Herein, we describe the surgical management of a patient with the diagnosis of cc-TGA, severe systemic atrioventricular (AV) valve insufficiency with Ebstein's anomaly and ventricular failure who underwent an urgent DSO with a temporary mechanical systemic ventricular support. Although the PAB was performed prior to admission of this patient, the LV was still untrained, and we had to proceed with a salvage DSO; otherwise, the expected mortality would be high due to severe biventricular heart failure and cardiogenic shock.
Figure 1: Chest X-ray showing significant cardiomegaly.
Atrial switch (modified Senning procedure) and arterial switch operations were performed. The interior flap was constituted with a polytetrafluoroethylene patch and the outer flap was enlarged with bovine pericardium. Arterial switch procedure was completed following a LeCompte maneuver. Pulmonary artery debanding was, then, performed. The aortic crossclamping and cardiopulmonary bypass times were 186 and 223 min, respectively. Although the patient was weaned from cardiopulmonary bypass with high dose inotropic support, the systemic ventricle failed at the first postoperative hour at the operating room. Therefore, a left atrium to the ascending aortic mechanical circulatory support was implemented with a centrifugal pump. The functions of the systemic ventricle gradually improved after eight days of mechanical circulatory support. The patient was weaned off, when transthoracic echocardiography revealed a LV mass index and Z-score of 115 g/m2 and 3, respectively (Figure 3). Both AV valves had mild incompetence with a systemic ventricular ejection fraction of 60% at the time of discharge. The patient is still uneventful three years after the DSO.
Double switch operation may be considered as a procedure of choice in the newborn or young infants presenting with congestive heart failure due to systemic valvular regurgitation. Furthermore, the DSO may be the only option to convert the failing tricuspid valve to a low-pressure environment, taking the challenging neonatal Ebsteinoid tricuspid valve repair into consideration.[9]
In conclusion, although congenitally corrected transposition of the great arteries is a rare cardiac malformation, its treatment mandates a meticulous surgical technique as well as a strict follow-up schedule. We believe that such salvage double switch operations may be encouraged in patients with early ventricular failure and atrioventricular insufficiency in cases where the systemic ventricle is not trained, yet. A mechanical circulatory support may also provide a time for the systemic ventricle to recover after the procedure.
Declaration of conflicting interests
The authors declared no conflicts of interest with respect to
the authorship and/or publication of this article.
Funding
The authors received no financial support for the research
and/or authorship of this article.
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