Neuropediatrics 2015; 46(06): 377-384
DOI: 10.1055/s-0035-1564618
Original Article
Georg Thieme Verlag KG Stuttgart · New York

A Multinational Survey on Actual Diagnostics and Treatment of Subacute Sclerosing Panencephalitis

Martin Häusler
1   Division of Pediatric Neurology and Social Pediatrics, Department of Pediatrics, University Hospital RWTH Aachen, Aachen, Germany
,
Ayse Aksoy
2   Clinics of Pediatric Neurology, Dr. Sami Ulus Research and Training Hospital of Women's and Children's Health and Diseases, Ankara, Turkey
,
Michael Alber
3   Department of Neuropaediatrics, University Children's Hospital, Tübingen, Germany
,
Sakir Altunbasak
4   Department of Pediatric Neurology, Cukurova University, Faculty of Medicine, Saricam/Adana, Turkey
,
Aydan Angay
5   Private Practice, Göztepe, Istanbul, Turkey
,
Oana Tarta Arsene
6   Pediatric Neurology Clinic, Professor Doctor Alexandru Obregia Clinical Hospital, Bucharest, Romania
,
Dana Craiu
6   Pediatric Neurology Clinic, Professor Doctor Alexandru Obregia Clinical Hospital, Bucharest, Romania
7   Department of Neurology, Pediatric Neurology, Psychiatry, Neurosurgery, Pediatric Neurology Clinic II, Carol Davila University of Medicine, Bucharest, Romania
,
Hans Hartmann
8   Department of Pediatrics, Hannover Medical School, Hannover, Germany
,
Semra Hiz-Kurul
9   Division of Child Neurology, Department of Pediatrics, Dokuz Eylül University Faculty of Medicine, İzmir, Turkey
,
Takashi Ichiyama
10   Department of Pediatrics, Tsudumigaura Handicapped Children's Hospital, Yamaguchi, Japan
,
Catrinel Iliescu
6   Pediatric Neurology Clinic, Professor Doctor Alexandru Obregia Clinical Hospital, Bucharest, Romania
7   Department of Neurology, Pediatric Neurology, Psychiatry, Neurosurgery, Pediatric Neurology Clinic II, Carol Davila University of Medicine, Bucharest, Romania
,
Bosanka Jocic-Jakubi
11   Department of Pediatric Neurology, Clinical Center Nis, Pediatric Clinic, Nis, Serbia
12   Department of Pediatrics, Al Sabah Hospital, Kuwait
,
Rudolf Korinthenberg
13   Division of Neuropediatrics and Muscular Diseases, Department of Pediatrics and Adolescent Medicine, University Medical Center Freiburg, Freiburg, Germany
,
Gülsen Köse
14   Department of Child Neurology, Health Ministery Şişli Hamidiye Etfal Education and Research Hospital, Istanbul, Turkey
,
Marissa B. Lukban
15   Manila Department of Pediatrics and Neurosciences, University of the Philippines College of Medicine, Manila, Philippines
,
Mehpare Ozkan
2   Clinics of Pediatric Neurology, Dr. Sami Ulus Research and Training Hospital of Women's and Children's Health and Diseases, Ankara, Turkey
,
Iliyana Patcheva
16   Department of Pediatrics and Medical Genetics, Medical University-Plovdiv, Plovdiv, Bulgaria
,
Jens Teichler
17   Department of Neuropediatrics, University Children's Hospital Zurich, Zürich, Switzerland
18   Department of Social Pediatrics, Konstanz General Hospital, Konstanz, Germany
,
Mihaela Vintan
19   Department of Neuroscience, Faculty of medicine, University of Medicine and Pharmacy, Cluj Napoca, Romania
,
Ahmet Yaramis
20   Pediatric Neurology Department, Dicle University, Diyarbakır, Turkey
,
Coskun Yarar
21   Child Neurology Unit, Eskisehir Osmangazi University, Eskisehir, Turkey
,
Uluc Yis
9   Division of Child Neurology, Department of Pediatrics, Dokuz Eylül University Faculty of Medicine, İzmir, Turkey
,
Deniz Yuksel
2   Clinics of Pediatric Neurology, Dr. Sami Ulus Research and Training Hospital of Women's and Children's Health and Diseases, Ankara, Turkey
,
Banu Anlar
22   Department of Pediatric Neurology, Hacettepe University Faculty of Medicine, Ankara, Turkey
› Author Affiliations
Further Information

Publication History

24 August 2014

28 July 2015

Publication Date:
19 October 2015 (online)

Abstract

Subacute sclerosing panencephalitis (SSPE) is a chronic infection of the central nervous system caused by the measles virus (MV). Its prevalence remains high in resource poor countries and is likely to increase in the Northern Europe as vaccination rates decrease. Clinical knowledge of this devastating condition, however, is limited. We therefore conducted this multinational survey summarizing experience obtained from more than 500 patients treated by 24 physicians in seven countries. SSPE should be considered in all patients presenting with otherwise unexplained acquired neurological symptoms. In most patients, the diagnosis will be established by the combination of typical clinical symptoms (characteristic repetitive myoclonic jerks), a strong intrathecal synthesis of antibodies to MV and typical electroencephalogram findings (Radermecker complexes). Whereas the therapeutic use of different antiviral (amantadine, ribavirin) and immunomodulatory drugs (isoprinosine, interferons) and of immunoglobulins has been reported repeatedly, optimum application regimen of these drugs has not been established. This is partly due to the absence of common diagnostic and clinical standards focusing on neurological and psychosocial aspects. Carbamazepine, levetiracetam, and clobazam are the drugs most frequently used to control myoclonic jerks. We have established a consensus on essential laboratory and clinical parameters that should facilitate collaborative studies. Those are urgently needed to improve outcome.

Supplementary Data

Supplementary data (Table S1 to S4) are available at: www.thieme-connect.com/products/ejournals/html/10.1055/s-0035-1564618.


Supplementary Material

 
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