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Inflammatory Bowel Disease and Pregnancy: Is It a Marker for Adverse Outcomes?

Objective  To assess obstetric/puerperal/neonatal outcomes in an inflammatory bowel disease (IBD) population and to analyze disease characteristics that may be associated to adverse outcomes. Methods  Retrospective descriptive analysis including 47 pregnant wom e n with IBD (28 with Crohn's dis...

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Autores principales: Costa, Rita Vicente, Simões, Carolina, Correia, Luís, Pinto, Luísa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Thieme Revinter Publicações Ltda. 2022
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9708404/
https://www.ncbi.nlm.nih.gov/pubmed/36446558
http://dx.doi.org/10.1055/s-0042-1756149
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author Costa, Rita Vicente
Simões, Carolina
Correia, Luís
Pinto, Luísa
author_facet Costa, Rita Vicente
Simões, Carolina
Correia, Luís
Pinto, Luísa
author_sort Costa, Rita Vicente
collection PubMed
description Objective  To assess obstetric/puerperal/neonatal outcomes in an inflammatory bowel disease (IBD) population and to analyze disease characteristics that may be associated to adverse outcomes. Methods  Retrospective descriptive analysis including 47 pregnant wom e n with IBD (28 with Crohn's disease – CD and 19 with ulcerative colitis – UC) who delivered between March 2012 and July 2018 in a tertiary hospital. We reviewed clinical records to extract demographic information, previous medical history, disease subtype, activity, severity, treatment, and obstetric, puerperal, and neonatal outcome measures. Results  Obstetric and neonatal complications (composite outcomes) occurred in 55.3% and 14.6% of the IBD population, respectively, and were more frequent in UC patients. Preterm birth (PTB), preeclampsia, anemia, low birth weight (LBW), and neonatal death were also more frequent in UC patients. The rate of postpartum hemorrhage (PPH) was 14.9%, and it was higher in CD patients. Women with active IBD had more obstetric/neonatal adverse outcomes (fetal growth restriction and LBW in particular) and cesarean sections. Patients with medicated IBD had less obstetric/neonatal complications (PTB and LBW in specific) and cesarean sections but more PPH. Conclusion  Women with IBD may have an increased risk of obstetric/puerperal/neonatal adverse outcomes. Ulcerative colitis patients had more obstetric and neonatal complications, whereas PPH was more frequent if CD patients. Other disease characteristics were considered, which allowed a better understanding of their possible influence. Although more research is needed, this work reinforces the importance of adequate surveillance to allow prompt recognition and treatment of complications.
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spelling pubmed-97084042022-12-01 Inflammatory Bowel Disease and Pregnancy: Is It a Marker for Adverse Outcomes? Costa, Rita Vicente Simões, Carolina Correia, Luís Pinto, Luísa Rev Bras Ginecol Obstet Objective  To assess obstetric/puerperal/neonatal outcomes in an inflammatory bowel disease (IBD) population and to analyze disease characteristics that may be associated to adverse outcomes. Methods  Retrospective descriptive analysis including 47 pregnant wom e n with IBD (28 with Crohn's disease – CD and 19 with ulcerative colitis – UC) who delivered between March 2012 and July 2018 in a tertiary hospital. We reviewed clinical records to extract demographic information, previous medical history, disease subtype, activity, severity, treatment, and obstetric, puerperal, and neonatal outcome measures. Results  Obstetric and neonatal complications (composite outcomes) occurred in 55.3% and 14.6% of the IBD population, respectively, and were more frequent in UC patients. Preterm birth (PTB), preeclampsia, anemia, low birth weight (LBW), and neonatal death were also more frequent in UC patients. The rate of postpartum hemorrhage (PPH) was 14.9%, and it was higher in CD patients. Women with active IBD had more obstetric/neonatal adverse outcomes (fetal growth restriction and LBW in particular) and cesarean sections. Patients with medicated IBD had less obstetric/neonatal complications (PTB and LBW in specific) and cesarean sections but more PPH. Conclusion  Women with IBD may have an increased risk of obstetric/puerperal/neonatal adverse outcomes. Ulcerative colitis patients had more obstetric and neonatal complications, whereas PPH was more frequent if CD patients. Other disease characteristics were considered, which allowed a better understanding of their possible influence. Although more research is needed, this work reinforces the importance of adequate surveillance to allow prompt recognition and treatment of complications. Thieme Revinter Publicações Ltda. 2022-11-29 /pmc/articles/PMC9708404/ /pubmed/36446558 http://dx.doi.org/10.1055/s-0042-1756149 Text en Federação Brasileira de Ginecologia e Obstetrícia. This is an open access article published by Thieme under the terms of the Creative Commons Attribution License, permitting unrestricted use, distribution, and reproduction so long as the original work is properly cited. ( https://creativecommons.org/licenses/by/4.0/ ) https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Costa, Rita Vicente
Simões, Carolina
Correia, Luís
Pinto, Luísa
Inflammatory Bowel Disease and Pregnancy: Is It a Marker for Adverse Outcomes?
title Inflammatory Bowel Disease and Pregnancy: Is It a Marker for Adverse Outcomes?
title_full Inflammatory Bowel Disease and Pregnancy: Is It a Marker for Adverse Outcomes?
title_fullStr Inflammatory Bowel Disease and Pregnancy: Is It a Marker for Adverse Outcomes?
title_full_unstemmed Inflammatory Bowel Disease and Pregnancy: Is It a Marker for Adverse Outcomes?
title_short Inflammatory Bowel Disease and Pregnancy: Is It a Marker for Adverse Outcomes?
title_sort inflammatory bowel disease and pregnancy: is it a marker for adverse outcomes?
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9708404/
https://www.ncbi.nlm.nih.gov/pubmed/36446558
http://dx.doi.org/10.1055/s-0042-1756149
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