Your browser doesn't support javascript.
Show: 20 | 50 | 100
Results 1 - 3 de 3
Filter
1.
Eur Heart J ; 42(11): 1053-1056, 2021 03 14.
Article in English | MEDLINE | ID: covidwho-1472268
2.
Medicina (Kaunas) ; 57(4)2021 Mar 25.
Article in English | MEDLINE | ID: covidwho-1241288

ABSTRACT

The prediction and prevention of sudden cardiac death is the philosopher's stone of clinical cardiac electrophysiology. Sports can act as triggers of fatal arrhythmias and therefore it is essential to promptly frame the athlete at risk and to carefully evaluate the suitability for both competitive and recreational sports activity. A history of syncope or palpitations, the presence of premature ventricular complexes or more complex arrhythmias, a reduced left ventricular systolic function, or the presence of known or familiar heart disease should prompt a thorough evaluation with second level examinations. In this regard, cardiac magnetic resonance and electrophysiological study play important roles in the diagnostic work-up. The role of genetics is increasing both in cardiomyopathies and in channelopathies, and a careful evaluation must be focused on genotype positive/phenotype negative subjects. In addition to being a trigger for fatal arrhythmias in certain cardiomyopathies, sports also play a role in the progression of the disease itself, especially in the case arrhythmogenic right ventricular cardiomyopathy. In this paper, we review the latest European guidelines on sport cardiology in patients with cardiovascular diseases, focusing on arrhythmic risk stratification and the management of cardiomyopathies and channelopathies.


Subject(s)
Cardiology , Cardiomyopathies , Cardiovascular Diseases , Channelopathies , Sports , Cardiomyopathies/complications , Channelopathies/complications , Channelopathies/genetics , Humans
3.
Orphanet J Rare Dis ; 15(1): 157, 2020 06 22.
Article in English | MEDLINE | ID: covidwho-610299

ABSTRACT

Inherited heart disease represent a very heterogenous group of cardiac disorders, characterized by inherited, acquired, and often rare disorders affecting the heart muscle (cardiomyopathies) or the cardiac electrical system (ion channel disease). They are often familial diseases, and are among the leading cause of juvenile sudden death and heart failure. The aim of this paper is to give a perspective on how to run a clinical service during an epidemic or pandemic emergency and to describe the potential COVID-19 associated risks for patients affected by inherited heart diseases.


Subject(s)
Betacoronavirus , Cardiomyopathies/complications , Cardiomyopathies/genetics , Channelopathies/complications , Channelopathies/genetics , Coronavirus Infections/complications , Pneumonia, Viral/complications , COVID-19 , Coronavirus Infections/epidemiology , Coronavirus Infections/prevention & control , Genetic Predisposition to Disease , Humans , Outpatient Clinics, Hospital/organization & administration , Pandemics/prevention & control , Pneumonia, Viral/epidemiology , Pneumonia, Viral/prevention & control , Rare Diseases/complications , Risk Factors , SARS-CoV-2 , Telemedicine/organization & administration
SELECTION OF CITATIONS
SEARCH DETAIL