Cone Reconstruction with Successful One and A Half Ventricle Repair for Ebstein Anomaly
Babürhan Özbek1, Kenan Öztürker2, Fatih Tomrukçu1, Kenan Abdurrahman Kara1, Ömer Faruk Şavluk3, Deniz Çevirme2, Eylem Tunçer1, Nihat Çine1, Hakan Ceyran1
1Department of Pediatric Cardiovascular Surgery, Kartal Koşuyolu High Specialization Training and Research Hospital, Istanbul, Turkey
2Department of Cardiovascular Surgery, Kartal Koşuyolu High Specialization Training and Research Hospital, Istanbul, Turkey
3Department of Anesthesiology and Reanimation, Kartal Koşuyolu High Specialization Training and Research Hospital, Istanbul, Turkey
Keywords: Cone reconstruction; Ebstein anomaly; one and a half ventricle repair
Abstract
Ebstein anomaly is a rare pathology among congenital cardiac diseases with a prevalance of 0.5%. Ebstein anomaly patients suffer from arrhytmia, severe right ventricular dysfunction and left ventricular dysfunction due to cyanosis and right ventricular involvement. Most of the patients are presented at infancy, childhood and rarely after adolescence ages. Biventricular repair has a high mortality and morbidity and unacceptable func- tional results in Ebstein anomaly patients with severe right ventricular dysfunction, one and a half ventricle repair yields better results. In our case, we presented a one and a half ventricle repair with a successful Cone type repair in a 34-year-old male patient who referred to our clinic with cardiac arrest presentation and was detected to have functional type C Ebstein anomaly.
Informed consent form was obtained from patient.
Externally peer-reviewed.
Concept/Design - BÖ, KÖ; Analysis/Interpretation - BÖ, ET; Data Collection - FT, KK; Writing - BÖ, DÇ; Critical Revision - ÖŞ, ET; Statistical Analysis - KÖ, FT; Obtained Funding - DÇ, KÖ; Overall Responsibility - BÖ, HC; Final Approval - All of authors.
The authors have no conflicts of interest to declare
The authors declared that this study has received no financial support.