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慢性疼痛的脑深部电刺激:两项多中心试验结果及系统评价

Deep brain stimulation for chronic pain: results of two multicenter trials and a structured review.

作者信息

Coffey R J

机构信息

Medtronic Drug Delivery, Bronxville, New York, USA.

出版信息

Pain Med. 2001 Sep;2(3):183-92. doi: 10.1046/j.1526-4637.2001.01029.x.

Abstract

OBJECTIVES

A U.S. Food and Drug Administration ruling required clinical trials to evaluate the safety and efficacy of deep brain stimulation devices, thereby limiting treatment to the investigational setting.

INTRODUCTION

As an investigator in two clinical trials of deep brain stimulation, I sought to determine why pain remained an unapproved indication despite regulatory approval of the same device for tremor.

METHODS

The results of two multicenter trials of deep brain stimulation for pain were analyzed, and the pertinent literature was reviewed using published guidelines for the evaluation of clinical trial reports.

RESULTS

The first-generation Model 3380 lead trial enrolled 196 patients; the current Model 3387 trial enrolled 50 patients. Prospectively defined criteria for success included at least half of patients reporting >/=50% pain relief at 1 year. Manufacture of the Model 3380 lead was discontinued, and the 3387 trial closed early because of slow enrollment, high attrition, and low efficacy. When results were analyzed according to the study plan, neither trial was successful. Consequently, deep brain stimulation has not been approved for pain control by the U.S. Food and Drug Administration.

CONCLUSIONS

Deep brain stimulation has not been shown to produce effective long-term pain relief. Future studies of motor cortex stimulation and similar therapies will require appropriate control groups and accepted methods of data collection and analysis to support claims that predictable and reliable analgesic effects are produced in humans.

摘要

目的

美国食品药品监督管理局的一项规定要求进行临床试验,以评估深部脑刺激设备的安全性和有效性,从而将治疗限制在研究环境中。

引言

作为两项深部脑刺激临床试验的研究者,我试图确定尽管同一设备已获震颤治疗的监管批准,但疼痛为何仍未被批准为适应症。

方法

分析了两项深部脑刺激治疗疼痛的多中心试验结果,并使用已发表的临床试验报告评估指南对相关文献进行了综述。

结果

第一代3380型电极试验招募了196名患者;当前的3387型试验招募了50名患者。预先确定的成功标准包括至少一半的患者在1年时报告疼痛缓解≥50%。3380型电极的生产已停止,3387型试验因入组缓慢、高损耗率和低疗效而提前结束。按照研究计划分析结果时,两项试验均未成功。因此,深部脑刺激尚未获得美国食品药品监督管理局的疼痛控制批准。

结论

深部脑刺激尚未被证明能产生有效的长期疼痛缓解。未来对运动皮层刺激及类似疗法的研究将需要适当的对照组以及可接受的数据收集和分析方法,以支持关于在人类中产生可预测和可靠镇痛效果的说法。

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