Title of article :
The unrestricted use of paclitaxel- versus sirolimus-eluting stents for coronary artery disease in an unselected population: One-year results of the Taxus-Stent Evaluated at Rotterdam Cardiology Hospital (T-SEARCH) registry Original Research Article
Author/Authors :
Andrew T.L. Ong، نويسنده , , Patrick W. Serruys، نويسنده , , Jiro Aoki، نويسنده , , Angela Hoye، نويسنده , , Carlos A.G. van Mieghem، نويسنده , , Gaston A. Rodriguez Granillo، نويسنده , , Marco Valgimigli، نويسنده , , Karel Sonnenschein، نويسنده , , Evelyn Regar، نويسنده , , Martin van der Ent، نويسنده , , Peter P.T. de Jaegere، نويسنده , , * Eugene P. McFadden، نويسنده , , Georgios Sianos، نويسنده , , Willem J. van der Giessen، نويسنده , , Pim J. De Feyter، نويسنده , , Ron T. van Domburg، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2005
Pages :
7
From page :
1135
To page :
1141
Abstract :
Objectives We investigated the efficacy of paclitaxel-eluting stents (PES) compared to sirolimus-eluting stents (SES) when used without restriction in unselected patients. Background Both SES and PES have been separately shown to be efficacious when compared to bare stents. In unselected patients, no direct comparison between the two devices has been performed. Methods Paclitaxel-eluting stents have been used as the stent of choice for all percutaneous coronary interventions in the prospective Taxus-Stent Evaluated At Rotterdam Cardiology Hospital (T-SEARCH) registry. A total of 576 consecutive patients with de novo coronary artery disease exclusively treated with PES were compared with 508 patients treated with SES from the Rapamycin-Eluting Stent Evaluated At Rotterdam Cardiology Hospital (RESEARCH) registry. Results The PES patients were more frequently male, more frequently treated for acute myocardial infarction, had longer total stent lengths, and more frequently received glycoprotein IIb/IIIa inhibitors. At one year, the raw cumulative incidence of major adverse cardiac events was 13.9% in the PES group and 10.5% in the SES group (unadjusted hazard ratio [HR] 1.33, 95% confidence interval [CI] 0.95 to 1.88, p = 0.1). Correction for differences in the two groups resulted in an adjusted HR of 1.16 (95% CI 0.81 to 1.64, p = 0.4, using significant univariate variables) and an adjusted HR of 1.20 (95% CI 0.85 to 1.70, p = 0.3, using independent predictors). The one-year cumulative incidence of clinically driven target vessel revascularization was 5.4% versus 3.7%, respectively (HR 1.38, 95% CI 0.79 to 2.43, p = 0.3). Conclusions The universal use of PES in an unrestricted setting is safe and is associated with a similar adjusted outcome compared to SES. The inferior trend in crude outcome seen in PES was due to its higher-risk population. A larger, randomized study enrolling an unselected population may assist in determining the relative superiority of either device.
Keywords :
BMS , myocardial infarction , Research , CK-MB , DES , Confidence interval , Hazard ratio , mace , SES , MI , PES , Sirolimus-eluting stent , Drug-eluting stent , CI , TVR , target vessel revascularization , HR , TIMI , Thrombolysis In Myocardial Infarction , creatine kinase-MB , major adverse cardiac event , paclitaxel-eluting stent , bare-metal stent , Rapamycin-Eluting Stent Evaluated At Rotterdam Cardiology Hospital , T-SEARCH , Taxus-Stent Evaluated At Rotterdam Cardiology Hospital
Journal title :
JACC (Journal of the American College of Cardiology)
Serial Year :
2005
Journal title :
JACC (Journal of the American College of Cardiology)
Record number :
459851
Link To Document :
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