在标准抗疟药物中加入青蒿琥酯可减少治疗失败

Timothy ME Davis (Commentary Author)
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引用次数: 1

摘要

问题在现有药物方案中添加青蒿琥酯对患有急性无并发症恶性疟原虫疟疾的人有什么影响?研究设计采用荟萃分析进行系统综述。主要结果16项试验符合纳入标准。试验中的标准抗疟药物各不相同(磺胺多辛-乙胺:7项随机对照试验;阿莫地喹:3项随机对照研究;氯喹:3个随机对照试验,甲氟喹:3次随机对照试验)。在标准抗疟药物中加入青蒿琥酯3天,与单独使用标准药物相比,显著降低了14天和28天的失败率(15项随机对照试验;14天失败的OR为0.20,95%CI为0.17至0.25;28天失败的OR0.23,95%CI 0.19至0.28),但与单独使用标准药物相比,失败率仍显著降低(6项随机对照试验;14天失败的OR为0.61,95%CI为0.48-0.77;28天失败的OR0.68,95%CI 0.53-0.89)。两组的副作用发生率相似。作者的结论:在标准抗疟药物方案中加入青蒿琥酯3天,无论使用何种标准抗疟药,在14天时治疗失败率都会持续降低。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Addition of artesunate to standard antimalarial drugs reduces treatment failure

Question

What is the effect of adding artesunate to existing drug regimens for people with acute uncomplicated Plasmodium falciparum malaria?

Study design

Systematic review with meta-analysis.

Main results

16 trials met inclusion criteria. Standard antimalarial drugs in the trials varied (sulfadoxine–pyrimethamine: 7 RCTs; amodiaquine: 3 RCTs; chloroquine: 3 RCTs; mefloquine: 3 RCTs). Adding artesunate for 3 days to standard antimalarial drugs significantly reduced 14 and 28 day's failure rates compared with standard drugs alone (15 RCTs; OR for failure by 14 day 0.20, 95% CI 0.17 to 0.25; OR for failure by 28 days 0.23, 95% CI 0.19 to 0.28). Addition of artesunate for 1 day was not as effective as 3 days, but still significantly reduced failure rates compared with standard drugs alone (6 RCTs; OR for failure by 14 days 0.61, 95% CI 0.48 to 0.77; OR for failure by 28 days 0.68, 95% CI 0.53 to 0.89). The incidence of side effects was similar in both groups.

Authors’ conclusions

Adding artesunate to a standard antimalarial drug regimen for 3 days leads to a consistent decrease in treatment failure at 14 days, irrespective of the standard antimalarial drug used.

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