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J Am Coll Cardiol, 2004; 44:1363-1367, doi:10.1016/j.jacc.2004.03.084
© 2004 by the American College of Cardiology Foundation
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Actinomycin-eluting stent for coronary revascularization

A randomized feasibility and safety study: The ACTION trial

Patrick W. Serruys, MD, PhD, FACC*,*, John A. Ormiston, MD{dagger}, Georgios Sianos, MD, PhD*, J. Eduardo Sousa, MD{ddagger}, Eberhard Grube, MD§, Peter den Heijer, MD||, Pim de Feyter, MD*, Pawel Buszman, MD, Albert Schömig, MD#, Jean Marco, MD**, Lech Polonski, MD, Leif Thuesen, MD{dagger}{dagger}, Andreas M. Zeiher, MD{ddagger}{ddagger}, J.H. Nicholas Bett, MD§§, Maarten J. Suttorp, MD||||, Helmut D. Glogar, MD¶¶, Mark Pitney, MD##, Gerard T. Wilkins, MD***, Robert Whitbourn, MD{dagger}{dagger}{dagger}, Susan Veldhof, RN{ddagger}{ddagger}{ddagger}, Karine Miquel, PhD{ddagger}{ddagger}{ddagger}, Rachel Johnson, BA{ddagger}{ddagger}{ddagger}, Leslie Coleman, DVM{ddagger}{ddagger}{ddagger}, Renu Virmani, PhD§§§ ACTION Investigators

* Erasmus Medical Center, Rotterdam, The Netherlands
{dagger} Green Lane Hospital, Auckland, Australia
{ddagger} Instituto Dante Pazzanese de Cardiologia, Sao Paulo, Brazil
§ Krankenhaus Siegburg, Siegburg, Germany
|| Amphia Ziekenhuis, Breda, The Netherlands
Silesian Heart Disease Center, Katowice, Poland
# Deutsches Herzzentrum München, Munich, Germany
** Clinique Pasteur, Toulouse, France
{dagger}{dagger} Skejby Syghus, Aarhus, Denmark
{ddagger}{ddagger} Klinikum de J. W. Goethe Universität, Frankfurt, Germany
§§ Prince Charles Hospital, Chermside, Australia
|||| Sint Antonius Ziekenhuis, Nieuwegein, The Netherlands
¶¶ Allgemeines Krankenhaus de Stadt Wien, Vienna, Austria
## Prince of Wales Hospital, Sydney, Australia
*** Dunedin Hospital, Dunedin, New Zealand
{dagger}{dagger}{dagger} St. Vincent's Hospital, Melbourne, Australia
{ddagger}{ddagger}{ddagger} Guidant Corporation, Diegim, Belgium
§§§ Armed Forces Institute of Pathology, Washington, DC



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Figure 1 Kaplan-Meier estimates of survival free of repeated target site revascularization up to 365 days among patients who received actinomycin-eluting 2.5 and 10 µg/cm2 stents and those who received the metallic stent. The rate of event-free survival was significantly higher in the control stent group than in the actinomycin stent groups (p < 0.05 by both the Wilcoxon and log-rank tests). Solid circles = control (n = 104); open circles = drug-coated, 2.5 µg/cm2 drug-eluting stent (n = 120); squares = drug-coated, 10 µg/cm2 drug-eluting stent (n = 119).

 





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