TY - JOUR
T1 - Inquadramento e gestione delle cardiomiopatie
T2 - il protocollo della Cardiologia di Trieste
AU - Merlo, Marco
AU - Cappelletto, Chiara
AU - De Angelis, Giulia
AU - Porcari, Aldostefano
AU - Caiffa, Thomas
AU - Lardieri, Gerardina
AU - Pagnan, Lorenzo
AU - Severini, Giovanni Maria
AU - Dal Ferro, Matteo
AU - Stolfo, Davide
AU - Vitrella, Giancarlo
AU - De Luca, Antonio
AU - Korkova, Renata
AU - Massa, Laura
AU - Tavcˇar, Irena
AU - Aleksova, Aneta
AU - Barbati, Giulia
AU - Zanchi, Cristiana
AU - Ramani, Federica
AU - Di Lenarda, Andrea
AU - Perkan, Andrea
AU - Mestroni, Luisa
AU - Zecchin, Massimo
AU - Pinamonti, Bruno
AU - Bussani, Rossana
AU - Sinagra, Gianfranco
N1 - Copyright:
This record is sourced from MEDLINE/PubMed, a database of the U.S. National Library of Medicine
PY - 2020/12/1
Y1 - 2020/12/1
N2 - Cardiomyopathies are primary myocardial disorders, genetically determined, with clinical onset between the third and the fifth decade of life. They represent the main causes of sudden cardiac death and heart failure in the youth. The more common myocardial diseases in clinical practice are dilated cardiomyopathy, arrhythmogenic cardiomyopathy and hypertrophic cardiomyopathy. Next generation sequencing techniques, recently available for genetics researches, together with the diffusion of advanced imaging techniques, permitted in the last years a deeper knowledge of these pathologies. Nevertheless, diagnosis, etiology and several aspects of patients' clinical management remain complex and controversial. This review paper aims to propose some operative flow-charts, derived from scientific evidences and the internal protocol of the Cardiothoracovascular Department of Trieste Hospital, Italian referral Center for cardiomyopathies and heart failure, with more than 30 years of experience in diagnosis and management of patients who suffer from primary myocardial disorders.
AB - Cardiomyopathies are primary myocardial disorders, genetically determined, with clinical onset between the third and the fifth decade of life. They represent the main causes of sudden cardiac death and heart failure in the youth. The more common myocardial diseases in clinical practice are dilated cardiomyopathy, arrhythmogenic cardiomyopathy and hypertrophic cardiomyopathy. Next generation sequencing techniques, recently available for genetics researches, together with the diffusion of advanced imaging techniques, permitted in the last years a deeper knowledge of these pathologies. Nevertheless, diagnosis, etiology and several aspects of patients' clinical management remain complex and controversial. This review paper aims to propose some operative flow-charts, derived from scientific evidences and the internal protocol of the Cardiothoracovascular Department of Trieste Hospital, Italian referral Center for cardiomyopathies and heart failure, with more than 30 years of experience in diagnosis and management of patients who suffer from primary myocardial disorders.
UR - http://www.scopus.com/inward/record.url?scp=85096738017&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85096738017&partnerID=8YFLogxK
U2 - 10.1714/3472.34548
DO - 10.1714/3472.34548
M3 - Articolo
C2 - 33231213
AN - SCOPUS:85096738017
VL - 21
SP - 935
EP - 953
JO - Giornale Italiano di Cardiologia
JF - Giornale Italiano di Cardiologia
SN - 1827-6806
IS - 12
ER -