Division of Neurology, Department of Pediatrics, Children's Mercy Kansas City, Kansas City, MO, USA.
University of Missouri Kansas City, Kansas City, MO, USA.
Epilepsia Open. 2021 Jan 15;6(1):112-119. doi: 10.1002/epi4.12453. eCollection 2021 Mar.
Patients with drug-resistant epilepsy (DRE) pose considerable management challenges for patients, their families, and providers. Both the vagus nerve stimulator (VNS) and the ketogenic diet (KD) have been shown to be safe and effective in treating DRE. Nevertheless, information is lacking regarding treatment with combination of both modalities. This study reports the efficacy and tolerability of combining VNS and KD in a pediatric cohort with intractable epilepsy.
This is a retrospective review of 33 patients (0-17 years) with DRE treated with VNS and KD at a single pediatric level IV epilepsy center. We compared seizure reduction rates for each patient at baseline and at every clinic visit for 24 months after adding the second nonpharmacological therapy. The frequency of adverse events on the combined therapy was collected to assess safety and tolerability.
There were a total of 170 visits for all patients while on the combined therapy. At 88% (95% CI: 83%-93%) of the visits, patients reported some reduction in seizure frequency. The proportion of patients reporting a greater than 50% seizure reduction over all visits was 62% (95% CI: 55%-69%). The proportion of a patient's visits with at least a greater than 50% reduction in seizure frequency had a median of 71% (IQR 33%-100%). Continued improvement was seen over time of combined treatment; for every one-unit time unit change (one month), there was a 6% increase in the odds of having a reduction in seizure frequency of >50% (OR = 1.06, 95% CI: 1.01-1.11).
This study shows that combining the VNS and KD in patients with drug-resistant epilepsy is well tolerated and reduces seizure frequency more than either one modality used alone and that the benefits in terms of seizure reduction continue to increase with the length of treatment.
耐药性癫痫(DRE)患者给患者、其家庭和医疗服务提供者带来了相当大的管理挑战。迷走神经刺激器(VNS)和生酮饮食(KD)已被证明在治疗 DRE 方面是安全有效的。然而,关于联合使用这两种方法的信息仍然缺乏。本研究报告了在一组难治性癫痫的儿科患者中联合使用 VNS 和 KD 的疗效和耐受性。
这是一项对在单一儿科四级癫痫中心接受 VNS 和 KD 治疗的 33 例 DRE 患者(0-17 岁)的回顾性研究。我们比较了每位患者在基线时和添加第二种非药物治疗后 24 个月的每次就诊时的癫痫发作减少率。收集联合治疗时的不良事件频率,以评估安全性和耐受性。
所有患者在联合治疗期间共有 170 次就诊。在 88%(95%CI:83%-93%)的就诊中,患者报告癫痫发作频率有所降低。在所有就诊中,报告癫痫发作减少 50%以上的患者比例为 62%(95%CI:55%-69%)。患者就诊中有至少 50%的癫痫发作减少的比例中位数为 71%(IQR 33%-100%)。随着联合治疗时间的延长,持续出现改善;每一个单位时间(一个月)的变化,癫痫发作频率减少 50%以上的可能性增加 6%(OR=1.06,95%CI:1.01-1.11)。
本研究表明,在耐药性癫痫患者中联合使用 VNS 和 KD 是耐受良好的,可降低癫痫发作频率,比单独使用任何一种方法都更有效,而且随着治疗时间的延长,癫痫发作减少的益处继续增加。