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The Global Enteric Multicenter Study (GEMS): Impetus, Rationale, and Genesis

Diarrheal disease remains one of the top 2 causes of young child mortality in the developing world. Whereas improvements in water/sanitation infrastructure and hygiene can diminish transmission of enteric pathogens, vaccines can also hasten the decline of diarrheal disease morbidity and mortality. F...

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Detalles Bibliográficos
Autores principales: Levine, Myron M., Kotloff, Karen L., Nataro, James P., Muhsen, Khitam
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3502311/
https://www.ncbi.nlm.nih.gov/pubmed/23169934
http://dx.doi.org/10.1093/cid/cis761
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author Levine, Myron M.
Kotloff, Karen L.
Nataro, James P.
Muhsen, Khitam
author_facet Levine, Myron M.
Kotloff, Karen L.
Nataro, James P.
Muhsen, Khitam
author_sort Levine, Myron M.
collection PubMed
description Diarrheal disease remains one of the top 2 causes of young child mortality in the developing world. Whereas improvements in water/sanitation infrastructure and hygiene can diminish transmission of enteric pathogens, vaccines can also hasten the decline of diarrheal disease morbidity and mortality. From 1980 through approximately 2004, various case/control and small cohort studies were undertaken to address the etiology of pediatric diarrhea in developing countries. Many studies had methodological limitations and came to divergent conclusions, making it difficult to prioritize the relative importance of different pathogens. Consequently, in the first years of the millennium there was no consensus on what diarrheal disease vaccines should be developed or implemented; however, there was consensus on the need for a well-designed study to obtain information on the etiology and burden of more severe forms of diarrheal disease to guide global investment and implementation decisions. Accordingly, the Global Enteric Multicenter Study (GEMS) was designed to overcome drawbacks of earlier studies and determine the etiology and population-based burden of pediatric diarrheal disease. GEMS, which includes one of the largest case/control studies of an infectious disease syndrome ever undertaken (target approximately 12 600 analyzable cases and 12 600 controls), was rolled out in 4 sites in sub-Saharan Africa (Gambia, Kenya, Mali, Mozambique) and 3 in South Asia (Bangladesh, India, Pakistan), with each site linked to a population under demographic surveillance (total approximately 467 000 child years of observation among children <5 years of age). GEMS data will guide investment and help prioritize strategies to mitigate the morbidity and mortality of pediatric diarrheal disease.
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spelling pubmed-35023112012-12-15 The Global Enteric Multicenter Study (GEMS): Impetus, Rationale, and Genesis Levine, Myron M. Kotloff, Karen L. Nataro, James P. Muhsen, Khitam Clin Infect Dis Supplement Articles Diarrheal disease remains one of the top 2 causes of young child mortality in the developing world. Whereas improvements in water/sanitation infrastructure and hygiene can diminish transmission of enteric pathogens, vaccines can also hasten the decline of diarrheal disease morbidity and mortality. From 1980 through approximately 2004, various case/control and small cohort studies were undertaken to address the etiology of pediatric diarrhea in developing countries. Many studies had methodological limitations and came to divergent conclusions, making it difficult to prioritize the relative importance of different pathogens. Consequently, in the first years of the millennium there was no consensus on what diarrheal disease vaccines should be developed or implemented; however, there was consensus on the need for a well-designed study to obtain information on the etiology and burden of more severe forms of diarrheal disease to guide global investment and implementation decisions. Accordingly, the Global Enteric Multicenter Study (GEMS) was designed to overcome drawbacks of earlier studies and determine the etiology and population-based burden of pediatric diarrheal disease. GEMS, which includes one of the largest case/control studies of an infectious disease syndrome ever undertaken (target approximately 12 600 analyzable cases and 12 600 controls), was rolled out in 4 sites in sub-Saharan Africa (Gambia, Kenya, Mali, Mozambique) and 3 in South Asia (Bangladesh, India, Pakistan), with each site linked to a population under demographic surveillance (total approximately 467 000 child years of observation among children <5 years of age). GEMS data will guide investment and help prioritize strategies to mitigate the morbidity and mortality of pediatric diarrheal disease. Oxford University Press 2012-12-15 /pmc/articles/PMC3502311/ /pubmed/23169934 http://dx.doi.org/10.1093/cid/cis761 Text en © The Author 2012. Published by Oxford University Press on behalf of the Infectious Diseases Society of America. http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Supplement Articles
Levine, Myron M.
Kotloff, Karen L.
Nataro, James P.
Muhsen, Khitam
The Global Enteric Multicenter Study (GEMS): Impetus, Rationale, and Genesis
title The Global Enteric Multicenter Study (GEMS): Impetus, Rationale, and Genesis
title_full The Global Enteric Multicenter Study (GEMS): Impetus, Rationale, and Genesis
title_fullStr The Global Enteric Multicenter Study (GEMS): Impetus, Rationale, and Genesis
title_full_unstemmed The Global Enteric Multicenter Study (GEMS): Impetus, Rationale, and Genesis
title_short The Global Enteric Multicenter Study (GEMS): Impetus, Rationale, and Genesis
title_sort global enteric multicenter study (gems): impetus, rationale, and genesis
topic Supplement Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3502311/
https://www.ncbi.nlm.nih.gov/pubmed/23169934
http://dx.doi.org/10.1093/cid/cis761
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