Abstract | BACKGROUND: OBJECTIVES: METHODS: RESULTS: In patients with MI/PAD and no prior stroke or transient ischemic attack, vorapaxar reduced first ischemic stroke (hazard ratio [HR]: 0.57, 95% confidence interval [CI]: 0.43 to 0.75; p < 0.001). The risk of hemorrhagic conversion after stroke (HR: 1.19, 95% CI: 0.49 to 2.91; p = 0.70) or death (HR: 1.09, 95% CI: 0.57 to 2.07; p = 0.79) during follow-up was not significantly increased with vorapaxar in patients who had a new ischemic stroke (n = 204). Although hemorrhagic stroke was increased (HR: 2.79, 95% CI: 1.00 to 7.73; p = 0.049), overall stroke was significantly reduced (HR: 0.67, 95% CI: 0.52 to 0.87; p = 0.002). CONCLUSIONS:
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Authors | Marc P Bonaca, Benjamin M Scirica, Eugene Braunwald, Stephen D Wiviott, Shinya Goto, Dennis W Nilsen, Vernon Bonarjee, Sabina A Murphy, David A Morrow |
Journal | Journal of the American College of Cardiology
(J Am Coll Cardiol)
Vol. 64
Issue 22
Pg. 2318-26
(Dec 09 2014)
ISSN: 1558-3597 [Electronic] United States |
PMID | 25465417
(Publication Type: Comparative Study, Journal Article, Multicenter Study, Randomized Controlled Trial, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't)
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Copyright | Copyright © 2014 American College of Cardiology Foundation. Published by Elsevier Inc. All rights reserved. |
Chemical References |
- Lactones
- Pyridines
- Receptors, Thrombin
- vorapaxar
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Topics |
- Aged
- Atherosclerosis
(diagnosis, drug therapy)
- Brain Ischemia
(diagnosis, drug therapy, epidemiology)
- Double-Blind Method
- Female
- Follow-Up Studies
- Humans
- Lactones
(administration & dosage)
- Male
- Middle Aged
- Myocardial Infarction
(diagnosis, drug therapy)
- Pyridines
(administration & dosage)
- Receptors, Thrombin
(antagonists & inhibitors)
- Stroke
(diagnosis, drug therapy, epidemiology)
- Treatment Outcome
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