Gonzalez-Martinez Jorge, Mullin Jeffrey, Bulacio Juan, Gupta Ajay, Enatsu Rei, Najm Imad, Bingaman William, Wyllie Elaine, Lachhwani Deepak
*Department of Neurosurgery and ‡Epilepsy Center, Neurological Institute, Cleveland Clinic, Cleveland, Ohio.
Neurosurgery. 2014 Sep;75(3):258-68; discussion 267-8. doi: 10.1227/NEU.0000000000000453.
BACKGROUND: Although stereoelectroencephalography (SEEG) has been shown to be a valuable tool for preoperative decision making in focal epilepsy, there are few reports addressing the utility and safety of SEEG methodology applied to children and adolescents. OBJECTIVE: To present the results of our early experience using SEEG in pediatric patients with difficult-to-localize epilepsy who were not considered candidates for subdural grid evaluation. METHODS: Thirty children and adolescents with the diagnosis of medically refractory focal epilepsy (not considered ideal candidates for subdural grids and strip placement) underwent SEEG implantation. Demographics, electrophysiological localization of the hypothetical epileptogenic zone, complications, and seizure outcome after resections were analyzed. RESULTS: Eighteen patients (60%) underwent resections after SEEG implantations. In patients who did not undergo resections (12 patients), reasons included failure to localize the epileptogenic zone (4 patients); multifocal epileptogenic zone (4 patients); epileptogenic zone located in eloquent cortex, preventing resection (3 patients); and improvement in seizures after the implantation (1 patient). In patients who subsequently underwent resections, 10 patients (55.5%) were seizure free (Engel class I) and 5 patients (27.7%) experienced seizure improvement (Engel class II or III) at the end of the follow-up period (mean, 25.9 months; range, 12 to 47 months). The complication rate in SEEG implantations was 3%. CONCLUSION: The SEEG methodology is safe and should be considered in children/adolescents with difficult-to-localize epilepsy. When applied to highly complex and difficult-to-localize pediatric patients, SEEG may provide an additional opportunity for seizure freedom in association with a low morbidity rate.
背景:尽管立体定向脑电图(SEEG)已被证明是局灶性癫痫术前决策的一种有价值的工具,但很少有报告涉及将SEEG方法应用于儿童和青少年的效用和安全性。 目的:介绍我们早期使用SEEG治疗难以定位癫痫的儿科患者的经验结果,这些患者不被认为是硬膜下网格评估的候选者。 方法:30名诊断为药物难治性局灶性癫痫(不被认为是硬膜下网格和条状电极放置的理想候选者)的儿童和青少年接受了SEEG植入。分析了人口统计学、假设致痫区的电生理定位、并发症以及切除术后的癫痫发作结果。 结果:18名患者(60%)在SEEG植入后接受了切除术。未接受切除术的患者(12名),原因包括未能定位致痫区(4名患者);多灶性致痫区(4名患者);致痫区位于功能区皮质,无法进行切除(3名患者);以及植入后癫痫发作改善(1名患者)。在随后接受切除术的患者中,10名患者(55.5%)在随访期结束时(平均25.9个月;范围12至47个月)无癫痫发作(Engel I级),5名患者(27.7%)癫痫发作改善(Engel II级或III级)。SEEG植入的并发症发生率为3%。 结论:SEEG方法是安全的,对于难以定位癫痫的儿童/青少年应予以考虑。当应用于高度复杂且难以定位的儿科患者时,SEEG可能提供额外的无癫痫发作机会,且发病率较低。
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