{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,10,12]],"date-time":"2025-10-12T19:55:28Z","timestamp":1760298928008},"reference-count":24,"publisher":"Wiley","issue":"2","license":[{"start":{"date-parts":[[2014,5,26]],"date-time":"2014-05-26T00:00:00Z","timestamp":1401062400000},"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":[[2015,2]]},"abstract":"<jats:sec><jats:title>Objectives<\/jats:title><jats:p>To assess the clinical outcome at 1\u2010year follow\u2010up of real\u2010world patients with long coronary lesions treated with the 38 mm Xience Prime (Abbott Vascular) everolimus\u2010eluting stent (EES).<\/jats:p><\/jats:sec><jats:sec><jats:title>Background<\/jats:title><jats:p>Long\u2010lesions present special challenges to the interventional cardiologists, including increased risk of restenosis, periprocedural injury, geographical miss, and stent deliverability. Indeed, results obtained with shorter stent in the treatment of simpler lesions are of limited applicability to longer stents.<\/jats:p><\/jats:sec><jats:sec><jats:title>Methods<\/jats:title><jats:p>Consecutive patients presenting with a long coronary lesion treated by percutaneous coronary intervention with at least one implanted 38 mm EES were enrolled in the study. Their clinical data were prospectively registered. Major adverse cardiac events (MACE) were defined as a composite of cardiac death, nonfatal myocardial infarction (according to the Universal Definition) and target vessel revascularization. Stent thrombosis was defined according to the Academic Research Consortium criteria.<\/jats:p><\/jats:sec><jats:sec><jats:title>Results<\/jats:title><jats:p>Overall, 203 real\u2010world patients (152 men, 68\u2009\u00b1\u20099 years) were enrolled in the P38 Study. At 1\u2010year follow\u2010up, 6 (3.0%) patients had died from cardiac causes, 7 (3.4%) had a nonfatal myocardial infarction and 8 (3.9%) underwent target vessel revascularization, yielding a 10.3% cumulative rate of MACE. Two patients had a stent thrombosis (one definite and one probable). No significant differences in event rates were found between patients with and without an additional stent implanted overlapping the 38 mm one.<\/jats:p><\/jats:sec><jats:sec><jats:title>Conclusions<\/jats:title><jats:p>The use of a new\u2010generation polymer\u2010based 38 mm EES in a real\u2010world population with unselected long lesions is associated with excellent procedural results and good clinical outcomes at 12\u2010month follow\u2010up. \u00a9 2014 Wiley Periodicals, Inc.<\/jats:p><\/jats:sec>","DOI":"10.1002\/ccd.25542","type":"journal-article","created":{"date-parts":[[2014,5,14]],"date-time":"2014-05-14T09:48:05Z","timestamp":1400060885000},"page":"218-224","source":"Crossref","is-referenced-by-count":9,"title":["One\u2010year follow\u2010up of patients treated with new\u2010generation polymer\u2010based 38 mm everolimus\u2010eluting stent: The P38 study"],"prefix":"10.1002","volume":"85","author":[{"given":"Gregory 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