Our mission is to become a worldwide reference for education in the field for all professionals involved in the process to disseminate knowledge & skills of Acute Cardiovascular Care.
Our mission is to promote excellence in clinical diagnosis, research, technical development, and education in cardiovascular imaging in Europe.
Our mission is to promote excellence in research, practice, education and policy in cardiovascular health, primary and secondary prevention.
Our mission is to reduce the burden of cardiovascular disease through percutaneous cardiovascular interventions.
Improving the quality of life and reducing sudden cardiac death by limiting the impact of heart rhythm disturbances.
Our mission is to improve quality of life and longevity, through better prevention, diagnosis and treatment of heart failure, including the establishment of networks for its management, education and research.
The ESC Working Groups' goal is to stimulate and disseminate scientific knowledge in different fields of cardiology.
The ESC Councils' goal is to share knowledge among medical professionals practicing in specific cardiology domains.
Munich, Germany, Sunday 31 August 2008: Sudden Cardiac Death (SCD) is a major contributor to mortality in industrialized nations, affecting ~500,000 individuals annually in the Western World, and causing more deaths than AIDS, lung and breast cancer and stroke together.
Frequently, autopsy becomes the principal diagnostic tool when macro and microscopic analyses provide a conclusive diagnosis in cardiomyopathies. However, on average one third of autopsies do not identify a pathologically defined cause of death and these deaths are classified as "natural" or arrhythmogenic. In the athlete, the most common causes of sudden cardiac death are of inherited origin. This represents a tremendous burden to families, community and health care.There has been considerable progress in the understanding of these genetic components thanks to research in familial forms of sudden death. Because these inherited diseases may remain undetected by conventional clinical investigations, genetic testing has been recently added to the clinical tools, improving significantly the detection of those individuals at risk. With that new information the physician, the proband and his family members can make an informed decision regarding their care and in the case of athletes, regarding continuation of competitive training.While genetic technology has become essential to the diagnosis and subsequent prevention strategies in carriers with borderline or abnormal phenotypes, the use of this technology to guide clinical decisions in asymptomatic genetic carriers with normal phenotype is not without controversy. These diseases have a low penetrance, indicating that only a small percentage of individuals with the genetic defect will develop the clinical features of the disease. Though to the physician genetic data are compelling evidence of having a risk for the development of the disease, and in several instances they tend to be overly aggressive with therapies. Genetic technology is useful to identify those at risk and those spared, but the clinical decisions have to be based on the clinical parametres and not solely on genetic testing.
This press release accompanies both a presentation and an ESC press conference given at the ESC Congress 2008. Written by the investigator himself/herself, this press release does not necessarily reflect the opinion of the European Society of Cardiology.
Our mission: To reduce the burden of cardiovascular disease
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