Early Dual Antiplatelet Therapy in Patients with Acute Minor Stroke Treated with Intravenous Thrombolysis
Author(s) -
Marina Mannino,
Salvatore Cottone
Publication year - 2020
Publication title -
european neurology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.573
H-Index - 77
eISSN - 1421-9913
pISSN - 0014-3022
DOI - 10.1159/000506592
Subject(s) - minor stroke , thrombolysis , medicine , stroke (engine) , acute stroke , anesthesia , fibrinolytic agent , cardiology , tissue plasminogen activator , myocardial infarction , mechanical engineering , stenosis , engineering
Dear Editor, We read the findings of Zhao et al. [1] with great interest. Recently, 2 independent, multicenter, randomized, double-blind, placebo-controlled trials (CHANCE and POINT) have established the efficacy of short-term dual antiplatelet therapy (DAPT) to prevent recurrent ischemic stroke in patients with minor stroke or high-risk TIA[2, 3]. Thus, starting DAPT (aspirin and clopidogrel) within 24 h after symptom onset is recommended by the most recent AHA guidelines [4] in patients presenting with minor noncardioembolic ischemic stroke (National Institutes of Health Stroke Scale [NIHSS] score ≤3) who did not receive intravenous alteplase. (Patients who are candidates for thrombolysis were not represented in these trials, so results cannot be generalized to this group.) Zhao et al. [1] treated 102 patients with aspirin and clopidogrel after intravenous thrombolysis for acute minor ischemic stroke and compared them with 105 patients treated with aspirin. Functional outcome was better in the dual antiplatelet group, without significant difference in terms of symptomatic intracerebral hemorrhage or mortality. However, in this study, minor stroke was defined as a score of ≤5 points on the National Institutes of Health Stroke Scale (NIHSS). About one-third of these patients harbor a large vessel occlusion [5] and potentially develop a medium to large infarction with increased risk of hemorrhagic conversion. Thus, it would be useful to know how many patients in the study had an ischemic lesion on follow-up imaging and the size of the lesions. Further, the half-life of alteplase is nearly 4 min, but its effect on the coagulation system persists much longer. The fibrinolytic activity of alteplase is associated with consumptive coagulopathy with hypofibrinogenemia that may last ≥24 h after completion of the alteplase infusion. Early hypofibrinogenemia (fibrinogen level <200 mg/dL at 2 h after alteplase infusion) occurs in about 20% of the patients after alteplase infusion and is associated with a substantially increased risk of symptomatic intracerebral hemorrhage [6]. In patients with minor stroke treated with intravenous thrombolysis, before starting early DAPT, it would be appropriate to consider the infarct size and exclude alteplase-related coagulopathy.
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