Causes of late mortality with dual antiplatelet therapy after coronary stents

التفاصيل البيبلوغرافية
العنوان: Causes of late mortality with dual antiplatelet therapy after coronary stents
المؤلفون: Stephan Windecker, Joseph M. Massaro, Sammy Elmariah, Laura Mauri, Eugene Braunwald, Dean J. Kereiakes, Stephen D. Wiviott, Robert W. Yeh, Ralph B. D'Agostino, David J. Cohen, Donald E. Cutlip, P. Gabriel Steg
المصدر: Mauri, Laura; Elmariah, Sammy; Yeh, Robert W; Cutlip, Donald E; Steg, P Gabriel; Windecker, Stephan; Wiviott, Stephen D; Cohen, David J; Massaro, Joseph M; D'Agostino, Ralph B; Braunwald, Eugene; Kereiakes, Dean J (2016). Causes of late mortality with dual antiplatelet therapy after coronary stents. European Heart Journal, 37(4), pp. 378-385. Oxford University Press 10.1093/eurheartj/ehv614 <http://dx.doi.org/10.1093/eurheartj/ehv614Test>
بيانات النشر: Oxford University Press, 2016.
سنة النشر: 2016
مصطلحات موضوعية: Male, medicine.medical_specialty, Ticlopidine, Thienopyridine, Pyridines, medicine.medical_treatment, Myocardial Infarction, Hemorrhage, 610 Medicine & health, Placebo, Percutaneous Coronary Intervention, Clinical Research, Cause of Death, Neoplasms, Humans, Medicine, Cause of death, Cancer Death Rate, Aspirin, business.industry, Mortality rate, Percutaneous coronary intervention, Drug-Eluting Stents, Middle Aged, Surgery, Treatment Outcome, Platelet aggregation inhibitor, Drug Therapy, Combination, Female, Cardiology and Cardiovascular Medicine, business, Platelet Aggregation Inhibitors, medicine.drug
الوصف: Aims In the dual antiplatelet therapy (DAPT) study, continued thienopyridine beyond 12 months after drug-eluting stent placement was associated with increased mortality compared with placebo. We sought to evaluate factors related to mortality in randomized patients receiving either drug-eluting or bare metal stents in the DAPT study. Methods and results Patients were enrolled after coronary stenting, given thienopyridine and aspirin for 12 months, randomly assigned to continued thienopyridine or placebo for an additional 18 months (while taking aspirin), and subsequently treated with aspirin alone for another 3 months. A blinded independent adjudication committee evaluated deaths. Among 11 648 randomized patients, rates of all-cause mortality rates were 1.9 vs. 1.5% (continued thienopyridine vs. placebo, P = 0.07), cardiovascular mortality, 1.0 vs. 1.0% ( P = 0.97), and non-cardiovascular mortality, 0.9 vs. 0.5% ( P = 0.01) over the randomized period (Months 12–30). Rates of fatal bleeding were 0.2 vs. 0.1% ( P = 0.81), and deaths related to any prior bleeding were 0.3 vs. 0.2% ( P = 0.36), Months 12–33). Cancer incidence did not differ (2.0 vs. 1.6%, P = 0.12). Cancer-related deaths occurred in 0.6 vs. 0.3% ( P = 0.02) and were rarely related to bleeding (0.1 vs. 0, P = 0.25). After excluding those occurring in patients with cancer diagnosed before enrolment, rates were 0.4 vs. 0.3% ( P = 0.16). Conclusion Bleeding accounted for a minority of deaths among patients treated with continued thienopyridine. Cancer-related death in association with thienopyridine therapy was mainly not related to bleeding and may be a chance finding. Caution is warranted when considering extended thienopyridine in patients with advanced cancer. Trial Registration clinicaltrials.gov Identifier: [NCT00977938][1]. [1]: /lookup/external-ref?link_type=CLINTRIALGOV&access_num=NCT00977938&atom=%2Fehj%2F37%2F4%2F378.atom
وصف الملف: application/pdf
اللغة: English
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1683e555eb3df139f51d0fc028b593c3Test
https://boris.unibe.ch/75897/1/378.full.pdfTest
حقوق: OPEN
رقم الانضمام: edsair.doi.dedup.....1683e555eb3df139f51d0fc028b593c3
قاعدة البيانات: OpenAIRE