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低剂量阿替普酶治疗南亚人群急性缺血性脑卒中:成本、疗效和安全性的系统评价。

Low-dose alteplase for the management of acute ischemic stroke in South Asians: A systematic review on cost, efficacy and safety.

机构信息

Rani Primary Health Care Centre, Biratnagar, Nepal.

Tribhuvan University Institute of Medicine, Maharajgunj, Kathmandu, Nepal.

出版信息

J Clin Neurosci. 2022 Sep;103:92-99. doi: 10.1016/j.jocn.2022.07.002. Epub 2022 Jul 16.

Abstract

INTRODUCTION

South Asia is responsible for more than 40% of the stroke burden and stroke mortality in the developing world. South Asia, which is home to one-fourth of the world's population, is the most densely populated and one of the poorest regions. The majority of patients in this region are unable to afford intravenous thrombolysis (IVT) for acute ischemic stroke (AIS). If low-dose alteplase proves effective and safe in South Asians, it may be a more cost-effective treatment option.

METHODS

The study was conducted according to the PRISMA (Preferred Reporting Items for Systematic Reviews and meta-Analyses) guideline. Researchers searched PubMed, EMBASE, and Google Scholar for English literature from 2005 to 2021. END, ENI, good functional outcome, SICH, and all-cause mortality were used to assess efficacy and safety.

RESULTS

In the low-dose alteplase treated patients, different studies reported 32 to 57% ENI 24 h after IVT, and 7% to 9.7% END. At 3 months follow-up, good functional outcome was achieved by 48%-76.92% of low-dose alteplase treated patients. SICH rates ranged from 0% to 16.6% across studies. Asymptomatic ICH occurred in 5-14% of patients. The mortality rate in all included studies varied from none to 25%.

CONCLUSION

Our systematic review demonstrates that the use of low-dose alteplase for AIS in the South Asians offer comparable efficacy and reduced risk of SICH at a significantly lower cost than standard alteplase dose. Future well-randomized clinical trials are necessary to validate the findings of our study.

摘要

简介

南亚承担了发展中国家 40%以上的中风负担和中风死亡率。南亚拥有世界四分之一的人口,是人口最密集、最贫穷的地区之一。该地区的大多数患者无法负担急性缺血性中风(AIS)的静脉内溶栓(IVT)治疗。如果低剂量阿替普酶在南亚人群中被证明有效且安全,那么它可能是一种更具成本效益的治疗选择。

方法

该研究按照 PRISMA(系统评价和荟萃分析的首选报告项目)指南进行。研究人员在 2005 年至 2021 年间从 PubMed、EMBASE 和 Google Scholar 搜索了英文文献。使用 END、ENI、良好的功能结局、SICH 和全因死亡率来评估疗效和安全性。

结果

在低剂量阿替普酶治疗的患者中,不同的研究报告 IVT 后 24 小时的 ENI 为 32%至 57%,END 为 7%至 9.7%。在 3 个月的随访中,低剂量阿替普酶治疗的患者中有 48%至 76.92%实现了良好的功能结局。SICH 发生率在不同的研究中从 0%到 16.6%不等。无症状性 ICH 发生在 5%至 14%的患者中。所有纳入研究的死亡率从无到 25%不等。

结论

我们的系统评价表明,低剂量阿替普酶用于南亚 AIS 患者,在显著降低成本的同时,提供了与标准阿替普酶剂量相当的疗效和降低 SICH 风险。未来需要进行良好的随机临床试验来验证我们研究的结果。

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