دانلود رایگان مقاله لاتین آسپرین از سایت الزویر


عنوان فارسی مقاله:

یک ارزیابی مجدد انتقادی از آسپرین برای پیشگیری ثانویه در بیماران مبتلا به بیماری های ایسکمیک قلب


عنوان انگلیسی مقاله:

A critical reappraisal of aspirin for secondary prevention in patients with ischemic heart disease


سال انتشار : 2016



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بخشی از مقاله انگلیسی :


Accepting that aspirin was a proven therapy for secondary prevention and acknowledging its relatively weak antiplatelet effect—the advent of adenosine diphosphate (ADP)—receptor blocking agents led to the investigation of the capacity to improve patient's outcomes through increased platelet inhibition with more potent agents or with the addition of a second antiplatelet agent on top of baseline aspirin. The Clopidogrel versus Aspirin in Patients at Risk of Ischaemic Events (CAPRIE) trial enrolled 19,195 stable patients with prior stroke (n = 12,083), MI (n = 11,630), or peripheral arterial disease (n = 11,592) to ASA 325 mg or clopidogrel 75 mg daily for approximately 2 years.13 The aspirin arm had a 5.83%/y event rate for the combined end point of vascular death, MI, or ischemic stroke. Clopidogrel monotherapy was associated with a modest reduction in the combined end point (5.32%/y) with a relative risk reduction of 8.7% (95% CI 0.3-16.5, P = .043) with no major differences in terms of safety. Aspirin in fact had numerically increased rates of severe bleeding (1.55% vs 1.38%, not significant), severe intracranial hemorrhage (0.43% vs 0.31%, not significant), and gastrointestinal hemorrhage (any 2.66% vs 1.99% [P b .05] and severe 0.71% vs 0.49% [P b .05]) over a mean duration of follow-up of 1.9 years.13,14 In patients with an acute stroke or transient ischemic attack (n = 13,199), ticagrelor monotherapy (180-mg loading dose followed by 90 mg twice daily) has recently been compared with aspirin monotherapy (300-mg loading dose followed by 100 mg daily) for 90 days.15 Ticagrelor was associated with a nonsignificant reduction in the combined end point of 90 day stroke, MI, or death (ticagrelor 6.7% vs clopidogrel 7.5%; hazard ratio [HR[ 0.87, 95% CI 0.76-1.01). Major bleeding occurred in 0.5% of ticagrelor-treated patients and in 0.6% of aspirin-treated patients with intracranial hemorrhage in 0.2% and 0.3% and fatal bleeding in 0.1% and 0.1%. Although this study was not in patients with established coronary artery disease, it demonstrates a similar safety profile of ticagrelor monotherapy to aspirin monotherapy despite ticagrelor's enhanced potency.



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