Neurology, Stroke Unit, IRCCS MultiMedica, Milano, Italy (M. Paciaroni).
Stroke Unit, Division of Cardiovascular Medicine, University of Perugia, Italy (M. Paciaroni, V.C., G.A., M.G.M., M.G., A.A., M.V., L.T., C.U.).
Stroke. 2022 Aug;53(8):2620-2627. doi: 10.1161/STROKEAHA.121.038239. Epub 2022 May 11.
In patients with atrial fibrillation who suffered an ischemic stroke while on treatment with nonvitamin K antagonist oral anticoagulants, rates and determinants of recurrent ischemic events and major bleedings remain uncertain.
This prospective multicenter observational study aimed to estimate the rates of ischemic and bleeding events and their determinants in the follow-up of consecutive patients with atrial fibrillation who suffered an acute cerebrovascular ischemic event while on nonvitamin K antagonist oral anticoagulant treatment. Afterwards, we compared the estimated risks of ischemic and bleeding events between the patients in whom anticoagulant therapy was changed to those who continued the original treatment.
After a mean follow-up time of 15.0±10.9 months, 192 out of 1240 patients (15.5%) had 207 ischemic or bleeding events corresponding to an annual rate of 13.4%. Among the events, 111 were ischemic strokes, 15 systemic embolisms, 24 intracranial bleedings, and 57 major extracranial bleedings. Predictive factors of recurrent ischemic events (strokes and systemic embolisms) included CHADS-VASc score after the index event (odds ratio [OR], 1.2 [95% CI, 1.0-1.3] for each point increase; =0.05) and hypertension (OR, 2.3 [95% CI, 1.0-5.1]; =0.04). Predictive factors of bleeding events (intracranial and major extracranial bleedings) included age (OR, 1.1 [95% CI, 1.0-1.2] for each year increase; =0.002), history of major bleeding (OR, 6.9 [95% CI, 3.4-14.2]; =0.0001) and the concomitant administration of an antiplatelet agent (OR, 2.8 [95% CI, 1.4-5.5]; =0.003). Rates of ischemic and bleeding events were no different in patients who changed or not changed the original nonvitamin K antagonist oral anticoagulants treatment (OR, 1.2 [95% CI, 0.8-1.7]).
Patients suffering a stroke despite being on nonvitamin K antagonist oral anticoagulant therapy are at high risk of recurrent ischemic stroke and bleeding. In these patients, further research is needed to improve secondary prevention by investigating the mechanisms of recurrent ischemic stroke and bleeding.
在接受非维生素 K 拮抗剂口服抗凝剂治疗的房颤患者中,发生缺血性卒中和主要出血的发生率和决定因素仍不确定。
本前瞻性多中心观察性研究旨在评估连续接受非维生素 K 拮抗剂口服抗凝剂治疗的房颤患者发生急性脑血管缺血性事件后的随访中缺血和出血事件的发生率及其决定因素。之后,我们比较了抗凝治疗改变和继续原治疗的患者的缺血和出血事件的估计风险。
平均随访 15.0±10.9 个月后,1240 例患者中有 192 例(15.5%)发生 207 次缺血或出血事件,年发生率为 13.4%。在这些事件中,111 次为缺血性脑卒中,15 次为系统性栓塞,24 次为颅内出血,57 次为主要颅外出血。复发性缺血事件(脑卒中及系统性栓塞)的预测因素包括事件后的 CHADS-VASc 评分(每增加 1 分,比值比 [OR] 1.2[95%可信区间,1.0-1.3];=0.05)和高血压(OR 2.3[95%可信区间,1.0-5.1];=0.04)。出血事件(颅内和主要颅外出血)的预测因素包括年龄(OR,每增加 1 年,1.1[95%可信区间,1.0-1.2];=0.002)、既往大出血史(OR,6.9[95%可信区间,3.4-14.2];=0.0001)和同时使用抗血小板药物(OR,2.8[95%可信区间,1.4-5.5];=0.003)。改变或不改变原非维生素 K 拮抗剂口服抗凝剂治疗的患者缺血和出血事件的发生率无差异(OR,1.2[95%可信区间,0.8-1.7])。
尽管接受了非维生素 K 拮抗剂口服抗凝剂治疗,房颤患者仍有发生缺血性卒中和出血的高风险。在这些患者中,需要进一步研究通过研究复发性缺血性卒中和出血的机制来改善二级预防。