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急性小缺血性卒中双联抗血小板治疗与静脉内组织型纤溶酶原激活剂治疗:安全性和疗效的系统评价和荟萃分析。

Dual antiplatelet therapy versus intravenous tissue plasminogen activator with acute minor ischemic stroke: A systematic review and meta-analysis of safety and efficacy.

机构信息

Faculty of Medicine, Al-Azhar University, Damietta, Egypt.

Faculty of Medicine, Menoufia University, Menoufia, Egypt.

出版信息

J Stroke Cerebrovasc Dis. 2024 Jul;33(7):107704. doi: 10.1016/j.jstrokecerebrovasdis.2024.107704. Epub 2024 Mar 30.

Abstract

OBJECTIVES

To compare the safety and efficacy of Dual Antiplatelet Therapy (DAPT) and Intravenous (IV) Tissue Plasminogen Activator (t-PA) in minor Acute Ischemic Stroke (AIS).

MATERIALS AND METHODS

Following Cochrane and PRISMA guidelines, we analyzed observational studies and clinical trials comparing DAPT and IV t-PA in patients with minor AIS. Databases included PubMed, Scopus, and Web of Science. Data extraction included study characteristics, patient demographics, and analyzed outcomes. RevMan 5.3 and OpenMetaAnalyst 2021 were used to analyze the data and assess heterogeneity, respectively. The risk of bias was determined using RoB 2.0 and the Newcastle-Ottawa scale.

RESULTS

This meta-analysis included five studies with 3,978 DAPT-treated patients and 2,224 IV t-PA-treated patients. We found no significant differences in achieving modified Rankin scale (mRS) scores of 0-1 (OR 1.11, 95 % CI: 0.79, 1.55, p = 0.56) and 0-2 (OR 0.90, 95 % CI: 0.61, 1.31, p = 0.57), as well as combined mRS scores (OR 1.05, 95 % CI: 0.82, 1.34, p = 0.72). Similarly, there were no significant disparities between the two treatment groups in NIHSS score change from baseline (MD 0.32, 95 % CI: -0.35, 0.98, p = 0.35) and in mortality rates (OR 0.87, 95 % CI: 0.26, 2.93, p = 0.83). Notably, in comparison to the IV t-PA group, the DAPT group exhibited a significantly lower incidence of bleeding (OR 0.31, 95 % CI: 0.14, 0.69, p = 0.004) and symptomatic intracranial hemorrhage (sICH) (OR 0.10, 95 % CI: 0.04, 0.26, p < 0.00001).

CONCLUSIONS

Our meta-analysis found no significant differences in efficacy between DAPT and IV t-PA. However, DAPT demonstrated a significantly lower risk of sICH and bleeding compared with IV t-PA.

摘要

目的

比较双联抗血小板治疗(DAPT)与静脉内(IV)组织型纤溶酶原激活剂(t-PA)在轻度急性缺血性卒中(AIS)中的安全性和疗效。

材料与方法

根据 Cochrane 和 PRISMA 指南,我们分析了比较 DAPT 和 IV t-PA 治疗轻度 AIS 患者的观察性研究和临床试验。纳入的数据库包括 PubMed、Scopus 和 Web of Science。数据提取包括研究特征、患者人口统计学和分析结果。RevMan 5.3 和 OpenMetaAnalyst 2021 分别用于分析数据和评估异质性。使用 RoB 2.0 和 Newcastle-Ottawa 量表评估偏倚风险。

结果

本荟萃分析纳入了五项研究,共纳入 3978 例 DAPT 治疗患者和 2224 例 IV t-PA 治疗患者。我们发现,在改良 Rankin 量表(mRS)评分 0-1 分(OR 1.11,95%CI:0.79,1.55,p=0.56)和 0-2 分(OR 0.90,95%CI:0.61,1.31,p=0.57)以及联合 mRS 评分(OR 1.05,95%CI:0.82,1.34,p=0.72)方面,两组之间无显著差异。同样,两组患者的 NIHSS 评分基线变化(MD 0.32,95%CI:-0.35,0.98,p=0.35)和死亡率(OR 0.87,95%CI:0.26,2.93,p=0.83)也无显著差异。值得注意的是,与 IV t-PA 组相比,DAPT 组的出血(OR 0.31,95%CI:0.14,0.69,p=0.004)和症状性颅内出血(sICH)(OR 0.10,95%CI:0.04,0.26,p<0.00001)发生率明显较低。

结论

我们的荟萃分析发现,DAPT 和 IV t-PA 在疗效方面无显著差异。然而,与 IV t-PA 相比,DAPT 显示出较低的 sICH 和出血风险。

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