Does the route of administration matter? Systematic review and meta-analysis of randomized clinical trials between vaginal versus intramuscular progesterone administration in the prevention of preterm birth
Descripción del Articulo
Objective. To determine the effectiveness of intramuscular progesterone compared to vaginal application in the prevention of asymptomatic preterm birth (PTB) in randomized clinical trials. Materials and Methods. A systematic search of electronic databases (Embase, PubMed and Scopus) was performed. R...
Autores: | , , , |
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Formato: | artículo |
Fecha de Publicación: | 2024 |
Institución: | Universidad Peruana de Ciencias Aplicadas |
Repositorio: | UPC-Institucional |
Lenguaje: | inglés |
OAI Identifier: | oai:repositorioacademico.upc.edu.pe:10757/673510 |
Enlace del recurso: | http://hdl.handle.net/10757/673510 |
Nivel de acceso: | acceso abierto |
Materia: | intramuscular Preterm birth prevention progesterone vaginal |
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dc.title.es_PE.fl_str_mv |
Does the route of administration matter? Systematic review and meta-analysis of randomized clinical trials between vaginal versus intramuscular progesterone administration in the prevention of preterm birth |
title |
Does the route of administration matter? Systematic review and meta-analysis of randomized clinical trials between vaginal versus intramuscular progesterone administration in the prevention of preterm birth |
spellingShingle |
Does the route of administration matter? Systematic review and meta-analysis of randomized clinical trials between vaginal versus intramuscular progesterone administration in the prevention of preterm birth Galdos-Bejar, Marcelo intramuscular Preterm birth prevention progesterone vaginal |
title_short |
Does the route of administration matter? Systematic review and meta-analysis of randomized clinical trials between vaginal versus intramuscular progesterone administration in the prevention of preterm birth |
title_full |
Does the route of administration matter? Systematic review and meta-analysis of randomized clinical trials between vaginal versus intramuscular progesterone administration in the prevention of preterm birth |
title_fullStr |
Does the route of administration matter? Systematic review and meta-analysis of randomized clinical trials between vaginal versus intramuscular progesterone administration in the prevention of preterm birth |
title_full_unstemmed |
Does the route of administration matter? Systematic review and meta-analysis of randomized clinical trials between vaginal versus intramuscular progesterone administration in the prevention of preterm birth |
title_sort |
Does the route of administration matter? Systematic review and meta-analysis of randomized clinical trials between vaginal versus intramuscular progesterone administration in the prevention of preterm birth |
author |
Galdos-Bejar, Marcelo |
author_facet |
Galdos-Bejar, Marcelo Mendoza-Rivera, Samantha Orco-Leon, Alipio Naranjo-Cáceres, Mónica |
author_role |
author |
author2 |
Mendoza-Rivera, Samantha Orco-Leon, Alipio Naranjo-Cáceres, Mónica |
author2_role |
author author author |
dc.contributor.author.fl_str_mv |
Galdos-Bejar, Marcelo Mendoza-Rivera, Samantha Orco-Leon, Alipio Naranjo-Cáceres, Mónica |
dc.subject.es_PE.fl_str_mv |
intramuscular Preterm birth prevention progesterone vaginal |
topic |
intramuscular Preterm birth prevention progesterone vaginal |
description |
Objective. To determine the effectiveness of intramuscular progesterone compared to vaginal application in the prevention of asymptomatic preterm birth (PTB) in randomized clinical trials. Materials and Methods. A systematic search of electronic databases (Embase, PubMed and Scopus) was performed. Randomized clinical trials comparing vaginal and Intramuscular progesterone (17-OHPC) in pregnant women at high risk of PTB. Additionally, bias and certainty assessment were performed. Results. Six clinical trials with a total of 1,408 randomized patients were included. The reported incidence of PTB < 37 weeks ranged from 10.9% to 43.9% for vaginal progesterone, and 14.0% to 38% for 17-OHPC. At the time of meta-analysis, patients receiving 17-OHPC was associated with a lower incidence of PTB < 28 weeks than vaginal use (Risk Difference 0.14; CI 0.01-0.29; I2 = 83.9%; T2 = 0.02) with no significant difference in differences in PTB < 37 and < 34 weeks. Additionally, on neonatal outcomes, the most common was admission to the neonatal ICU independent of the method of administration (6.1% and 7.7%), followed by APGAR < 7 (4.1% and 5.2%), with no significant differences in neonatal outcomes. Conclusions. Both the use of vaginal progesterone and 17-OHPC in the prevention of PTB in singleton high-risk gestations are reasonable options, with similar incidence of PTB and no additional impact on short-term neonatal complications. Thus, costs, resource availability and patient preferences should be considered when choosing a route of administration. |
