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The underlying etiology of infantile spasms (West syndrome): Information from the United Kingdom Infantile Spasms Study (UKISS) on contemporary causes and their classification2
Authors:John P. Osborne  Andrew L. Lux  Stuart W. Edwards  Eleanor Hancock  Anthony L. Johnson  Colin R. Kennedy  Richard W. Newton  Christopher M. Verity  Finbar J. K. O’Callaghan
Affiliation:1. The School for Health, University of Bath, Claverton Down, Bath, United Kingdom;2. The Royal United Hospital, Bath NHS Trust, Combe Park, Bath, United Kingdom;3. These two authors are joint first authors.;4. Department of Paediatric Neurology, Frenchay Hospital and the Bristol Royal Hospital for Children, Bristol, United Kingdom;5. Child and Family Health Services, Goldsworth Park, Woking, United Kingdom;6. Medical Research Council Biostatistics Unit, University of Cambridge Institute of Public Health, Cambridge, and MRC Clinical Trials Unit, London, United Kingdom;7. Paediatric Neurology, Clinical Neurosciences, University of Southampton, Southampton, United Kingdom;8. Department of Paediatric Neurology, Royal Manchester Children’s Hospital, Manchester, United Kingdom;9. Department of Paediatrics, Addenbrooke’s Hospital, Cambridge, United Kingdom;10. Department of Child Health, University of Bristol, Bristol, United Kingdom
Abstract:Purpose: To examine the underlying etiology of infantile spasms from the United Kingdom Infantile Spasms Study (UKISS), using the pediatric adaptation of ICD 10. Methods: Infants were enrolled in a randomized controlled trial or a parallel epidemiologic study. Etiological information included history, examination, and investigations. The infants were classified as proven etiology, if a neurologic disease was identified; as no identified etiology, if no neurologic disease was identified; and as not fully investigated, if a major piece of information was missing. Proven etiology was subclassified using the pediatric adaptation of ICD 10. The results were then examined to identify further methods of classification. Results: Of 207 infants, 127 (61%) had proven etiology, 68 (33%) had no identified etiology, and 12 (6%) were not fully investigated. Etiologies were prenatal in 63, perinatal in 38, postnatal in 8, and 18 other. The most common etiologies were: hypoxic–ischemic encephalopathy (HIE) 21 (10%), chromosomal 16 (8%), malformations 16 (8%), stroke 16 (8%), tuberous sclerosis complex (TSC) 15 (7%), and periventricular leukomalacia or hemorrhage 11 (5%). The remaining 32 etiologies were all individually uncommon. Response to treatment is given for individual etiologies. Discussion: Our method of classification allows the reporting of results by individual diseases, disease groups, or categories and is structured and clear. It avoids the use of poorly defined terms such as symptomatic and cryptogenic. It can adapt to new neurologic diseases, such as gene defects, and can be used for comparison of different groups of infants, thereby aiding meta‐analysis.
Keywords:Infantile spasms  West syndrome  Etiology  Classification  United Kingdom Infantile Spasms Study
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