A hybrid effectiveness-implementation study protocol to assess the effectiveness and chemoprevention efficacy of implementing seasonal malaria chemoprevention in five districts in Karamoja region, Uganda.

Gates Open Research Pub Date : 2023-12-18 eCollection Date: 2023-01-01 DOI:10.12688/gatesopenres.14287.2
Richard Kajubi, Jennifer Ainsworth, Kevin Baker, Sol Richardson, Craig Bonnington, Christian Rassi, Jane Achan, Godfrey Magumba, Denis Rubahika, Jane Nabakooza, James Tibenderana, Anthony Nuwa, Jimmy Opigo
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Abstract

Background: The World Health Organization (WHO) recommends seasonal malaria chemoprevention (SMC) with sulfadoxine-pyrimethamine and amodiaquine (SPAQ) for children aged 3 to 59 months, living in areas where malaria transmission is highly seasonal. However, due to widespread prevalence of resistance markers, SMC has not been implemented at scale in East and Southern Africa. An initial study in Uganda showed that SMC with SPAQ was feasible, acceptable, and protective against malaria in eligible children in Karamoja region. Nonetheless, exploration of alternative regimens is warranted since parasite resistance threats persist.

Objective: The study aims to test the effectiveness of SMC with Dihydroartemisinin-piperaquine (DP) or SPAQ (DP-SMC & SPAQ-SMC), chemoprevention efficacy as well as the safety and tolerability of DP compared to that of SPAQ among 3-59 months old children in Karamoja region, an area of Uganda where malaria transmission is highly seasonal.

Methods: A Type II hybrid effectiveness-implementation study design consisting of four components: 1) a cluster randomized controlled trial (cRCT) using passive surveillance to establish confirmed malaria cases in children using both SPAQ and DP; 2a) a prospective cohort study to determine the chemoprevention efficacy of SPAQ and DP (if SPAQ or DP clears sub-patent infection and provides 28 days of protection from new infection) and whether drug concentrations and/or resistance influence the ability to clear and prevent infection; 2b) a sub study examining pharmacokinetics of DP in children between 3 to <6 months; 3) a resistance markers study in children 3-59 months in the research districts plus the standard intervention districts to measure changes in resistance marker prevalence over time and finally; 4) a process evaluation.

Discussion: This study evaluates the effects of SPAQ-SMC versus DP-SMC on clinical malaria in vulnerable children in the context of high parasite SP resistance, whilst informing on the best implementation strategies.

Conclusion: This study will inform malaria policy in high-burden countries, specifically on utility of SMC outside the sahel, and contribute to progress in malaria control.

在乌干达卡拉莫贾地区的五个县实施季节性疟疾化学预防的有效性和化学预防效果评估混合有效性-实施研究方案。
背景:世界卫生组织(WHO)建议对生活在疟疾传播季节性强的地区的 3 至 59 个月大的儿童使用磺胺乙胺嘧啶和阿莫地喹(SPAQ)进行季节性疟疾化学预防(SMC)。然而,由于抗药性标记普遍存在,SMC 尚未在东部和南部非洲大规模实施。在乌干达进行的一项初步研究表明,在卡拉莫贾地区符合条件的儿童中,使用 SPAQ 的 SMC 是可行的、可接受的,而且对疟疾有保护作用。然而,由于寄生虫抗药性的威胁依然存在,因此有必要探索替代方案:本研究旨在测试卡拉莫贾地区 3-59 个月大的儿童使用双氢青蒿素-哌喹(DP)或 SPAQ(DP-SMC 和 SPAQ-SMC)进行 SMC 治疗的有效性、化学预防效果以及 DP 与 SPAQ 相比的安全性和耐受性:方法:采用由四个部分组成的第二类效果-实施混合研究设计:1)一项群集随机对照试验(cRCT),利用被动监测确定使用 SPAQ 和 DP 的儿童疟疾确诊病例;2a)一项前瞻性队列研究,以确定 SPAQ 和 DP 的化学预防效果(SPAQ 或 DP 是否能清除亚专利感染并提供 28 天的新感染保护),以及药物浓度和/或耐药性是否会影响清除和预防感染的能力;2b)一项子研究,检查 3 至讨论期儿童的 DP 药代动力学:本研究评估了 SPAQ-SMC 与 DP-SMC 在寄生虫 SP 抗药性高的情况下对易感儿童临床疟疾的影响,同时为最佳实施策略提供了信息:这项研究将为疟疾高负担国家的疟疾政策,特别是萨赫勒地区以外的 SMC 实用性提供信息,并促进疟疾控制工作的进展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Gates Open Research
Gates Open Research Immunology and Microbiology-Immunology and Microbiology (miscellaneous)
CiteScore
3.60
自引率
0.00%
发文量
90
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