Abstract

IntroductionComplete endocardial cushion defect is a congenital heart disease characterized by a variable deficiency of the atrioventricular area in the developing heart. The mortality rate for an unrepaired endocardial cushion defect in pregnancy and the postpartum period is high.Case presentationWe present a rare case of a pregnant woman with complete endocardial cushion defect. A 20-year-old Chinese woman with unrepaired complete endocardial cushion defect delivered a premature male baby at 33 weeks and six days of pregnancy in our hospital. The baby had a normal human karyotype and a birth defect of hypospadias deformity. Our patient died from heart failure 10 minutes after delivery. She had severe pulmonary hypertension and suspected trisomy 21.ConclusionOur experience further emphasizes the necessity of prenatal screening for congenital heart defects and of prompt surgical correction for endocardial cushion defects during infancy. Mortality for endocardial cushion defect during pregnancy and the postpartum period is high and women with complete endocardial cushion defect should avoid pregnancy, especially those women who cannot intellectually judge their risks.

Highlights

  • Complete endocardial cushion defect is a congenital heart disease characterized by a variable deficiency of the atrioventricular area in the developing heart

  • Our experience further emphasizes the necessity of prenatal screening for congenital heart defects and of prompt surgical correction for endocardial cushion defects during infancy

  • It is thought that more than 50% of complete endocardial cushion defect (ECD) occur in conjunction with trisomy 21 [1]

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Summary

Conclusion

Women with a complete ECD should avoid pregnancy, especially those women who cannot intellectually judge their risks. Doi:10.1186/1752-1947-8-91 Cite this article as: Chen et al.: Complete endocardial cushion defects in pregnancy: a case report. Journal of Medical Case Reports 2014 8:91. Consent Written informed consent was obtained from the patient and patient’s family for publication of this case report and any accompanying images. HZ proposed the study and helped to draft the manuscript. All authors read and approved the final manuscript. Author details 1Department of Obstetrics and Gynecology, The First Affiliated Hospital of Wenzhou Medical University, 2# Fuxue Road, Wenzhou 325000, People’s Republic of China.

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