%0 Journal Article
%A Charron, Philippe
%A Elliott, Perry M
%A Gimeno, Juan R
%A Caforio, Alida L P
%A Kaski, Juan Pablo
%A Tavazzi, Luigi
%A Tendera, Michal
%A Maupain, Carole
%A Laroche, Cecile
%A Rubis, Pawel
%A Jurcut, Ruxandra
%A Calo, Leonardo
%A Heliö, Tiina M
%A Sinagra, Gianfranco
%A Zdravkovic, Marija
%A Kavoliuniene, Aušra
%A Felix, Stephan B
%A Grzybowski, Jacek
%A Losi, Maria-Angela
%A Asselbergs, Folkert W
%A Garcia-Pinilla, Jose Manuel
%A Salazar-Mendiguchia, Joel
%A Mizia-Stec, Katarzyna
%A Maggioni, Aldo P
%A EORP Cardiomyopathy Registry Investigators
%T The Cardiomyopathy Registry of the EURObservational Research Programme of the European Society of Cardiology: baseline data and contemporary management of adult patients with cardiomyopathies.
%D 2018
%U http://hdl.handle.net/10668/12058
%X The Cardiomyopathy Registry of the EURObservational Research Programme is a prospective, observational, and multinational registry of consecutive patients with four cardiomyopathy subtypes: hypertrophic cardiomyopathy (HCM), dilated cardiomyopathy (DCM), arrhythmogenic right ventricular cardiomyopathy (ARVC), and restrictive cardiomyopathy (RCM). We report the baseline characteristics and management of adults enrolled in the registry. A total of 3208 patients were enrolled by 69 centres in 18 countries [HCM (n = 1739); DCM (n = 1260); ARVC (n = 143); and RCM (n = 66)]. Differences between cardiomyopathy subtypes (P  By providing contemporary observational data on characteristics and management of patients with cardiomyopathies, the registry provides a platform for the evaluation of guideline implementation. Potential gaps with existing recommendations are discussed as well as some suggestions for improvement of health care provision in Europe.
%K Valor
%K Lang
%K Defibrillators
%K Cardiomyopathy, Restrictive
%~