scholarly journals Partial atrioventricular canal defect with cor triatriatum sinister: report of three cases

2004 ◽  
Vol 127 (2) ◽  
pp. 572-573 ◽  
Author(s):  
Praveen K. Varma ◽  
Girish Warrier ◽  
Padmakumar Ramachandran ◽  
Praveen Kumar Neema ◽  
Soman Rema Krishna Manohar ◽  
...  
2014 ◽  
Vol 6 (1) ◽  
pp. 86-89 ◽  
Author(s):  
Pankaj Garg ◽  
Amit Mishra ◽  
Ritesh Shah ◽  
Jigar Panchal ◽  
Divyakant Parmar

2017 ◽  
Vol 4 (1) ◽  
pp. 110
Author(s):  
Camila Carneiro Araujo ◽  
Ercília Maria Carvalho ◽  
Amanda Luiza Nascimento ◽  
Sheila Sousa Santos ◽  
Paula Priscila Correia

O Cor triatriatum é uma anomalia congênita de ocorrência rara em cães. Nesta, identifica-se a presença de três átrios no coração, sendo denominado Cor triatriatum dexter quando há um átrio a mais do lado direito e Cor triatriatum sinister quando esta anomalia ocorre do lado esquerdo. A causa da doença ainda não está conhecida, mas é sabido que ocorre falhas na embriogênese do animal acometido por esta enfermidade. Os animais que possuem a doença apresentam sinais de insuficiência cardíaca direita ou esquerda. O diagnóstico é realizado por meio de exames complementares, dentre estes, se destaca o ecodopplercardiograma como método de escolha. O tratamento baseia-se na correção cirúrgica e/ou tratamento para a insuficiência cardíaca. Para evitar o surgimento desta anomalia, recomenda-se a castração destes animais, a não repetição do cruzamento que gerou este filhote, assim como, cruzamento consanguíneos.


2015 ◽  
Vol 44 (8) ◽  
pp. 964-969 ◽  
Author(s):  
Nicolas Borenstein ◽  
Vassiliki Gouni ◽  
Luc Behr ◽  
Emilie Trehiou-Sechi ◽  
Amandine Petit ◽  
...  

Circulation ◽  
2020 ◽  
Vol 142 (Suppl_3) ◽  
Author(s):  
Ilias P Doulamis ◽  
Supreet P Marathe ◽  
Breanna L Piekarski ◽  
Rebecca S Beroukhim ◽  
Gerald R Marx ◽  
...  

Hypothesis: Biventricular conversion (BiVC) following takedown of Fontan circulation is feasible and results in improved hemodynamics. Methods: Retrospective analysis of patients who had takedown of Fontan circulation and conversion to BiV circulation at a single center from September 2007 to April 2020. Failing Fontan physiology was defined as Fontan circulation pressure >15 mmHg. Results: There were 23 patients (median age: 10.0 (7.5-13.0) years); 15 (65%) had failing Fontan physiology and 8 (35%) underwent elective takedown of their Fontan circulation. Of the 15 patients with failing Fontan physiology, 4 had exercise intolerance or cyanosis, 3 had hepatic congestion or cirrhosis, 3 had end-organ damage and 1 patient had protein losing enteropathy; the rest 4 patients had no other sign of SVP complications. A subset of patients (n=6) underwent recruitment of the non-dominant ventricle prior to conversion. HLHS (p<0.01) and sub-/aortic stenosis (p<0.01) were more common in these patients. BiVC with or without staged ventricular recruitment led to a significant increase in indexed end-diastolic volume (p<0.01), indexed end-systolic volume (p<0.01) and ventricular mass (p<0.01) of the non-dominant ventricle (14 RV, 9 LV). There were 1 (4%) early and 4 (17%) late deaths. All who underwent elective BiVC survived, while 2-year survival rate for patients with a failing Fontan circulation was 72.7% (95% CI: 37-90%) (Figure 1). The overall, 1-year reintervention free survival was 44.1% (95% CI: 21-65%). Left dominant atrioventricular canal defect (p<0.01) and early year of BiVC (p=0.02) were significant predictors for mortality. Conclusions: BiVC is feasible in patients with failing Fontans, and has promising outcomes after elective takedown of Fontan circulation. A staged approach for ventricular recruitment does not seem inferior to primary BiVC. The optimal timing for BiVC in Fontan patients needs further evaluation.


Author(s):  
Ahmadreza Karimianpour ◽  
Amanda W. Cai ◽  
Frank A. Cuoco ◽  
J. Lacy Sturdivant ◽  
Sheldon E. Litwin ◽  
...  

2018 ◽  
Vol 9 (6) ◽  
pp. 645-650
Author(s):  
David Blitzer ◽  
Jeremy L. Herrmann ◽  
John W. Brown

Background: Mitral valve replacement (MVR) with a pulmonary autograft (Ross II) may be a useful technique for pediatric and young adult patients who wish to avoid anticoagulation. Our aim was to evaluate the long-term outcomes of the Ross II procedure at our institution. Methods: Patients undergoing the Ross II procedure between June 2002 and April 2008 were included. Preoperative diagnoses included rheumatic disease (n = 5), congenital mitral valve (MV) pathology (partial atrioventricular canal defect [n = 2], complete atrioventricular canal defect [n = 1], Shone's complex [n = 1]), and myocarditis (n = 1). Results: Ten patients (eight females and two males) between 7 months and 46 years were included. Mean age at surgery was 25.2 ± 15.7 years. There were no in-hospital deaths. Mean follow-up was 11.7 ± 5.2 years. There were three late deaths at 11 months, 5 years, and 11 years, respectively. Causes of death included right heart failure, sepsis, and sudden cardiac arrest. Three patients required subsequent mechanical MVR a median of two years after the Ross II procedure (range: 1-4 years). There was no mortality with reoperation. Echocardiographic follow-up demonstrated mean MV gradients ranging from 2.2 to 9.6 mm Hg. Two patients had greater than mild MV regurgitation postoperatively, and all others had minimal mitral regurgitation or less. Two patients developed moderate MV stenosis. Conclusions: The Ross II procedure is an option for select older children and young adults desiring a durable tissue MVR to avoid long-term anticoagulation.


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