for ADEM in children require further investigation.
- Differentiating ADEM from other demyelinating disorders like multiple sclerosis is crucial for appropriate management.
Purpose of the Study:
- To investigate prognostic factors for relapse in pediatric ADEM.
- To evaluate diagnostic criteria for ADEM and related disorders in children.
- To assess long-term outcomes and disease course in pediatric ADEM.
Main Methods:
- Retrospective study of 24 Italian children diagnosed with ADEM.
- Mean age at onset 6.9 years, mean follow-up 52.8 months.
- Analysis of clinical, neurophysiologic, cerebrospinal fluid (CSF), and neuroradiologic data.
Main Results:
- Most patients (22/24) met International Pediatric Multiple Sclerosis Study Group criteria for ADEM.
- Three patients experienced relapses at 3 months, 2 years, and 8 years.
- Early findings of oligoclonal IgG bands in CSF and persistent visual-evoked potential abnormalities correlated with poor outcomes.
- No initial features predicted outcomes; however, revised McDonald criteria aided diagnosis by the second attack.
Conclusions:
- Early prognostic indicators for pediatric ADEM include CSF oligoclonal bands and visual-evoked potential abnormalities.
- Revised diagnostic criteria facilitate early identification of multiple sclerosis and multiphasic ADEM.
- Long-term follow-up is essential to characterize the disease course in pediatric ADEM.
Abstract:
This study investigated the possible prognostic factors for relapse, and the diagnostic criteria for multiple sclerosis and related disorders, in pediatric acute disseminated encephalomyelitis. The study population comprised 24 Italian children with a mean age at onset of 6.9 years, and a mean follow-up time of 52.8 months (range, 12-180). Clinical, neurophysiologic, spinal-fluid, neuroradiologic, and outcome features were investigated. All patients but 2, who were reclassified as exhibiting clinically isolated syndromes, fulfilled the new classification criteria for acute disseminated encephalomyelitis recently proposed by the International Pediatric Multiple Sclerosis Study Group. Three patients relapsed after 3 months, 2 years, and 8 years, respectively. By the second attack, the diagnosis of multiple sclerosis, as well as of multiphasic disseminated encephalomyelitis, could be rendered using the revised criteria of McDonald et al. Long-term follow-up seemed to confirm a chronic disease course in 2 children. We could not identify features at onset to predict outcomes of patients. However, early in follow-up, the appearance of oligoclonal immunoglobulin G bands in spinal fluid and the persistence of visual-evoked potential abnormalities were associated with poor outcomes.
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