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在马里班迪加拉,开展了一项评估双氢青蒿素-哌喹用于学龄儿童季节性疟疾化学预防的安全性和有效性的随机现场试验。

Randomized Field Trial to Assess the Safety and Efficacy of Dihydroartemisinin-Piperaquine for Seasonal Malaria Chemoprevention in School-Aged Children in Bandiagara, Mali.

机构信息

Malaria Research and Training Center, University of Sciences, Techniques, and Technologies, Bamako, Mali.

出版信息

J Infect Dis. 2024 Jan 12;229(1):189-197. doi: 10.1093/infdis/jiad387.

Abstract

BACKGROUND

Owing to the increased cases of malaria in older children, the World Health Organization has recently recommended extending seasonal malaria chemoprevention (SMC) to children >5 years of age and using other effective drugs for malaria. In this study, we report the safety and efficacy of dihydroartemisinin-piperaquine (DHA-PQ) for SMC in school-aged children in Mali.

METHOD

This randomized, controlled trial included 345 participants aged 6-15 years randomized to receive DHA-PQ, sulfadoxine-pyrimethamine plus amodiaquine (SP-AQ), or no chemoprevention (albendazole) at a 1:1:1 ratio. Four rounds of SMC were conducted from September to December 2021. The participants were assessed 7 days after each round for safety and efficacy of the interventions.

RESULTS

Abdominal pain (11.8% vs 29.2%), headache (11.2% vs 19.2%), and vomiting (5.7% vs 15.2%) were frequently reported in the DHA-PQ and SP-AQ arms. On Day 120 of follow up, the incidence of clinical malaria was 0.01 episodes/person-month in the DHA-PQ and SP-AQ arms and 0.17 episodes/person-month in the control arm (P < .0001). Gametocytes were detected in 37 participants in all arms.

CONCLUSIONS

Children in DHA-PQ arm reported less adverse events compared to the SP-AQ arm. Both drugs were effective against clinical malaria and infection.

摘要

背景

由于儿童疟疾病例增多,世界卫生组织最近建议将季节性疟疾化学预防(SMC)扩展到 5 岁以上儿童,并使用其他有效抗疟药物。在这项研究中,我们报告了二氢青蒿素-哌喹(DHA-PQ)在马里学龄儿童中进行 SMC 的安全性和疗效。

方法

这是一项随机、对照试验,纳入了 345 名年龄在 6-15 岁的参与者,按照 1:1:1 的比例随机分为 DHA-PQ 组、磺胺多辛-乙胺嘧啶加阿莫地喹(SP-AQ)组和无预防组(阿苯达唑)。从 2021 年 9 月至 12 月进行了四轮 SMC。参与者在每轮后 7 天接受安全性和干预效果评估。

结果

DHA-PQ 和 SP-AQ 组常见的不良反应有腹痛(11.8%比 29.2%)、头痛(11.2%比 19.2%)和呕吐(5.7%比 15.2%)。在随访的第 120 天,DHA-PQ 和 SP-AQ 组的临床疟疾发病率为 0.01 例/人/月,对照组为 0.17 例/人/月(P<0.0001)。所有组均有 37 名参与者检测到配子体。

结论

DHA-PQ 组报告的不良反应少于 SP-AQ 组。两种药物对临床疟疾和感染均有效。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6d8/10786242/3c9a602c7324/jiad387f1.jpg

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