Colonna Paolo, Ammirati Fabrizio
U.O. Cardiologia Ospedaliera, Azienda Ospedaliero-Universitaria Consorziale Policlinico, Bari.
U.O. Cardiologia, Ospedale G.B. Grassi, Ostia (RM).
G Ital Cardiol (Rome). 2016 Nov;17(11):932-939. doi: 10.1714/2498.26202.
Atrial fibrillation-related stroke prevention with anticoagulant drugs is currently evolving towards the introduction into clinical practice of the new oral anticoagulants, including rivaroxaban. Our aim was to evaluate in a real-life setting the characteristics and management of patients with nonvalvular atrial fibrillation to whom Italian doctors decided to prescribe rivaroxaban.
Between January and February 2014, a group of 95 physicians collected aggregate retrospective data, through an online questionnaire, on 1127 patients with nonvalvular atrial fibrillation receiving rivaroxaban. Descriptive statistics were performed based on the data collected.
Mean age of patients was 76 years; 20% of patients suffered a previous transient ischemic attack and 16% a previous stroke; 16% was anemic or at risk of bleeding. Over 40% of patients was unable to have a good control of the previous antithrombotic therapy, 22% was also taking antiplatelet drugs or nonsteroidal anti-inflammatory drugs, and 85% had been on a previous stroke prevention therapy; among the latter the main causes for switching to rivaroxaban were patient choice (30%), problems in maintaining the prothromin time-international normalized ratio (PT-INR) within the therapeutic range (27%), and logistic problems in attending the PT-INR follow-up visits (20%). Rivaroxaban was prescribed at a dosage of 15 mg in 37.8% of patients and 20 mg in 62.2%; the 15 mg dose was prescribed to 264 of 354 patients with creatinine clearance <50 ml/h (74.6%) and in older patients with more comorbidities.
In this real-life analysis, patient characteristics were similar to those of patients enrolled in large randomized trials, whereas differences in dose prescriptions were observed.
使用抗凝药物预防房颤相关性卒中目前正朝着将包括利伐沙班在内的新型口服抗凝药引入临床实践的方向发展。我们的目的是在实际临床环境中评估意大利医生决定为非瓣膜性房颤患者处方利伐沙班时这些患者的特征及治疗情况。
在2014年1月至2月期间,一组95名医生通过在线问卷收集了1127例接受利伐沙班治疗的非瓣膜性房颤患者的汇总回顾性数据。基于收集到的数据进行描述性统计分析。
患者的平均年龄为76岁;20%的患者曾有过短暂性脑缺血发作,16%的患者曾发生过卒中;16%的患者贫血或有出血风险。超过40%的患者此前无法很好地控制抗栓治疗,22%的患者同时服用抗血小板药物或非甾体类抗炎药,85%的患者此前接受过卒中预防治疗;在后者中,改用利伐沙班的主要原因是患者选择(30%)、难以将凝血酶原时间国际标准化比值(PT-INR)维持在治疗范围内(27%)以及进行PT-INR随访存在后勤问题(20%)。37.8%的患者服用利伐沙班的剂量为15mg,62.2%的患者为20mg;15mg剂量用于354例肌酐清除率<50ml/h的患者中的264例(74.6%)以及合并症更多的老年患者。
在这项实际临床分析中,患者特征与大型随机试验中纳入的患者相似,但在剂量处方方面存在差异。