The Stenting Coronary Arteries in Non-stress/benestent Disease (SCANDSTENT) Trial
Henning Kelbæk, MD*,*,
Leif Thuesen, MD ,
Steffen Helqvist, MD*,
Lene Kløvgaard, RN*,
Erik Jørgensen, MD*,
Samir Aljabbari, MD*,
Kari Saunamäki, MD*,
Lars R. Krusell, MD ,
Gunnar V.H. Jensen, MD ,
Hans E. Bøtker, MD ,
Jens F. Lassen, MD ,
Henning R. Andersen, MD ,
Per Thayssen, MD ,
Anders Galløe, MD||,
Anton van Weert, PhD¶ SCANDSTENT Investigators
* Rigshospitalet, Copenhagen, Denmark
Skejby Sygehus, Skejby, Denmark
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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