Time Course for Benefit and Risk of Clopidogrel and Aspirin After Acute Transient Ischemic Attack and Minor Ischemic Stroke A Secondary Analysis from the POINT Randomized Trial

被引:81
作者
Johnston, S. Claiborne [1 ]
Elm, Jordan J. [2 ]
Easton, J. Donald [3 ]
Farrant, Mary [3 ]
Barsan, William G. [4 ]
Kim, Anthony S. [3 ]
Lindblad, Anne S. [5 ]
Palesch, Yuko Y. [2 ]
Zurita, Karla G. [3 ]
Albers, Gregory W. [6 ]
Cucchiara, Brett L. [7 ]
Kleindorfer, Dawn O. [8 ]
Lutsep, Helmi L. [9 ]
Pearson, Claire [10 ]
Sethi, Pramod [11 ]
Vora, Nirali [6 ]
机构
[1] Univ Texas Austin, Dell Med Sch, Deans Off, Austin, TX 78712 USA
[2] Med Univ South Carolina, Data Coordinat Unit, Dept Publ Hlth Sci, Charleston, SC 29425 USA
[3] Univ Calif San Francisco, Dept Neurol, San Francisco, CA 94143 USA
[4] Univ Michigan, Dept Emergency Med, Ann Arbor, MI 48109 USA
[5] Emmes Corp, Rockville, MD USA
[6] Stanford Univ, Dept Neurol & Neurol Sci, Stanford Stroke Ctr, Palo Alto, CA 94304 USA
[7] Univ Penn, Dept Neurol, Philadelphia, PA 19104 USA
[8] Univ Cincinnati, Coll Med, Dept Neurol & Rehabil Med, Cincinnati, OH 45221 USA
[9] Oregon Hlth & Sci Univ, Dept Neurol, Portland, OR 97201 USA
[10] Wayne State Univ, Sch Med, Dept Emergency Med, Detroit, MI USA
[11] Guilford Neurol Associates, Cone Hlth Comprehens Stroke Ctr, Greensboro, NC USA
基金
美国国家卫生研究院;
关键词
aspirin; clopidogrel; ischemic attack; transient; platelet aggregation inhibitors; stroke; PREVENTION; EFFICACY; TIA;
D O I
10.1161/CIRCULATIONAHA.119.040713
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: In patients with acute minor ischemic stroke or high-risk transient ischemic attack enrolled in the POINT trial (Platelet-Oriented Inhibition in New TIA and Minor Ischemic Stroke [POINT] Trial), the combination of clopidogrel and aspirin for 90 days reduced major ischemic events but increased major hemorrhage in comparison to aspirin alone. Methods: In a secondary analysis of POINT (N=4881), we assessed the time course for benefit and risk from the combination of clopidogrel and aspirin. The primary efficacy outcome was a composite of ischemic stroke, myocardial infarction, or ischemic vascular death. The primary safety outcome was major hemorrhage. Risks and benefits were estimated for delayed times of treatment initiation using left-truncated models. Results: Through 90 days, the rate of major ischemic events was initially high then decreased markedly, whereas the rate of major hemorrhage remained low but relatively constant throughout. With the use of a model-based approach, the optimal change point for major ischemic events was 21 days (0-21 days hazard ratio 0.65 for clopidogrel-aspirin versus aspirin; 95% CI, 0.50-0.85; P=0.0015, in comparison to 22-90 days hazard ratio, 1.38; 95% CI, 0.81-2.35; P=0.24). Models showed benefits of clopidogrel-aspirin for treatment delayed as long as 3 days after symptom onset. Conclusions: The benefit of clopidogrel-aspirin occurs predominantly within the first 21 days, and outweighs the low, but ongoing risk of major hemorrhage. When considered with the results of the CHANCE trial (Clopidogrel in High-Risk Patients With Non-disabling Cerebrovascular Events), a similar trial treating with clopidogrel-aspirin for 21 days and showing no increase in major hemorrhage, these results suggest that limiting clopidogrel-aspirin use to 21 days may maximize benefit and reduce risk after high-risk transient ischemic attack or minor ischemic stroke.
引用
收藏
页码:658 / 664
页数:7
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