Department of Dental Anesthesiology, Faculty of Dental Medicine and Graduate School of Dental Medicine, Hokkaido University, Sapporo, Hokkaido, Japan.
Medicine (Baltimore). 2023 Jan 27;102(4):e32709. doi: 10.1097/MD.0000000000032709.
Dravet syndrome (DS) is a rare and severe myoclonic epilepsy, with onset commonly occurring in infancy. Seizures are triggered by various causes, including fever, bathing, and light stimulus. DS is refractory to drug treatment. Moreover, status epilepticus (SE) can cause serious encephalopathy and epilepsy-related deaths. There are very few reports of general anesthesia in DS patients. Herein, we report our experience with the anesthetic management of a pediatric patient with DS.
A 5-year-old boy (height, 112 cm; weight, 19 kg) was diagnosed with DS through SCN1A genetic testing, which revealed a de novo novel missense mutation. His medical history included drug-resistant epilepsy, developmental delay, and hypotonia. His seizures tended to be triggered daily by a rise in body temperature (BT), bathing, and light stimulus. He could not receive adequate dental treatment due to DS, although he had previously undergone dental treatment under restraint at the pediatric dentistry department of our hospital.
The patient was scheduled for intensive dental treatment under general anesthesia due to noncooperation, and DS-related limitations. By considering the risk posed by elevated BT, seizure-inducing drugs were avoided, and general anesthesia was completed as planned, uneventfully. Although fluctuation of BT occurred during the procedure, it was finally controlled at the end of anesthesia at about the same level as at anesthesia induction. However, small seizures and a single generalized convulsion were observed accompanied by fever on postoperative day 1. The patient was discharged from the hospital without major problems on postoperative day 3, because of detailed planning and close preoperative cooperation with the attending pediatrician.
It is essential to pay attention to managing BT and to avoid drugs that induce seizures during anesthesia for patients with DS. Cautious preoperative planning for anesthesia based on evaluation of the patient and rapid postoperative response in collaboration with the attending pediatrician is necessary in case an epileptic seizure occurs.
Dravet 综合征(DS)是一种罕见且严重的肌阵挛性癫痫,发病通常发生在婴儿期。癫痫发作可由多种原因引发,包括发热、洗澡和光刺激。DS 对抗癫痫药物治疗反应差。此外,癫痫持续状态(SE)可导致严重的脑病和与癫痫相关的死亡。DS 患者全身麻醉的报告非常少。在此,我们报告了我们对 1 例 DS 患儿进行麻醉管理的经验。
一名 5 岁男孩(身高 112cm,体重 19kg)通过 SCN1A 基因检测诊断为 DS,检测结果显示一种新的错义突变。他的病史包括耐药性癫痫、发育迟缓伴肌张力低下。他的癫痫发作常由体温升高(BT)、洗澡和光刺激诱发,每日发作。尽管他之前在我院儿科牙科部门接受过约束下的牙科治疗,但由于 DS,他无法接受足够的牙科治疗。
由于不配合和 DS 相关的限制,患儿需要在全身麻醉下进行强化牙科治疗。考虑到 BT 升高的风险,避免使用致痫药物,并按计划完成全身麻醉,过程顺利。尽管在手术过程中 BT 波动,但最终在麻醉结束时控制在与麻醉诱导时大致相同的水平。然而,术后第 1 天观察到小发作和单次全身强直-阵挛发作,同时伴有发热。由于详细的术前计划和与主治儿科医生的密切合作,患儿在术后第 3 天无重大问题出院。
在为 DS 患儿进行麻醉时,需要注意管理 BT,避免使用致痫药物。根据患者评估和与主治儿科医生的快速术后反应进行谨慎的麻醉术前计划,以应对癫痫发作的发生。