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MR CLEAN 登记研究中急性缺血性卒中血管内取栓治疗时的动脉内溶栓。

Intra-arterial thrombolytics during endovascular thrombectomy for acute ischaemic stroke in the MR CLEAN Registry.

机构信息

Department of Radiology, Medical Imaging Centre, University Medical Centre Groningen, University of Groningen, Groningen, the Netherlands

Department of Radiology, Medical Imaging Centre, University Medical Centre Groningen, University of Groningen, Groningen, the Netherlands.

出版信息

Stroke Vasc Neurol. 2023 Feb;8(1):17-25. doi: 10.1136/svn-2022-001677. Epub 2022 Aug 4.

Abstract

INTRODUCTION

The efficacy and safety of local intra-arterial (IA) thrombolytics during endovascular thrombectomy (EVT) for large-vessel occlusions is uncertain. We analysed how often IA thrombolytics were administered in the Multicenter Randomized Clinical Trial of Endovascular Treatment for Acute Ischemic Stroke in the Netherlands (MR CLEAN) Registry, whether it was associated with improved functional outcome and assessed technical and safety outcomes compared with EVT without IA thrombolytics.

METHODS

In this observational study, we included patients undergoing EVT for an acute ischaemic stroke in the anterior circulation from the MR CLEAN Registry (March 2014-November 2017). The primary endpoint was favourable functional outcome, defined as an modified Rankin Scale score ≤2 at 90 days. Secondary endpoints were reperfusion status, early neurological recovery and symptomatic intracranial haemorrhage (sICH). Subgroup analyses for IA thrombolytics as primary versus adjuvant revascularisation attempt were performed.

RESULTS

Of the 2263 included patients, 95 (4.2%) received IA thrombolytics during EVT. The IA thrombolytics administered were urokinase (median dose, 250 000 IU (IQR, 1 93 750-2 50 000)) or alteplase (median dose, 20 mg (IQR, 12-20)). No association was found between IA thrombolytics and favourable functional outcome (adjusted OR (aOR), 1.16; 95% CI 0.71 to 1.90). Successful reperfusion was less often observed in those patients treated with IA thrombolytics (aOR, 0.57; 95% CI 0.36 to 0.90). The odds of sICH (aOR, 0.82; 95% CI 0.32 to 2.10) and early neurological recovery were comparable between patients treated with and without IA thrombolytics. For primary and adjuvant revascularisation attempts, IA thrombolytics were more often administered for proximal than for distal occlusions. Functional outcomes were comparable for patients receiving IA thrombolytics as a primary versus adjuvant revascularisation attempt.

CONCLUSION

Local IA thrombolytics were rarely used in the MR CLEAN Registry. In the relatively small study sample, no statistical difference was observed between groups in the rate of favourable functional outcome or sICH. Patients whom required and underwent IA thrombolytics were patients less likely to achieve successful reperfusion, probably due to selection bias.

摘要

介绍

血管内血栓切除术(EVT)期间局部动脉内(IA)溶栓的疗效和安全性尚不确定。我们分析了荷兰多中心急性缺血性卒中血管内治疗随机临床试验(MR CLEAN)登记处中IA 溶栓的应用频率,以及与未接受 IA 溶栓的 EVT 相比,IA 溶栓是否与改善功能结局相关,并评估了技术和安全性结局。

方法

在这项观察性研究中,我们纳入了来自 MR CLEAN 登记处的接受急性前循环缺血性卒中 EVT 的患者(2014 年 3 月至 2017 年 11 月)。主要终点是功能结局良好,定义为 90 天时改良 Rankin 量表评分≤2。次要终点为再灌注状态、早期神经恢复和症状性颅内出血(sICH)。对 IA 溶栓作为主要或辅助血管再通尝试进行了亚组分析。

结果

在 2263 例纳入患者中,95 例(4.2%)在 EVT 期间接受了 IA 溶栓。使用的 IA 溶栓药物为尿激酶(中位数剂量 250000IU(IQR 193750-250000))或阿替普酶(中位数剂量 20mg(IQR 12-20))。IA 溶栓与功能结局良好无关联(调整后比值比[aOR],1.16;95%置信区间[CI]0.71 至 1.90)。接受 IA 溶栓的患者成功再灌注的比例较低(aOR,0.57;95%CI 0.36 至 0.90)。接受 IA 溶栓与未接受 IA 溶栓的患者的 sICH (aOR,0.82;95%CI 0.32 至 2.10)和早期神经恢复的几率相当。对于主要和辅助血管再通尝试,IA 溶栓更多地用于近端而非远端闭塞。接受 IA 溶栓作为主要或辅助血管再通尝试的患者,其功能结局相当。

结论

在 MR CLEAN 登记处,IA 溶栓的应用很少。在相对较小的研究样本中,两组在功能结局良好或 sICH 的发生率方面无统计学差异。需要并接受 IA 溶栓的患者,其成功再灌注的可能性较低,这可能是由于选择偏倚。

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