Study design and rationale of the pAtients pResenTing with cOngenital heaRt dIseAse Register (ARTORIA‐R)

Autor: Christoph Sinning, Elvin Zengin, Gerhard‐Paul Diller, Francesco Onorati, María‐Angeles Castel, Thibault Petit, Yih‐Sharng Chen, Mauro Lo Rito, Carmelina Chiarello, Romain Guillemain, Karine Nubret‐Le Coniat, Christina Magnussen, Dorit Knappe, Peter Moritz Becher, Benedikt Schrage, Jacqueline M. Smits, Andreas Metzner, Christoph Knosalla, Felix Schoenrath, Oliver Miera, Mi‐Young Cho, Alexander Bernhardt, Jessica Weimann, Alina Goßling, Amedeo Terzi, Antonio Amodeo, Sara Alfieri, Emanuela Angeli, Luca Ragni, Carlo Pace Napoleone, Gino Gerosa, Nicola Pradegan, Inez Rodrigus, Julia Dumfarth, Michel dePauw, Katrien François, Olivier Van Caenegem, Arnaut Ancion, Johan Van Cleemput, Davor Miličić, Ajay Moza, Peter Schenker, Josef Thul, Michael Steinmetz, Gregor Warnecke, Fabio Ius, Susanne Freyt, Murat Avsar, Tim Sandhaus, Assad Haneya, Sandra Eifert, Diyar Saeed, Michael Borger, Henryk Welp, László Ablonczy, Bastian Schmack, Arjang Ruhparwar, Shiho Naito, Xiaoqin Hua, Nina Fluschnik, Moritz Nies, Laura Keil, Juliana Senftinger, Djemail Ismaili, Shinwan Kany, Dora Csengeri, Massimo Cardillo, Alessandra Oliveti, Giuseppe Faggian, Richard Dorent, Carine Jasseron, Alicia Pérez Blanco, José Manuel Sobrino Márquez, Raquel López‐Vilella, Ana García‐Álvarez, María Luz Polo López, Alvaro Gonzalez Rocafort, Óscar González Fernández, Raquel Prieto‐Arevalo, Eduardo Zatarain‐Nicolás, Katrien Blanchart, Aude Boignard, Pascal Battistella, Soulef Guendouz, Lucile Houyel, Marylou Para, Erwan Flecher, Arnaud Gay, Éric Épailly, Camille Dambrin, Kaitlyn Lam, Cally Ho Ka‐lai, Yang Hyun Cho, Jin‐Oh Choi, Jae‐Joong Kim, Louise Coats, David Steven Crossland, Lisa Mumford, Samer Hakmi, Cumaraswamy Sivathasan, Larissa Fabritz, Stephan Schubert, Jan Gummert, Michael Hübler, Peter Jacksch, Andreas Zuckermann, Günther Laufer, Helmut Baumgartner, Alessandro Giamberti, Hermann Reichenspurner, Paulus Kirchhof

Publikováno v: ESC Heart Failure, Vol 8, Iss 6, Pp 5542-5550 (2021)

Abstract Aim Due to improved therapy in childhood, many patients with congenital heart disease reach adulthood and are termed adults with congenital heart disease (ACHD). ACHD often develop heart failure (HF) as a consequence of initial palliative su

Externí odkaz: https://doaj.org/article/a39a61b29a124f8abe25af33d95cbfcd

Candidacy for heart transplantation in adult congenital heart disease patients: A cohort study

Autor: Emanuela Angeli, Emanuela Concetta D'Angelo, Luca Ragni, Gaetano Domenico Gargiulo, Andrea Donti, Luciano Potena, Federica Tonoli, Ylenia Bartolacelli, Ambra Bulgarelli, Lucio Careddu, Cristina Ciuca, Rossana Zanoni, Gabriele Egidy Assenza

Publikováno v: International Journal of Cardiology Congenital Heart Disease, Vol 8, Iss , Pp 100363- (2022)

Objective: The object of the present study is to evaluate factors precluding heart transplantation (HTx) in adult congenital heart disease patients (ACHD) with end-stage heart failure (HF) referred for HTx evaluation. Methods: This retrospective coho

Externí odkaz: https://doaj.org/article/54561c0cf4754298ad78278e4c584198

Pediatric Restrictive Cardiomyopathies

Autor: Raffaello Ditaranto, Angelo Giuseppe Caponetti, Valentina Ferrara, Vanda Parisi, Matteo Minnucci, Chiara Chiti, Riccardo Baldassarre, Federico Di Nicola, Simone Bonetti, Tammam Hasan, Luciano Potena, Nazzareno Galiè, Luca Ragni, Elena Biagini

Publikováno v: Frontiers in Pediatrics, Vol 9 (2022)

Restrictive cardiomyopathy (RCM) is the least frequent phenotype among pediatric heart muscle diseases, representing only 2.5–3% of all cardiomyopathies diagnosed during childhood. Pediatric RCM has a poor prognosis, high incidence of pulmonary hyp

Externí odkaz: https://doaj.org/article/74831a10c9e24f2da3dddabc55a96b1b

Hypertrophic Cardiomyopathy with Biventricular Involvement and Coronary Anomaly: A Case Report

Autor: Ylenia Bartolacelli, Simone Bonetti, Anna Balducci, Ambra Bulgarelli, Luca Ragni, Andrea Donti

Publikováno v: Life, Vol 12, Iss 10, p 1608 (2022)

Although hypertrophic cardiomyopathy (HCM) is classically considered a disease of the left ventricle, right ventricular (RV) involvement has also been reported, though still not extensively characterized. We present a case of biventricular HCM with s

Externí odkaz: https://doaj.org/article/c1a936386e8943708d6b81b8aeac9286

Left Ventricular Myocardial Noncompaction with Advanced Atrioventricular Conduction Disorder and Ventricular Arrhythmias in a Young Patient: Role of MIB1 Gene

Autor: Cristina Balla, Martina De Raffele, Maria Angela Deserio, Mariabeatrice Sanchini, Marianna Farnè, Cecilia Trabanelli, Luca Ragni, Mauro Biffi, Alessandra Ferlini, Claudio Rapezzi, Francesca Gualandi, Matteo Bertini

Publikováno v: Journal of Cardiovascular Development and Disease, Vol 8, Iss 9, p 109 (2021)

Left ventricular noncompaction (LVNC) is a structural abnormality of the left ventricle, usually described as an isolated condition, or sometimes associated with other structural cardiac diseases. LVNC is generally asymptomatic, although it may prese

Externí odkaz: https://doaj.org/article/bea361b0dc7a4e089a294c8a08f67873