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 in Europe through percutaneous cardiovascular interventions.
Our mission is to improve the quality of life of the population by reducing the impact of cardiac rhythm disturbances and reduce sudden cardiac death.
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 practising in specific cardiology domains.
OUR MISSION: TO REDUCE THE BURDEN OF CARDIOVASCULAR DISEASE
Prof. Antoine Lafont,
In 2006, the issue of safety of DES was deeply questioned, with reports on over-mortality and very late DES thrombosis. This has led to a huge work in order to find common definitions of DES thrombosis in order to compare stents, and evaluate clinical trials and registries.
Virmani showed the occurrence of thrombosis in arteries in which healing did not occur (struts in the lumen) more than one year after deployment. She insisted on the thrombosis protection by neointimal hyperplasia, advocating for some late loss. Basically less than 50% of the DES were reendothelialised after more than 40 months whereas BMS were endothelialised at 6 months. She showed occurrence of atherogenesis within DES. She underlined the DES thrombosis when used during STEMI. Pocock defined the rules of methodology regarding safety, efficacy, and use of meta analysis. Clinical endpoints must not be replaced by surrogate end points and major adverse events must distinguish hard (acute MI, death) from soft (revascularisation, restenosis) endpoints. Lefevre showed several trials about to be published without confirmation regarding overmortality with DES. In particular the SCAAR trial did not confirm the overmortality with any DES. Late thrombosis occurs, but the amplitude of the threat is not confirmed at this stage. Simoons gives strong recommendations on behalf of the ESC in order to avoid misunderstanding of the delivered message. Basically, he blames errors in misinterpretation, misuse of the raw data, leading to contradictory metaanalysis even published by prestigious journals which increases the lack of guidance. All data should be available for an independent academic analysis.
Safety of Drug-eluting-stents: 1 year after Barcelona
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