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      Safety and Effectiveness of Coronary Intravascular Lithotripsy for Treatment of Severely Calcified Coronary Stenoses : The Disrupt CAD II Study

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          Abstract

          The feasibility of intravascular lithotripsy (IVL) for modification of severe coronary artery calcification (CAC) was demonstrated in the Disrupt CAD I study (Disrupt Coronary Artery Disease). We next sought to confirm the safety and effectiveness of IVL for these lesions.

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          Most cited references26

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          2011 ACCF/AHA/SCAI Guideline for Percutaneous Coronary Intervention: a report of the American College of Cardiology Foundation/American Heart Association Task Force on Practice Guidelines and the Society for Cardiovascular Angiography and Interventions.

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            High-speed rotational atherectomy before paclitaxel-eluting stent implantation in complex calcified coronary lesions: the randomized ROTAXUS (Rotational Atherectomy Prior to Taxus Stent Treatment for Complex Native Coronary Artery Disease) trial.

            This study sought to determine the effect of rotational atherectomy (RA) on drug-eluting stent (DES) effectiveness.
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              Mechanisms of stent thrombosis analysed by optical coherence tomography: insights from the national PESTO French registry.

              Angiography has limited value for identifying the causes of stent thrombosis (ST). We studied a large cohort of patients by optical coherence tomography (OCT) to explore ST characteristics and mechanisms.
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                Author and article information

                Journal
                Circulation: Cardiovascular Interventions
                Circ: Cardiovascular Interventions
                Ovid Technologies (Wolters Kluwer Health)
                1941-7640
                1941-7632
                October 2019
                October 2019
                : 12
                : 10
                Affiliations
                [1 ]St. Francis Hospital, Roslyn, NY (Z.A.A.).
                [2 ]NewYork-Presbyterian Hospital, Columbia University (Z.A.A., A.M.).
                [3 ]Clinical Trials Center, Cardiovascular Research Foundation, New York, NY (Z.A.A., G.W.S., A.C., M. Matsumura, A.M.).
                [4 ]Department of Cardiology, University of Giessen, Frankfurt, Germany (H.N.).
                [5 ]Hospital Clínico San Carlos IDISSC, Complutense University of Madrid, Spain (J.E.).
                [6 ]Krankenhaus der Barmherzigen Brüder Trier, Germany (N.W.).
                [7 ]Department of Cardiology, Oxford University Hospitals, United Kingdom (A.P.B.).
                [8 ]King’s College Hospital, London, United Kingdom (J.M.H.).
                [9 ]Department of Cardiology, Cardiovascular Research Centre, OLV Hospital, Aalst, Belgium (B.D.B.).
                [10 ]San Raffaele Hospital, Milan, Italy (M. Montorfano).
                [11 ]Institut Cardiovasculaire Paris Sud, Hôpital Privé Jacques Cartier, Générale de Santé, Massy, France (T.L.).
                [12 ]The Zena and Michael A. Wiener Cardiovascular Institute, Icahn School of Medicine at Mount Sinai, New York, NY (G.W.S.).
                [13 ]Yale University Medical Center, New Haven, CT (A.J.L.).
                [14 ]Clinique Pasteur, Toulouse, France (J.F.).
                [15 ]Structural Interventional Cardiology, Careggi University Hospital, Florence, Italy (C.D.M.).
                Article
                10.1161/CIRCINTERVENTIONS.119.008434
                31553205
                41406ce3-9417-420e-a178-2fdd34d95345
                © 2019
                History

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