Kikuchi Kenjiro, Kuki Ichiro, Nishiyama Masahiro, Ueda Yuki, Matsuura Ryuki, Shiohama Tadashi, Nagase Hiroaki, Akiyama Tomoyuki, Sugai Kenji, Hayashi Kitami, Murakami Kiyotaka, Yamamoto Hitoshi, Fukuda Tokiko, Kashiwagi Mitsuru, Maegaki Yoshihiro
Working Group for the Revision of Treatment Guidelines for Pediatric Status Epilepticus/Convulsive Status Epilepticus, Japanese Society of Child Neurology, Tokyo, Japan; Division of Neurology, Pediatric Epilepsy Center, Saitama Children 's Medical Center, Saitama, Japan.
Working Group for the Revision of Treatment Guidelines for Pediatric Status Epilepticus/Convulsive Status Epilepticus, Japanese Society of Child Neurology, Tokyo, Japan; Division of Pediatric Neurology, Osaka City General Hospital, Osaka, Japan.
Brain Dev. 2025 Feb;47(1):104306. doi: 10.1016/j.braindev.2024.104306. Epub 2024 Dec 2.
The updated definition of status epilepticus (SE) by the International League Against Epilepsy in 2015 included two critical time points (t: at which the seizure should be regarded as an "abnormally prolonged seizure"; and t: beyond which the ongoing seizure activity can pose risk of long-term consequences) to aid in diagnosis and management and highlights the importance of early treatment of SE more clearly than ever before. Although Japan has witnessed an increasing number of pre-hospital drug treatment as well as first- and second-line treatments, clinical issues have emerged regarding which drugs are appropriate. To address these clinical concerns, a revised version of the "Japanese Guidelines for the Treatment of Pediatric Status Epilepticus 2023" (GL2023) was published. For pre-hospital treatment, buccal midazolam is recommended. For in-hospital treatment, if an intravenous route is unobtainable, buccal midazolam is also recommended. If an intravenous route can be obtained, intravenous benzodiazepines such as midazolam, lorazepam, and diazepam are recommended. However, the rates of seizure cessation were reported to be the same among the three drugs, but respiratory depression was less frequent with lorazepam than with diazepam. For established SE, phenytoin/fosphenytoin and phenobarbital can be used for pediatric SE, and levetiracetam can be used in only adults in Japan. Coma therapy is recommended for refractory SE, with no recommended treatment for super-refractory SE. GL2023 lacks adequate recommendations for the treatment of nonconvulsive status epilepticus (NCSE). Although electrographic seizure and electrographic SE may lead to brain damages, it remains unclear whether treatment of NCSE improves outcomes in children. We plan to address this issue in an upcoming edition of the guideline.
国际抗癫痫联盟在2015年对癫痫持续状态(SE)的定义进行了更新,其中纳入了两个关键时间点(t:此时发作应被视为“异常延长的发作”;以及t:超过该时间点,持续的发作活动可能会带来长期后果的风险),以辅助诊断和管理,并且比以往任何时候都更清晰地凸显了SE早期治疗的重要性。尽管日本院前药物治疗以及一线和二线治疗的数量不断增加,但关于哪些药物合适的临床问题还是出现了。为解决这些临床问题,发布了《2023年日本小儿癫痫持续状态治疗指南》(GL2023)的修订版。对于院前治疗,推荐使用咪达唑仑口腔黏膜给药。对于院内治疗,如果无法建立静脉通路,也推荐使用咪达唑仑口腔黏膜给药。如果可以建立静脉通路,推荐使用静脉注射苯二氮䓬类药物,如咪达唑仑、劳拉西泮和地西泮。然而,据报道这三种药物的癫痫发作停止率相同,但劳拉西泮引起呼吸抑制的频率低于地西泮。对于确诊的SE,苯妥英钠/磷苯妥英钠和苯巴比妥可用于小儿SE,在日本左乙拉西坦仅可用于成人。对于难治性SE,推荐昏迷治疗,对于超难治性SE则没有推荐的治疗方法。GL2023对于非惊厥性癫痫持续状态(NCSE)的治疗缺乏充分的推荐。尽管脑电图发作和脑电图SE可能会导致脑损伤,但NCSE的治疗是否能改善儿童的预后仍不清楚。我们计划在该指南的下一版中解决这个问题。