The underlying etiology of infantile spasms (West syndrome): Information from the United Kingdom Infantile Spasms Study (UKISS) on contemporary causes and their classification

被引:195
作者
Osborne, John P. [1 ,2 ]
Lux, Andrew L. [3 ,4 ]
Edwards, Stuart W. [2 ]
Hancock, Eleanor [9 ]
Johnson, Anthony L. [10 ,11 ]
Kennedy, Colin R. [8 ]
Newton, Richard W. [7 ]
Verity, Christopher M. [6 ]
O'Callaghan, Finbar J. K. [3 ,4 ,5 ]
机构
[1] Royal United Hosp, Childrens Ctr, Bath NHS Trust, Bath BA1 3NG, Avon, England
[2] Univ Bath, Sch Hlth, Bath BA2 7AY, Avon, England
[3] Bristol Royal Hosp Children, Bristol, Avon, England
[4] Frenchay Hosp, Dept Paediat Neurol, Bristol BS16 1LE, Avon, England
[5] Univ Bristol, Dept Child Hlth, Bristol, Avon, England
[6] Addenbrookes Hosp, Dept Paediat, Cambridge CB2 2QQ, England
[7] Royal Manchester Childrens Hosp, Dept Paediat Neurol, Manchester M27 1HA, Lancs, England
[8] Univ Southampton, Southampton, Hants, England
[9] Child & Family Hlth Serv, Woking, Surrey, England
[10] Univ Cambridge, Inst Publ Hlth, MRC, Biostat Unit, Cambridge, England
[11] MRC Clin Trials Unit, London, England
基金
英国惠康基金;
关键词
Infantile spasms; West syndrome; Etiology; Classification; United Kingdom Infantile Spasms Study; MULTICENTER RANDOMIZED-TRIAL; TUBEROUS SCLEROSIS; EPILEPSY OUTCOMES; VIGABATRIN; MUTATIONS; SEIZURES;
D O I
10.1111/j.1528-1167.2010.02695.x
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
P>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.
引用
收藏
页码:2168 / 2174
页数:7
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