房颤患者长期坚持和坚持服用非维生素K口服抗凝剂及其与卒中风险的关系

Joris J Komen, Eibert R Heerdink, Olaf H Klungel, Aukje K Mantel-Teeuwisse, Tomas Forslund, Björn Wettermark, Paul Hjemdahl
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引用次数: 30

摘要

目的:关于非维生素K口服抗凝剂(NOAC)治疗依从性和持久性的研究依赖于NOAC早期可用性的数据。我们的目的是研究NOACs的长期依从性和持久性及其与卒中风险的关系。方法和结果:从斯德哥尔摩医疗保健数据库中,我们纳入了2011年7月至2018年10月期间首次服用NOAC处方的21 028例房颤患者,其中1000多例患者随访时间超过5年(中位数:2.0,四分位数间距:1.0-3.2)。坚持率,定义为在90天间隔内继续要求NOAC处方,在随访结束时下降到70%。然而,85%的患者在研究结束时因再启动而接受了治疗。依从性,以持续服用者3个月和6个月的药物持有率(MPR)计算,保持稳定在90%,75%的患者在整个研究期间的MPR >95%。采用病例对照设计,我们计算了持久性和依从性与中风风险的关联,并对潜在的混杂因素进行了调整。结果是缺血性或未明确的中风和短暂性缺血性发作的综合结果。不坚持治疗和依从性差均与卒中风险增加相关[非坚持治疗调整优势比(aOR): 2.05;95%置信区间(CI): 1.49 ~ 2.82, MPR aOR降低1%:1.03;置信区间:1.01—-1.05)。非持续性或不良依从性与伪造终点之间没有关联;分数和呼吸道感染,表明没有“健康粘附”效果。结论:坚持率随时间缓慢下降,但坚持患者的坚持率较高。不坚持和依从性差都与卒中风险增加有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Long-term persistence and adherence with non-vitamin K oral anticoagulants in patients with atrial fibrillation and their associations with stroke risk.

Long-term persistence and adherence with non-vitamin K oral anticoagulants in patients with atrial fibrillation and their associations with stroke risk.

Long-term persistence and adherence with non-vitamin K oral anticoagulants in patients with atrial fibrillation and their associations with stroke risk.

Long-term persistence and adherence with non-vitamin K oral anticoagulants in patients with atrial fibrillation and their associations with stroke risk.

Aims: Studies on adherence and persistence with non-vitamin K oral anticoagulant (NOAC) treatment have relied on data from the early years of NOAC availability. We aimed to study long-term adherence and persistence with NOACs and their association with stroke risk.

Methods and results: From the Stockholm Healthcare database, we included 21 028 atrial fibrillation patients claiming a first NOAC prescription from July 2011 until October 2018, with more than 1000 patients having more than 5 years of follow-up (median: 2.0, interquartile range: 1.0-3.2). Persistence rates, defined as continuing to claim NOAC prescriptions within a 90-day gap, decreased to 70% at the end of follow-up. However, 85% of the patients were treated at the end of the study due to reinitiations. Adherence, calculated as medication possession rate (MPR) in 3 and 6-month intervals among persistent users, remained stable at 90%, with 75% of patients having an MPR >95% throughout the study period. Using a case-control design, we calculated associations of persistence and adherence with stroke risk, adjusting for potential confounders. The outcome was a composite of ischaemic or unspecified stroke and transient ischaemic attack. Non-persistence and poor adherence were both associated with increased stroke risk [non-persistence adjusted odds ratio (aOR): 2.05; 95% confidence interval (CI): 1.49-2.82, 1% reduction MPR aOR: 1.03; CI: 1.01-1.05]. There was no association between non-persistence or poor adherence and the falsification endpoints; fractions and respiratory infections, indicating no 'healthy-adherer' effect.

Conclusion: Persistence rates decreased slowly over time, but persistent patients had high adherence rates. Both non-persistence and poor adherence were associated with an increased stroke risk.

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