首页> 外文期刊>Seminars in Thrombosis and Hemostasis >Nonvitamin K Antagonist Oral Anticoagulants Use in Patients with Atrial Fibrillation and Bioprosthetic Heart Valves/Prior Surgical Valve Repair: A Multicenter Clinical Practice Experience
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Nonvitamin K Antagonist Oral Anticoagulants Use in Patients with Atrial Fibrillation and Bioprosthetic Heart Valves/Prior Surgical Valve Repair: A Multicenter Clinical Practice Experience

机译:非viTamin K拮抗剂口腔抗凝剂用于心房颤动和生物假体心脏瓣膜/先前外科瓣膜修复的患者:多中心临床实践经验

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摘要

This is an observational study to investigate the efficacy and safety of nonvitamin K antagonist oral anticoagulants (NOACs) in atrial fibrillation (AF) patients with bioprosthetic valves or prior surgical valve repair in clinical practice. A total of 122 patients (mean age: 74.1 +/- 13.2; 54 females) with bioprosthetic heart valve or surgical valve repair and AF treated with NOACs were included in the analysis. The mean CHA (2) DS (2) -VASc (Congestive heart failure, Hypertension, Age 75 years, Diabetes mellitus, prior Stroke or transient ischemic attack, Vascular disease) and HAS-BLED (Hypertension, Abnormal renal and liver function, Stroke, Bleeding, Labile INR [international normalized ratio], Elderly, Drugs or alcohol) score values were 3.6 +/- 1.2 and 2.6 +/- 1.4, respectively. Of the total study population, 28.6% was taking apixaban 5mg twice daily (BID), 24.5% apixaban 2.5mg BID, 18% dabigatran 150mg BID, 13% dabigatran 110mg BID, 9.8% rivaroxaban 20mg daily (QD), and 5.7% rivaroxaban 15mg QD. Also, 92% of the study population previously had warfarin replaced with NOACs due to lack compliance and labile INR control (time in therapeutic range60%). NOAC therapy for AF was started on average 934 +/- 567 days after bioprosthetic heart valve implantation or surgical repair for an average duration of 835 +/- 203 days. The study population included 24 (19.6%) patients with bioprosthetic mitral valve, 52 (43%) patients with bioprosthetic aortic valve, 41 (33.6%) patients with previous surgical mitral repair, 5 (4%) patients with previous surgical aortic repair, and concomitant use of NOACs. All patients were evaluated for thromboembolic events (ischemic stroke, transient ischemic attack, systemic embolism) as well as major bleeding events during the follow-up period. In our study population, we recorded a low mean annual incidence of thromboembolism (0.8%) and major bleeding (1.3%). According to our data, anticoagulation therapy with NOACs seems to be an effective and a safe treatment strategy for nonvalvular AF patients with bioprosthetic valves or prior surgical valve repair.
机译:这是一种观察性研究,以研究非富特敏素K拮抗剂口腔抗凝血剂(NOAC)在心房颤动(AF)的生物假瓣或先前手术瓣膜修复患者中的非禽素K拮抗剂口腔抗凝血剂(NOAC)的疗效和安全性。分析中,共有122名患者(平均年龄:74.1 +/- 13.2; 54雌性),分析中包括巨大术治疗。平均CHA(2)DS(2)-VASC(充血性心力衰竭,高血压,年龄& 75岁,糖尿病,前卒中或短暂性缺血性发作,血管疾病)和血液疾病(高血压,异常肾和肝功能,中风,出血,不稳定的INR [国际标准化比率],老年人,药物或酒精)得分值分别为3.6 +/- 1.2和2.6 +/- 1.4。在总研究人群中,28.6%正在服用每日两次(BID),24.5%Apixaban 2.5mg BID,18%Dabigatran 150mg BID,13%Dabigatran 110mg BID,9.8%Rivaroxaban 20mg Daily(QD),5.7%Rivaroxaban和5.7%Rivaroxaban 15mg QD。此外,由于缺乏符合和不稳定的INR控制(治疗范围的时间& 60%),92%的研究人群以前用Noacs取代了Noacs。在生物假心心脏瓣膜植入或手术修复后,平均止血患者的2934 +/- 567天,平均持续时间为835 +/- 203天。研究人群包括24例(19.6%)的生物假体二尖瓣患者,52例(43%)生物假体主动脉瓣,41名(33.6%)患者以前的外科二尖瓣修复,5例(4%)患者以前的外科主动脉修复,并伴随着Noacs。在随访期间评估所有患者对血栓栓塞事件(缺血性脑卒中,短暂性缺血性发作,全身栓塞)以及主要出血事件。在我们的研究人口中,我们记录了血栓栓塞的低于平均年发病率(0.8%)和重大出血(1.3%)。根据我们的数据,Noacs的抗凝治疗似乎是一种有效的和安全的非血管瓣膜患者或先前手术瓣膜修复的安全处理策略。

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