Arrhythmia surgery in association with complex congenital heart repairs excluding patients with fontan conversion

Author(s):  
Constantine Mavroudis ◽  
Barbara J. Deal ◽  
Carl L. Backer
2011 ◽  
Vol 21 (S2) ◽  
pp. 169-176 ◽  
Author(s):  
Carl L. Backer

AbstractBetween 1994 and 2011, we performed 133 Fontan conversions with arrhythmia surgery. Most patients had tricuspid atresia or double-inlet left ventricle with prior atriopulmonary connection. Operative mortality was 1.5%, and mean length of stay was 14 days. A total of eight patients (6%) have had late cardiac transplantation. Freedom from arrhythmia recurrence is 85% at 10 years. For properly selected patients with a functionally univentricular heart who have had an atriopulmonary Fontan procedure, Fontan conversion with arrhythmia surgery significantly improves quality of life.


2003 ◽  
Vol 41 (6) ◽  
pp. 486
Author(s):  
Tim S. Hornung ◽  
Sam C. Siu ◽  
Mark Osten ◽  
Kristin Honshorst ◽  
William G. Williams ◽  
...  

2020 ◽  
Vol 9 (19) ◽  
Author(s):  
Charlotte A. Houck ◽  
Natasja M. S. de Groot ◽  
Isabella Kardys ◽  
Christa D. Niehot ◽  
Ad J. J. C. Bogers ◽  
...  

Background The improved life expectancy of patients with congenital heart disease is often accompanied by the development of atrial tachyarrhythmias. Similarly, the number of patients requiring redo operations is expected to continue to rise as these patients are aging. Consequently, the role of arrhythmia surgery in the treatment of atrial arrhythmias is likely to become more important in this population. Although atrial arrhythmia surgery is a well‐established part of Fontan conversion procedures, evidence‐based recommendations for arrhythmia surgery for macroreentrant atrial tachycardia and atrial fibrillation in other patients with congenital heart disease are still lacking. Methods and Results Twenty‐eight studies were included in this systematic review. The median reported arrhythmia recurrence was 13% (interquartile range, 4%–26%) during follow‐up ranging from 3 months to 15.2 years. A large variation in surgical techniques was observed. Based on the acquired data, biatrial lesions are more effective in the treatment of atrial fibrillation than exclusive right‐sided lesions. Right‐sided lesions may be more appropriate in the treatment of macroreentrant atrial tachycardia; evidence for the superiority of additional left‐sided lesions is lacking. There are not enough data to support the use of exclusive left‐sided lesions. Theoretically, prophylactic atrial arrhythmia surgery may be beneficial in this population, but evidence is currently limited. Conclusions To be able to provide recommendations for arrhythmia surgery in patients with congenital heart disease, future studies should report outcomes according to the type of preoperative arrhythmia, underlying congenital heart disease, lesion set, and energy source. This is essential for determining which surgical techniques should ideally be applied under which circumstances.


2008 ◽  
Vol 86 (3) ◽  
pp. 857-868 ◽  
Author(s):  
Constantine Mavroudis ◽  
Barbara J. Deal ◽  
Carl L. Backer ◽  
Sabrina Tsao

Author(s):  
Constantine Mavroudis ◽  
Barbara J. Deal ◽  
Carl L. Backer ◽  
Christopher L. Johnsrude

2012 ◽  
Vol 3 (2) ◽  
pp. 165-170 ◽  
Author(s):  
Carl Lewis Backer ◽  
Hyde M. Russell ◽  
Barbara J. Deal

This review will outline the optimal, initial palliation for children who are born with a functionally univentricular heart. Optimizing the initial palliation is of critical importance in this patient population to prevent potential problems such as systemic outflow and pulmonary vein obstruction that may complicate further surgical intervention. The palliative techniques that are discussed include pulmonary artery banding, modified Blalock-Taussig shunt, Damus-Kaye-Stansel procedure, modified Norwood, hybrid, and early bidirectional Glenn. Our recommendations for optimal palliation for children with a univentricular heart are based on our experience with nearly 200 patients who had either a lateral tunnel or extracardiac Fontan procedure and 130 patients who had Fontan conversion with arrhythmia surgery.


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