<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><submitter>Ramlakhan KP</submitter><funding>Edwards Lifesciences</funding><funding>Boston Scientific Corporation</funding><funding>Fondazione Internazionale Menarini</funding><funding>Stichting Zabawas</funding><funding>Bristol-Myers Squibb</funding><funding>Amgen</funding><funding>De Hoop Foundation</funding><funding>Vifor Pharma</funding><funding>Pfizer</funding><funding>Novartis Pharma</funding><funding>Bayer</funding><funding>Gedeon Richter</funding><funding>Eli Lilly and Company</funding><funding>ResMed Foundation</funding><funding>Boehringer Ingelheim</funding><funding>Daiichi Sankyo Company</funding><funding>AstraZeneca</funding><funding>Servier</funding><funding>Sanofi</funding><funding>Abbott Vascular Int.</funding><funding>Merck Sharp and Dohme</funding><pubmed_abstract>&lt;h4>Objective&lt;/h4>Pregnancy in women with aortic coarctation (CoA) has an estimated moderately increased risk (mWHO II-III) of adverse cardiovascular, obstetric or fetal events, but prospective data to validate this risk classification are scarce. We examined pregnancy outcomes and identified associations with adverse outcomes.&lt;h4>Methods&lt;/h4>Pregnancies in women with CoA were selected from the worldwide prospective Registry of Pregnancy and Cardiac Disease (ROPAC, n=303 out of 5739), part of the European Society of Cardiology EURObservational Research Programme. The frequency of and associations with major adverse cardiac events (MACE) and hypertensive disorders (pregnancy-induced hypertension, (pre-)eclampsia or haemolysis, elevated liver enzymes and low platelets syndrome) were analysed</pubmed_abstract><journal>Heart (British Cardiac Society)</journal><pagination>heartjnl-2020-317513</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7873427</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Pregnancy outcomes in women with aortic coarctation.</pubmed_title><pmcid>PMC7873427</pmcid><pubmed_authors>Manga P</pubmed_authors><pubmed_authors>Tobler D</pubmed_authors><pubmed_authors>Johnson MR</pubmed_authors><pubmed_authors>Ramlakhan KP</pubmed_authors><pubmed_authors>Nihoyannopoulos P</pubmed_authors><pubmed_authors>Schwerzmann M</pubmed_authors><pubmed_authors>Hall R</pubmed_authors><pubmed_authors>Maggioni AP</pubmed_authors><pubmed_authors>Baris L</pubmed_authors><pubmed_authors>Greutmann M</pubmed_authors><pubmed_authors>Roos-Hesselink JW</pubmed_authors><pubmed_authors>ROPAC investigators group</pubmed_authors><pubmed_authors>Yetman AT</pubmed_authors><pubmed_authors>Boersma E</pubmed_authors></additional><is_claimable>false</is_claimable><name>Pregnancy outcomes in women with aortic coarctation.</name><description>&lt;h4>Objective&lt;/h4>Pregnancy in women with aortic coarctation (CoA) has an estimated moderately increased risk (mWHO II-III) of adverse cardiovascular, obstetric or fetal events, but prospective data to validate this risk classification are scarce. We examined pregnancy outcomes and identified associations with adverse outcomes.&lt;h4>Methods&lt;/h4>Pregnancies in women with CoA were selected from the worldwide prospective Registry of Pregnancy and Cardiac Disease (ROPAC, n=303 out of 5739), part of the European Society of Cardiology EURObservational Research Programme. The frequency of and associations with major adverse cardiac events (MACE) and hypertensive disorders (pregnancy-induced hypertension, (pre-)eclampsia or haemolysis, elevated liver enzymes and low platelets syndrome) were analysed</description><dates><release>2020-01-01T00:00:00Z</release><publication>2020 Oct</publication><modification>2026-07-16T00:40:51.042Z</modification><creation>2026-07-09T10:25:58.677Z</creation></dates><accession>S-EPMC7873427</accession><cross_references><pubmed>33122301</pubmed><doi>10.1136/heartjnl-2020-317513</doi></cross_references></HashMap>