Role of echocardiography in atrioventricular canal defects assessment

Le résumé fourni par la source

Introduction: Atrioventricular (AV) canal defects are a group of congenital cardiac defects involving the AV septum and AV valves (ie.mitral and tricuspid valves).Combinations of these anatomic abnormalities result in complete (both atrial and ventricular septal defects [ASD/VSD] and partial (only ASD) forms that are manifested in varying clinical presentations.1-4 Case 1: 35-year-old patient with Down syndrome and untreated complete AV canal defect who developed Eisenmenger syndrome and has been treated with bosentan (Figure 1).Complete AV canal defect is a result of complete failure of fusion between the superior and inferior endocardial cushions.It is characterized by a primum ASD that is contiguous with a posterior (or inlet) VSD and a common AV valve.Case 2: 61-year-old patient with partial AV canal defect who undergone surgical correction 2 years ago and is now in NYHA I class status (Figure 2).Partial AV canal defect is due to incomplete fusion of the superior and inferior endocardial cushions and consists of a primum ASD and a single AV valve annulus with two separate valve orifices.Due to abnormal fusion of the left tubercle of the superior and inferior cushions, the anterior leaflet of the mitral valve typically is cleft.Case 3: 26-year-old patient with transitional AV canal defect.Due to 1.5:1 left to right shunt without signs of significant right ventricle volume overload, she will undergo further evaluation in 6 months (Figure 3).Transitional AV canal defect is anatomically a subtype of complete AV canal defect as it consists of a large primum defect, cleft mitral valve and inlet VSD.However, dense chordal attachments to the ventricular septum lead to small insignificant ventricular shunting and delineation of distinct left and right AV valve orifices, resulting in a defect that is similar to the physiology of a partial AV canal defect.Case 4: 48-year-old patient undergone surgical correction 2 months ago due to development of bidirectional shunt (dominantly left to right with Qp/Qs 2.1:1) (Figure 4).

Ce résumé expose les affirmations des auteurs. BNTIC ne l’interprète pas comme une validation indépendante des résultats.