| Literature DB >> 26135488 |
Zeinelabdien Elsherif1, Naveed Mahmood2, Shazia Jamil3, Hadeel Wagas3.
Abstract
A single ventricle is a rare congenital heart disease that accounts for less than 1% of all congenital heart diseases. A woman was assessed in our obstetric clinic for the first time at the gestational age of 28 weeks and found to have placental bleeding. She also had complex congenital heart disease and atrial fibrillation requiring anticoagulation. Echocardiography revealed double-inlet single ventricle with right and left atrioventricular valves entering into this chamber and levo-transposition of the great arteries. After an extensive discussion with the patient regarding the risks and benefits of anticoagulation including risk of stroke, the agreed plan was to start her on intravenous heparin with close observation and to continue pregnancy for at least 32 weeks in order to reduce the postpartum risk for the fetus. The pregnancy progressed without any further complications and the patient had elective caesarean section at 33 weeks of gestation and delivered a healthy baby boy. 2015 BMJ Publishing Group Ltd.Entities:
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Year: 2015 PMID: 26135488 PMCID: PMC4493255 DOI: 10.1136/bcr-2015-209388
Source DB: PubMed Journal: BMJ Case Rep ISSN: 1757-790X