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一项关于替罗非班30毫克/天与阿司匹林100毫克/天治疗中风患者的随机、双盲、平行组研究的原理与设计:替罗非班预防有缺血性中风或短暂性脑缺血发作病史患者的缺血性脑血管和心血管事件(PERFORM)研究

Rationale and design of a randomized, double-blind, parallel-group study of terutroban 30 mg/day versus aspirin 100 mg/day in stroke patients: the prevention of cerebrovascular and cardiovascular events of ischemic origin with terutroban in patients with a history of ischemic stroke or transient ischemic attack (PERFORM) study.

作者信息

Bousser M G, Amarenco P, Chamorro A, Fisher M, Ford I, Fox K, Hennerici M G, Mattle H P, Rothwell P M

机构信息

Hôpital Lariboisière (AP-HP), INSERM U-740, Paris, France.

出版信息

Cerebrovasc Dis. 2009;27(5):509-18. doi: 10.1159/000212671. Epub 2009 Apr 16.

Abstract

BACKGROUND

Ischemic stroke is the leading cause of mortality worldwide and a major contributor to neurological disability and dementia. Terutroban is a specific TP receptor antagonist with antithrombotic, antivasoconstrictive, and antiatherosclerotic properties, which may be of interest for the secondary prevention of ischemic stroke. This article describes the rationale and design of the Prevention of cerebrovascular and cardiovascular Events of ischemic origin with teRutroban in patients with a history oF ischemic strOke or tRansient ischeMic Attack (PERFORM) Study, which aims to demonstrate the superiority of the efficacy of terutroban versus aspirin in secondary prevention of cerebrovascular and cardiovascular events.

METHODS AND RESULTS

The PERFORM Study is a multicenter, randomized, double-blind, parallel-group study being carried out in 802 centers in 46 countries. The study population includes patients aged > or =55 years, having suffered an ischemic stroke (< or =3 months) or a transient ischemic attack (< or =8 days). Participants are randomly allocated to terutroban (30 mg/day) or aspirin (100 mg/day). The primary efficacy endpoint is a composite of ischemic stroke (fatal or nonfatal), myocardial infarction (fatal or nonfatal), or other vascular death (excluding hemorrhagic death of any origin). Safety is being evaluated by assessing hemorrhagic events. Follow-up is expected to last for 2-4 years. Assuming a relative risk reduction of 13%, the expected number of primary events is 2,340. To obtain statistical power of 90%, this requires inclusion of at least 18,000 patients in this event-driven trial. The first patient was randomized in February 2006.

CONCLUSIONS

The PERFORM Study will explore the benefits and safety of terutroban in secondary cardiovascular prevention after a cerebral ischemic event.

摘要

背景

缺血性中风是全球范围内导致死亡的主要原因,也是导致神经功能障碍和痴呆的主要因素。特鲁曲班是一种具有抗血栓形成、抗血管收缩和抗动脉粥样硬化特性的特异性TP受体拮抗剂,可能对缺血性中风的二级预防具有重要意义。本文介绍了用特鲁曲班预防缺血性中风或短暂性脑缺血发作病史患者的脑血管和心血管事件(PERFORM)研究的基本原理和设计,该研究旨在证明特鲁曲班在预防脑血管和心血管事件方面的疗效优于阿司匹林。

方法与结果

PERFORM研究是一项在46个国家的802个中心进行的多中心、随机、双盲、平行组研究。研究人群包括年龄≥55岁、患有缺血性中风(≤3个月)或短暂性脑缺血发作(≤8天)的患者。参与者被随机分配到特鲁曲班组(30毫克/天)或阿司匹林组(100毫克/天)。主要疗效终点是缺血性中风(致命或非致命)、心肌梗死(致命或非致命)或其他血管性死亡(不包括任何原因的出血性死亡)的复合终点。通过评估出血事件来评估安全性。随访预计持续2至4年。假设相对风险降低13%,主要事件的预期数量为2340例。为了获得90%的统计效力,在这项事件驱动的试验中至少需要纳入18000名患者。第一位患者于2006年2月随机分组。

结论

PERFORM研究将探讨特鲁曲班在脑缺血事件后二级心血管预防中的益处和安全性。

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