Background: To investigate the impact of residual lesion score (RLS) on the long-term outcomes of 5 common congenital heart operations.
Methods: All infants who underwent definitive surgery for complete atrioventricular septal defect (AVSD), tetralogy of Fallot (TOF), dextro-transposition of the great arteries (d-TGA), single ventricle (Norwood procedure), and coarctation with ventricular septal defect (CoA/VSD) between 2000 and 2012 who survived until discharge were studied. RLS scores (1 - no/trivial, 2 - minor, 3 - major or in-hospital reinterventions/reoperations for such lesions) were assigned based on post-repair clinical and echocardiographic evaluation. The time to events was summarized using the Kaplan-Meier survival method and competing risk models.
Results: 1027 patients were included (213 AVSDs, 358 TOFs, 308 d-TGAs, 127 single ventricles, and 21 CoA/VSDs) with a median follow-up time of 15 years (IQR 11-18.4 years). Overall, 227 patients (22.1%) had RLS of 1, 556 patients (54.1%) had RLS of 2, and 244 patients (23.8%) had RLS of 3. Freedom from late death/transplantation was 93.7% at 15 years. RLS was not associated with late death/transplantation. Male sex, TOF and ASO had the lowest risk for late death/transplantation. Late reintervention/reoperations were present in 14.5% at 15 years. Younger age, TOF/PS repair, ASO, RLS of 3 (HR 2.02, CI 1.17-3.51, p=0.012), intraoperative surgical revision, and in-hospital reintervention/reoperation associated with late reintervention/reoperation.
Conclusions: The RLS does not predict late mortality but predicts late reintervention/reoperation after congenital cardiac repair and can be used to target at-risk patients for follow-up.
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http://dx.doi.org/10.1016/j.athoracsur.2025.01.034 | DOI Listing |
Ann Thorac Surg
February 2025
Division of Cardiovascular Surgery, The Labatt Family Heart Centre, The Hospital for Sick Children, University of Toronto, Toronto, Ontario, Canada. Electronic address:
Background: To investigate the impact of residual lesion score (RLS) on the long-term outcomes of 5 common congenital heart operations.
Methods: All infants who underwent definitive surgery for complete atrioventricular septal defect (AVSD), tetralogy of Fallot (TOF), dextro-transposition of the great arteries (d-TGA), single ventricle (Norwood procedure), and coarctation with ventricular septal defect (CoA/VSD) between 2000 and 2012 who survived until discharge were studied. RLS scores (1 - no/trivial, 2 - minor, 3 - major or in-hospital reinterventions/reoperations for such lesions) were assigned based on post-repair clinical and echocardiographic evaluation.
Front Cardiovasc Med
March 2022
Department of Congenital Heart Disease/Pediatric Cardiology, German Heart Centre Berlin, Berlin, Germany.
Objectives: Despite the outstanding success of the Fontan operation, it is a palliative procedure and a substantial number of patients experience late failure of the Fontan circulation. Clinical presentation and hemodynamic phenotypes of Fontan failure are considerably variable. While various parameters have been identified as risk factors for late Fontan failure, a feasible score to classify Fontan failure and possibly allow timely risk stratification is lacking.
View Article and Find Full Text PDFJ Thorac Cardiovasc Surg
October 2019
The Heart Centre for Children, The Children's Hospital at Westmead, Westmead, Australia; The University of Sydney, Sydney, Australia. Electronic address:
Objectives: D-transposition of the great arteries and l-transposition of the great arteries with ventricular septal defect and left ventricular outflow tract obstruction are complex biventricular congenital heart diseases for which decision-making regarding surgical strategy remains challenging. We investigated the intermediate-term outcomes of Fontan versus biventricular procedures in these patients.
Methods: We analyzed 129 patients with d-transposition of the great arteries/ventricular septal defect/left ventricular outflow tract obstruction (n = 85) or l-transposition of the great arteries/ventricular septal defect/left ventricular outflow tract obstruction (n = 44) and 2 functional ventricles from Australia who had primary surgical management (29 Fontan, 100 biventricular repair) undertaken between 1990 and 2015.
JACC Cardiovasc Imaging
July 2019
Cardiovascular Division, Department of Medicine, Brigham and Women's Hospital, Boston, Massachusetts; Harvard Medical School, Boston, Massachusetts. Electronic address:
Objectives: The aim of this study was to assess the utility of left ventricular (LV) entropy, a novel measure of myocardial heterogeneity, for predicting cardiovascular events in patients with dilated cardiomyopathy (DCM).
Background: Current risk stratification for ventricular arrhythmia in patients with DCM is imprecise. LV entropy is a measure of myocardial heterogeneity derived from cardiac magnetic resonance imaging that assesses the probability distribution of pixel signal intensities in the LV myocardium.
Circulation
July 2018
Department of Cardiology, Royal Children's Hospital (M.C., A.M.D., R.G.W.).
Background: Long-term outcomes for childhood left ventricular noncompaction (LVNC) are uncertain. We examined late outcomes for children with LVNC enrolled in a national population-based study.
Methods: The National Australian Childhood Cardiomyopathy Study includes all children in Australia with primary cardiomyopathy diagnosed before 10 years of age between 1987 and 1996.
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