...
首页> 外文期刊>BMC Infectious Diseases >Efficacy and safety of artemisinin-based combination therapies for the treatment of uncomplicated malaria in pediatrics: a systematic review and meta-analysis
【24h】

Efficacy and safety of artemisinin-based combination therapies for the treatment of uncomplicated malaria in pediatrics: a systematic review and meta-analysis

机译:基于青蒿素的组合疗法治疗儿科的外语的疗效和安全性:系统审查和荟萃分析

获取原文

摘要

Malaria is a major cause of morbidity and mortality in pediatrics in malaria endemic areas. Artemisinin-based combination therapies (ACTs) are the drugs of choice for malaria management particularly across malaria-endemic countries. This systematic review and meta-analysis was performed to assess efficacy and safety of ACTs for uncomplicated malaria in pediatric populations. A body of evidence was searched for published ACT trials until March 06, 2020. The search was focused on efficacy and safety studies of ACTs for uncomplicated malaria in pediatrics. PubMed library was searched using best adapted search terms after multiple trials. References were exported to the endnote library and then to Covidence for screening. Data was extracted using the Covidence platform. The per-protocol analysis report for the efficacy and the intention-to-treat analysis for the safety were synthesized. Met-analysis was carried using Open Meta-Analyst software. Random effects model was applied and the heterogeneity of studies was evaluated using I2 statistic. Nineteen studies were included in the final analysis. Overall, crude, PCR-corrected P. falciparum malaria treatment success rate was 96.3 and 93.9% for day 28 and 42, respectively. In the subgroup analysis, PCR-corrected adequate clinical and parasitological response (ACPR) of dihydroartemisinin-piperaquine (DP) was 99.6% (95% CI: 99.1 to 100%, I2?=?0%; 4 studies) at day 28 and 99.6% (95% CI of 99 to 100%, I2?=?0%; 3 studies) at day 42. Nine studies reported ACT related adverse drug reactions (ADR) (8.3%, 356/4304). The reported drug related adverse reactions ranged from 1.8% in DP (two studies) to 23.3% in artesunate-pyronaridine (AP). Gastrointestinal symptoms were the most common ACT related adverse effects, and all ADRs were reported to resolve spontaneously. ACTs demonstrated a high crude efficacy and tolerability against P. falciparum. The high treatment success and tolerability with low heterogeneity conferred by DP has implication for policy makers who plan the use of ACTs for uncomplicated falciparum malaria treatment in pediatrics.
机译:疟疾是疟疾流行区域儿科的发病率和死亡率的主要原因。基于青蒿素的组合疗法(行为)是疟疾管理的首选药物,特别是在疟疾流行国家。进行了这种系统审查和荟萃分析,以评估儿科人群不复杂的疟疾行为的疗效和安全性。在2020年3月6日之前搜索了发表的法案试验的证据。该搜索专注于儿科对外语不复杂的疟疾行为的疗效和安全研究。在多次试验后使用最佳调整搜索条件搜索PubMed库。参考文献出口到终端图书馆,然后进入筛选的科维依附力。使用Covidend平台提取数据。合成了对效力的每协定分析报告以及对安全性的意图分析进行了合成。使用Open Meta-Analyst软件进行待遇分析。应用随机效果模型,使用I2统计评估研究的异质性。在最终分析中包括19项研究。总体而言,PCR校正的P.Malciparum疟疾治疗成功率分别为96.3和93.9%,分别为第28和42天。在亚组分析中,PCR校正的临床和寄生虫学反应(DP)的二氢氨苄蛋白 - 滴点(DP)为99.6%(95%CI:99.1至100%,I2?= 0%; 4研究) 99.6%(99%CI为99至100%,I2?= 0%; 3研究)在第42天。9项研究报告了ACT相关的不良药物反应(ADR)(8.3%,356/4304)。报告的药物相关的不良反应在Artesunate-Pyronaridine(AP)中的DP(两项研究)中的1.8%至23.3%。胃肠道症状是最常见的行为相关的不良反应,据报道所有ADR都自发地解决。作用表展示了对P. falciparum的高粗疗效和耐受性。 DP赋予低异质性的高治疗成功和耐受性对计划在儿科学中使用行为的政策制定者的政策制定者有所意义。

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