Ebstein's anomaly with total anomalous pulmonary venous connection in an adult.

Ebstein's anomaly is a rare congenital cardiac disease which is often associated with various other cardiac anomalies. However, its association with total anomalous pulmonary venous connection is extremely rare with only one case reported so far in the English literature. We report the first successful surgical correction of both Ebstein's anomaly and total anomalous pulmonary venous connection in an adult patient. Such complex scenarios may pose unique challenges in management which require a judicious approach. Supplementary information: The online version contains supplementary material available at 10.1007/s12055-023-01664-8.

Single-stage repair of complex aortic arch anomaly with aortic regurgitation.

Aneurysm of the aberrant left subclavian artery arising from Kommerell's diverticulum is very rare. Early intervention is recommended in such a case to avoid complications. Rarely, such an aneurysm may present with a concomitant cardiac pathology. Surgical approach in this complex scenario is difficult as anatomically distant areas have to be exposed and usually a staged approach is preferred. There are only a few published reports about the same. We report, for the first time, successful single-stage intervention in a patient with aortic regurgitation, right aortic arch, and aneurysmal aberrant left subclavian artery from Kommerell's diverticulum, exclusively through median sternotomy. A 37-year-old gentleman presented with the complaints of palpitations (New York Heart Association grade II) and left-sided neck swelling of 4 months' duration. He also had history of hoarseness of voice for 2 weeks. He was diagnosed to have aortic regurgitation, right aortic arch, and aneurysmal aberrant left subclavian artery from Kommerell's diverticulum and was treated by single-stage repair of the aneurysm and aortic valve replacement with mechanical prosthesis via median sternotomy. Single-stage intervention through midline sternotomy provides excellent outcomes and can be a feasible option for such a complex aortic anomaly.

Total transatrial correction of tetralogy of Fallot: no outflow patch technique.

BACKGROUND: The aim of this study was to analyze the feasibility and early results of transatrial total correction of tetralogy of Fallot (TOF). METHODS: Of the 860 patients undergoing total correction for TOF between January 2000 and July 2005, 334 patients were considered morphologically suitable for transatrial total correction. The ventricular septal defect (VSD) closure, infundibular resection, and pulmonary valvotomy were performed through the right atrium without a right ventriculotomy. Age ranged from 6 months to 40 years (median, 2.8 years), and weight ranged from 5.5 to 70 kg (median, 14 kg). RESULTS: Peroperatively, 34 patients required right ventriculotomy and transannular patch; hence, they were excluded from the study. In addition, pulmonary arteriotomy was required in 71 patients (22.9%). There were 4 hospital deaths. There were 4 early reoperations (residual/additional VSD in 3 and tricuspid regurgitation in 1). Two patients had complete heart block requiring permanent pacemaker. Echocardiography at discharge showed a peak right ventricular outflow tract gradient of 20 +/- 5.2 mm Hg. Mean follow-up was 26.8 +/- 4.2 months (range, 1 to 52 months). The right ventricular outflow tract gradients reduced to 13 +/- 4.2 mm Hg after a mean interval of 18.8 +/- 5.2 months. Follow-up New York Heart Association class was I in 240 cases (82%), II in 49 (16%), and III in 7 (2%). There were no late deaths or reoperations. CONCLUSIONS: Transatrial total correction of TOF can be accomplished in selected patients with good early results. In 300 cases (90%), the feasibility of transatrial total correction could be predicted accurately.