Abstract:Editorial
Às vésperas da reunião do Food and Drug Administration (FDA), que acontecerá neste mês de julho, para avaliar o requerimento para a aprovação pré-comercial nos Estados Unidos da prótese Edwards-SAPIEN TM (Edwards Lifesciences, Irvine, Estados Unidos) para o tratamento percutâneo da estenose aórtica, duas sociedades médicas -American College of Cardiology (ACC) Foundation e Society of Thoracic Surgeons (STS) -publicaram documento de consenso que menciona pontos fundamentais que devem ser observados an… Show more
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