Geisel School of Medicine at Dartmouth, Hanover, New Hampshire, U.S.A.
NeuroPace, Inc., Mountain View, California, U.S.A.
Epilepsia. 2017 Jun;58(6):1005-1014. doi: 10.1111/epi.13739. Epub 2017 Apr 7.
Evaluate the seizure-reduction response and safety of brain-responsive stimulation in adults with medically intractable partial-onset seizures of neocortical origin.
Patients with partial seizures of neocortical origin were identified from prospective clinical trials of a brain-responsive neurostimulator (RNS System, NeuroPace). The seizure reduction over years 2-6 postimplantation was calculated by assessing the seizure frequency compared to a preimplantation baseline. Safety was assessed based on reported adverse events. Additional analyses considered safety and seizure reduction according to lobe and functional area (e.g., eloquent cortex) of seizure onset.
There were 126 patients with seizures of neocortical onset. The average follow-up was 6.1 implant years. The median percent seizure reduction was 70% in patients with frontal and parietal seizure onsets, 58% in those with temporal neocortical onsets, and 51% in those with multilobar onsets (last observation carried forward [LOCF] analysis). Twenty-six percent of patients experienced at least one seizure-free period of 6 months or longer and 14% experienced at least one seizure-free period of 1 year or longer. Patients with lesions on magnetic resonance imaging (MRI; 77% reduction, LOCF) and those with normal MRI findings (45% reduction, LOCF) benefitted, although the treatment response was more robust in patients with an MRI lesion (p = 0.02, generalized estimating equation [GEE]). There were no differences in the seizure reduction in patients with and without prior epilepsy surgery or vagus nerve stimulation. Stimulation parameters used for treatment did not cause acute or chronic neurologic deficits, even in eloquent cortical areas. The rates of infection (0.017 per patient implant year) and perioperative hemorrhage (0.8%) were not greater than with other neurostimulation devices.
Brain-responsive stimulation represents a safe and effective treatment option for patients with medically intractable epilepsy, including adults with seizures of neocortical onset, and those with onsets from eloquent cortex.
评估大脑反应性刺激对药物难治性皮质起源部分性发作成人患者的发作减少反应和安全性。
从大脑反应性神经刺激器(RNS 系统,NeuroPace)的前瞻性临床试验中确定皮质起源部分性发作的患者。通过评估植入后 2-6 年的发作频率与植入前基线相比,计算发作减少。根据报告的不良事件评估安全性。其他分析根据发作起始的脑叶和功能区(如语言皮质)考虑安全性和发作减少。
共有 126 例皮质起源的癫痫发作患者。平均随访时间为 6.1 年。在有额极和顶极发作起始的患者中,中位数的发作减少率为 70%,在有颞极皮质发作起始的患者中为 58%,在有多脑叶起始的患者中为 51%(末次观察推进[LOCF]分析)。26%的患者至少有一次 6 个月或更长时间的无发作期,14%的患者至少有一次 1 年或更长时间的无发作期。磁共振成像(MRI)上有病变的患者(77%的减少,LOCF)和 MRI 结果正常的患者(45%的减少,LOCF)均受益,尽管 MRI 病变患者的治疗反应更显著(p=0.02,广义估计方程[GEE])。在有和没有既往癫痫手术或迷走神经刺激的患者中,发作减少没有差异。用于治疗的刺激参数不会导致急性或慢性神经功能缺损,即使在语言皮质区也是如此。感染率(0.017 例患者植入年)和围手术期出血率(0.8%)与其他神经刺激装置相比没有更高。
大脑反应性刺激为药物难治性癫痫患者提供了一种安全有效的治疗选择,包括皮质起源的癫痫发作患者和语言皮质起源的癫痫发作患者。