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European Journal of Cardio-Thoracic Surgery, Vol 10, 443-448, Copyright © 1996 by European Association for Cardio-thoracic Surgery
M Szufladowicz, P Horvath, M de Leval, M Elliott, R Wyse and J Stark
OBJECTIVE: Discordant atrioventricular (AV) connection is a rare congenital
cardiac anomaly. Associated cardiac defects modify the physiology, clinical
presentation, and surgical management of these patients. We have reviewed
our overall experience with 90 patients operated for lesions associated
with AV discordance between 1975-1990. METHODS: 90 patients, consecutively
operated between 1975-1990, were reviewed. Patients' charts, angiograms and
echocardiograms were studied. Follow-up was obtained from our records or
was requested from referring cardiologists/paediatricians. It was completed
in December 1992. For the analysis of risk factors of early death we used P
values by chi-squared and Fisher's exact test. For the analysis of the
triangulated events, we used the Kaplan-Meier method. Variables associated
with P value over 0.20 were eliminated. RESULTS: 90 patients aged 6
months-30 years (mean 9.1 year) underwent repair of cardiac anomalies
associated with AV discordance. Three patients had total cavopulmonary
connection; the remainder received biventricular repair. Most important
associated malformations were ventricular septal defect (77), subpulmonary
obstruction (68) and tricuspid valve anomaly (21). 59 patients received
extracardiac valved conduit, 10 had tricuspid valve replacement. Thirteen
patients died in hospital (14%). One year and 10 year actuarial survival
rate was 84% and 70% respectively. The most significant factors for early
death were: anatomically abnormal tricuspid valve (P < 0.0001),
tricuspid valve regurgitation (P < 0.002), date of operation (P <
0.012), preoperative or perioperative complete heart block (P < 0.015),
and tricuspid valve surgery (P < 0.05). Complete heart block developed
in 17 (20%) out of 85 patients who did not have it preoperatively. During
the follow-up, 22 intracardiac reoperations were necessary (4 died). 63
patients of 73 survivors (86%) remain in NYHA Class 1, 6 in Class 2 and 4
in Class 3. CONCLUSIONS: The operative mortality was 14%. Twenty per cent
of patients developed complete heart block. These results improved in the
later part of the series (1985-1990); mortality decreased to 5% and
incidence of heart block to 14%. Cardiac anomalies associated with AV
discordance still present a surgical challenge. The data reported in our
study should serve as a useful baseline for evaluation of newer surgical
techniques, such as the "double switch" operation.
ARTICLES
Intracardiac repair of lesions associated with atrioventricular discordance
Cardiothoracic Unit, Hospital for Children, London, UK.
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