<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>194(6)</volume><submitter>Malinowski AK</submitter><pubmed_abstract>We aimed to identify risk factors for adverse outcomes in pregnancies of women with sickle cell disease (SCD) and develop risk prediction models. Models were derived from a retrospective cohort of pregnant women with SCD and constructed using generalised estimating equation logistic regression, with clustering by woman. Maternal event(s) consisted of acute anaemia; cardiac, pulmonary, hepatobiliary, musculoskeletal, skin, splenic, neurological or renal complications, multi-organ failure, venous thromboembolism, admission-requiring vaso-occlusive events (VOE), red cell transfusion, mortality or hypertensive disorder of pregnancy. Fetal events included preterm birth, small-for-gestational-age or perinatal mortality. Of 199 pregnancies, 71% and 45% resulted in adverse maternal and fetal outco</pubmed_abstract><journal>British journal of haematology</journal><pagination>1063-1073</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8518407</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Distinct maternal and fetal pregnancy outcomes in women with sickle cell disease can be predicted using routine clinical and laboratory data.</pubmed_title><pmcid>PMC8518407</pmcid><pubmed_authors>Shehata N</pubmed_authors><pubmed_authors>Kuo KHM</pubmed_authors><pubmed_authors>Palcu P</pubmed_authors><pubmed_authors>Malinowski AK</pubmed_authors><pubmed_authors>Tomlinson GA</pubmed_authors><pubmed_authors>Ward R</pubmed_authors></additional><is_claimable>false</is_claimable><name>Distinct maternal and fetal pregnancy outcomes in women with sickle cell disease can be predicted using routine clinical and laboratory data.</name><description>We aimed to identify risk factors for adverse outcomes in pregnancies of women with sickle cell disease (SCD) and develop risk prediction models. Models were derived from a retrospective cohort of pregnant women with SCD and constructed using generalised estimating equation logistic regression, with clustering by woman. Maternal event(s) consisted of acute anaemia; cardiac, pulmonary, hepatobiliary, musculoskeletal, skin, splenic, neurological or renal complications, multi-organ failure, venous thromboembolism, admission-requiring vaso-occlusive events (VOE), red cell transfusion, mortality or hypertensive disorder of pregnancy. Fetal events included preterm birth, small-for-gestational-age or perinatal mortality. Of 199 pregnancies, 71% and 45% resulted in adverse maternal and fetal outco</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Sep</publication><modification>2026-03-27T17:06:06.832Z</modification><creation>2025-05-18T12:31:17.687Z</creation></dates><accession>S-EPMC8518407</accession><cross_references><pubmed>34124774</pubmed><doi>10.1111/bjh.17607</doi></cross_references></HashMap>