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人尿激肽原酶治疗急性缺血性脑卒中血管内治疗患者的有效性和安全性。

The effectiveness and safety of human urinary kallidinogenase in acute ischemic stroke patients undergoing endovascular therapy.

机构信息

Department of Neurology, Weihai Municipal Hospital, Cheeloo College of Medicine, Shandong University, Shandong Province, China.

Clinical College, Weifang Medical University, Weifang, China.

出版信息

J Cereb Blood Flow Metab. 2024 Sep;44(9):1565-1576. doi: 10.1177/0271678X241238033. Epub 2024 Mar 9.

Abstract

The effectiveness and safety of human urinary kallidinogenase (HUK) in acute ischemic stroke (AIS) patients undergoing endovascular therapy (EVT) due to large vessel occlusion (LVO) was unclear. A pooled analysis was performed using individual data from the DEVT and RESCUE BT trials. Patients were divided into two groups based on HUK treatment. The primary outcome was the 90-day modified Rankin Scale (mRS) score. Safety outcomes included 90-day mortality and symptomatic intracranial hemorrhage (sICH) within 48 hours. A total of 1174 patients were included in the study. Of these, 150 (12.8%) patients received HUK. The adjusted common odds ratio (OR) of the mRS score was 1.458 (95% confidence interval [CI] = 1.072-1.983; 0.016) favoring HUK. The incidence of sICH (2.0% 8.6%; adjusted OR: 0.198; 95% CI: 0.061-0.638; 0.007) and mortality (11.3% 18.5%; adjusted OR: 0.496; 95% CI: 0.286-0.862; 0.013) was lower in HUK group than non-HUK group. This association was consistent with propensity score-matching and the inverse probability of treatment weighting analysis. In conclusion, HUK was safe and associated with a preferable prognosis in AIS patients due to LVO in the anterior circulation.

摘要

人尿激肽原酶(HUK)在接受血管内治疗(EVT)的大动脉闭塞(LVO)急性缺血性卒中(AIS)患者中的有效性和安全性尚不清楚。使用 DEVT 和 RESCUE BT 试验的个体数据进行了汇总分析。根据 HUK 治疗将患者分为两组。主要结局是 90 天改良 Rankin 量表(mRS)评分。安全性结局包括 90 天死亡率和 48 小时内症状性颅内出血(sICH)。共纳入 1174 例患者。其中,150 例(12.8%)患者接受了 HUK。mRS 评分的调整后常见比值比(OR)为 1.458(95%置信区间 [CI] = 1.072-1.983;0.016),有利于 HUK。sICH(2.0% 8.6%;调整 OR:0.198;95% CI:0.061-0.638;0.007)和死亡率(11.3% 18.5%;调整 OR:0.496;95% CI:0.286-0.862;0.013)在 HUK 组低于非 HUK 组。这种关联与倾向评分匹配和治疗权重反概率分析一致。总之,HUK 是安全的,与前循环 LVO 的 AIS 患者预后较好相关。

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