根据心房颤动患者的肾功能确定口服抗凝剂的疗效和安全性。

IF 5.3 1区 医学 Q1 CARDIAC & CARDIOVASCULAR SYSTEMS
Casper Binding, Paul Blanche, Gregory Y H Lip, Anne-Lise Kamper, Christina J Y Lee, Laila Staerk, Gunnar Gislason, Christian Torp-Pedersen, Jonas Bjerring Olesen, Anders Nissen Bonde
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引用次数: 0

摘要

背景和目的:肾功能严重减退的患者被排除在随机对照试验之外,根据肾功能评价直接口服抗凝药(DOACs)的安全性和有效性的数据仍然很少。该研究旨在评估不同肾功能亚组 DOAC 的安全性和有效性:利用丹麦全国范围内的多个登记册和实验室数据库,我们纳入了开始服用口服抗凝药(OACs)的心房颤动患者和肌酐水平可用的患者,并对患者进行了为期 2 年的随访,以评估中风/血栓栓塞症(TE)和大出血的发生率:在纳入的 26,686 名患者中,3667 人(13.7%)的估计肾小球滤过率(eGFR)为 30-49 mL/min/1.73m2,596 人(2.2%)的 eGFR 低于 30 mL/min/1.73m2。我们没有发现证据表明 OACs 之间在卒中/TE 风险方面存在差异(所有 OACs 的交互值均大于 0.05)。与 VKA 相比,阿哌沙班的 2 年大出血风险较低(风险比为 0.79,95% 置信区间 (CI)为 0.67-0.93),肾功能减退患者的风险差异明显更大(p 值交互作用为 0.018)。在 eGFR 为 30-49 mL/min/1.73m2 的患者中,利伐沙班的出血风险高于阿哌沙班(风险比为 1.78,95%CI 为 1.32-2.39):总体而言,我们没有发现中风/TE 风险方面的差异,但与 VKA 相比,阿哌沙班的大出血相对风险降低了 21%。如果在 eGFR 为 15-30 mL/min/1.73m2 的患者中比较阿哌沙班和利伐沙班,以及在 eGFR 为 30-49 mL/min/1.73m2 的患者中比较阿哌沙班和达比加群及利伐沙班,这种风险降低幅度更大。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Efficacy and safety of oral anticoagulants according to kidney function among patients with atrial fibrillation.

Background and aims: Patients with severely reduced kidney function have been excluded from randomized controlled trials and data on the safety and efficacy of direct oral anticoagulants (DOACs) according to kidney function remain sparse. The aim was to evaluate the safety and efficacy of the DOACs across subgroups of kidney function.

Methods: Using multiple Danish nationwide registers and laboratory databases, we included patients initiated on oral anticoagulants (OACs) with atrial fibrillation and available creatinine level and followed patients for 2 years to evaluate occurrence of stroke/thromboembolism (TE) and major bleeding.

Results: Among 26 686 included patients, 3667 (13.7%) had an estimated glomerular filtration rate (eGFR) of 30-49 mL/min/1.73 m2 and 596 (2.2%) had an eGFR below 30 mL/min/1.73 m2. We found no evidence of differences regarding the risk of stroke/TE between the OACs (P-value interaction >0.05 for all). Apixaban was associated with a lower 2-year risk of major bleeding compared to vitamin K antagonists (VKA) [hazard ratio 0.79, 95% confidence interval (CI) 0.67-0.93], and the risk difference was significantly larger among patients with reduced kidney function (P-value interaction 0.018). Rivaroxaban was associated with a higher risk of bleeding compared to apixaban (hazard ratio 1.78, 95%CI 1.32-2.39) among patients with eGFR 30-49 mL/min/1.73 m2.

Conclusions: Overall, we found no differences regarding the risk of stroke/TE, but apixaban was associated with a 21% lower relative risk of major bleeding compared to VKA. This risk reduction was even greater when comparing apixaban to VKA among patients with eGFR 15-30 mL/min/1.73 m2, and when comparing apixaban to dabigatran and rivaroxaban among patients with eGFR 30-49 mL/min/1.73 m2.

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来源期刊
European Heart Journal - Cardiovascular Pharmacotherapy
European Heart Journal - Cardiovascular Pharmacotherapy Medicine-Cardiology and Cardiovascular Medicine
CiteScore
10.10
自引率
14.10%
发文量
65
期刊介绍: The European Heart Journal - Cardiovascular Pharmacotherapy (EHJ-CVP) is an international, peer-reviewed journal published in English, specifically dedicated to clinical cardiovascular pharmacology. EHJ-CVP publishes original articles focusing on clinical research involving both new and established drugs and methods, along with meta-analyses and topical reviews. The journal's primary aim is to enhance the pharmacological treatment of patients with cardiovascular disease by interpreting and integrating new scientific developments in this field. While the emphasis is on clinical topics, EHJ-CVP also considers basic research articles from fields such as physiology and molecular biology that contribute to the understanding of cardiovascular drug therapy. These may include articles related to new drug development and evaluation, the physiological and pharmacological basis of drug action, metabolism, drug interactions, and side effects.
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