首页> 外文期刊>Drug Design, Development and Therapy >Different doses of tenecteplase vs alteplase in thrombolysis therapy of acute ischemic stroke: evidence from randomized controlled trials
【24h】

Different doses of tenecteplase vs alteplase in thrombolysis therapy of acute ischemic stroke: evidence from randomized controlled trials

机译:急性缺血性脑卒中溶栓治疗中不同剂量的替奈普酶和阿替普酶的剂量:随机对照试验的证据

获取原文
           

摘要

Background: Recent studies showed inconsistent results of tenecteplase vs alteplase for acute ischemic stroke (AIS) with safety and efficacy. Methods: A meta-analysis was performed to explore the value of tenecteplase and alteplase in AIS treatment. Medline, Embase, and Cochrane Library from January 2001 to April 2018 were searched for randomized controlled trials (RCTs) with tenecteplase vs alteplase for AIS. Results: The primary outcomes were early neurological improvement at 24?h and functional outcome at 3?months. We pooled 1,390 patients from four RCTs. Tenecteplase showed a significant early neurological improvement ( P =0.035) compared with alteplase. In addition, tenecteplase showed a neutral effect on excellent outcome ( P =0.309), good functional outcome ( P =0.275), and recanalization ( P =0.3). No significant differences in safety outcomes were demonstrated. In subgroup analysis, 0.25?mg/kg dose of tenecteplase showed a significantly increased early neurological improvement ( P 12) subgroup, tenecteplase showed a dramatic early neurological improvement ( P =0.002) and low risks of any intracranial hemorrhage (ICH) ( P =0.027). Conclusion: Tenecteplase provided better early neurological improvement than alteplase. The 0.25?mg/kg dose of tenecteplase subgroup specially showed better early neurological improvement and lower any ICH tendency than that of alteplase. In addition, in serious stroke at baseline subgroup, tenecteplase showed a lower risk of any ICH.
机译:背景:最近的研究表明,替奈普酶与阿替普酶治疗急性缺血性中风(AIS)的结果不一致,且具有安全性和有效性。方法:进行荟萃分析,探讨替奈普酶和阿替普酶在AIS治疗中的价值。搜索2001年1月至2018年4月在Medline,Embase和Cochrane库中进行的替奈普酶和阿替普酶用于AIS的随机对照试验(RCT)。结果:主要结果是24小时时的早期神经功能改善和3小时时的功能结果。我们从四个RCT中汇集了1,390名患者。与阿替普酶相比,替奈普酶显示出明显的早期神经学改善(P = 0.035)。此外,替奈普酶对中毒效果(P = 0.309),良好的功能性结果(P = 0.275)和再通(P = 0.3)有中性作用。没有显示出安全性结果有显着差异。在亚组分析中,0.25?mg / kg剂量的替奈普酶显示出明显的早期神经功能改善(P 12)亚组,替奈普酶显示出明显的早期神经功能改善(P = 0.002),颅内出血(ICH)的风险较低(P = 0.027)。结论:替奈普酶比阿替普酶能提供更好的早期神经功能改善。奈替普酶亚组的0.25?mg / kg剂量特别显示出比阿替普酶更好的早期神经功能改善和更低的ICH趋势。此外,在基线亚组的严重中风中,替奈普酶显示出发生任何ICH的风险较低。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号