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Infantile spasms: Neurological and developmental follow-up – A comparison between two ethnic groups: Israeli Jews and Bedouin in the South of Israel

机译:小儿痉挛:神经学和发育方面的跟进–以色列南部的以色列犹太人和贝都因人这两个种族之间的比较

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Background: The aim of this study was to examine all cases of infantile spasms (IS) diagnosed at the Soroka University Medical Center, Ben Gurion University, Israel during 1981–1997.Material/Methods: 31 children, 17 (55%) males. 17 (55%) were Jews and 14 (45%) Bedouins. Four (13%) died. Data was gathered from hospital fi les, neuropediatric unit and Zusman Child Development Center. Demographic and ethnic data, characteristics of the disease type of seizures, EEG pattern imaging studies, type of treatment, psychomotor development, rehabilitation and educational services were analysed.Results: Mean age at diagnosis 7.22 months. Etiology for one third was pre- or perinatal insult, one third postnatal and one third unknown. 26 (84%) were symptomatic and fi ve (16%) cryptogenic. Signifi cant statistical difference was found with more Bedouin children symptomatic with moderate or severe mental retardation, cerebral palsy with severe motor diffi culties and recurrence of the disease.Statistically signifi cant correlation existed between poor response to initial treatment and placement in special education, recurrence of disease and cerebral palsy with moderate or severe motor diffi culties, the appearence of a different type of epilepsy during follow-up and placement in special education. 18 children (58%) received fi rst treatment with ACTH, 10 (32%) children with IVIG (immunoglobolin iv), 3 (10%) with neither ACTH nor IVIG. Regarding therapy response we found no signifi cant difference between Jews and Bedouins.Conclusions: No signifi cant statistical difference was found between the two treatments concerning clinical course or developmental follow-up. Due to small numbers multi-center research is needed.
机译:背景:本研究的目的是检查1981-1997年在以色列本古里安大学索罗卡大学医学中心诊断出的所有婴儿痉挛(IS)病例。材料/方法:31名儿童,17名(55%)男性。犹太人17人(55%),贝都因人14人(45%)。四人(13%)死亡。数据来自医院文件,神经儿科和祖斯曼儿童发展中心。分析人口和种族数据,癫痫发作的疾病类型特征,脑电图成像研究,治疗类型,精神运动发育,康复和教育服务。结果:诊断时的平均年龄为7.22个月。病因中有三分之一是产前或围产期的侮辱,三分之一是产后的,三分之一是未知的。有症状(26%(84%)有症状,有五个(16%)有隐源性。在多贝多因儿童中度或重度智力低下症状,脑瘫伴重度运动困难和疾病复发中发现显着统计学差异。对初始治疗的不良反应与特殊教育的安置,复发,复发之间存在统计学意义的相关性。疾病和患有中度或重度运动困难的脑瘫,在随访和特殊教育期间出现了不同类型的癫痫病。 18例儿童(58%)接受了ACTH的首次治疗,10例(32%)的IVIG(免疫球蛋白iv)儿童,3例(10%)既没有ACTH也没有IVIG的儿童。关于治疗反应,我们发现犹太人和贝都因人之间没有显着差异。结论:两种疗法在临床过程或发育随访方面均未发现显着统计学差异。由于数量少,需要进行多中心研究。

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