{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,10,30]],"date-time":"2025-10-30T22:20:46Z","timestamp":1761862846278},"reference-count":29,"publisher":"Wiley","issue":"1","license":[{"start":{"date-parts":[[2009,6,23]],"date-time":"2009-06-23T00:00:00Z","timestamp":1245715200000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Cathet Cardio Intervent"],"published-print":{"date-parts":[[2010,1]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:sec><jats:title>Objectives:<\/jats:title><jats:p>This study was designed to compare long\u2010term clinical outcomes of drug\u2010eluting stents (DES) versus bare metal stents (BMS) in patients with saphenous vein graft (SVG) disease in the \u201creal world.\u201d<\/jats:p><\/jats:sec><jats:sec><jats:title>Background:<\/jats:title><jats:p>The safety and efficacy of DES versus BMS in SVG remains uncertain due to contradictory reports of either lower revascularization rates with DES; or clinical equivalence to BMS; or even an excess of clinical events associated with DES use.<\/jats:p><\/jats:sec><jats:sec><jats:title>Methods:<\/jats:title><jats:p>We identified consecutive patients who underwent stent placement within a de novo SVG lesion between May 1, 2003 and July 31, 2007. Follow\u2010up was obtained at regular intervals. The Kaplan\u2013Meier method was used to produce actuarial survival estimates. Cox regression analysis was used to predict the risk associated with stent type, and propensity scores were generated to risk\u2010adjust the results.<\/jats:p><\/jats:sec><jats:sec><jats:title>Results:<\/jats:title><jats:p>The study group included 379 stent recipients (284 DES; 95 BMS) with 410 stented lesions. BMS were placed more frequently in current smokers, acute myocardial infarctions, larger vessels, and longer lesions. In\u2010hospital mortality was higher in BMS recipients than in their DES counterparts (3.2% vs. 0, respectively; <jats:italic>P<\/jats:italic> = 0.015). At 3 years, there was no significant difference in clinical adverse event rates between DES and BMS recipients, even after risk adjustment.<\/jats:p><\/jats:sec><jats:sec><jats:title>Conclusions:<\/jats:title><jats:p>Three\u2010year adverse event rates are similar among patients treated with DES or BMS in SVG lesions. Therefore, while DES are safe, they do not appear to offer an advantage in terms of long\u2010term graft patency. \u00a9 2009 Wiley\u2010Liss, Inc.<\/jats:p><\/jats:sec>","DOI":"10.1002\/ccd.22194","type":"journal-article","created":{"date-parts":[[2009,6,23]],"date-time":"2009-06-23T21:25:03Z","timestamp":1245792303000},"page":"93-100","source":"Crossref","is-referenced-by-count":20,"title":["Long\u2010term outcomes of drug\u2010eluting stents versus bare\u2010metal stents in saphenous vein graft disease: Results from the Prairie \u201cReal World\u201d Stent Registry"],"prefix":"10.1002","volume":"75","author":[{"given":"Nilesh 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