publishDate |
2024 |
dc.date.accessioned.none.fl_str_mv |
2024-05-08T14:58:23Z |
dc.date.available.none.fl_str_mv |
2024-05-08T14:58:23Z |
dc.date.issued.fl_str_mv |
2024-03-01 |
dc.type.es_PE.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
dc.identifier.doi.none.fl_str_mv |
10.36129/jog.2023.139 |
dc.identifier.uri.none.fl_str_mv |
http://hdl.handle.net/10757/673510 |
dc.identifier.eissn.none.fl_str_mv |
23850868 |
dc.identifier.journal.es_PE.fl_str_mv |
Italian Journal of Gynaecology and Obstetrics |
dc.identifier.eid.none.fl_str_mv |
2-s2.0-85188521976 |
dc.identifier.scopusid.none.fl_str_mv |
SCOPUS_ID:85188521976 |
dc.identifier.isni.none.fl_str_mv |
0000 0001 2196 144X |
dc.identifier.ror.none.fl_str_mv |
047xrr705 |
identifier_str_mv |
10.36129/jog.2023.139 23850868 Italian Journal of Gynaecology and Obstetrics 2-s2.0-85188521976 SCOPUS_ID:85188521976 0000 0001 2196 144X 047xrr705 |
url |
http://hdl.handle.net/10757/673510 |
dc.language.iso.es_PE.fl_str_mv |
eng |
language |
eng |
dc.rights.es_PE.fl_str_mv |
info:eu-repo/semantics/openAccess |
dc.rights.*.fl_str_mv |
Attribution-NonCommercial-NoDerivatives 4.0 International |
dc.rights.uri.*.fl_str_mv |
http://creativecommons.org/licenses/by-nc-nd/4.0/ |
eu_rights_str_mv |
openAccess |
rights_invalid_str_mv |
Attribution-NonCommercial-NoDerivatives 4.0 International http://creativecommons.org/licenses/by-nc-nd/4.0/ |
dc.format.es_PE.fl_str_mv |
application/pdf |
dc.publisher.es_PE.fl_str_mv |
EDRA S.p.A |
dc.source.es_PE.fl_str_mv |
Universidad Peruana de Ciencias Aplicadas (UPC) Repositorio Academico - UPC |
dc.source.none.fl_str_mv |
reponame:UPC-Institucional instname:Universidad Peruana de Ciencias Aplicadas instacron:UPC |
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Universidad Peruana de Ciencias Aplicadas |
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UPC |
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UPC-Institucional |
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UPC-Institucional |
dc.source.journaltitle.none.fl_str_mv |
Italian Journal of Gynaecology and Obstetrics |
dc.source.volume.none.fl_str_mv |
36 |
dc.source.issue.none.fl_str_mv |
1 |
dc.source.beginpage.none.fl_str_mv |
27 |
dc.source.endpage.none.fl_str_mv |
37 |
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Six clinical trials with a total of 1,408 randomized patients were included. The reported incidence of PTB < 37 weeks ranged from 10.9% to 43.9% for vaginal progesterone, and 14.0% to 38% for 17-OHPC. At the time of meta-analysis, patients receiving 17-OHPC was associated with a lower incidence of PTB < 28 weeks than vaginal use (Risk Difference 0.14; CI 0.01-0.29; I2 = 83.9%; T2 = 0.02) with no significant difference in differences in PTB < 37 and < 34 weeks. Additionally, on neonatal outcomes, the most common was admission to the neonatal ICU independent of the method of administration (6.1% and 7.7%), followed by APGAR < 7 (4.1% and 5.2%), with no significant differences in neonatal outcomes. Conclusions. Both the use of vaginal progesterone and 17-OHPC in the prevention of PTB in singleton high-risk gestations are reasonable options, with similar incidence of PTB and no additional impact on short-term neonatal complications. 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Nota importante:
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La información contenida en este registro es de entera responsabilidad de la institución que gestiona el repositorio institucional donde esta contenido este documento o set de datos. El CONCYTEC no se hace responsable por los contenidos (publicaciones y/o datos) accesibles a través del Repositorio Nacional Digital de Ciencia, Tecnología e Innovación de Acceso Abierto (ALICIA).