季节性疟疾化学预防在阿奇霉素对儿童死亡率影响中的作用:CHAT聚类随机临床试验的二次分析

IF 2.5
PLOS global public health Pub Date : 2025-09-29 eCollection Date: 2025-01-01 DOI:10.1371/journal.pgph.0004653
Elisabeth A Gebreegziabher, Mamadou Ouattara, Mamadou Bountogo, Boubacar Coulibaly, Valentin Boudo, Thierry Ouedraogo, Elodie Lebas, Huiyu Hu, Kieran S O'Brien, Michelle S Hsiang, David V Glidden, Benjamin F Arnold, Thomas M Lietman, Ali Sié, Catherine E Oldenburg
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引用次数: 0

摘要

本研究的目的是探讨阿奇霉素(AZ)的大量分布对5岁以下儿童全因死亡率的影响是否随季节疟疾化学预防(SMC)给药季节或覆盖率的变化而变化。这是对阿奇霉素社区卫生试验(CHAT)的二次分析,这是一项在布基纳法索Nouna区341个社区进行的每年两次阿奇霉素治疗的聚类随机、安慰剂对照试验。所有社区都接受SMC作为标准护理。SMC的管理和覆盖数据来自国家疟疾控制规划。SMC季节被定义为SMC期间和之后的时期(7 - 12月)与无SMC季节(1 - 6月)。SMC的覆盖率是根据所覆盖人口的比例以及低于或高于80%的阈值来评估的。我们使用泊松回归模型,将人时间风险作为补偿和稳健标准误差来分析治疗组和SMC亚组的死亡率,并在乘法和加性尺度上评估相互作用。两组的死亡率在SMC季节均较高。与安慰剂相比,SMC季节AZ群的死亡率为0.77 (95% CI: 0.60至0.98),而非SMC季节的死亡率为0.89 (95% CI: 0.68至1.15)。在集群中
本文章由计算机程序翻译,如有差异,请以英文原文为准。

The role of seasonal malaria chemoprevention in the effect of azithromycin on child mortality: A secondary analysis of the CHAT cluster randomized clinical trial.

The role of seasonal malaria chemoprevention in the effect of azithromycin on child mortality: A secondary analysis of the CHAT cluster randomized clinical trial.

The role of seasonal malaria chemoprevention in the effect of azithromycin on child mortality: A secondary analysis of the CHAT cluster randomized clinical trial.

The role of seasonal malaria chemoprevention in the effect of azithromycin on child mortality: A secondary analysis of the CHAT cluster randomized clinical trial.

The objective of this study was to examine whether the effect of mass Azithromycin (AZ) distribution on all-cause mortality among children under 5 varies with seasonal malaria chemoprevention (SMC) administration season or coverage. This was a secondary analysis of the Community Health with Azithromycin Trial (CHAT), a cluster-randomized, placebo-controlled trial of twice-yearly AZ treatment in 341 communities in the Nouna District, Burkina Faso. All communities received SMC as standard-of-care. SMC administration and coverage data were provided from National Malaria Control Program. SMC season was defined as the period during and following SMC (July-December) versus the no SMC season (January-June). SMC coverage was assessed as proportion of the population covered and by whether it was below or above a threshold of 80%. We used Poisson regression models with person-time at risk as an offset and robust standard error to analyze mortality rates by treatment group and SMC subgroups and assessed interaction on both multiplicative and additive scales. Mortality was higher in SMC seasons for both arms. Compared to placebo, the mortality rate in AZ clusters was 0.77 (95% CI: 0.60 to 0.98) during SMC season, while it was 0.89 (95% CI: 0.68 to 1.15) during the non-SMC seasons. In clusters with <80% SMC coverage, the effect of AZ was 0.73 95%CI (0.56 to 0.96) and in clusters with ≥80% SMC coverage, it was 1.0 95%CI (0.59 to 1.69). The interaction between AZ and SMC season or coverage was not statistically significant on the additive or multiplicative scales. While our findings did not reach statistical significance, they raise the question of whether prioritizing MDA AZ during high transmission periods or in regions with low SMC coverage could be beneficial. Further research is needed to determine if targeting these periods or areas could further reduce child mortality.

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