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Sökning: WFRF:(Fowkes F. Gerry R.) > Ticagrelor versus C...

Ticagrelor versus Clopidogrel in Symptomatic Peripheral Artery Disease

Hiatt, William R (författare)
University of Colorado
Fowkes, F Gerry R (författare)
University of Edinburgh
Heizer, Gretchen (författare)
Duke University
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Berger, Jeffrey S (författare)
New York University
Baumgartner, Iris (författare)
University of Bern
Held, Peter (författare)
AstraZeneca, Sweden
Katona, Brian G (författare)
AstraZeneca, US
Mahaffey, Kenneth W (författare)
Stanford University
Norgren, Lars (författare)
Örebro University
Jones, W Schuyler (författare)
Duke University
Blomster, Juuso (författare)
Millegård, Marcus (författare)
Reist, Craig (författare)
Patel, Manesh R (författare)
Gottsäter, Anders (creator_code:cre_t)
Lund University,Lunds universitet,Internmedicin - epidemiologi,Forskargrupper vid Lunds universitet,Internal Medicine - Epidemiology,Lund University Research Groups
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 (creator_code:org_t)
 
2017
2017
Engelska.
Ingår i: The New England journal of medicine. - 0028-4793 .- 1533-4406. ; 376, s. 32-40
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • BACKGROUND: Peripheral artery disease is considered to be a manifestation of systemic atherosclerosis with associated adverse cardiovascular and limb events. Data from previous trials have suggested that patients receiving clopidogrel monotherapy had a lower risk of cardiovascular events than those receiving aspirin. We wanted to compare clopidogrel with ticagrelor, a potent antiplatelet agent, in patients with peripheral artery disease.METHODS: In this double-blind, event-driven trial, we randomly assigned 13,885 patients with symptomatic peripheral artery disease to receive monotherapy with ticagrelor (90 mg twice daily) or clopidogrel (75 mg once daily). Patients were eligible if they had an ankle-brachial index (ABI) of 0.80 or less or had undergone previous revascularization of the lower limbs. The primary efficacy end point was a composite of adjudicated cardiovascular death, myocardial infarction, or ischemic stroke. The primary safety end point was major bleeding. The median follow-up was 30 months.RESULTS: The median age of the patients was 66 years, and 72% were men; 43% were enrolled on the basis of the ABI and 57% on the basis of previous revascularization. The mean baseline ABI in all patients was 0.71, 76.6% of the patients had claudication, and 4.6% had critical limb ischemia. The primary efficacy end point occurred in 751 of 6930 patients (10.8%) receiving ticagrelor and in 740 of 6955 (10.6%) receiving clopidogrel (hazard ratio, 1.02; 95% confidence interval [CI], 0.92 to 1.13; P=0.65). In each group, acute limb ischemia occurred in 1.7% of the patients (hazard ratio, 1.03; 95% CI, 0.79 to 1.33; P=0.85) and major bleeding in 1.6% (hazard ratio, 1.10; 95% CI, 0.84 to 1.43; P=0.49).CONCLUSIONS: In patients with symptomatic peripheral artery disease, ticagrelor was not shown to be superior to clopidogrel for the reduction of cardiovascular events. Major bleeding occurred at similar rates among the patients in the two trial groups. (Funded by AstraZeneca; EUCLID ClinicalTrials.gov number, NCT01732822 .).

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Kardiologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Cardiac and Cardiovascular Systems (hsv//eng)

Nyckelord

Adenosine/adverse effects
Aged
Cardiovascular Diseases/mortality
Clopidogrel
Double-Blind Method
Female
Hemorrhage/chemically induced
Humans
Intermittent Claudication/drug therapy
Ischemia/drug therapy
Kaplan-Meier Estimate
Leg/blood supply
Male
Middle Aged
Peripheral Arterial Disease/drug therapy
Platelet Aggregation Inhibitors/adverse effects
Purinergic P2Y Receptor Antagonists/therapeutic use
Ticagrelor
Ticlopidine/adverse effects

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