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Published on: September 5, 2011
Pregnancy in a Previously Conjoined Thoracopagus Twin with a Crisscross Heart
Bassam H Rimawi1, Iris Krishna1, Anurag Sahu2
1Division of Maternal-Fetal Medicine, Department of Gynecology and Obstetrics, Emory University School of Medicine, 8th Floor, 550 Peachtree Street, Atlanta, GA 30308, USA.
Insights
A rare maternal cardiac defect, crisscross heart (CCH), was successfully managed, leading to a healthy vaginal delivery. This case highlights the importance of a multidisciplinary team for managing complex congenital heart conditions during pregnancy.
Area of Science:
- Cardiology
- Maternal-Fetal Medicine
- Congenital Abnormalities
Background:
- Crisscross heart (CCH) is a rare congenital cardiac abnormality (<0.1% of CHDs) involving abnormal ventricular inflow.
- Maternal CCH cases are previously unreported in medical literature.
Purpose of the Study:
- To report the first case of a successful pregnancy in a patient with maternal crisscross heart.
- To emphasize the role of a multidisciplinary approach in managing complex cardiac conditions during pregnancy.
Main Methods:
- A primigravida patient with CCH, separated from a conjoined twin at birth, was managed by a specialized team.
- Pregnancy care involved congenital cardiology, maternal-fetal medicine, anesthesiology, and obstetrics.
- The patient underwent a successful 39-week vaginal delivery.
Main Results:
- The pregnancy and delivery were managed without maternal or neonatal complications.
- A successful term pregnancy outcome was achieved despite the complex cardiac condition.
Conclusions:
- A multidisciplinary approach is crucial for managing patients with crisscross heart during pregnancy.
- Successful term pregnancy and delivery are achievable in women with CCH.
Abstract:
Background. Crisscross heart (CCH) is a complex, rare, congenital, rotational, cardiac abnormality that accounts for <0.1% of congenital heart defects (CHD). CCH is characterized by the crossing of the inflow streams of the two ventricles due to an abnormal twisting of the heart. A case of maternal CCH has not been previously reported. Case. We report a case of a primigravida with a CCH, who was separated at birth from her thoracopagus conjoined twin. Pregnancy was managed by congenital cardiology, maternal-fetal medicine, anesthesiology, and obstetrics. She underwent a 39-week vaginal delivery without maternal or neonatal complication. Conclusion. A successful term pregnancy outcome was achieved in a patient with CCH using a multidisciplinary approach to address her cardiac condition.
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