Abstract
From the first quarter of 2014, a new generation of transcatheter valves (Fig. 8.1) has CE mark approval for clinical use in Europe and under scrutiny for FDA approval in the United States. These new valves aim to overcome or to reduce the major limitations of first-generation valves (Edwards XT and CoreValve) as paravalvular leak, vascular complications, cardiac rhythm disturbances, and stroke. We describe below the technical features and the first clinical results of the new transfemoral devices.
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Bedogni, F., Agnifili, M., Testa, L. (2017). Current and Next Generation of Transcatheter Valves. In: Reimers, B., Moussa, I., Pacchioni, A. (eds) Percutaneous Interventions for Structural Heart Disease. Springer, Cham. https://doi.org/10.1007/978-3-319-43757-6_8
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DOI: https://doi.org/10.1007/978-3-319-43757-6_8
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