2006
DOI: 10.1016/j.ahj.2006.04.012
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Evaluation of prasugrel compared with clopidogrel in patients with acute coronary syndromes: design and rationale for the TRial to assess Improvement in Therapeutic Outcomes by optimizing platelet InhibitioN with prasugrel Thrombolysis In Myocardial Infarction 38 (TRITON-TIMI 38)

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Cited by 297 publications
(222 citation statements)
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“…Inclusion and exclusion criteria for the main trial have previously been published in detail. 24 Briefly, subjects were eligible for enrollment if they had moderate-to high-risk unstable angina (UA/NSTEMI), after medical treatment for ST-segment elevation MI (STEMI) with coronary anatomy known to be suitable for PCI, or before cardiac catheterization with planned primary PCI for STEMI. Key exclusion criteria included increased risk of bleeding and any thienopyridine within 5 days before enrollment.…”
Section: Study Populationmentioning
confidence: 99%
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“…Inclusion and exclusion criteria for the main trial have previously been published in detail. 24 Briefly, subjects were eligible for enrollment if they had moderate-to high-risk unstable angina (UA/NSTEMI), after medical treatment for ST-segment elevation MI (STEMI) with coronary anatomy known to be suitable for PCI, or before cardiac catheterization with planned primary PCI for STEMI. Key exclusion criteria included increased risk of bleeding and any thienopyridine within 5 days before enrollment.…”
Section: Study Populationmentioning
confidence: 99%
“…25,26 The key safety end point was noncoronary artery bypass grafting (CABG)-related TIMI major bleeding; secondary analysis was of non-CABG-related TIMI major or minor bleeding as previously defined. 24 Net clinical benefit was defined as the composite of all-cause mortality, nonfatal MI, nonfatal stroke, or nonfatal TIMI major bleeding not related to CABG. 18 Efficacy event rates are calculated from intention-to-treat analyses, and safety analyses are based on the safety cohort.…”
Section: End Pointsmentioning
confidence: 99%
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“…Prasugrel has the advantage of more efficient and consistent active metabolite production compared to clopidogrel and therefore achieves higher mean levels of inhibition of platelet aggregation with less variability [24]. However, prasugrel also possesses the limitation of delayed recovery of platelet reactivity following cessation, which can lead to increased rates of major bleeding in patients managed with CABG surgery [25].…”
Section: Unmet Need In Antiplatelet Therapymentioning
confidence: 99%
“…In STEMI patients, an initial delay in the onset of newer P2Y12 antiplatelet action was observed and ticagrelor did not appear superior to prasugrel [3]. However, patients with Cardiogenic Shock (CS) or after Cardio Pulmonary Resuscitation (CPR) were mostly excluded from randomized studies and data on the clinical efficacy of these drugs comparing to clopidogrel in these patients is sparse [11][12][13].CS has a profound effect on drug absorption and metabolism due to the disturbance of microcirculation, the use of catecholamines and opioids which results in slower platelet inhibition [13][14][15]. The pharmacological properties of the newer P2Y12 are promising in a CS setting since their bioactivation is more rapid and consistent when compared to clopidogrel [2,13].…”
mentioning
confidence: 99%