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      Understanding atrioventricular septal defect: Anatomoechocardiographic correlation

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          Abstract

          Objective

          Correlate the anatomic features of atrioventricular septal defect with echocardiographic images.

          Materials and methods

          Sixty specimen hearts were studied by sequential segmental analysis. Echocardiograms were performed on 34 patients. Specimen hearts with findings equivalent to those of echocardiographic images were selected in order to establish an anatomo-echocardiographic correlation.

          Results

          Thirty-three specimen hearts were in situs solitus, 19 showed dextroisomerism, 6 were in situs inversus and 2 levoisomerism. Fifty-eight had a common atrioventricular valve and 2 had two atrioventricular valves. Rastelli types were determined in 21 hearts. Nine were type A, 2 intermediate between A and B, 1 mixed between A and B, 4 type B and 5 type C. Associated anomalies included pulmonary stenosis, pulmonary atresia atrial septal defect, patent ductus arteriosus and anomalous connection of pulmonary veins. Echocardiograms revealed dextroisomerism in 12 patients, situs solitus in 11, levoisomerism in 7 and situs inversus in 4. Thirty-one patients had common atrioventricular valves and three two atrioventricular valves. Rastelli types were established in all cases with common atrioventricular valves; 17 had type A canal defects, 10 type B, 3 intermediate between A and B, 1 mixed between A and B and 3 type C. Associated anomalies included regurgitation of the atrioventricular valve, pulmonary stenosis, anomalous connection of pulmonary veins, pulmonary hypertension and pulmonary atresia.

          Conclusion

          Anatomo-echocardiographic correlation demonstrated a high degree of diagnostic precision with echocardiography.

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          Most cited references31

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          Nomenclature and classification of congenital heart disease.

          At present there is no universally accepted nomenclature for congenital cardiac malformations. Much of the controversy results from failure to distinguish the structural connections of the heart from the morphology and spatial relations of its components. The confusion is compounded by an abundance of individual definitions, many of them speculative. The present article proposes a totally descriptive nomenclature. It describes in turn the connections of the cardiac segments, their morphology, their relations, and additional anomalies in any segment. Each step in the segmental approach is discrete. The overall effect is to force a succinct and comprehensive description of any cardiac malformation, no matter how complex.
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            Non-compacted cardiomyopathy: clinical-echocardiographic study

            The aim of the present study was to describe the clinical and echocardiographic findings of ventricular noncompaction in adult patients. Fifty-three patients underwent complete clinical history, electrocardiogram, Holter and transthoracic echocardiogram. Forty patients (75%) were in class I/II of the New York Heart Association, and 13 (25%) in class III/IV. Ventricular and supraventricular escape beats were found in 40% and 26.4%, respectively. Holter showed premature ventricular contractions in 32% and sustained ventricular tachycardia in 7.5%. Ventricular noncompaction was an isolated finding in 74% of cases and was associated with other congenital heart disease in 26%. Noncompacted ventricular myocardium involved only left ventricle in 62% of the patients and both ventricles in 38%. The mean ratio of noncompacted to compacted myocardial layers at the site of maximal wall thickness was 3.4 ± 0.87 mm (range 2.2–7.5). The presence of ventricular noncompaction in more than three segments was associated with a functional class greater than II and ventricular arrhythmia with demonstrable statistical significance by χ2(p < 0.003). Conclusion a) Noncompacted cardiomyopathy is a congenital pathological entity that can occur in isolated form or associated with other heart disease and often involves both ventricles. b) A ratio of noncompacted to compacted myocardium greater than 3 and involvement of three or more segments are indicators of poor prognosis. c) Since the clinical manifestations are not sufficient to establish diagnosis, echocardiography is the diagnostic tool that makes it possible to document ventricular noncompaction and establish prognostic factors.
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              Anatomic observations on complete form of persistent common atrioventricular canal with special reference to atrioventricular valves.

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                Author and article information

                Journal
                Cardiovasc Ultrasound
                Cardiovascular Ultrasound
                BioMed Central
                1476-7120
                2008
                24 June 2008
                : 6
                : 33
                Affiliations
                [1 ]Echocardiography in Out Patients Clinic, Instituto Nacional de Cardiología Ignacio Chávez, Juan Badiano N°1, Colonia Sección XVI, Mexico City, Mexico
                [2 ]Embryology Department, Instituto Nacional de Cardiología Ignacio Chávez, Juan Badiano N°1, Colonia Sección XVI, Mexico City, Mexico
                [3 ]Morphology Department, Escuela Superior de Medicina – IPN, Díaz-Mirón y Plan de San Luís, Colonia Casco de Santo Tomás, Tacuba, Mexico City, Mexico
                Article
                1476-7120-6-33
                10.1186/1476-7120-6-33
                2453104
                18573220
                c3b28b22-9eba-4404-9383-d52e16cbd7ee
                Copyright © 2008 Espinola-Zavaleta et al; licensee BioMed Central Ltd.

                This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 4 June 2008
                : 24 June 2008
                Categories
                Research

                Cardiovascular Medicine
                Cardiovascular Medicine

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