Retrospective Evaluation of Patients with Infantile Spasm Diagnosis

Mahmut Aslan, Serdal Gungor
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Abstract

Introduction: Infantile spasm (West Syndrome) (IS) is an age-dependent epileptic encephalopathy clinic specific to the first two years of life. Infantile spasm is the most known epileptic syndrome of infancy with typical seizures in the form of spasm, psychomotor retardation and hypsarrhythmia on electroencephalography. Typical spasms are in the form of flexor/extensor contractions that last for about 2-5 seconds, which usually symmetrically involves all muscle groups in the body.    Material and Method: In this study, the data of patients, who were followed up with the diagnosis of "infantile spasm" in the Pediatric Neurology Clinic of Mersin City Training and Research Hospital between 2020 and 2022, were retrospectively analyzed. Demographic characteristics, clinical, EEG and MRI findings of the patients were analyzed. Results: Eighteen patients were included in the study. Ten (55.5%) of our patients were male and 8 (44.5%) were female. The mean age of patients was ……. years. 11 (61.1%) patients were in the symptomatic group, 5 (27.7%) patients were in the cryptogenic group, and 2 (11.1%) patients were in the idiopathic group. At the time of diagnosis, there was flexor spasm, extensor spasm, mixt spasm, tonic seizure, myoclonic seizure in 5 (27,7%), 4 (22,2%), 4 (22,2%), 3 (16,6%), and 2 (11,1%) patients, respectively. Hypsarrhythmia, suppression-burst pattern, focal epileptic abnormality and generalized epileptic abnormality was observed in 8 (44,4%), 4 (22,2%), 3 (16,6%), and 3 (16,6%) patients, respectively. Of the 14 patients who were first diagnosed, 8 (57.1%) were treated with ACTH, 4 (28.6%) with phenobarbital, 2 (14.3%) with vigabatrin. Conclusion: Infantile spasm is an important age-related encephalopathy with severe neurological sequelae, resistant seizures, and high morbidity and mortality all over the world and in our country. Spasms cause further damage to the central nervous system, which continues to develop. For this reason, a positive contribution can be made in terms of prognosis with early and appropriate treatment.
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小儿痉挛诊断患者的回顾性评价
简介:婴儿痉挛(西综合征)(IS)是一种年龄依赖性癫痫性脑病临床,具体到生命的头两年。婴儿痉挛是最著名的婴儿癫痫综合征,典型的癫痫发作形式为痉挛、精神运动迟缓和脑电图上的心律失常。典型的痉挛表现为屈肌/伸肌收缩,持续约2-5秒,通常对称地涉及全身所有肌肉群。材料与方法:本研究回顾性分析梅尔辛市培训与研究医院儿科神经内科2020 - 2022年随访诊断为“婴儿痉挛”的患者资料。分析患者的人口学特征、临床、脑电图及MRI表现。结果:18例患者纳入研究。其中男性10例(55.5%),女性8例(44.5%)。患者平均年龄为.......年。症状组11例(61.1%),隐原组5例(27.7%),特发性组2例(11.1%)。诊断时出现屈肌痉挛5例(27.7%),伸肌痉挛4例(22.2%),强直性发作4例(22.2%),16.6% 3例,11.1% 2例。低心律失常8例(44.4%),抑制-爆发型4例(22.2%),局灶性癫痫异常3例(16.6%),全面性癫痫异常3例(16.6%)。在首次诊断的14例患者中,8例(57.1%)接受ACTH治疗,4例(28.6%)接受苯巴比妥治疗,2例(14.3%)接受维加巴比林治疗。结论:婴幼儿痉挛是一种重要的年龄相关性脑病,具有严重的神经系统后遗症、顽固性癫痫发作,在国内外发病率和死亡率均较高。痉挛会进一步损害中枢神经系统,使其继续发展。因此,通过早期和适当的治疗,可以对预后做出积极的贡献。
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