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坦桑尼亚临床严重感染的低龄婴儿补充锌的疗效:一项随机对照试验的研究方案

Efficacy of zinc supplementation for young infants with clinical severe infection in Tanzania: study protocol for a randomised controlled trial.

作者信息

Manji Karim P, Somji Sarah, Bakari Mohamed, Fawzi Wafaie W, Kibwana Upendo, Kisenge Rodrick, Kisumuni Abuu S, Liu Enju, Mafie Neema, Maleko Fredrick A, Salim Nahya, Duggan Christopher P, Sudfeld Christopher R

机构信息

Department of Pediatrics and Child Health, Muhimbili University of Health and Allied Sciences, Dar es Salaam, Tanzania.

Center for Child, Adolescent, and Maternal Health Research, Faculty of Medicine and Health Technology, Tampere University, Tampere, Finland.

出版信息

BMJ Paediatr Open. 2025 Aug 14;9(1):e003804. doi: 10.1136/bmjpo-2025-003804.

Abstract

INTRODUCTION

Innovative interventions will be essential for countries in sub-Saharan Africa to achieve the 2030 Sustainable Development Goal for child mortality. Infections among young infants, including sepsis, meningitis and pneumonia, continue to cause a large burden of morbidity and mortality in low-income and middle-income countries. Zinc is an essential micronutrient with a well-established role in human health and immune system function, and supplementation may improve survival and treatment outcomes for infants with bacterial infections.

METHODS AND ANALYSIS

We will conduct an individually randomised, quadruple-blind trial of zinc supplementation among 3250 infants 0-59 days old with clinical severe infection (CSI) in Dar es Salaam, Tanzania. Infants with CSI will be randomised to receive either (1) zinc citrate supplementation consisting of 5 mg elemental zinc taken two times per day for 14 days or (2) a matching placebo supplementation taken two times per day for 14 days. Infants will be followed for 90 days postrandomisation. The coprimary outcomes are (1) infant death (all-cause mortality to 90 days) and (2) treatment failure (composite outcome of death during initial hospitalisation, need for additional respiratory support, use of vasoactive medicines or change of antibiotics). Secondary outcomes include important infant health and nutritional outcomes.

ETHICS AND DISSEMINATION

The trial protocol was approved by Harvard T. H. Chan School of Public Health Institutional Review Board, the Muhimbili University of Health and Allied Sciences Institutional Review Board, the National Health Research Ethics Sub-Committee and the Tanzania Medicine and Medical Device Authority. Findings will be disseminated locally, regionally and internationally at scientific conference presentations and as peer-reviewed publications.

TRIAL REGISTRATION NUMBER

NCT06102044; ClinicalTrials.gov identifier.

摘要

引言

创新干预措施对于撒哈拉以南非洲国家实现2030年儿童死亡率可持续发展目标至关重要。在低收入和中等收入国家,包括败血症、脑膜炎和肺炎在内的年幼儿童感染继续造成巨大的发病和死亡负担。锌是一种必需的微量营养素,在人类健康和免疫系统功能中具有既定作用,补充锌可能会改善细菌感染婴儿的存活率和治疗效果。

方法与分析

我们将在坦桑尼亚达累斯萨拉姆对3250名0至59日龄患有临床严重感染(CSI)的婴儿进行一项单独随机、四重盲法的锌补充试验。患有CSI的婴儿将被随机分配接受以下两种治疗之一:(1)柠檬酸锌补充剂,每天服用两次,每次5毫克元素锌,共14天;或(2)匹配的安慰剂补充剂,每天服用两次,共14天。随机分组后将对婴儿进行90天的随访。共同主要结局是:(1)婴儿死亡(至90天的全因死亡率)和(2)治疗失败(初始住院期间死亡、需要额外呼吸支持、使用血管活性药物或更换抗生素的综合结局)。次要结局包括重要的婴儿健康和营养结局。

伦理与传播

该试验方案已获得哈佛T.H. Chan公共卫生学院机构审查委员会、穆希姆比利健康与联合科学大学机构审查委员会、国家卫生研究伦理小组委员会以及坦桑尼亚药品和医疗器械管理局的批准。研究结果将在当地、区域和国际科学会议上发表,并作为同行评审出版物进行传播。

试验注册号

NCT06102044;ClinicalTrials.gov标识符。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a6a3/12352140/de5fa504c241/bmjpo-9-1-g001.jpg

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