新型迷走神经刺激疗法(VNS Therapy®)发生器AspireSR®的植入:植入及更换手术中的注意事项与建议——与传统系统的比较

Implantation of a new Vagus Nerve Stimulation (VNS) Therapy® generator, AspireSR®: considerations and recommendations during implantation and replacement surgery--comparison to a traditional system.

作者信息

Schneider Ulf C, Bohlmann Katrin, Vajkoczy Peter, Straub Hans-Beatus

机构信息

Department of Neurosurgery, Charité-Universitätsmedizin Berlin, Hindenburgdamm 30, 12203, Berlin, Germany,

出版信息

Acta Neurochir (Wien). 2015 Apr;157(4):721-8. doi: 10.1007/s00701-015-2362-3. Epub 2015 Feb 13.

Abstract

INTRODUCTION

The most widely used neuro-stimulation treatment for drug-resistant epilepsy is Vagus Nerve Stimulation (VNS) Therapy®. Ictal tachycardia can be an indicator of a seizure and, if monitored, can be used to trigger an additional on-demand stimulation, which may positively influence seizure severity or duration. A new VNS Therapy generator model, AspireSR®, was introduced and approved for CE Mark in February 2014. In enhancement of former models, the AspireSR has incorporated a cardiac-based seizure-detection (CBSD) algorithm that can detect ictal tachycardia and automatically trigger a defined auto-stimulation. To evaluate differences in preoperative, intraoperative and postoperative handling, we compared the AspireSR to a conventional generator model (Demipulse®).

METHOD

Between February and September 2014, seven patients with drug-resistant epilepsy and ictal tachycardia were implanted with an AspireSR. Between November 2013 and September 2014, seven patients were implanted with a Demipulse and served as control group. Operation time, skin incision length and position, and complications were recorded. Handling of the new device was critically evaluated.

RESULTS

The intraoperative handling was comparable and did not lead to a significant increase in operation time. In our 14 operations, we had no significant short-term complications. Due to its larger size, patients with the AspireSR had significantly larger skin incisions. For optimal heart rate detection, the AspireSR had to be placed significantly more medial in the décolleté area than the Demipulse. The preoperative testing is a unique addition to the implantation procedure of the AspireSR, which may provide minor difficulties, and for which we provide several recommendations and tips. The price of the device is higher than for all other models.

CONCLUSIONS

The new AspireSR generator offers a unique technical improvement over the previous Demipulse. Whether the highly interesting CBSD feature will provide an additional benefit for the patients, and will rectify the additional costs, respectively, cannot be answered in the short-term. The preoperative handling is straightforward, provided that certain recommendations are taken into consideration. The intraoperative handling is equivalent to former models-except for the placement of the generator, which might cause cosmetic issues and has to be discussed with the patient carefully. We recommend the consideration of the AspireSR in patients with documented ictal tachycardia to provide a substantial number of patients for later seizure outcome analysis.

摘要

引言

用于耐药性癫痫的最广泛使用的神经刺激治疗方法是迷走神经刺激(VNS)疗法。发作期心动过速可能是癫痫发作的一个指标,如果进行监测,可用于触发额外的按需刺激,这可能对癫痫发作的严重程度或持续时间产生积极影响。一种新的VNS疗法发生器模型AspireSR于2014年2月推出并获得CE标志认证。在改进以前的模型时,AspireSR纳入了一种基于心脏的癫痫发作检测(CBSD)算法,该算法可以检测发作期心动过速并自动触发确定的自动刺激。为了评估术前、术中和术后操作的差异,我们将AspireSR与传统发生器模型(Demipulse)进行了比较。

方法

2014年2月至9月期间,7例耐药性癫痫和发作期心动过速患者植入了AspireSR。2013年11月至2014年9月期间,7例患者植入了Demipulse并作为对照组。记录手术时间、皮肤切口长度和位置以及并发症。对新设备的操作进行了严格评估。

结果

术中操作相当,并未导致手术时间显著增加。在我们的14例手术中,没有明显的短期并发症。由于AspireSR尺寸较大,植入该设备的患者皮肤切口明显更大。为了实现最佳心率检测,AspireSR在锁骨上区的放置位置必须比Demipulse更偏向内侧。术前测试是AspireSR植入过程中的一个独特补充,可能会带来一些小困难,对此我们提供了一些建议和提示。该设备的价格高于所有其他型号。

结论

新型AspireSR发生器相对于以前的Demipulse有独特的技术改进。高度有趣的CBSD功能是否会为患者带来额外益处,并分别弥补额外成本,短期内无法给出答案。术前操作很简单,前提是考虑某些建议。术中操作与以前的模型相当——除了发生器的放置位置可能会引起美观问题,必须与患者仔细讨论。我们建议对有记录的发作期心动过速患者考虑使用AspireSR,以便为以后的癫痫发作结果分析提供大量患者。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索