Please use this identifier to cite or link to this item: http://cmuir.cmu.ac.th/jspui/handle/6653943832/58847
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dc.contributor.authorPreeyaporn Jirakittidulen_US
dc.contributor.authorSupatra Sirichotiyakulen_US
dc.contributor.authorChidchanok Ruengornen_US
dc.contributor.authorKitirat Techatraisaken_US
dc.contributor.authorBusaba Wiriyasirivajen_US
dc.date.accessioned2018-09-05T04:33:58Z-
dc.date.available2018-09-05T04:33:58Z-
dc.date.issued2018-09-01en_US
dc.identifier.issn14320711en_US
dc.identifier.issn09320067en_US
dc.identifier.other2-s2.0-85049117968en_US
dc.identifier.other10.1007/s00404-018-4821-6en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85049117968&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/58847-
dc.description.abstract© 2018, Springer-Verlag GmbH Germany, part of Springer Nature. Objective: To investigate the association between iron supplementation during early pregnancy and the presence of de novo hypertension after 20 weeks’ gestation (either gestational hypertension or pre-eclampsia). Study design: Retrospective cohort study. Methods: This study retrospectively reviewed the medical records of non-anemic pregnant women who received first antenatal care at the Department of Obstetrics and Gynecology, Faculty of Medicine Vajira Hospital, Navamindradhiraj University, Bangkok, Thailand, during the June 2009–December 2010 study period. All included women had blood pressure and urine albumin level data that were recorded at each antenatal visit. The study population was divided into one of the two following groups: iron supplementation starting at gestational age (GA) < 16 weeks (study group) or GA ≥ 16 weeks (control group). A comparison of the proportion of de novo hypertension arising after 20 weeks’ gestation was then performed between groups. Results: Four hundred non-anemic pregnant women were included, with 200 patients allocated to each groups. The overall incidence of de novo hypertension after 20 weeks’ gestation was 10% (40/400), with significantly higher prevalence in the study group than that in the control group [13.5% (27/200) vs. 6.5% (13/200); relative risk: 2.14, 95%, CI 1.22–3.73; p = 0.008]. None of the women in this study developed anemia at time of delivery. There was no significant difference between groups for GA at delivery, birth weight, or birth asphyxia. Conclusion: In our study population, iron supplementation before 16 weeks’ GA was significantly associated with increased risk of developing de novo hypertension after 20 weeks’ gestation.en_US
dc.subjectMedicineen_US
dc.titleEffect of iron supplementation during early pregnancy on the development of gestational hypertension and pre-eclampsiaen_US
dc.typeJournalen_US
article.title.sourcetitleArchives of Gynecology and Obstetricsen_US
article.volume298en_US
article.stream.affiliationsMahidol Universityen_US
article.stream.affiliationsChiang Mai Universityen_US
article.stream.affiliationsVajira Hospitalen_US
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