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华法林治疗心房颤动患者的国际标准化比值控制与后续临床结局。

International normalized ratio control and subsequent clinical outcomes in patients with atrial fibrillation using warfarin.

机构信息

Duke Clinical Research Institute, Durham, NC, 27705, USA.

Uppsala Clinical Research Center, Department of Medical Sciences, Cardiology, Uppsala University, Uppsala, Sweden.

出版信息

J Thromb Thrombolysis. 2019 Jul;48(1):27-34. doi: 10.1007/s11239-019-01858-1.

DOI:10.1007/s11239-019-01858-1
PMID:30972712
Abstract

We explored associations between INR measures and clinical outcomes in patients with AF using warfarin, and whether INR history predicted future INR measurements. We included patients in ARISTOTLE who were randomized to and received warfarin. Among patients who had events, we included those with ≥ 3 INR values in the 180 days prior to the event, with the most recent ≤ 60 days prior to the event, who were on warfarin at the time of event (n = 545). Non-event patients were included in the control group if they had ≥ 180 days of warfarin exposure with ≥ 3 INR measurements (n = 7259). The median (25th, 75th) number of INR values per patient was 29 (21, 38) over a median follow-up of 1.8 years. A total of 87% had at least one INR value < 1.5; 49% had at least one value > 4.0. The last INRs before events (median 14 [24, 7] days) were < 3.0 for at least 75% of patients with major bleeding and > 2.0 for half of patients with ischemic stroke. Historic time in therapeutic range (TTR) was weakly associated with future TTR (R = 0.212). Historic TTR ≥ 80% had limited predictive ability to discriminate future TTR ≥ 80% (C index 0.61). In patients with AF receiving warfarin, most bleeding events may not have been preventable despite careful INR control. Our findings suggest that INRs collected through routine management are not sufficiently predictive to provide reassurance about future time in therapeutic range or to prevent subsequent outcomes, and might be over-interpreted in clinical practice.

摘要

我们使用华法林研究了房颤患者 INR 指标与临床结局之间的关系,以及 INR 历史是否可以预测未来的 INR 测量值。我们纳入了 ARISTOTLE 研究中接受华法林治疗的随机分组患者。对于发生事件的患者,纳入了在事件发生前 180 天内有≥3 次 INR 值,且最近一次 INR 值在事件发生前 60 天内,在事件发生时正在服用华法林的患者(n=545)。非事件患者纳入对照组的标准为有≥180 天的华法林暴露史和≥3 次 INR 测量值(n=7259)。在中位 1.8 年的随访期间,每位患者的 INR 值中位数(25 分位数,75 分位数)为 29(21,38)。共有 87%的患者至少有一次 INR 值<1.5;49%的患者至少有一次 INR 值>4.0。事件前最后一次 INR 值(中位数 14[24,7]天),大出血患者中至少 75%的 INR 值<3.0,缺血性卒中患者中一半患者的 INR 值>2.0。既往治疗范围内时间(TTR)与未来 TTR 呈弱相关(R=0.212)。既往 TTR≥80%对预测未来 TTR≥80%的能力有限(C 指数 0.61)。在接受华法林治疗的房颤患者中,尽管 INR 控制仔细,大多数出血事件可能仍无法预防。我们的研究结果表明,通过常规管理收集的 INR 并不能充分预测未来的治疗范围内时间或预防后续结局,并且在临床实践中可能被过度解释。

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Time in the Therapeutic Range for Patients Taking Warfarin in Clinical Trials: Useful, but Also Misleading, Misused, and Overinterpreted.临床试验中服用华法林患者处于治疗范围内的时间:有用,但也具有误导性、被滥用且被过度解读。
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