Basit öğe kaydını göster

dc.contributor.authorKohli, Payal
dc.contributor.authorWallentin, Lars
dc.contributor.authorReyes, Eric
dc.contributor.authorHorrow, Jay
dc.contributor.authorHusted, Steen
dc.contributor.authorAngiolillo, Dominick J.
dc.contributor.authorArdissino, Diego
dc.contributor.authorMaurer, Gerald
dc.contributor.authorMorais, Joao
dc.contributor.authorNicolau, Jose C.
dc.contributor.authorOto, Ali
dc.contributor.authorStorey, Robert F.
dc.contributor.authorJames, Stefan K.
dc.contributor.authorCannon, Christopher P.
dc.date.accessioned2019-12-10T11:23:46Z
dc.date.available2019-12-10T11:23:46Z
dc.date.issued2013
dc.identifier.issn0009-7322
dc.identifier.urihttps://doi.org/10.1161/CIRCULATIONAHA.112.124248
dc.identifier.urihttp://hdl.handle.net/11655/15593
dc.description.abstractBackground-We sought to evaluate the effect of potent platelet inhibition after acute coronary syndrome on total (ie, first and recurrent) occurrences of any of the primary outcome events (eg, cardiovascular death, myocardial infarction, and stroke) as well as on other ischemic events, such as urgent revascularization, (severe) recurrent ischemia, transient ischemic attacks, and arterial thrombotic events. Methods and Results-In the PLATelet inhibition and patient Outcomes (PLATO) study, 18 624 patients presenting with acute coronary syndromes randomly received ticagrelor (n=9333) or clopidogrel (n=9291). Cox proportional hazard models were used to calculate time to first event and hazard ratios. Total events were compared using a Poisson regression model, and time to second event or death was calculated with the Wei Lin Weissfeld method. Patients randomized to ticagrelor had 1057 total primary end point events versus 1225 for patients on clopidogrel (rate ratio, 0.86; 95% confidence interval, 0.79-0.93; P=0.003). The number of additional events was numerically lower for ticagrelor (189 versus 205; P=0.40), resulting in a hazard for time to second event/death of 0.80 (95% confidence interval, 0.70-0.90; P<0.001) and a number needed to treat of 54. For cardiovascular death/myocardial infarction/stroke/(severe) recurrent ischemia/transient ischemic attack/arterial thrombotic events, total events were fewer with ticagrelor (2030 versus 2290; rate ratio, 0.88; 95% confidence interval, 0.82-0.95; P<0.001), with fewer recurrent events with ticagrelor (740 versus 834; P=0.01) and a highly significant concurrent reduction in hazard for time to second event or death of 0.83 (95% confidence interval, 0.75-0.91; P<0.001). Recurrent PLATO major or Thrombolysis in Myocardial Infarction (TIMI) major non-coronary artery bypass graft bleeding events were infrequent and not different between the two therapies (P=0.96 and 0.38, respectively). Conclusions-In PLATO, treatment with ticagrelor compared with clopidogrel resulted in a reduction in total events, including first and subsequent recurrent cardiovascular events, when compared with clopidogrel. These types of analyses demonstrate an even greater absolute benefit of ticagrelor over clopidogrel than previously reported.
dc.language.isoen
dc.publisherLippincott Williams & Wilkins
dc.relation.isversionof10.1161/CIRCULATIONAHA.112.124248
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectCardiovascular System & Cardiology
dc.titleReduction in First and Recurrent Cardiovascular Events with Ticagrelor Compared with Clopidogrel in the Plato Study
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion
dc.relation.journalCirculation
dc.contributor.departmentKardiyoloji
dc.identifier.volume127
dc.identifier.issue6
dc.identifier.startpage673
dc.identifier.endpage+
dc.description.indexWoS
dc.description.indexScopus


Bu öğenin dosyaları:

Bu öğe aşağıdaki koleksiyon(lar)da görünmektedir.

Basit öğe kaydını göster