Our experience of pediatric epilepsy surgery

Kostiantyn R. Kostiuk, Viacheslav M. Buniakin
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Abstract

Objective: to evaluate the effectiveness and safety of different operations in children with drug-resistant epilepsy. Materials and Method. 91 children with drug-resistant epilepsy were enrolled in a retrospective study. Mean age was 10.3±5.1 years. Anterior temporal lobectomy was performed in 16 (57.1%) patients, lesionectomy – in 9 (10.0%), microsurgical callosotomy in 18 (19.8%), stereotactic callosotomy in 7 (7.7%), multifocal resections in 4 (4.4%), functional hemispherotomy in 14 (15.6%). Stereotactic radiofrequency callosotomy was performed on a CRW Stereotactic frame (Radionics Inc., USA). Ultrasound navigation and neuronavigation were used in 6 (7%) and 14 (15%) cases correspondingly. Intraoperative corticography was applied in 8 (9%) cases. Postoperative long-term follow-up lasted from 1 to 17 years (mean - 8.2±2.1 years). Results. An epileptogenic zone within single hemisphere was indentified in 66 (72.2%) cases, while bilateral epileptiform activity was observed in 25 (27.5%) children. The most common etiologies of epilepsy included hypoxic-ischemic encephalopathy, intracerebral hemorrhage, meningoencephalitis, Rasmussen syndrome, cortical dysplasia, tumors.After surgery 51 (56%) patients became seizures free (Engel 1), 14 (15.4%) patients had rare auras or focal seizures (Engel 2). In 25 (27.5%) cases, seizure frequency reduction was less than 75% or did not change significantly. The most favorable outcomes were associated with resection procedures, resulting in complete seizure control in 46 (69.7%) out of 66 children, with significant improvement observed in 9 (13.6%) cases. After callosotomy drop-attacks stopped in 14 (78%) out of 18 who had them before surgery. Operative complications were encountered in 6 (6.6%) cases, postoperative mortality occurred in 1 (1.1%) case. Conclusions. The key to the effectiveness of surgical treatment of childhood epilepsy is early surgical intervention, which leads to the control of epileptic seizures, correction of psychological and cognitive emotional disorders and improvement of quality of life. The combination of resection procedures and disconnections contributes to the reduction of epileptogenic neurons and suppression of epileptic discharges.
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我们对小儿癫痫手术的经验
目的:评价不同手术方式治疗儿童耐药癫痫的有效性和安全性。材料与方法:91例耐药癫痫患儿纳入回顾性研究。平均年龄10.3±5.1岁。前颞叶切除术16例(57.1%),病变切除9例(10.0%),显微胼胝体切开术18例(19.8%),立体定向胼胝体切开术7例(7.7%),多灶切除4例(4.4%),功能性半球切开术14例(15.6%)。在CRW立体定向支架(Radionics Inc., USA)上进行立体定向射频胼胝体切开术。超声导航6例(7%),神经导航14例(15%)。术中应用皮质造影8例(9%)。术后长期随访1 ~ 17年(平均- 8.2±2.1年)。结果。66例(72.2%)患儿在单半球内发现癫痫区,25例(27.5%)患儿双侧出现癫痫样活动。癫痫最常见的病因包括缺氧缺血性脑病、脑出血、脑膜脑炎、拉斯穆森综合征、皮质发育不良、肿瘤。术后51例(56%)患者无癫痫发作(Engel 1), 14例(15.4%)患者出现罕见的先兆或局灶性癫痫发作(Engel 2)。25例(27.5%)患者癫痫发作频率降低小于75%或无明显变化。最有利的结果与切除手术有关,66例儿童中有46例(69.7%)癫痫发作完全控制,9例(13.6%)有显著改善。在胼胝体切开术后,18例患者中有14例(78%)在手术前停止了跌落。手术并发症6例(6.6%),术后死亡1例(1.1%)。结论。儿童癫痫手术治疗效果的关键是早期手术干预,从而控制癫痫发作,纠正心理和认知情绪障碍,提高生活质量。切除手术和断开连接的结合有助于减少致痫神经元和抑制癫痫放电。
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