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Evaluating progestogens for prevention of preterm birth international collaborative (EPPPIC) individual participant data (IPD) meta-analysis: protocol

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dc.contributor.author Stewart, Lesley A.
dc.contributor.author Simmonds, Mark
dc.contributor.author Duley, Lelia
dc.contributor.author Dietz, Kristina Charlotte
dc.contributor.author Harden, Melissa
dc.contributor.author Hodkinson, Alex
dc.contributor.author Llewellyn, Alexis
dc.contributor.author Sharif, Sahar
dc.contributor.author Walker, Ruth
dc.contributor.author Wright, Kath
dc.date.accessioned 2021-06-10T20:51:13Z
dc.date.available 2021-06-10T20:51:13Z
dc.date.issued 2017
dc.identifier.citation STEWART, Lesley A., SIMMONDS, Mark, DULEY, Lelia, et al. Evaluating progestogens for prevention of preterm birth international collaborative (EPPPIC) individual participant data (IPD) meta-analysis: protocol. In: Buletin de perinatologie. 2017, nr. 4(76), pp. 61-76. ISSN 1810-5289. en_US
dc.identifier.issn 1810-5289
dc.identifier.uri https://ibn.idsi.md/sites/default/files/j_nr_file/Buletin%20de%20Perinatologie_4_2017.pdf
dc.identifier.uri http://repository.usmf.md/handle/20.500.12710/17675
dc.description EPPPIC group en_US
dc.description.abstract Background: Preterm birth is the most common cause of death and harm to newborn babies. Babies that are born early may have difficulties at birth and experience health problems during early childhood. Despite extensive study, there is still uncertainty about the effectiveness of progestogen (medications that are similar to the natural hormone progesterone) in preventing or delaying preterm birth, and in improving birth outcomes. The Evaluating Progestogen for Prevention of Preterm birth International Collaborative (EPPPIC) project aims to reduce uncertainty about the specific conditions in which progestogen may (or may not) be effective in preventing or delaying preterm birth and improving birth outcomes. Methods: The design of the study involves international collaborative individual participant data meta-analysis comprising systematic review, re-analysis, and synthesis of trial datasets. Inclusion criteria are as follows: randomized controlled trials comparing progestogen versus placebo or nonintervention, or comparing different types of progestogen, in asymptomatic women at risk of preterm birth. Main outcomes are as follows; fetal/infant death, preterm birth or fetal death (<=37 weeks, <=34 weeks, <= 28 weeks), serious neonatal complications or fetal/infant death, neurosensory disability (measured at 18 months or later) or infant/child death, important maternal morbidity, or maternal death. In statistical methods, IPD will be synthesized across trials using meta-analysis. Both ‘two-stage’ models (where effect estimates are calculated for each trial and subsequently pooled in a meta-analysis) and ‘one-stage’ models (where all IPD from all trials are analyzed in one step, while accounting for the clustering of participants within trials) will be used. If sufficient suitable data are available, a network meta-analysis will compare all types of progesterone and routes of administration extending the one-stage models to include multiple treatment arms. Discussion: EPPPIC is an international collaborative project being conducted by the forming EPPPIC group, which includes trial investigators, an international secretariat, and the research project team. Results, which are intended to contribute to improvements in maternal and child health, are expected to be publicly available in mid 2018. en_US
dc.language.iso en en_US
dc.publisher Instituţia Medico-Sanitară Publică Institutul Mamei și Copilului en_US
dc.relation.ispartof Buletin de perinatologie en_US
dc.subject Preterm birth en_US
dc.subject Progestogen en_US
dc.subject Individual participant data en_US
dc.subject IPD en_US
dc.subject Meta-analysis en_US
dc.title Evaluating progestogens for prevention of preterm birth international collaborative (EPPPIC) individual participant data (IPD) meta-analysis: protocol en_US
dc.type Article en_US


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