Disability After Minor Stroke and Transient Ischemic Attack in the POINT Trial

被引:51
作者
Cucchiara, Brett [1 ]
Elm, Jordan [2 ]
Easton, J. Donald [3 ]
Coutts, Shelagh B. [4 ]
Willey, Joshua Z. [5 ]
Biros, Michelle H. [6 ]
Ross, Michael A. [7 ]
Johnston, S. Claiborne [8 ]
机构
[1] Univ Penn, Dept Neurol, Philadelphia, PA 19104 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 USA
[4] Univ Calgary, Dept Clin Neurosci Radiol & Community Hlth Sci, Hotchkiss Brain Inst, Calgary, AB, Canada
[5] Columbia Univ, Dept Neurol, New York, NY USA
[6] Univ Minnesota, Emergency Med, Minneapolis, MN USA
[7] Emory Univ, Dept Neurol, Atlanta, GA 30322 USA
[8] Univ Texas Austin, Emergency Med Deans Off, Dell Med Sch, Austin, TX 78712 USA
基金
美国国家卫生研究院;
关键词
aspirin; diabetes mellitus; humans; ischemic attack; transient; stroke; ASPIRIN; SEVERITY; RISK;
D O I
10.1161/STROKEAHA.119.027465
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background and Purpose-While combination aspirin and clopidogrel reduces recurrent stroke compared with aspirin alone in patients with transient ischemic attack (TIA) or minor stroke, the effect on disability is uncertain. Methods-The POINT trial (Platelet-Oriented Inhibition in New TIA and Minor Ischemic Stroke) randomized patients with TIA or minor stroke (National Institutes of Health Stroke Scale score <= 3) within 12 hours of onset to dual antiplatelet therapy (DAPT) with aspirin plus clopidogrel versus aspirin alone. The primary outcome measure was a composite of stroke, myocardial infarction, or vascular death. We performed a post hoc exploratory analysis to examine the effect of treatment on overall disability (defined as modified Rankin Scale score >1) at 90 days, as well as disability ascribed by the local investigator to index or recurrent stroke. We also evaluated predictors of disability. Results-At 90 days, 188 of 1964 (9.6%) of patients enrolled with TIA and 471 of 2586 (18.2%) of those enrolled with stroke were disabled. Overall disability was similar between patients assigned DAPT versus aspirin alone (14.7% versus 14.3%; odds ratio, 0.97 [95% CI, 0.82-1.14]; P=0.69). However, there were numerically fewer patients with disability in conjunction with a primary outcome event in the DAPT arm (3.0% versus 4.0%; odds ratio, 0.73 [95% CI, 0.53-1.01]; P=0.06) and significantly fewer patients in the DAPT arm with disability attributed by the investigators to either the index event or recurrent stroke (5.9% versus 7.4%; odds ratio, 0.78 [95% CI, 0.62-0.99]; P=0.04). Notably, disability attributed to the index event accounted for the majority of this difference (4.5% versus 6.0%; odds ratio, 0.74 [95% CI, 0.57-0.96]; P=0.02). In multivariate analysis, age, subsequent ischemic stroke, serious adverse events, and major bleeding were significantly associated with disability in TIA; for those with stroke, female sex, hypertension, or diabetes mellitus, National Institutes of Health Stroke Scale score, recurrent ischemic stroke, subsequent myocardial infarction, and serious adverse events were associated with disability. Conclusions-In addition to reducing recurrent stroke in patients with acute minor stroke and TIA, DAPT might reduce stroke-related disability.
引用
收藏
页码:792 / 799
页数:8
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