Please use this identifier to cite or link to this item: http://cmuir.cmu.ac.th/jspui/handle/6653943832/59884
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dc.contributor.authorSuchaya Luewanen_US
dc.contributor.authorKasemsri Srisupunditen_US
dc.contributor.authorTheera Tongsongen_US
dc.date.accessioned2018-09-10T03:23:01Z-
dc.date.available2018-09-10T03:23:01Z-
dc.date.issued2009-01-01en_US
dc.identifier.issn00207292en_US
dc.identifier.other2-s2.0-66549125438en_US
dc.identifier.other10.1016/j.ijgo.2008.10.012en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=66549125438&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/59884-
dc.description.abstractObjective: To assess the outcomes of pregnancies affected by beta-thalassemia/hemoglobin E (β-thal/HbE) disease. Methods: A retrospective cohort study was conducted with 54 women with singleton pregnancies complicated by β-thal/HbE disease only. The controls-to-cases ratio was 2:1. Results: Although maternal outcomes were similar in both groups, gestational age at birth and birth weight were significantly lower in the study group and the cesarean delivery rate was significantly higher in that group (relative risk [RR], 2.1). The incidences of fetal growth restriction, preterm birth, and low birth weight were also significantly higher in the study group, with RRs of 2.8, 2.7, and 5.6, respectively. Conclusion: Pregnancies affected by β-thal/HbE disease were significantly associated with an increased risk of fetal growth restriction, preterm birth, and low birth weight. © 2008 Elsevier Ireland Ltd. All rights reserved.en_US
dc.subjectMedicineen_US
dc.titleOutcomes of pregnancies complicated by beta-thalassemia/hemoglobin E diseaseen_US
dc.typeJournalen_US
article.title.sourcetitleInternational Journal of Gynecology and Obstetricsen_US
article.volume104en_US
article.stream.affiliationsChiang Mai Universityen_US
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