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6.2. Five-year clinical follow-up of a randomized comparison of a polymer-free sirolimuseluting<br />
stent versus a polymer-based paclitaxel-eluting stent in patients with diabetes<br />
mellitus (LIPSIA Yukon trial).<br />
Stiermaier T, Heinz A, Schloma D, Kleinertz K, Dänschel W, Erbs S, Linke Axel, Boudriot E, Lauer B,<br />
Schuler G, Thiele H, Desch S.<br />
Source<br />
Department of Internal Medicine - Cardiology, University of Leipzig - Heart Center, Leipzig, Germany.<br />
Abstract<br />
OBJECTIVES:<br />
The long-term performance of polymer-free stent systems in patients with diabetes mellitus has not<br />
been investigated extensively. This study reports long-term results of the LIPSIA Yukon trial which<br />
compared the polymer-free sirolimus-eluting Yukon Choice stent with the polymer-based paclitaxeleluting<br />
Taxus Liberté stent in this subpopulation. At 9 months, the Yukon Choice stent failed to show<br />
non-inferiority in terms of the primary end point late lumen loss, while no significant difference in<br />
clinical outcome was detected.<br />
METHODS AND RESULTS:<br />
The LIPSIA Yukon trial randomized 240 patients with diabetes mellitus to a polymer-free sirolimus<br />
eluting stent (Yukon Choice, Translumina) versus a polymer-based paclitaxel-eluting stent (Taxus<br />
Liberté, Boston Scientific). Clinical follow-up was conducted with a standardized telephone follow-up<br />
and all events were centrally adjudicated. Follow-up was available for 98.3% of patients after a<br />
median of 5.0 years. The incidence of all-cause death (16.9% versus 14.0%, P = 0.67), respectively<br />
definite or presumed cardiovascular death (7.6% versus 8.8%, P = 0.94) were similar in the Yukon<br />
Choice and the Taxus Liberté group. There were no significant differences in the rates of myocardial<br />
infarction (9.3% versus 7.9%, P = 0.88), definite stent thrombosis (0.8% versus 0.9%, P = 1.0),<br />
target lesion revascularization (15.3% versus 15.8%, P = 1.0), target vessel revascularization (18.6%<br />
versus 23.7%, P = 0.44), non-target vessel revascularization (18.6% versus 26.3%, P = 0.21), and<br />
stroke (3.4% versus 4.4%, P = 0.96) between patients assigned to the Yukon Choice and the Taxus<br />
Liberté stent.<br />
CONCLUSION:<br />
At 5 years of follow-up, clinical outcome was similar between the polymer-free sirolimus-eluting Yukon<br />
Choice stent and the polymer-based paclitaxel-eluting Taxus Liberté stent. © 2013 Wiley Periodicals,<br />
Inc.<br />
Copyright © 2013 Wiley Periodicals, Inc.<br />
KEYWORDS:<br />
coronary artery disease, drug-eluting stent, paclitaxel, polymer-free, sirolimus<br />
PMID:<br />
23873579<br />
[PubMed - as supplied by publisher]<br />
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