急性缺血性脑卒中患者血管再通治疗中,联合使用支架回吸管和接触式抽吸器与单独使用支架回吸管的疗效和安全性对比:系统综述和荟萃分析

Wei Li, Guo-hui Lin, Hong-hong Li, Peng-Bo Zhou, Yue-yang Chen, Hong-tao Sun, He-cheng Chen
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引用次数: 0

摘要

在大血管闭塞性卒中患者的血管再通治疗中,联合支架留置术和接触式抽吸术(S + A)的疗效是否优于单纯支架留置术(S)仍不确定。我们在 PubMed、Embase、Web of Science 和 Cochrane Library 数据库中系统检索了 2023 年 10 月 1 日之前发表的随机对照试验和观察性研究(病例对照和队列研究),比较了联合支架回流器和接触式抽吸与单独支架回流器在大血管闭塞性卒中患者中的疗效。这项荟萃分析研究观察的主要疗效终点是首次近完全或完全再通畅率(mTICI 2c-3)。次要疗效节点为:首次成功再通率(mTICI 2b-3)、术后血管近乎完全或完全再通率、术后血管成功再通率、90 天内 MRS 0-2。安全性终点为术中栓塞、无症状性颅内出血和90天内死亡率。本次荟萃分析共纳入了16项研究,共计7320名患者(S+C组:3406人,S组:3914人)。对所纳入文献的综合分析表明,联合使用支架回纳器和接触式抽吸术的术后血管近乎完全或完全再通率更高[OR = 1.53,95% CI (1.24, 1.88),P < 0.0001]和术后血管成功再通率与单纯支架回流术相比[OR = 1.83,95% CI (1.55,2.17),P < 0.00001];两组在首次近完全或完全再通率[OR = 1.00,95% CI (0.83,1.19),P = 0.96]、首次成功再通率[OR = 1.02,95% CI (0.85,1.24),P = 0.81]、术中栓塞[OR = 0.93,95% CI (0.72,1.20),P = 0.56]、无症状性颅内出血[OR = 1.14,95% CI (0.87,1.48),P = 0.33]、90 天内 MRS 0-2 [OR = 0.89,95% CI (0。在大血管闭塞性卒中患者中,联合使用支架回吸管和接触式抽吸与单独使用支架回吸管相比,术后血管再通率(mTICI 2c-3/mTICI 2b-3)更高。此外,就首通再通率(mTICI 2c-3/mTICI 2b-3)、术中栓塞、无症状颅内出血、90 天内功能预后良好率和 90 天内死亡率而言,该方法均不优于单纯支架植入术。
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Efficacy and safety of combined stent retriever and contact aspiration vs. stent retriever alone on revascularization in patients with acute ischemic stroke: a systematic review and meta-analysis
Whether the efficacy of combined stent retriever and contact aspiration (S + A) is superior to stent retriever (S) alone for revascularisation in patients with large vessel occlusive stroke remains uncertain. The aim of this meta-analysis was to assess the safety and efficacy of combined stent retriever and contact aspiration for the treatment of acute ischaemic stroke with large vessel occlusion by comparing it with stent retriever alone.We systematically searched the PubMed, Embase, Web of Science, and The Cochrane Library databases for randomised controlled trials and observational studies (case-control and cohort studies) published before 1 October 2023 comparing the efficacy of combined stent retriever and contact aspiration versus tent retriever alone in patients with large vessel occlusive stroke. The end point of the primary efficacy observed in this meta-analysis study was the rate of first pass nearly complete or complete recanalisation (mTICI 2c-3). Secondary effectiveness nodes were: rate of first pass successful recanalisation (mTICI 2b-3), rate of near-complete or complete recanalisation of the postoperative vessel, rate of successful recanalisation of the postoperative vessel, and MRS 0–2 within 90 days. Safety endpoints were interoperative embolism, symptomatic intracranial haemorrhage, and mortality within 90 days.A total of 16 studies were included in the literature for this meta-analysis, with a total of 7,320 patients (S + C group: 3,406, S group: 3,914). A comprehensive analysis of the included literature showed that combined stent retriever and contact aspiration had a higher rate of near-complete or complete recanalisation of the postoperative vessel [OR = 1.53, 95% CI (1.24, 1.88), p < 0.0001] and rate of successful recanalisation of the postoperative vessel compared to stent retriever alone [OR = 1.83, 95% CI (1.55, 2.17), p < 0.00001]; there were no statistically significant differences between the two groups in terms of the rate of first pass nearly complete or complete recanalisation [OR = 1.00, 95% CI (0.83, 1.19), p = 0.96], rate of first pass successful recanalisation [OR = 1.02, 95% CI (0.85, 1.24), p = 0.81], interoperative embolism [OR = 0.93, 95% CI (0.72, 1.20), p = 0.56], symptomatic intracranial haemorrhage [OR = 1.14, 95% CI (0.87, 1.48), p = 0.33], MRS 0–2 within 90 days [OR = 0.89, 95% CI (0.76, 1.04), p = 0.14] and mortality within 90 days [OR = 1.11, 95% CI (0.94, 1.31), p = 0.22].Combined stent retriever and contact aspiration has a higher rate of postprocedural revascularisation (mTICI 2c-3/mTICI 2b-3) compared with stent retriever alone in patients with large vessel occlusion stroke. In addition, it was not superior to stenting alone in terms of the rate of first pass recanalisation (mTICI 2c-3/mTICI 2b-3), interoperative embolisation, symptomatic intracranial haemorrhage, good functional prognosis within 90 days and mortality within 90 days.
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