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J Am Coll Cardiol, 2006; 47:449-455, doi:10.1016/j.jacc.2005.10.045 (Published online 13 December 2005).
© 2006 by the American College of Cardiology Foundation
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The Stenting Coronary Arteries in Non-stress/benestent Disease (SCANDSTENT) Trial

Henning Kelbæk, MD*,*, Leif Thuesen, MD{dagger}, Steffen Helqvist, MD*, Lene Kløvgaard, RN*, Erik Jørgensen, MD*, Samir Aljabbari, MD*, Kari Saunamäki, MD*, Lars R. Krusell, MD{dagger}, Gunnar V.H. Jensen, MD{ddagger}, Hans E. Bøtker, MD{dagger}, Jens F. Lassen, MD{dagger}, Henning R. Andersen, MD{dagger}, Per Thayssen, MD§, Anders Galløe, MD||, Anton van Weert, PhD for the SCANDSTENT Investigators

* Rigshospitalet, Copenhagen, Denmark
{dagger} Skejby Sygehus, Skejby, Denmark
{ddagger} Roskilde Amtssygehus, Roskilde, Denmark
§ Odense Universitets hospital, Odense, Denmark
|| Gentofte Amtssygehus, Gentofte, Denmark
Heart Core, Leiden, the Netherlands



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  		Figure 1 Cumulative frequency of the minimal lumen diameter before (pre), immediately after (post), and six months after (follow-up) stent implantation in patients who received sirolimus-eluting and bare-metal stents.

 


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  		Figure 2 Kaplan-Meier estimates of event-free survival among patients who received sirolimus-eluting and bare-metal stents.

 


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  		Figure 3 Subgroup analysis for the six-month rate of target lesion revascularization. CI = confidence interval; CX = circumflex; LAD = left anterior descending; RCA = right coronary artery.

 




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Copyright © 2006 by the American College of Cardiology Foundation.