[Comparison of therapy adherence in patients suffering from atrial fibrillation treated with direct oral anticoagulants based on data from years 2015-2018].

IF 0.8 4区 医学 Q3 MEDICINE, GENERAL & INTERNAL
Gábor Simonyi, András Paksy, Mihály Medvegy, Kristína Gencsiová, Erzsébet Evelyn Sipos, Gergő Csitári, Roland Gasparics, Ervin Finta
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引用次数: 0

Abstract

Introduction: Direct oral anticoagulants are playing a significant role in the treatment of non-valvular atrial fibrillation for stroke prevention. Previous studies have demonstrated that adherence to direct anticoagulant therapy is better than that of vitamin K antagonists, however, it remains suboptimal. Objective: The authors aimed to examine the persistence of direct anticoagulant therapy in patients with atrial fibrillation by analyzing the National Health Insurance Fund Administration database. Method: We analyzed data from patients receiving direct anticoagulant therapy between 2015 and 2018 using the database of the National Health Insurance Fund Administration. The study considered both newly treated patients and those previously receiving direct anticoagulant therapy. Patients’ medication refills were tracked for 14 months, and persistence changes were evaluated using Kaplan–Meier analysis. The average duration of drug intake and its 95% confidence interval were determined for each active substance. Results: The one-year persistence of newly initiated direct anticoagulant therapy was 63.4% on average, while it was 71.1% among previously treated patients. The one-year average persistence was 7.7 percentage points higher in previously treated patients compared to those newly initiated on direct anticoagulant therapy. This advantage was +4.9 percentage points for apixaban, +9.5 percentage points for dabigatran, and +9.4 percentage points for rivaroxaban. The best one-year persistence in both groups was observed in 2017 (65.7% and 72.5%, respectively). Among newly treated patients, the average persistence rates were 61.5% for apixaban, 57.7% for dabigatran, and 62.9% for rivaroxaban. In previously treated patients, the one-year average persistence rates were 66.4% for apixaban, 67.4% for dabigatran, and 72.3% for rivaroxaban. The mean duration of drug intake over a 360-day period was 299 days for new patients and 322 days for previously treated patients. Conclusion: Differences were observed in one-year persistence among the various direct anticoagulants. However, in general, therapy adherence to direct anticoagulants has increased since 2016. Nonetheless, significant efforts are required to further improve persistence rates. Orv Hetil. 2025; 166(21): 808–816.

[2015-2018年直接口服抗凝药物治疗心房颤动患者治疗依从性的比较]。
前言:直接口服抗凝剂在治疗非瓣膜性房颤预防脑卒中中发挥着重要作用。先前的研究表明,直接抗凝治疗的依从性优于维生素K拮抗剂,然而,它仍然不是最佳的。目的:通过分析国家健康保险基金管理局的数据库,了解房颤患者直接抗凝治疗的持续性。方法:使用国家健康保险基金管理局数据库,对2015年至2018年接受直接抗凝治疗的患者数据进行分析。该研究考虑了新治疗的患者和先前接受直接抗凝治疗的患者。随访患者用药14个月,使用Kaplan-Meier分析评估持续性变化。测定每一种活性物质的平均服药时间及其95%置信区间。结果:新开始直接抗凝治疗的患者1年平均坚持率为63.4%,而以前接受过直接抗凝治疗的患者平均坚持率为71.1%。与新开始直接抗凝治疗的患者相比,先前接受治疗的患者一年平均持续时间高出7.7个百分点。阿哌沙班为+4.9个百分点,达比加群为+9.5个百分点,利伐沙班为+9.4个百分点。两组患者的最佳一年持久性均在2017年(分别为65.7%和72.5%)。在新治疗的患者中,阿哌沙班的平均持续率为61.5%,达比加群为57.7%,利伐沙班为62.9%。在先前接受治疗的患者中,阿哌沙班的一年平均持续率为66.4%,达比加群为67.4%,利伐沙班为72.3%。在360天的时间内,新患者的平均服药时间为299天,先前接受治疗的患者为322天。结论:不同直接抗凝剂的1年持久性存在差异。然而,总体而言,自2016年以来,直接抗凝药物的治疗依从性有所增加。尽管如此,仍需要作出重大努力来进一步提高持久性。Orv Hetil. 2025;166(21): 808 - 816。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Orvosi hetilap
Orvosi hetilap MEDICINE, GENERAL & INTERNAL-
CiteScore
1.20
自引率
50.00%
发文量
274
期刊介绍: The journal publishes original and review papers in the fields of experimental and clinical medicine. It covers epidemiology, diagnostics, therapy and the prevention of human diseases as well as papers of medical history. Orvosi Hetilap is the oldest, still in-print, Hungarian publication and also the one-and-only weekly published scientific journal in Hungary. The strategy of the journal is based on the Curatorium of the Lajos Markusovszky Foundation and on the National and International Editorial Board. The 150 year-old journal is part of the Hungarian Cultural Heritage.
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