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SWIFT 研究:急性缺血性脑卒中患者应用 Solitaire 血流恢复装置与 Merci 取栓装置的随机、平行分组、非劣效试验

Solitaire flow restoration device versus the Merci Retriever in patients with acute ischaemic stroke (SWIFT): a randomised, parallel-group, non-inferiority trial.

机构信息

Department of Neurology and Stroke Center, University of California, Los Angeles, CA 90095, USA.

出版信息

Lancet. 2012 Oct 6;380(9849):1241-9. doi: 10.1016/S0140-6736(12)61384-1. Epub 2012 Aug 26.

Abstract

BACKGROUND

The Solitaire Flow Restoration Device is a novel, self-expanding stent retriever designed to yield rapid flow restoration in acute cerebral ischaemia. We compared the efficacy and safety of Solitaire with the standard, predicate mechanical thrombectomy device, the Merci Retrieval System.

METHODS

In this randomised, parallel-group, non-inferiority trial, we enrolled patients from 18 sites (17 in the USA and one in France). Patients were eligible for inclusion if they had acute ischaemic stroke with moderate to severe neurological deficits and were treatable by thrombectomy within 8 h of stroke symptom onset. We used a computer-generated randomisation sequence to randomly allocate patients to receive thrombectomy treatment with either Solitaire or Merci (1:1; block sizes of four and stratified by centre and stroke severity). The primary endpoint was Thrombolysis In Myocardial Ischemia (TIMI) scale 2 or 3 flow in all treatable vessels without symptomatic intracranial haemorrhage, after up to three passes of the assigned device, as assessed by an independent core laboratory, which was masked to study assignment. Primary analysis was done by intention to treat. A prespecified efficacy stopping rule triggered an early halt to the trial. The study is registered with ClinicalTrials.gov, number NCT 01054560.

RESULTS

Between February, 2010, and February, 2011, we randomly allocated 58 patients to the Solitaire group and 55 patients to the Merci group. The primary efficacy outcome was achieved more often in the Solitaire group than it was in the Merci group (61%vs 24%; difference 37% [95% CI 19-53], odds ratio [OR] 4·87 [95% CI 2·14-11·10]; p(non-inferiority)<0·0001, p(superiority)=0·0001). More patients had good 3-month neurological outcome with Solitaire than with Merci (58%vs 33%; difference 25% [6-43], OR 2·78 [1·25-6·22]; p(non-inferiority)=0·0001, p(superiority)=0·02). 90-day mortality was lower in the Solitaire group than it was in the Merci group (17 vs 38; difference -21% [-39 to -3], OR 0·34 [0·14-0·81]; p(non-inferiority)=0·0001, p(superiority)=0·02).

INTERPRETATION

The Solitaire Flow Restoration Device achieved substantially better angiographic, safety, and clinical outcomes than did the Merci Retrieval System. The Solitaire device might be a future treatment of choice for endovascular recanalisation in acute ischaemic stroke.

FUNDING

Covidien/ev3.

摘要

背景

Solitaire 血流恢复装置是一种新型、自膨式支架取栓器,旨在快速恢复急性脑缺血患者的血流。我们比较了 Solitaire 与标准、预测性机械血栓切除术装置——Merci 取栓系统的疗效和安全性。

方法

在这项随机、平行组、非劣效性试验中,我们从 18 个地点(美国 17 个,法国 1 个)招募了患者。如果患者有中度至重度神经功能缺损的急性缺血性脑卒中,且在脑卒中发病后 8 小时内可进行血栓切除术治疗,那么患者就有资格入组。我们使用计算机生成的随机序列,将患者随机分配接受 Solitaire 或 Merci(1:1;块大小为 4 个,按中心和卒中严重程度分层)治疗。主要终点是在至多三次使用指定装置后,由独立的核心实验室评估的所有可治疗血管中无症状性颅内出血的血栓溶解心肌梗死(TIMI)分级 2 或 3 级血流,核心实验室对研究分组情况设盲。主要分析采用意向治疗。预先规定的疗效终止规则触发了试验的提前终止。本研究在 ClinicalTrials.gov 注册,编号为 NCT 01054560。

结果

在 2010 年 2 月至 2011 年 2 月期间,我们将 58 名患者随机分配到 Solitaire 组,55 名患者分配到 Merci 组。主要疗效结局在 Solitaire 组更常见(61% vs 24%;差值 37%[95%CI 19-53],比值比[OR] 4.87[95%CI 2.14-11.10];p(非劣效性)<0.0001,p(优效性)=0.0001)。与 Merci 相比,Solitaire 治疗组有更多患者获得良好的 3 个月神经功能结局(58% vs 33%;差值 25%[6-43],OR 2.78[1.25-6.22];p(非劣效性)=0.0001,p(优效性)=0.02)。Solitaire 组 90 天死亡率低于 Merci 组(17% vs 38%;差值 -21%[-39 至-3],OR 0.34[0.14-0.81];p(非劣效性)=0.0001,p(优效性)=0.02)。

解释

Solitaire 血流恢复装置在血管造影、安全性和临床结局方面的表现明显优于 Merci 取栓系统。Solitaire 装置可能成为急性缺血性脑卒中血管内再通治疗的未来选择。

资金来源

Covidien/ev3。

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