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社区卫生工作者对7至59日龄幼儿快速呼吸性肺炎的管理:一项多中心整群随机对照试验方案

Management of fast breathing pneumonia in young infants aged 7 to 59 days by community level health workers: protocol for a multi-centre cluster randomized controlled trial.

作者信息

Mothabbir Golam, Rana Shohel, Baqui Abdullah H, Ahmed Salahuddin, Ahmed Asm Nawshad, Taneja Sunita, Mundra Sudarshan, Bhandari Nita, Dalpath Suresh, Tigabu Zemene, Andargie Gashaw, Teklu Alemayehu, Tazebew Ashenafi, Alemu Kassahun, Awoke Tadese, Gebeyehu Abebaw, Jenda Gomezgani, Nsona Humphreys, Mathanga Don, Nisar Yasir Bin, Bahl Rajiv, Sadruddin Salim, Muhe Lulu, Moschovis Peter, Aboubaker Samira, Qazi Shamim

机构信息

Save the Children US, Bangladesh Office.

Johns Hopkins University, USA.

出版信息

Int J Clin Trials. 2020 Apr-Jun;7(2):83-93. doi: 10.18203/2349-3259.ijct20201715.

Abstract

BACKGROUND

WHO does not recommend community-level health workers (CLHWs) using integrated community case management (iCCM) to treat 7-59 days old infants with fast breathing with oral amoxicillin, whereas World Health Organization (WHO) integrated management of childhood illness (IMCI) recommends it. We want to collect evidence to help harmonization of both protocols.

METHODS

A cluster, randomized, open-label trial will be conducted in Africa and Asia (Ethiopia, Malawi, Bangladesh and India) using a common protocol with the same study design, inclusion criteria, intervention, comparison, and outcomes to contribute to the overall sample size. This trial will also identify hypoxaemia in young infants with fast breathing. CLHWs will assess infants for fast breathing, which will be confirmed by a study supervisor. Enrolled infants in the intervention clusters will be treated with oral amoxicillin, whereas in the control clusters they will be managed as per existing iCCM protocol. An independent outcome assessor will assess all enrolled infants on days 6 and 14 of enrolment for the study outcomes in both intervention and control clusters. Primary outcome will be clinical treatment failure by day 6. This trial will obtain approval from the WHO and site institutional ethics committees.

CONCLUSIONS

If the research shows that CLHWs can effectively and safely treat fast breathing pneumonia in 7-59 days old young infants, it will increase access to pneumonia treatment substantially for infants living in communities with poor access to health facilities. Additionally, this evidence will contribute towards the review of the current iCCM protocol and its harmonization with IMCI protocol.

TRIAL REGISTRATION

The trial is registered at AZNCTR International Trial Registry as ACTRN12617000857303.

摘要

背景

世界卫生组织(WHO)不建议社区卫生工作者(CLHWs)采用综合社区病例管理(iCCM)使用口服阿莫西林治疗7至59日龄呼吸急促的婴儿,而世界卫生组织(WHO)的儿童疾病综合管理(IMCI)则推荐这样做。我们希望收集证据以帮助协调这两种方案。

方法

将在非洲和亚洲(埃塞俄比亚、马拉维、孟加拉国和印度)进行一项整群、随机、开放标签试验,采用相同的研究设计、纳入标准、干预措施、对照和结局的通用方案,以形成总体样本量。该试验还将识别呼吸急促的幼儿中的低氧血症。社区卫生工作者将评估婴儿是否呼吸急促,这将由研究监督员确认。干预组中登记的婴儿将接受口服阿莫西林治疗,而对照组中的婴儿将按照现有的iCCM方案进行管理。一名独立的结局评估者将在入组的第6天和第14天对干预组和对照组中所有登记的婴儿进行研究结局评估。主要结局将是第6天的临床治疗失败。该试验将获得WHO和各研究点机构伦理委员会的批准。

结论

如果研究表明社区卫生工作者能够有效且安全地治疗7至59日龄幼儿的呼吸急促性肺炎,将大大增加生活在难以获得卫生设施社区的婴儿获得肺炎治疗的机会。此外,这一证据将有助于对当前的iCCM方案进行审查,并使其与IMCI方案协调一致。

试验注册

该试验已在AZNCTR国际试验注册中心注册,注册号为ACTRN12617000857303。

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