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随机临床试验比较使用 Amplatzer PFO 封堵器经皮闭合卵圆孔未闭(PFO)与药物治疗在隐源性栓塞患者中的效果(PC-Trial):原理与设计。

Randomized clinical trial comparing percutaneous closure of patent foramen ovale (PFO) using the Amplatzer PFO Occluder with medical treatment in patients with cryptogenic embolism (PC-Trial): rationale and design.

机构信息

Cardiology Department, Bern University Hospital, Bern, Switzerland.

出版信息

Trials. 2011 Feb 28;12:56. doi: 10.1186/1745-6215-12-56.

Abstract

BACKGROUND

Several studies have shown an association of cryptogenic stroke and embolism with patent foramen ovale (PFO), but the question how to prevent further events in such patients is unresolved. Options include antithrombotic treatment with warfarin or antiplatelet agents or surgical or endovascular closure of the PFO. The PC-Trial was set up to compare endovascular closure and best medical treatment for prevention of recurrent events.

METHODS

The PC-Trial is a randomized clinical trial comparing the efficacy of percutaneous closure of the PFO using the Amplatzer PFO occluder with best medical treatment in patients with cryptogenic embolism, i.e. mostly cryptogenic stroke. Warfarin for 6 months followed by antiplatelet agents is recommended as medical treatment. Randomization is stratified according to patients age (<45 versus ≥45 years), presence of atrial septal aneurysm (ASA yes or no) and number of embolic events before randomization (one versus more than one event). Primary endpoints are death, nonfatal stroke and peripheral embolism.

DISCUSSION

patients were randomized in 29 centers of Europe, Canada, and Australia. Randomization started February 2000. Enrollment of 414 patients was completed in February 2009. All patients will be followed-up longitudinally. Follow-up is maintained until the last enrolled patient is beyond 2.5 years of follow-up (expected in 2011).

摘要

背景

多项研究表明卵圆孔未闭(PFO)与隐源性卒中及栓塞之间存在关联,但如何预防此类患者的进一步发病仍未解决。治疗选择包括华法林或抗血小板药物的抗血栓治疗,或 PFO 的手术或血管内封堵。PC 试验旨在比较血管内封堵与最佳药物治疗对预防复发事件的效果。

方法

PC 试验是一项随机临床试验,比较使用 Amplatzer PFO 封堵器经皮封堵 PFO 与最佳药物治疗在隐源性栓塞(即大多数隐源性卒中)患者中的疗效。推荐华法林治疗 6 个月,继之以抗血小板药物。随机分组根据患者年龄(<45 岁与≥45 岁)、房间隔瘤(有或无)和随机分组前栓塞事件的数量(单发与多发)分层。主要终点是死亡、非致死性卒中及外周栓塞。

讨论

患者在欧洲、加拿大和澳大利亚的 29 个中心被随机分组。随机分组始于 2000 年 2 月。2009 年 2 月完成了 414 例患者的入组。所有患者将进行长期随访。随访将持续至最后入组患者的随访时间超过 2.5 年(预计在 2011 年)。

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