Objectives: This study sought to characterize the echocardiographic features of straddling mitral valve (SMV) and to determine its surgical implications and midterm outcome in a large clinical cohort.
Background: Despite a relatively large body of literature on the postmortem anatomy of SMV, there is a paucity of information regarding its echocardiographic features, surgical implications and preoperative predictors of outcome.
Methods: A retrospective review identified 46 patients with SMV between 1982 and 1999 who underwent echocardiography and surgery and had follow-up data. A detailed review of the echocardiograms, surgical reports and all pertinent records was undertaken.
Results: Review of the echocardiograms revealed a widely varying anatomy among the study patients. However, four distinct groups with relatively uniform morphologic features could be distinguished on the basis of segmental analysis. Cardiac malposition associated with right ventricular hypoplasia, superior-inferior ventricles and criss-cross atrioventricular relations were common among patients with [S,D,L] (S = visceroatrial situs solitus, D = D-ventricular loop, L = L-malposition of the great arteries) (n = 6) and [S,L,D] (n = 5) segmental combinations but were rare among patients with [S,D,D] (n = 26) and [S,L,L] (n = 9) combinations. Surgical management consisted of a functional single-ventricle palliation in 38 patients (83%) and biventricular repair in 8 patients (17%). Overall mortality was 22%, but none of the seven patients who were operated on during the cohort's last five years (1994 to 1999) has died. By multivariate analysis, noncommitted ventricular septal defect was the strongest independent predictor of death (relative risk = 10.2), followed by multiple ventricular septal defects (relative risk = 4.7).
Conclusions: This study demonstrates that echocardiography provides detailed noninvasive imaging of the complex anatomic features of SMV and its associated anomalies. Anatomic classification based on segmental analysis allows the distinction of four groups with more uniform morphologic features. Although a biventricular approach is feasible in selected patients, a functional univentricular palliation is indicated in those with major straddling and markedly hypoplastic ventricles.
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http://dx.doi.org/10.1016/s0735-1097(01)01441-3 | DOI Listing |
Eur Heart J Case Rep
January 2025
Department of Cardiovascular Medicine, Sendai Kousei Hospital, 1-20 Tsutsumidori-amamiya, Aoba Ward, Sendai, Miyagi 9810914, Japan.
World J Pediatr Congenit Heart Surg
November 2024
Pediatric Cardiothoracic Surgery, Children's Medical Center Dallas/UT Southwestern, Dallas, TX, USA.
Biventricular repair of a straddling mitral valve (MV) can involve relocating ectopic papillary muscles and chordae. However, this increases operative complexity and risks MV incompetence. We describe a nine-month-old with D-transposition of the great arteries and straddling MV.
View Article and Find Full Text PDFWorld J Pediatr Congenit Heart Surg
July 2024
Institute of Genetic Medicine, Newcastle University, Newcastle upon Tyne, UK.
We describe an unusual example of double-outlet right atrium with separate atrioventricular junctions. The straddling and overriding tricuspid valve had two orifices, and the mitral valve was morphologically normal. An appropriate understanding of the morphology of the atrioventricular junctions, the valves, and the subvalvar apparatus, along with the location of the atrioventricular conduction axis, allowed for successful biventricular repair.
View Article and Find Full Text PDFIndian J Thorac Cardiovasc Surg
November 2022
Department of Pediatric Cardiac Surgery, Kumamoto City Hospital, 4-1-60, Higashimachi, Higashi-ku, Kumamoto, 862-8505 Japan.
Although atrioventricular septal defects are categorized according to the anatomical atrioventricular orifice, the location of the intracardiac shunt in atrioventricular septal defects is important from a surgical perspective. Herein, we report three cases of atrioventricular septal defects with a small or no ostium primum defect. Case 1 (3-month-old girl) was diagnosed preoperatively with a ventricular septal defect, secundum atrial septal defect, and mitral valve cleft.
View Article and Find Full Text PDFJ Cardiovasc Dev Dis
February 2021
MD FRCP FRCPCH, Royal Brompton Hospital, London SW3 6NP, UK.
Robert Anderson has made a huge contribution to almost all aspects of morphology and understanding of congenital cardiac malformations, none more so than the group of anomalies that many of those in the practice of paediatric cardiology and adult congenital heart disease now call 'Atrioventricular Septal Defect' (AVSD). In 1982, with Anton Becker working in Amsterdam, their hallmark 'What's in a name?' editorial was published in the . At that time most described the group of lesions as 'atrioventricular canal malformation' or 'endocardial cushion defect'.
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