Impact of body mass index on 90-day warfarin requirements: a retrospective chart review.

IF 2.6 Q2 CARDIAC & CARDIOVASCULAR SYSTEMS Therapeutic Advances in Cardiovascular Disease Pub Date : 2021-01-01 DOI:10.1177/17539447211012803
Bolanle M Soyombo, Ashley Taylor, Christopher Gillard, Candice Wilson, Janel Bailey Wheeler
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引用次数: 2

Abstract

Background: Rates of obesity continue to rise worldwide as evidenced in the 2017 Centers for Disease Control and Prevention (CDC) report that indicated over 35% of United States (US) citizens are obese, with Louisiana ranked as the fifth most obese state in America. Since large clinical trials tend to exclude obese patients, health care providers are faced with concerns of under- or overdosing these patients on warfarin.

Methods: This retrospective chart review evaluated patients who reported to a community anticoagulation clinic for warfarin management between 1 June 2017 and 30 September 2017. Along with baseline demographics, chronic use of drugs that have clinically significant interactions with warfarin, social activity such as tobacco use and alcohol consumption, were collected. Body mass indexes (BMI) were collected and categorized according to the World Health Organization definitions as follows: Normal (BMI 18-24.9 kg/m2), Overweight (25-29.9 kg/m2), Obesity Class I (30-34.9 kg/m2), Obesity Class II (35-39.9 kg/m2), Obesity Class III (⩾40 kg/m2). The primary outcome was the mean 90-day warfarin dose required to maintain "intermediate control" or "good control" of international normalized ratio (INR), stratified by BMI classifications. The secondary outcome was the time in therapeutic range (TTR) stratified by BMI classifications.

Results: A total of 433 patient encounters were included in this study. There was a total of 43 encounters in the Normal BMI category, 111 Overweight encounters, 135 Obesity Class I encounters, 45 Obesity Class II encounters, and 99 Obesity Class III encounters. Approximately 63% of the study population were male, and over 90% the patients were African American. The Obesity Class I and Obesity Class II class required an average of 11.47 mg and 17.10 mg more warfarin, respectively, to maintain a therapeutic INR when compared with the Normal BMI category. These findings were statistically significant with p values of 0.007 and <0.001, respectively. Additionally, upon comparing the Overweight BMI category with the Obesity Class II category, there was a mean warfarin dose difference of 11.22 mg (p = 0.010) more in Obesity Class II encounters to maintain a therapeutic INR. In the secondary analysis of TTR, Overweight category encounters had the highest TTR, whereas encounters in the Normal BMI category had the lowest TTR.

Conclusion: As BMI increases, there is an increased chronic warfarin requirement to maintain "intermediate control" or "good control" of INR between 2 and 3 in an ambulatory care setting.

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体重指数对90天华法林需用量的影响:回顾性图表回顾。
背景:2017年美国疾病控制与预防中心(CDC)的报告显示,全球肥胖率持续上升,超过35%的美国公民肥胖,路易斯安那州是美国第五大肥胖州。由于大型临床试验倾向于排除肥胖患者,卫生保健提供者面临着对这些患者华法林剂量不足或过量的担忧。方法:本回顾性图表回顾评估了2017年6月1日至2017年9月30日期间到社区抗凝诊所报告使用华法林治疗的患者。除了基线人口统计数据外,还收集了与华法林有临床显著相互作用的药物的长期使用情况、社会活动(如吸烟和饮酒)。根据世界卫生组织的定义收集和分类体重指数(BMI)如下:正常(BMI 18-24.9 kg/m2),超重(25-29.9 kg/m2),肥胖I类(30-34.9 kg/m2),肥胖II类(35-39.9 kg/m2),肥胖III类(大于或等于40 kg/m2)。主要终点是维持国际标准化比率(INR)“中间控制”或“良好控制”所需的平均90天华法林剂量,按BMI分类分层。次要终点是按BMI分类分层的治疗范围时间(TTR)。结果:本研究共纳入433例患者。BMI正常的共有43例,超重的有111例,I类肥胖的有135例,II类肥胖的有45例,III类肥胖的有99例。大约63%的研究人群是男性,超过90%的患者是非裔美国人。与正常BMI组相比,肥胖I类和肥胖II类患者平均需要分别多服用11.47 mg和17.10 mg华法林来维持治疗INR。这些发现具有统计学意义(p值分别为0.007和p = 0.010), II类肥胖患者更能维持治疗INR。在TTR的二次分析中,超重组的TTR最高,而正常BMI组的TTR最低。结论:随着BMI的增加,在门诊环境中维持INR在2到3之间的“中间控制”或“良好控制”的慢性华法林需求增加。
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来源期刊
Therapeutic Advances in Cardiovascular Disease
Therapeutic Advances in Cardiovascular Disease CARDIAC & CARDIOVASCULAR SYSTEMS-
CiteScore
3.50
自引率
0.00%
发文量
11
审稿时长
9 weeks
期刊介绍: The journal is aimed at clinicians and researchers from the cardiovascular disease field and will be a forum for all views and reviews relating to this discipline.Topics covered will include: ·arteriosclerosis ·cardiomyopathies ·coronary artery disease ·diabetes ·heart failure ·hypertension ·metabolic syndrome ·obesity ·peripheral arterial disease ·stroke ·arrhythmias ·genetics
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