Assessment of Platelet Function in Acute Ischemic Stroke Patients Previously Treated with Aspirin

被引:3
|
作者
Lago, Aida [1 ]
Parkhutik, Vera [1 ]
Ignacio Tembl, Jose [1 ]
Valles, Juana [2 ]
Teresa Santos, Maria [2 ]
Moscardo, Antonio [2 ]
机构
[1] Hosp Univ La Fe, Dept Neurol, Valencia 46026, Spain
[2] Hosp Univ La Fe, Res Ctr, Valencia 46026, Spain
来源
关键词
Antiplatelet; ischemic stroke; aspirin; clopidogrel; ANTIPLATELET THERAPY; SECONDARY PREVENTION; VASCULAR-DISEASE; REACTIVITY; ERYTHROCYTES; NONRESPONDER; ASSOCIATION; CLOPIDOGREL; GUIDELINES; RESISTANCE;
D O I
10.1016/j.jstrokecerebrovasdis.2014.07.007
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Background: Platelet inhibition measured by platelet function tests could be critical to understand the reasons for early recurrence and to guide therapeutic recommendations. We assess the platelet function during the acute phase of ischemic stroke in patients pretreated with aspirin who continue their treatment with aspirin only, are started on clopidogrel only, or add clopidogrel to aspirin. Methods: Sixty-four patients were taking aspirin before the stroke. Depending on the administered antiplatelet, 3 groups were defined: ASA: patients who continued on aspirin orally or intravenous acetylsalicylate of lysine, n = 30; CLO: patients who discontinued aspirin and were started on clopidogrel, n = 16; and ASA + CLO: patients who were prescribed both aspirin and clopidogrel, n = 10. Collagen-induced thromboxane A(2) (TXA(2)) synthesis, ADP (adenosine diphosphate)-induced aggregation, and occlusion time (PF-100) were measured. Results: CLO group only had a marked elevation of TXA(2) (17.44 +/- 15.62 ng/mL, P = .000) and a shortening of the platelet function analyzer (PFA)-100 closure time (157.13 +/- 88 seconds, P = .047) compared with the other 2 groups (ASA: TXA(2), .62 +/- 1.59 ng/mL; ASA + CLO: TXA(2) 1.79 +/- 4.59 ng/mL). They achieved a small (13%) but significant reduction of ADP-induced aggregation (87.00 +/- 23.06 mm, P = .008) compared with the ASA group (102.82 +/- 22.38 seconds). Conclusions: Stopping aspirin intake within the first 72 hours of the acute stroke drastically increases TXA(2) synthesis. During the same time window, the freshly prescribed clopidogrel manages to reduce the ADP-induced aggregation only slightly (13%). This study offers analytic proof that the common practice of replacing aspirin with clopidogrel does not leave stroke patients fully protected during the first days after an ischemic stroke. Possible solutions could be to preserve aspirin during a few days or to use loading doses of clopidogrel at hospital admission.
引用
收藏
页码:2794 / 2799
页数:6
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