心房颤动患者治疗范围内的华法林和直接口服抗凝药:全国队列研究。

Annals of medicine Pub Date : 2024-12-01 Epub Date: 2024-06-14 DOI:10.1080/07853890.2024.2364825
Mika Lehto, Alex Luojus, Olli Halminen, Jari Haukka, Jukka Putaala, Miika Linna, Pirjo Mustonen, Janne Kinnunen, Ossi Lehtonen, Konsta Teppo, Paula Tiili, Elis Kouki, Saga Itäinen-Strömberg, Mikko Niemi, Aapo L Aro, Juha Hartikainen, K E Juhani Airaksinen
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引用次数: 0

摘要

背景:与直接口服抗凝药(DOACs)相比,人们对心房颤动(AF)患者个人治疗范围内时间(TTR)如何影响华法林治疗的有效性和安全性知之甚少:比较标准剂量 DOAC 与华法林对房颤患者的有效性和安全性,同时根据患者的 TTR 将接受华法林治疗的患者分为四等分:我们在全国范围内开展了一项研究,研究对象包括 2011 年至 2018 年间芬兰所有新发房颤患者。使用Cox回归分析和逆治疗概率加权法计算危险比(HR),以评估阿哌沙班(n = 12,426)、达比加群(n = 4545)、利伐沙班(n = 12,950)和华法林(n = 43,548)使用者发生缺血性卒中(IS)、颅内出血(ICH)和死亡的风险:华法林使用者的中位TTR为72%。与TTR第二好的四分位数(参考值)相比,TTR最差的两个四分位数的IS风险较高,TTR最好的四分位数和服用利伐沙班的IS风险较低[2.35(95%置信区间,1.85-2.85)、1.44(1.18-1.75)、0.60(0.47-0.77)和0.72(0.56-0.92)]。阿哌沙班和达比加群则差异不显著。与参照组相比,两个TTR最差组的ICH HR分别为6.38(4.88-8.35)和1.87(1.41-2.49),利伐沙班为1.44(1.02-1.93),TTR最佳组为0.58(0.40-0.85)。两个TTR最差组的死亡率较高,而TTR最佳组的死亡率最低:结论:在TTR最低的两个四分位数中,有一半的患者接受了华法林治疗,其结果并不令人满意。高TTR组与标准剂量DOAC之间没有差异或差异不大。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Time-in-therapeutic-range defined warfarin and direct oral anticoagulants in atrial fibrillation: a Nationwide Cohort Study.

Background: Little is known how individual time-in-therapeutic-range (TTR) impacts the effectiveness and safety of warfarin therapy compared to direct oral anticoagulants (DOACs) in patients with atrial fibrillation (AF).

Objective: To compare the effectiveness and safety of standard dose DOACs to warfarin in patients with AF, while categorizing warfarin treated patients into quartiles based on their individual TTR.

Materials and methods: We conducted a nationwide study including all patients with new-onset AF between 2011 and 2018 in Finland. Hazard ratios (HR) were calculated using Cox regression analysis with the inverse probability of treatment weighted method to assess the risks of ischaemic stroke (IS), intracranial haemorrhage (ICH) and mortality for users of apixaban (n = 12,426), dabigatran (n = 4545), rivaroxaban (n = 12,950) and warfarin (n = 43,548).

Results: The median TTR for warfarin users was 72%. Compared to the second best TTR quartile (reference), the risk of IS was higher in the two poorest TTR quartiles, and lower in the best TTR quartile and on rivaroxaban [2.35 (95% confidence interval, 1.85-2.85), 1.44 (1.18-1.75), 0.60 (0.47-0.77) and 0.72 (0.56-0.92)]. These differences were non-significant for apixaban and dabigatran. HR of ICH was 6.38 (4.88-8.35) and 1.87 (1.41-2.49) in the two poorest TTR groups, 1.44 (1.02-1.93) on rivaroxaban, and 0.58 (0.40-0.85) in the best TTR group compared to the reference group. Mortality was higher in the two poorest TTR groups and lowest in the best TTR group.

Conclusions: The outcome was unsatisfactory in the two lowest TTR quartiles - in half of the patients treated with warfarin. The differences between the high TTR groups and standard dose DOACs were absent or modest.

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