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当前及提议的扩大年龄范围的常年疟疾化学预防措施对公共卫生的影响:一项建模研究

Public health impact of current and proposed age-expanded perennial malaria chemoprevention: a modelling study.

作者信息

Sen Swapnoleena, Braunack-Mayer Lydia, Kelly Sherrie L, Masserey Thiery, Malinga Josephine, Moehrle Joerg J, Penny Melissa A

机构信息

Swiss Tropical and Public Health Institute, Allschwil, Switzerland.

University of Basel, Basel, Switzerland.

出版信息

Sci Rep. 2025 Mar 26;15(1):10488. doi: 10.1038/s41598-025-93623-z.

Abstract

In 2022, the World Health Organization extended their guidelines for perennial malaria chemoprevention (PMC) from infants to children up to 24 months old. However, evidence for PMC's public health impact is primarily limited to children under 15 months. Further research is needed to assess the public health impact and cost-effectiveness of PMC, and the added benefit of further age-expansion. We integrated an individual-based model of malaria with pharmacological models of drug action to address these questions for PMC and a proposed age-expanded schedule (referred as PMC+, for children 03-36 months). Across malaria prevalence settings of 5-70% and different drug sensitivity assumptions, we predicted PMC and PMC+'s median efficacy (interquartile range) of 18.6% (12.2-25.0%) and 21.9% (14.3-29.5%) against clinical disease and 9.0% (2.0-16.0%) and 10.8% (3.2-18.4%) against severe malaria, respectively, in children under three years. PMC's total impact outweighed the risk of delayed malaria in children up to age five and remained cost-effective across currently recommended transmission intensities (over 10% prevalence) when delivered through the existing Expanded Program on Immunization channels. Further empirical evidence of likely added benefit, operational feasibility and sustainability of age-expanded PMC will be essential to complement our model-based findings.

摘要

2022年,世界卫生组织将其常年疟疾化学预防(PMC)指南从婴儿扩展至24个月以下的儿童。然而,PMC对公共卫生影响的证据主要限于15个月以下的儿童。需要进一步研究来评估PMC的公共卫生影响和成本效益,以及进一步扩大年龄范围带来的额外益处。我们将基于个体的疟疾模型与药物作用的药理学模型相结合,以解决PMC以及拟议的扩大年龄范围时间表(称为PMC+,适用于3至36个月的儿童)的这些问题。在疟疾流行率为5%至70%的环境以及不同的药物敏感性假设下,我们预测在三岁以下儿童中,PMC和PMC+预防临床疾病的中位效力(四分位间距)分别为18.6%(12.2%至25.0%)和21.9%(14.3%至29.5%),预防重症疟疾的中位效力分别为9.0%(2.0%至16.0%)和10.8%(3.2%至18.4%)。在五岁以下儿童中,PMC的总体影响超过了疟疾延迟发生的风险,并且通过现有的扩大免疫规划渠道实施时,在目前推荐的传播强度(流行率超过10%)范围内仍具有成本效益。扩大年龄范围的PMC可能带来的额外益处、操作可行性和可持续性的进一步实证证据对于补充我们基于模型的研究结果至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a977/11947144/9fb1569d2f42/41598_2025_93623_Fig1_HTML.jpg

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