Whole genome sequencing of M. tuberculosis for disease control in high-burden settings: study protocol for a cluster randomized controlled trial evaluating different community-wide intervention strategies in rural Madagascar.

IF 2 4区 医学 Q3 MEDICINE, RESEARCH & EXPERIMENTAL
Trials Pub Date : 2024-10-25 DOI:10.1186/s13063-024-08537-4
Emmanuelle Sandra Adjoa Ametepe, Noela Andriamanoha, Fanantenana Randria Andrianomanana, Floriane Point, Reziky Tiandraza Mangahasimbola, Alina Dyachenko, Michael Hall, Theodora Mayouya Gamana, Astrid M Knoblauch, Yemimah Yededyah Razafindrasoa, Arianminpathy Nimalan, Marcel Behr, Madeleine Durand, Mira Johri, Zamin Iqbal, Andry Rivo Rakotoarivelo, Rindra Vatosoa Randremanana, Niaina Rakotosamimanana, Simon Grandjean Lapierre
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引用次数: 0

Abstract

Background: Retrospective and descriptive molecular epidemiology studies have shown that Mycobacterium tuberculosis whole genome sequencing can identify outbreaks and disease transmission events with higher resolution than conventional epidemiological investigations. Those studies have strengthened our understanding of genomic polymorphisms correlating with person-to-person transmission and helped resolve putative transmission clusters. To date, systematic genomic surveillance programs implemented for M. tuberculosis were only implemented in low-incidence settings. The purpose of this study is to determine whether there is an impact of routine M. tuberculosis whole genome sequencing on tuberculosis case detection in a high-incidence setting.

Methods: A cluster randomized controlled trial will be performed. Forty-eight rural village groups (or Fokontany) in the Vohibato district of Madagascar will be randomized to one of three interventions arms. Arm 1 (standard of care) involves healthcare facility-based passive case detection with smear microscopy testing. Arm 2 (best practice) consists of active case finding and Xpert MTB/RIF Ultra PCR testing followed by household contact investigations. Arm 3 (novel intervention) includes the same interventions as arm 2, with addition of sputum culture and M. tuberculosis whole genome sequencing for all newly diagnosed cases. In arm 3, molecular suggested putative outbreaks are investigated, and additional TB suspects are appropriately tested. The intervention observational period will be 2 years. The primary outcome will be the number of detected cases/100,000/year in each arm after 1 year of intervention.

Discussion: This study is designed to determine whether there is an impact of prospective whole genome sequencing-based molecular typing on tuberculosis case detection in high-incidence settings. Investigating potential outbreaks and focusing active case finding in spatiotemporal settings where disease transmission is suggested by genomic typing is hypothesized to improve case detection in rural communities.

Trial registration: ClinicalTrials.gov NCT05406453 . Retrospectively registered on June 6, 2022.

结核杆菌全基因组测序用于高负担环境下的疾病控制:评估马达加斯加农村地区不同社区干预策略的分组随机对照试验研究方案。
背景:回顾性和描述性分子流行病学研究表明,结核分枝杆菌全基因组测序能够以比传统流行病学调查更高的分辨率识别疾病爆发和传播事件。这些研究加强了我们对与人际传播相关的基因组多态性的了解,并有助于解决假定的传播集群问题。迄今为止,针对结核杆菌的系统基因组监测计划仅在低发病率地区实施。本研究的目的是确定常规结核杆菌全基因组测序对高发病率环境中结核病病例检测是否有影响:方法:将进行分组随机对照试验。马达加斯加 Vohibato 地区的 48 个农村小组(或 Fokontany)将被随机分配到三个干预组中的一个。干预组 1(标准护理)包括以医疗机构为基础,通过涂片显微镜检测进行病例被动检测。干预措施 2(最佳实践)包括主动病例发现和 Xpert MTB/RIF Ultra PCR 检测,然后进行家庭接触调查。第三组(新型干预措施)包括与第二组相同的干预措施,但对所有新诊断病例增加了痰培养和结核杆菌全基因组测序。在第 3 组中,将对分子建议的潜在疫情进行调查,并对其他肺结核疑似病例进行适当检测。干预观察期为 2 年。主要结果将是干预 1 年后各组的检出病例数/100,000/年:本研究旨在确定基于全基因组测序的前瞻性分子分型是否会对高发病率地区的结核病例检测产生影响。根据假设,在基因组分型显示疾病传播的时空环境中调查潜在的疫情并集中开展积极的病例发现工作,可提高农村社区的病例发现率:试验注册:ClinicalTrials.gov NCT05406453。追溯注册于 2022 年 6 月 6 日。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Trials
Trials 医学-医学:研究与实验
CiteScore
3.80
自引率
4.00%
发文量
966
审稿时长
6 months
期刊介绍: Trials is an open access, peer-reviewed, online journal that will encompass all aspects of the performance and findings of randomized controlled trials. Trials will experiment with, and then refine, innovative approaches to improving communication about trials. We are keen to move beyond publishing traditional trial results articles (although these will be included). We believe this represents an exciting opportunity to advance the science and reporting of trials. Prior to 2006, Trials was published as Current Controlled Trials in Cardiovascular Medicine (CCTCVM). All published CCTCVM articles are available via the Trials website and citations to CCTCVM article URLs will continue to be supported.
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