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一些影响全球肠道多中心研究(GEMS)设计和实施的流行病学、临床、微生物学和组织学假设。

Some epidemiologic, clinical, microbiologic, and organizational assumptions that influenced the design and performance of the Global Enteric Multicenter Study (GEMS).

机构信息

Center for Vaccine Development, University of Maryland School of Medicine, Baltimore, MD 21201, USA.

出版信息

Clin Infect Dis. 2012 Dec;55 Suppl 4(Suppl 4):S225-31. doi: 10.1093/cid/cis787.

DOI:10.1093/cid/cis787
PMID:23169935
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3502315/
Abstract

The overall aim of the Global Enteric Multicenter Study-1 (GEMS-1) is to identify the etiologic agents associated with moderate-to-severe diarrhea (MSD) among children <5 years of age, and thereby the attributable pathogen-specific population-based incidence of MSD, to guide investments in research and public health interventions against diarrheal disease. To accomplish this, 9 core assumptions were vetted through widespread consultation: (1) a limited number of etiologic agents may be responsible for most MSD; (2) a definition of MSD can be crafted that encompasses cases that might otherwise be fatal in the community without treatment; (3) MSD seen at sentinel centers is a proxy for fatal diarrheal disease in the community; (4) matched case/control is the appropriate epidemiologic design; (5) methods across the sites can be standardized and rigorous quality control maintained; (6) a single 60-day postenrollment visit to case and control households creates mini-cohorts, allowing comparisons; (7) broad support for GEMS-1 messages can be achieved by incorporating advice from public health spokespersons; (8) results will facilitate the setting of investment and intervention priorities; and (9) wide acceptance and dissemination of the GEMS-1 results can be achieved.

摘要

全球肠道疾病多中心研究 1 期(GEMS-1)的总体目标是确定与 5 岁以下儿童中度至重度腹泻(MSD)相关的病原体,从而明确导致 MSD 的病原体在特定人群中的发病率,为腹泻病的研究和公共卫生干预措施提供指导。为了实现这一目标,经过广泛协商,对 9 项核心假设进行了审查:(1)可能只有少数病原体是导致大多数 MSD 的原因;(2)可以制定一个 MSD 的定义,涵盖在没有治疗的情况下可能在社区中致命的病例;(3)哨点中心看到的 MSD 是社区中致命腹泻病的代表;(4)匹配的病例对照是适当的流行病学设计;(5)各站点的方法可以标准化,并保持严格的质量控制;(6)对病例和对照家庭进行单次 60 天的随访访问可创建小型队列,从而进行比较;(7)通过纳入公共卫生发言人的建议,可以获得对 GEMS-1 信息的广泛支持;(8)研究结果将有助于确定投资和干预措施的优先顺序;(9)广泛接受和传播 GEMS-1 的结果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/79f1/3502315/9834c2e39078/cis78701.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/79f1/3502315/9834c2e39078/cis78701.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/79f1/3502315/9834c2e39078/cis78701.jpg

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