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达比加群血浆浓度和患者特征对房颤患者缺血性卒中和大出血发生率的影响:RE-LY 试验(随机评估长期抗凝治疗)。

The effect of dabigatran plasma concentrations and patient characteristics on the frequency of ischemic stroke and major bleeding in atrial fibrillation patients: the RE-LY Trial (Randomized Evaluation of Long-Term Anticoagulation Therapy).

机构信息

Departments of Clinical Development and Clinical Biostatistics, Boehringer Ingelheim Pharmaceuticals, Ridgefield, Connecticut.

Departments of Translational Medicine and Biometry, Boehringer Ingelheim Pharma GmbH & Co. KG, Biberach, Germany; Saarland University, Saarbrücken, Germany.

出版信息

J Am Coll Cardiol. 2014 Feb 4;63(4):321-8. doi: 10.1016/j.jacc.2013.07.104. Epub 2013 Sep 27.

Abstract

OBJECTIVES

The goal of this study was to analyze the impact of dabigatran plasma concentrations, patient demographics, and aspirin (ASA) use on frequencies of ischemic strokes/systemic emboli and major bleeds in atrial fibrillation patients.

BACKGROUND

The efficacy and safety of dabigatran etexilate were demonstrated in the RE-LY (Randomized Evaluation of Long-Term Anticoagulation Therapy) trial, but a therapeutic concentration range has not been defined.

METHODS

In a pre-specified analysis of RE-LY, plasma concentrations of dabigatran were determined in patients treated with dabigatran etexilate 110 mg twice daily (bid) or 150 mg bid and correlated with the clinical outcomes of ischemic stroke/systemic embolism and major bleeding using univariate and multivariate logistic regression and Cox regression models. Patient demographics and ASA use were assessed descriptively and as covariates.

RESULTS

Plasma concentrations were obtained from 9,183 patients, with 112 ischemic strokes/systemic emboli (1.3%) and 323 major bleeds (3.8%) recorded. Dabigatran levels were dependent on renal function, age, weight, and female sex, but not ethnicity, geographic region, ASA use, or clopidogrel use. A multiple logistic regression model (c-statistic 0.657, 95% confidence interval [CI]: 0.61 to 0.71) showed that the risk of ischemic events was inversely related to trough dabigatran concentrations (p = 0.045), with age and previous stroke (both p < 0.0001) as significant covariates. Multiple logistic regression (c-statistic 0.715, 95% CI: 0.69 to 0.74) showed major bleeding risk increased with dabigatran exposure (p < 0.0001), age (p < 0.0001), ASA use (p < 0.0003), and diabetes (p = 0.018) as significant covariates.

CONCLUSIONS

Ischemic stroke and bleeding outcomes were correlated with dabigatran plasma concentrations. Age was the most important covariate. Individual benefit-risk might be improved by tailoring dabigatran dose after considering selected patient characteristics. (Randomized Evaluation of Long Term Anticoagulant Therapy [RE-LY] With Dabigatran Etexilate; NCT00262600).

摘要

目的

本研究旨在分析达比加群血浆浓度、患者特征和阿司匹林(ASA)使用对房颤患者缺血性卒中和全身性栓塞以及大出血发生频率的影响。

背景

达比加群酯在 RE-LY(随机评估长期抗凝治疗)试验中已证实其疗效和安全性,但尚未确定其治疗浓度范围。

方法

在 RE-LY 的一项预设分析中,对接受达比加群酯 110 mg 每日 2 次(bid)或 150 mg bid 治疗的患者测定达比加群血浆浓度,并使用单变量和多变量逻辑回归及 Cox 回归模型将其与缺血性卒中和全身性栓塞以及大出血的临床结局相关联。对患者特征和 ASA 使用进行描述性评估和作为协变量。

结果

共纳入 9183 例患者,记录到 112 例缺血性卒中和全身性栓塞(1.3%)和 323 例大出血(3.8%)。达比加群水平依赖于肾功能、年龄、体重和性别,但与种族、地理位置、ASA 使用或氯吡格雷使用无关。多变量逻辑回归模型(C 统计量 0.657,95%置信区间[CI]:0.61 至 0.71)显示,缺血事件风险与达比加群谷浓度呈反比关系(p = 0.045),年龄和既往卒中(均 p < 0.0001)为显著协变量。多变量逻辑回归(C 统计量 0.715,95%CI:0.69 至 0.74)显示,达比加群暴露量增加与大出血风险相关(p < 0.0001),年龄(p < 0.0001)、ASA 使用(p < 0.0003)和糖尿病(p = 0.018)为显著协变量。

结论

缺血性卒中和出血结局与达比加群血浆浓度相关。年龄是最重要的协变量。考虑到某些患者特征后,通过调整达比加群剂量可能会改善个体的获益-风险比。(RE-LY 研究:达比加群酯的随机长期抗凝治疗评估;NCT00262600)。

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