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社区环境中接受华法林治疗患者的酒精滥用、遗传学与严重出血情况

Alcohol misuse, genetics, and major bleeding among warfarin therapy patients in a community setting.

作者信息

Roth Joshua A, Bradley Katharine, Thummel Kenneth E, Veenstra David L, Boudreau Denise

机构信息

Group Health Research Institute, Group Health, Seattle, WA, USA.

Hutchinson Institute for Cancer Outcomes Research, Fred Hutchinson Cancer Research Center, Seattle, WA, USA.

出版信息

Pharmacoepidemiol Drug Saf. 2015 Jun;24(6):619-27. doi: 10.1002/pds.3769. Epub 2015 Apr 8.

Abstract

PURPOSE

Little is known about the impact of alcohol consumption on warfarin safety, or whether demographic, clinical, or genetic factors modify risk of adverse events. We conducted a case-control study to assess the association between screening positive for moderate/severe alcohol misuse and the risk of major bleeding in a community sample of patients using warfarin.

METHODS

The study sample consisted of 570 adult patients continuously enrolled in Group Heath for at least 2 years and receiving warfarin. The main outcome was major bleeding validated through medical record review. Cases experienced major bleeding, and controls did not experience major bleeding. Exposures were Alcohol Use Disorders Identification Test Consumption Questionnaire (AUDIT-C) scores and report of heavy episodic drinking (≥5 drinks on an occasion). The odds of major bleeding were estimated with multivariate logistic regression models. The overall sample was 55% male, 94% Caucasian, and had a mean age of 70 years.

RESULTS

Among 265 cases and 305 controls, AUDIT-C scores indicative of moderate/severe alcohol misuse and heavy episodic drinking were associated with increased risk of major bleeding (OR = 2.10, 95% CI = 1.08-4.07; and OR = 2.36, 95% CI = 1.24-4.50, respectively). Stratified analyses demonstrated increased alcohol-related major bleeding risk in patients on warfarin for ≥1 year and in those with a low-dose genotype (CYP2C9*2/3, VKORC1(1173G>A), CYP4F21), but not in other sub-groups evaluated.

CONCLUSIONS

Alcohol screening questionnaires, potentially coupled with genetic testing, could have clinical utility in selecting patients for warfarin therapy, as well as refining dosing and monitoring practices.

摘要

目的

关于饮酒对华法林安全性的影响,或者人口统计学、临床或遗传因素是否会改变不良事件风险,目前所知甚少。我们开展了一项病例对照研究,以评估在使用华法林的社区患者样本中,中度/重度酒精滥用筛查呈阳性与大出血风险之间的关联。

方法

研究样本包括570名成年患者,他们连续参加健康集团至少2年并接受华法林治疗。主要结局是通过病历审查验证的大出血。病例组经历了大出血,对照组未经历大出血。暴露因素为酒精使用障碍识别测试消费问卷(AUDIT-C)得分和大量饮酒报告(一次饮酒≥5杯)。采用多变量逻辑回归模型估计大出血的几率。总体样本中男性占55%,白种人占94%,平均年龄为70岁。

结果

在265例病例和305例对照中,表明中度/重度酒精滥用和大量饮酒的AUDIT-C得分与大出血风险增加相关(比值比分别为2.10,95%置信区间为1.08 - 4.07;以及比值比为2.36,95%置信区间为1.24 - 4.50)。分层分析表明,使用华法林≥1年的患者以及具有低剂量基因型(CYP2C9*2/3、VKORC1(1173G>A)、CYP4F21)的患者中,与酒精相关的大出血风险增加,但在评估的其他亚组中未增加。

结论

酒精筛查问卷,可能结合基因检测,在选择接受华法林治疗的患者以及完善剂量调整和监测实践方面可能具有临床实用性。

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