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Updated: May 18, 2026

Induction and Clinical Scoring of Chronic-Relapsing Experimental Autoimmune Encephalomyelitis
Published on: July 4, 2007
[Clinical outcome of the hyperacute form of acute disseminated encephalomyelitis]
R Reig Sáenz1, C Zazo Santidrián, P Martín Medina
1Unidad de Cuidados Intensivos Pediátricos, Servicio de Medicina Intensiva, Hospital General Universitario de Alicante, Alicante, España. reig_rob@gva.es
Introduction:
Acute disseminated encephalomyelitis (ADEM) is an inflammatory disease that damages the white matter of the central nervous system. Its clinical course is monophasic and multifocal. The outcome is usually favourable. We report our experience in the management of the hyperacute form of ADEM.
Patients And Methods:
A retrospective chart review was performed on five patients admitted in coma with a diagnosis of ADEM in the Paediatric Intensive Care Unit (PICU). We describe their epidemiological, clinical, microbiological, magnetic resonance imaging features and their treatment and outcomes.
Results:
The mean age was 5.2 years and all were male. None of them fulfilled radiologic criteria for acute haemorrhagic leukoencephalitis. At admission all patients were in a coma, and all were on controlled mechanical ventilation support. Before their admission all patients had fever. In all cases the time between the first neurological symptom and coma was ≤ 24hours. The cerebrospinal fluid examination was abnormal in three patients, and in one case, oligoclonal bands were detected. The first brain magnetic resonance imaging (MRI) showed white matter and basal ganglia lesions in all patients, and in three cases the spinal medulla was affected by demyelination. All patients were treated with a course of high-dose methylprednisolone. Four patients were also treated with high-dose immunoglobulins, and one of them received plasmapheresis. Two patients died, and one patient had severe sequelae at discharge from the PICU. At discharge the lesions in the white matter were still present in the MRI. After nine months the three survivors had a Glasgow Outcome Scale score of five and no one relapsed.
Conclusions:
There is a hyperacute clinical form of ADEM which has a high mortality rate. In the short term, the clinical improvement of hyperacute ADEM is not accompanied by a decrease of severity of the brain MRI.
Insights
A severe, rapid form of acute disseminated encephalomyelitis (ADEM) presents with high mortality. Early treatment with methylprednisolone and immunoglobulins may improve outcomes, but MRI lesions persist short-term.
Area of Science:
- Neurology
- Pediatric Intensive Care
- Neuroimmunology
Context:
- Acute disseminated encephalomyelitis (ADEM) is an inflammatory demyelinating disease of the central nervous system.
- The hyperacute form of ADEM presents a diagnostic and therapeutic challenge, often with severe neurological deficits.
Purpose:
- To describe the clinical characteristics, management, and outcomes of five pediatric patients with hyperacute ADEM admitted to the Paediatric Intensive Care Unit (PICU).
- To evaluate the short-term and long-term outcomes in a cohort of children with severe ADEM.
Summary:
- Five male patients with a mean age of 5.2 years presented with coma and mechanical ventilation requirements within 24 hours of initial neurological symptoms.
- Brain MRI revealed white matter and basal ganglia lesions, with spinal cord involvement in three cases. Treatment included high-dose methylprednisolone, immunoglobulins, and plasmapheresis in one patient.
- Two patients died, one had severe sequelae, but survivors showed significant neurological recovery at nine months, despite persistent MRI lesions.
Impact:
- Highlights the existence of a hyperacute ADEM variant with significant mortality and morbidity.
- Suggests that aggressive immunosuppressive therapy may lead to clinical recovery despite persistent radiological evidence of disease activity.
- Emphasizes the need for prompt recognition and intensive management of hyperacute ADEM in pediatric critical care settings.
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