Okumura Taro, Usui Naotaka, Kondo Akihiko, Ogawa Hiroshi, Hashiguchi Mitsuru, Kuromi Yosuke, Yamaguchi Tokito, Otani Hideyuki, Imai Katsumi, Ishizaki Tomotaka, Tanei Takafumi, Maesawa Satoshi, Saito Ryuta
National Epilepsy Center, NHO Shizuoka Institute of Epilepsy and Neurological Disorders, Shizuoka, Japan.
Department of Neurosurgery, Nagoya University School of Medicine, Nagoya, Japan.
Epilepsia. 2025 Apr;66(4):1084-1096. doi: 10.1111/epi.18249. Epub 2024 Dec 27.
At our institute, most pediatric patients undergo epilepsy surgery following a thorough presurgical evaluation without intracranial electroencephalography (EEG). We conducted an initial validation of our noninvasive presurgical strategy by assessing the seizure and developmental outcomes of 135 children.
All 135 pediatric patients were <15 years old, had undergone curative surgery, and were followed for at least 2 years postoperatively. Presurgical evaluations and postoperative seizure and developmental outcomes were investigated. Thorough noninvasive evaluation included 3-T magnetic resonance imaging (MRI) and fluorodeoxyglucose positron emission tomography (FDG-PET) in all patients. Intracranial EEG was mainly indicated for patients whose MRIs were negative or subtle. We defined Engel class I as favorable and Engel classes II-IV as unfavorable seizure outcomes. Intelligence quotient (IQ) and developmental quotient (DQ) before and 2 years after surgery were used to assess developmental/neuropsychological outcomes.
MRI was positive in 130 of 135 patients (96.3%), including 39 of 40 with focal cortical dysplasia (FCD) type II and 30 of 33 with FCD type I. FDG-PET revealed concordant localizing findings in 119 of 132 patients (90.2%). Ictal single photon emission computed tomography provided concordant localizing information in 85 of 91 patients (93.4%). Intracranial EEG was performed in only 10 of 135 patients (7.4%). Ninety-seven of 135 patients (71.9%) were seizure-free 2 years after surgery. The final seizure-free rate was 99 of 135 (73.3%). Temporal lobe surgery predicted a favorable seizure outcome by multivariate analysis, whereas FCD type I and preoperative IQ/DQ < 70 predicted an unfavorable outcome. The mean IQ change was +1.3 points, and the mean DQ change was +1.0 points. Mean DQ significantly improved following extratemporal surgery (multivariate regression, p < .05), and mean DQ significantly decreased in patients with epileptic spasms (multivariate regression, p < .01).
Thorough noninvasive presurgical evaluation enables detection of subtle MRI lesions and curative epilepsy surgery without intracranial EEG in most patients, including those with FCD type II and type I, and leads to favorable seizure and developmental/neuropsychological outcomes.
在我们研究所,大多数儿科患者在经过全面的术前评估(不包括颅内脑电图[EEG])后接受癫痫手术。我们通过评估135名儿童的癫痫发作和发育结局,对我们的非侵入性术前策略进行了初步验证。
所有135名儿科患者年龄均小于15岁,均接受了根治性手术,并在术后至少随访2年。对术前评估以及术后癫痫发作和发育结局进行了调查。全面的非侵入性评估包括对所有患者进行3-T磁共振成像(MRI)和氟脱氧葡萄糖正电子发射断层扫描(FDG-PET)。颅内EEG主要用于MRI结果为阴性或不明显的患者。我们将恩格尔I级定义为良好的癫痫发作结局,将恩格尔II-IV级定义为不良的癫痫发作结局。使用手术前和手术后2年的智商(IQ)和发育商(DQ)来评估发育/神经心理结局。
135例患者中有130例(96.3%)MRI结果呈阳性,其中40例II型局灶性皮质发育不良(FCD)患者中有39例,33例I型FCD患者中有30例。132例患者中有119例(90.2%)FDG-PET显示出一致的定位结果。91例患者中有85例(93.4%)发作期单光子发射计算机断层扫描提供了一致的定位信息。135例患者中仅10例(7.4%)进行了颅内EEG检查。135例患者中有97例(71.9%)在术后2年无癫痫发作。最终无癫痫发作率为135例中的99例(73.3%)。多因素分析显示颞叶手术预示着良好的癫痫发作结局,而I型FCD和术前IQ/DQ<70预示着不良结局。IQ平均变化为+1.3分,DQ平均变化为+1.0分。颞叶外手术后DQ平均显著改善(多因素回归,p<0.05),癫痫痉挛患者的DQ平均显著下降(多因素回归,p<0.01)。
全面的非侵入性术前评估能够在大多数患者中检测到细微的MRI病变,并在不进行颅内EEG的情况下进行根治性癫痫手术,包括II型和I型FCD患者,并带来良好的癫痫发作以及发育/神经心理结局。