Auvichayapat Narong, Tassniyom Sompon, Treerotphon Sutthinee, Auvichayapat Paradee
Division of Pediatric Neurology, Department of Pediatrics, Faculty of Medicine, Khon Kaen University, Khon Kaen 40002, Thailand.
J Med Assoc Thai. 2007 Sep;90(9):1809-14.
To review the result of the infantile spasms' treatment with sodium valproate followed by nitrazepam or clonazepam.
Descriptive retrospective study.
Srinagarind Hospital, Department of Pediatrics, Faculty of Medicine, Khon Kaen University, Khon Kaen, Thailand.
Twenty-four infantile spasms admitted between January 1994 and December 2003 were analyzed. The inclusion criteria were the patients with infantile spasms clinically diagnosed by the pediatric neurologist, having hypsarrhythmic pattern EEG, and receiving sodium valproate with or without nitrazepam or clonazepam. The patients who had an uncertain diagnosis, incomplete medical record, or that were incompletely followed up were excluded. Data were collected on sex, age at onset of seizure, type of infantile spasms, associated type of seizure, predisposing etiological factor, neuroimaging study, and the result of treatment including cessation of spasms, subsequent development of other seizure types, quantitative reduction of spasms, relapse rates of spasms, psychomotor development, and adverse effects of AEDs.
The mean age at onset was 177 days. The male-to-female ratio was 1:1.2. There were 13 cryptogenic (54.2%) and 11 symptomatic (45.8%) infantile spasms. The most common predisposing etiological factors in symptomatic cases were hypoxic ischemic encephalopathy (45.5%) and microcephaly (36.4%), respectively. Ten patients received sodium valproate (41.7%), another 10 received sodium valproate with clonazepam (41.7%), and four received sodium valproate with nitrazepam (16.7%). Both, the complete cessation rate and the 50% reduction of spasms rate were 45.8%. The duration to complete cessation was 70 days. The relapse rate was 18.2%. The rate of delayed psychomotor development was 83.3%. The mean duration of follow-up was 49.6 months.
The authors propose to use sodium valproate concomitantly with benzodiazepines, especially clonazepam, in situations such as unavailability, intolerability, or adverse effects of ACTH or vigabatrin, or in a patient who does not respond to ACTH or vigabatrin.
回顾丙戊酸钠联合硝西泮或氯硝西泮治疗婴儿痉挛症的效果。
描述性回顾性研究。
泰国孔敬府孔敬大学医学院儿科学系诗里拉吉医院。
分析1994年1月至2003年12月收治的24例婴儿痉挛症患者。纳入标准为经儿科神经科医生临床诊断为婴儿痉挛症、脑电图呈高峰节律紊乱图形且接受丙戊酸钠治疗(联合或不联合硝西泮或氯硝西泮)的患者。排除诊断不明确、病历不完整或随访不完整的患者。收集的数据包括性别、癫痫发作起始年龄、婴儿痉挛症类型、相关癫痫发作类型、诱发病因、神经影像学检查以及治疗结果,包括痉挛停止情况、其他癫痫发作类型的后续发展、痉挛定量减少情况、痉挛复发率、精神运动发育情况以及抗癫痫药物的不良反应。
发作的平均年龄为177天。男女比例为1:1.2。有13例隐源性婴儿痉挛症(54.2%)和11例症状性婴儿痉挛症(45.8%)。症状性病例中最常见的诱发病因分别是缺氧缺血性脑病(45.5%)和小头畸形(36.4%)。10例患者接受丙戊酸钠治疗(41.7%),另外10例接受丙戊酸钠联合氯硝西泮治疗(41.7%),4例接受丙戊酸钠联合硝西泮治疗(16.7%)。痉挛完全停止率和痉挛减少50%的比率均为45.8%。完全停止的持续时间为70天。复发率为18.2%。精神运动发育延迟率为83.3%。平均随访时间为49.6个月。
作者建议在促肾上腺皮质激素(ACTH)或氨己烯酸不可用、不耐受或有不良反应,或患者对ACTH或氨己烯酸无反应等情况下,将丙戊酸钠与苯二氮䓬类药物(尤其是氯硝西泮)联合使用。