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Rundbrief - IBO-Verein

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Rundbrief - IBO-Verein

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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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