Neuropediatrics 2009; 40(5): 211-217
DOI: 10.1055/s-0030-1247518
Original Article

© Georg Thieme Verlag KG Stuttgart · New York

Clinical Outcome of Children Presenting with a Severe Manifestation of Acute Disseminated Encephalomyelitis

K. Rostásy1 , A. Nagl1 , S. Lütjen2 , K. Roll2 , S. Zotter1 , A. Blaschek3 , G.C. Korenke4 , M. Karenfort5 , T. Gotwald6 , H. Holthausen2
  • 1Department of Pediatrics IV, Division of Pediatric Neurology, Inherited Metabolic Disorders and Developmental Neurology, Medical University Innsbruck, Innsbruck, Austria
  • 2Behandlungszentrum Vogtareuth, Vogtareuth, Germany
  • 3Department of Pediatric Neurology and Developmental Medicine, Dr. von Hauner's Children's Hospital, University of Munich, Munich, Germany
  • 4Department of Neuropediatrics, Children's Hospital, Klinikum Oldenburg,Oldenburg, Germany
  • 5Department of General Pediatrics, Pediatric Neurology, Heinrich Heine University Düsseldorf, Düsseldorf, Germany
  • 6Department of Neuroradiology, Medical University Innsbruck, Innsbruck,Austria
Further Information

Publication History

received 18.08.2009

accepted 07.01.2010

Publication Date:
10 March 2010 (online)

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Abstract

Background: Acute disseminated encephalomyelitis (ADEM) is an acute, inflammatory-demyelinating disorder of the CNS with a favourable outcome in the majority of cases.

Objective: The aim of this study was to examine the long-term outcome of children with an initially severe form of ADEM.

Methods: Children with ADEM according to the criteria of the International Pediatric MS Study Group (IPMSSG) referred to the rehabilitation centre Vogtareuth were included. Neurological impairment was evaluated with a standardized telephone-based interview assessing the EDSS score. Neuropsychological outcome was assessed with review of the medical records and a standardized parental questionnaire (KOPKIJ).

Results: Twelve children (1 year 9 months to 13 years of age) were included. All children had focal-neurological signs and changes in mental status at presentation and an MRI of the brain showing a range of white and gray matter lesions. 11/12 patients with a mean follow-up of 6.2 years (2–13.6 years) had a monophasic course of the disease. One child had a multiphasic ADEM. Two children had an EDSS score of 0, three an EDSS of 2, five an EDSS between 3 and 5 and two children had an EDSS score of 6 and 9. Results of a standardized parental questionnaire (KOPKIJ) revealed that 7 children had deficits in the categories alertness, memory, school performance, visual-spatial skills and/or impulse control.

Conclusion: The results of our study indicate that children with an initially severe manifestation of ADEM continue to have in the majority of cases neurological and neuropsychological handicaps.

References

Correspondence

Kevin RostásyMD 

Department of Pediatrics IV

Division of Pediatric Neurology

Medical University Innsbruck

Anichstraße 35

6062 Innsbruck

Austria

Phone: +43/512/504 23517

Fax: +43/512/504 24941

Email: Kevin.Rostasy@uki.at