Department of Neurology, Sahlgrenska University Hospital, Gothenburg, Sweden.
Epilepsy Behav. 2013 Nov;29(2):416-9. doi: 10.1016/j.yebeh.2013.08.014. Epub 2013 Sep 24.
Vagus nerve stimulation (VNS) is an accepted therapy for the treatment of drug-resistant epilepsy. A new VNS system ("FitNeS"; manufactured by BioControl Medical (B.C.M.) Ltd., Yehud, Israel) was implanted in 5 patients with refractory focal epilepsy. The system is composed of a programmable pulse generator and a cuff electrode that is able to provide unidirectional stimulation, both of which are implanted in the left chest and in the neck, respectively. FitNeS is based on the CardioFit vagus nerve stimulation system, which is intended for the treatment of heart failure and which is currently in a randomized controlled phase III clinical trial. Long-term stimulation in the 5 patients resulted in a 50% seizure reduction in 2 patients, 25% in 2 patients, and no effect in one patient, with few reports concerning side effects. There were no complaints of hoarseness at levels of stimulation below 2mA nor were there any reports of dysphagia or cough. The lack of perceived stimulation effects might finally allow for the design of a truly blinded randomized controlled study to evaluate the efficacy of VNS compared to placebo.
迷走神经刺激术(VNS)是一种被广泛接受的治疗耐药性癫痫的方法。5 名难治性局灶性癫痫患者接受了一种新的迷走神经刺激系统(“FitNeS”;由以色列耶胡德的 BioControl Medical(B.C.M.)有限公司制造)的植入。该系统由一个可编程脉冲发生器和一个袖带电极组成,能够提供单向刺激,两者分别植入左侧胸部和颈部。FitNeS 基于 CardioFit 迷走神经刺激系统,该系统旨在治疗心力衰竭,目前正在进行一项随机对照 III 期临床试验。5 名患者的长期刺激导致 2 名患者的癫痫发作减少了 50%,2 名患者减少了 25%,1 名患者没有效果,副作用报告很少。在低于 2mA 的刺激水平下,没有出现声音嘶哑的投诉,也没有出现吞咽困难或咳嗽的报告。缺乏感知到的刺激效果最终可能允许设计一项真正的盲法随机对照研究,以评估 VNS 与安慰剂相比的疗效。