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急性缺血性脑卒中血管内取栓治疗的收缩压管理方案:MASTERSTROKE 试验 随机临床试验

Protocol for the MAnagement of Systolic blood pressure during Thrombectomy by Endovascular Route for acute ischemic STROKE randomized clinical trial: The MASTERSTROKE trial.

机构信息

Department of Anaesthesia and Perioperative Medicine, Auckland City Hospital, Auckland, New Zealand.

Department of Physiology, University of Auckland, Auckland, New Zealand.

出版信息

Int J Stroke. 2022 Aug;17(7):810-814. doi: 10.1177/17474930211059029. Epub 2021 Nov 22.

DOI:10.1177/17474930211059029
PMID:34806930
Abstract

REGISTRATION

Australian New Zealand Clinical Trials Registry: ACTRN12619001274167p.

RATIONALE

Cerebral blood flow is blood pressure-dependent when cerebral autoregulation is impaired. Cerebral ischemia and anesthetic drugs impair cerebral autoregulation. In ischemic stroke patients treated with endovascular thrombectomy, induced hypertension is a plausible intervention to increase blood flow in the ischemic penumbra until reperfusion is achieved. This could potentially reduce final infarct size and improve functional recovery.

AIM

To test if patients with large vessel occlusion stroke treated with endovascular thrombectomy will benefit from induced hypertension.

DESIGN

Prospective, randomized, parallel group, open label, multicenter clinical trial with blinded assessment of outcomes.

PROCEDURES

Patients with anterior circulation stroke treated with endovascular thrombectomy with general anesthesia within 6 h of symptom onset, and patients with 'wake up' stroke or presenting within 6 to 24 h with potentially salvageable tissue on computed tomography perfusion scanning, are included. Participants are randomized to a systolic blood pressure target of 140 mmHg or 170 mmHg from procedure initiation until recanalization. Methods to maintain the blood pressure are at the discretion of the procedural anesthesiologist.

STUDY OUTCOMES

The primary efficacy outcome is improvement in disability measured by modified Rankin Scale score at 90 days. The primary safety outcome is all-cause mortality at 90 days.

ANALYSIS

The Mann-Whitney U test will be used to test the ordinal shift in the seven-category modified Rankin Scale score. All-cause mortality will be estimated using the Kaplan-Meier method and compared using a log-rank test.

摘要

注册

澳大利亚和新西兰临床试验注册中心:ACTRN12619001274167p。

背景

当脑自动调节受损时,脑血流与血压相关。脑缺血和麻醉药物会损害脑自动调节。在接受血管内血栓切除术治疗的缺血性脑卒中患者中,诱导性高血压是一种增加缺血半影区血流的合理干预措施,直到实现再灌注。这可能会减少最终的梗死体积并改善功能恢复。

目的

测试接受血管内血栓切除术治疗的大血管闭塞性脑卒中患者是否会从诱导性高血压中获益。

设计

前瞻性、随机、平行组、开放标签、多中心临床试验,结局评估采用盲法。

程序

在症状发作后 6 小时内接受血管内血栓切除术和全身麻醉治疗的前循环脑卒中患者,以及在“苏醒”性脑卒中或在 CT 灌注扫描上出现潜在可挽救组织的 6 至 24 小时内就诊的患者,均纳入本研究。参与者随机分为从手术开始到再通时的收缩压目标为 140mmHg 或 170mmHg。维持血压的方法由手术麻醉师决定。

研究结果

主要疗效结局是 90 天时残疾程度的改善,用改良 Rankin 量表评分来衡量。主要安全性结局是 90 天时的全因死亡率。

分析

将使用曼-惠特尼 U 检验来检验改良 Rankin 量表七分类评分的有序变化。全因死亡率将使用 Kaplan-Meier 方法进行估计,并使用对数秩检验进行比较。

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Acta Neurol Belg. 2024 Apr;124(2):523-531. doi: 10.1007/s13760-023-02399-4. Epub 2023 Oct 19.
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