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The PRECISE (PREgnancy Care Integrating translational Science, Everywhere) Network’s first protocol: deep phenotyping in three sub-Saharan African countries
BACKGROUND: The PRECISE (PREgnancy Care Integrating translational Science, Everywhere) Network is a new and broadly-based group of research scientists and health advocates based in the UK, Africa and North America. METHODS: This paper describes the protocol that underpins the clinical research activ...
Autores principales: | , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7191688/ https://www.ncbi.nlm.nih.gov/pubmed/32354357 http://dx.doi.org/10.1186/s12978-020-0872-9 |
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author | von Dadelszen, Peter Flint-O’Kane, Meriel Poston, Lucilla Craik, Rachel Russell, Donna Tribe, Rachel M. d’Alessandro, Umberto Roca, Anna Jah, Hawanatu Temmerman, Marleen Koech Etyang, Angela Sevene, Esperança Chin, Paulo Lawn, Joy E. Blencowe, Hannah Sandall, Jane Salisbury, Tatiana T. Barratt, Benjamin Shennan, Andrew H. Makanga, Prestige Tatenda Magee, Laura A. |
author_facet | von Dadelszen, Peter Flint-O’Kane, Meriel Poston, Lucilla Craik, Rachel Russell, Donna Tribe, Rachel M. d’Alessandro, Umberto Roca, Anna Jah, Hawanatu Temmerman, Marleen Koech Etyang, Angela Sevene, Esperança Chin, Paulo Lawn, Joy E. Blencowe, Hannah Sandall, Jane Salisbury, Tatiana T. Barratt, Benjamin Shennan, Andrew H. Makanga, Prestige Tatenda Magee, Laura A. |
author_sort | von Dadelszen, Peter |
collection | PubMed |
description | BACKGROUND: The PRECISE (PREgnancy Care Integrating translational Science, Everywhere) Network is a new and broadly-based group of research scientists and health advocates based in the UK, Africa and North America. METHODS: This paper describes the protocol that underpins the clinical research activity of the Network, so that the investigators, and broader global health community, can have access to ‘deep phenotyping’ (social determinants of health, demographic and clinical parameters, placental biology and agnostic discovery biology) of women as they advance through pregnancy to the end of the puerperium, whether those pregnancies have normal outcomes or are complicated by one/more of the placental disorders of pregnancy (pregnancy hypertension, fetal growth restriction and stillbirth). Our clinical sites are in The Gambia (Farafenni), Kenya (Kilifi County), and Mozambique (Maputo Province). In each country, 50 non-pregnant women of reproductive age will be recruited each month for 1 year, to provide a final national sample size of 600; these women will provide culturally-, ethnically-, seasonally- and spatially-relevant control data with which to compare women with normal and complicated pregnancies. Between the three countries we will recruit ≈10,000 unselected pregnant women over 2 years. An estimated 1500 women will experience one/more placental complications over the same epoch. Importantly, as we will have accurate gestational age dating using the TraCer device, we will be able to discriminate between fetal growth restriction and preterm birth. Recruitment and follow-up will be primarily facility-based and will include women booking for antenatal care, subsequent visits in the third trimester, at time-of-disease, when relevant, during/immediately after birth and 6 weeks after birth. CONCLUSIONS: To accelerate progress towards the women’s and children’s health-relevant Sustainable Development Goals, we need to understand how a variety of social, chronic disease, biomarker and pregnancy-specific determinants health interact to result in either a resilient or a compromised pregnancy for either mother or fetus/newborn, or both. This protocol has been designed to create such a depth of understanding. We are seeking funding to maintain the cohort to better understand the implications of pregnancy complications for both maternal and child health. |
format | Online Article Text |
