Comparison of Everolimus-Eluting and Sirolimus-Eluting Coronary Stents: 1-Year Outcomes from the Randomized Evaluation of Sirolimus-Eluting Versus Everolimus-Eluting Stent Trial (RESET)

Several recent randomized trials comparing everolimus-eluting stent (EES) and sirolimus-eluting stent (SES) reported similar outcomes. However, only 1 trial was powered for a clinical end point, and no trial was powered for evaluating target-lesion revascularization. Randomized Evaluation of Sirolim...

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Veröffentlicht in:Circulation (New York, N.Y.) N.Y.), 2012-09, Vol.126 (10), p.1225-1236
Hauptverfasser: KIMURA, Takeshi, MORIMOTO, Takeshi, NISHIKAWA, Hideo, YAMAMOTO, Yoshito, NAKAGAWA, Yoshihisa, HAYASHI, Yasuhiko, IWABUCHI, Masashi, UMEDA, Hisashi, KAWAI, Kazuya, OKADA, Hisayuki, KIMURA, Kazuo, SIMONTON, Charles A, NATSUAKI, Masahiro, KOZUMA, Ken, SHIOMI, Hiroki, IGARASHI, Keiichi, KADOTA, Kazushige, TANABE, Kengo, MORINO, Yoshihiro, AKASAKA, Takashi, TAKATSU, Yoshiki
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Sprache:eng
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Zusammenfassung:Several recent randomized trials comparing everolimus-eluting stent (EES) and sirolimus-eluting stent (SES) reported similar outcomes. However, only 1 trial was powered for a clinical end point, and no trial was powered for evaluating target-lesion revascularization. Randomized Evaluation of Sirolimus-eluting versus Everolimus-eluting stent Trial is a prospective multicenter randomized open-label trial comparing EES with SES in Japan. The trial was powered for evaluating noninferiority of EES relative to SES in terms of target-lesion revascularization. From February and July 2010, 3197 patients were randomly assigned to receive either EES (1597 patients) or SES (1600 patients). At 1 year, the primary efficacy end point of target-lesion revascularization occurred in 65 patients (4.3%) in the EES group and in 76 patients (5.0%) in the SES group, demonstrating noninferiority of EES to SES (P(noninferiority)
ISSN:0009-7322
1524-4539
DOI:10.1161/circulationaha.112.104059