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采用环介导等温扩增技术(LAMP)主动检测和治疗妊娠疟疾(LAMPREG):一项实用随机诊断结局试验研究方案。

Active case detection and treatment of malaria in pregnancy using LAMP technology (LAMPREG): a pragmatic randomised diagnostic outcomes trial-study protocol.

机构信息

Armauer Hansen Research Institute, Addis Ababa, Ethiopia.

Pathology and Laboratory Medicine, University of Calgary Cumming School of Medicine, Calgary, Alberta, Canada.

出版信息

BMJ Open. 2022 Jul 18;12(7):e058397. doi: 10.1136/bmjopen-2021-058397.

Abstract

INTRODUCTION

Malaria is one of the major public health problems in sub-Saharan Africa. It contributes significantly to maternal and fetal morbidity and mortality in affected countries. This study aims to evaluate the impact of enhanced case detection using molecular testing called loop-mediated isothermal amplification (LAMP) on birth outcomes in a prospective study design.

METHODS AND ANALYSIS

A pragmatic randomised diagnostic outcomes trial will be conducted in several health institutes in different Ethiopian regions. Women (n=2583) in their first and second trimesters of pregnancy will be included in the study and individually randomised to the standard of care or enhanced case detection arms, and followed until delivery. Enrolment will encompass the malaria peak transmission seasons. In the standard of care arm, a venous blood sample will be collected for malaria diagnosis only in symptomatic patients. In contrast, in the intervention arm, mothers will be tested by a commercially available Conformité Européene (CE)-approved LAMP malaria test, microscopy and rapid diagnostic test for malaria regardless of their symptoms at each antenatal care visit. The primary outcome of the study is to measure birth weight.

ETHICS AND DISSEMINATION

The study was approved by the following ethical research boards: Armauer Hansen Research Institute/ALERT Ethics Review Committee (FORM AF-10-015.1, Protocol number PO/05/20), the Ethiopia Ministry of Science and Higher Education National Research Ethics Review Committee (approval SRA/11.7/7115/20), the Ethiopia Food and Drug Administration (approval 02/25/33/I), UCalgary Conjoint Health Research Ethics Board (REB21-0234). The study results will be shared with the institutions and stakeholders such as the Ethiopia Ministry of Health, the Foundation for Innovative Diagnostics, WHO's Multilateral initiative on Malaria - Tropical Diseases Research (TDR-MIM), Roll Back Malaria and the Malaria in Pregnancy Consortium. The study results will also be published in peer-reviewed journals and presented at international conferences.

TRIAL REGISTRATION NUMBER

NCT03754322.

摘要

简介

疟疾是撒哈拉以南非洲地区的主要公共卫生问题之一。它在受影响的国家中对母婴发病率和死亡率有重大影响。本研究旨在评估使用称为环介导等温扩增(LAMP)的分子检测增强病例检测对前瞻性研究设计中出生结局的影响。

方法和分析

将在埃塞俄比亚不同地区的多个卫生机构进行一项实用随机诊断结局试验。将在妊娠第一和第二 trimester 的妇女(n=2583)纳入研究,并对她们进行个体随机分配到标准护理或增强病例检测组,并随访至分娩。招募将涵盖疟疾高峰传播季节。在标准护理组中,仅在有症状的患者中采集静脉血样进行疟疾诊断。相比之下,在干预组中,无论母亲在每次产前保健就诊时的症状如何,都将使用市售的符合欧洲标准(CE)的 LAMP 疟疾检测、显微镜检查和快速诊断检测进行检测。研究的主要结局是测量出生体重。

伦理和传播

该研究得到了以下伦理研究委员会的批准:Armauer Hansen 研究所/警报伦理审查委员会(FORM AF-10-015.1,方案编号 PO/05/20)、埃塞俄比亚科学技术高等教育部国家伦理审查委员会(批准 SRA/11.7/7115/20)、埃塞俄比亚食品和药品管理局(批准 02/25/33/I)、卡尔加里联合健康伦理审查委员会(REB21-0234)。研究结果将与埃塞俄比亚卫生部、创新诊断基金会、世界卫生组织疟疾-热带病研究多边倡议(TDR-MIM)、减少疟疾伙伴关系和妊娠疟疾联盟等机构和利益相关者共享。研究结果也将发表在同行评议的期刊上,并在国际会议上展示。

试验注册编号

NCT03754322。

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