id | pubmed-7191688 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-71916882020-05-04 The PRECISE (PREgnancy Care Integrating translational Science, Everywhere) Network’s first protocol: deep phenotyping in three sub-Saharan African countries von Dadelszen, Peter Flint-O’Kane, Meriel Poston, Lucilla Craik, Rachel Russell, Donna Tribe, Rachel M. d’Alessandro, Umberto Roca, Anna Jah, Hawanatu Temmerman, Marleen Koech Etyang, Angela Sevene, Esperança Chin, Paulo Lawn, Joy E. Blencowe, Hannah Sandall, Jane Salisbury, Tatiana T. Barratt, Benjamin Shennan, Andrew H. Makanga, Prestige Tatenda Magee, Laura A. Reprod Health Study Protocol BACKGROUND: The PRECISE (PREgnancy Care Integrating translational Science, Everywhere) Network is a new and broadly-based group of research scientists and health advocates based in the UK, Africa and North America. METHODS: This paper describes the protocol that underpins the clinical research activity of the Network, so that the investigators, and broader global health community, can have access to ‘deep phenotyping’ (social determinants of health, demographic and clinical parameters, placental biology and agnostic discovery biology) of women as they advance through pregnancy to the end of the puerperium, whether those pregnancies have normal outcomes or are complicated by one/more of the placental disorders of pregnancy (pregnancy hypertension, fetal growth restriction and stillbirth). Our clinical sites are in The Gambia (Farafenni), Kenya (Kilifi County), and Mozambique (Maputo Province). In each country, 50 non-pregnant women of reproductive age will be recruited each month for 1 year, to provide a final national sample size of 600; these women will provide culturally-, ethnically-, seasonally- and spatially-relevant control data with which to compare women with normal and complicated pregnancies. Between the three countries we will recruit ≈10,000 unselected pregnant women over 2 years. An estimated 1500 women will experience one/more placental complications over the same epoch. Importantly, as we will have accurate gestational age dating using the TraCer device, we will be able to discriminate between fetal growth restriction and preterm birth. Recruitment and follow-up will be primarily facility-based and will include women booking for antenatal care, subsequent visits in the third trimester, at time-of-disease, when relevant, during/immediately after birth and 6 weeks after birth. CONCLUSIONS: To accelerate progress towards the women’s and children’s health-relevant Sustainable Development Goals, we need to understand how a variety of social, chronic disease, biomarker and pregnancy-specific determinants health interact to result in either a resilient or a compromised pregnancy for either mother or fetus/newborn, or both. This protocol has been designed to create such a depth of understanding. We are seeking funding to maintain the cohort to better understand the implications of pregnancy complications for both maternal and child health. BioMed Central 2020-04-30 /pmc/articles/PMC7191688/ /pubmed/32354357 http://dx.doi.org/10.1186/s12978-020-0872-9 Text en © The Author(s). 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Study Protocol von Dadelszen, Peter Flint-O’Kane, Meriel Poston, Lucilla Craik, Rachel Russell, Donna Tribe, Rachel M. d’Alessandro, Umberto Roca, Anna Jah, Hawanatu Temmerman, Marleen Koech Etyang, Angela Sevene, Esperança Chin, Paulo Lawn, Joy E. Blencowe, Hannah Sandall, Jane Salisbury, Tatiana T. Barratt, Benjamin Shennan, Andrew H. Makanga, Prestige Tatenda Magee, Laura A. The PRECISE (PREgnancy Care Integrating translational Science, Everywhere) Network’s first protocol: deep phenotyping in three sub-Saharan African countries |
title | The PRECISE (PREgnancy Care Integrating translational Science, Everywhere) Network’s first protocol: deep phenotyping in three sub-Saharan African countries |
title_full | The PRECISE (PREgnancy Care Integrating translational Science, Everywhere) Network’s first protocol: deep phenotyping in three sub-Saharan African countries |
title_fullStr | The PRECISE (PREgnancy Care Integrating translational Science, Everywhere) Network’s first protocol: deep phenotyping in three sub-Saharan African countries |
title_full_unstemmed | The PRECISE (PREgnancy Care Integrating translational Science, Everywhere) Network’s first protocol: deep phenotyping in three sub-Saharan African countries |
title_short | The PRECISE (PREgnancy Care Integrating translational Science, Everywhere) Network’s first protocol: deep phenotyping in three sub-Saharan African countries |
title_sort | precise (pregnancy care integrating translational science, everywhere) network’s first protocol: deep phenotyping in three sub-saharan african countries |
topic | Study Protocol |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7191688/ https://www.ncbi.nlm.nih.gov/pubmed/32354357 http://dx.doi.org/10.1186/s12978-020-0872-9 |
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