华法林使用与国际标准化比率增加的关系:FDA不良事件报告系统(FAERS)的系统分析

Robert Morris, Megan Todd, Nicole Zapata Aponte, Milagros Salcedo, Matthew Bruckner, Alfredo Suarez Garcia, Rachel Webb, Kun Bu, Weiru Han, Feng Cheng
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引用次数: 0

摘要

导读:国际标准化比率(INR)升高通常被报道为华法林抗凝治疗患者的药物不良事件(ADE)。目的:本研究的目的是通过使用FDA不良事件报告系统(FAERS)的药物警戒数据来确定INR升高与华法林使用之间的关系。方法:采用FAERS数据对服用华法林的77010例患者的ade进行分析。关联规则挖掘用于识别与INR升高最相关的华法林相关ade (n = 15,091),以及与INR升高相关的可能的药物-药物相互作用(ddi)。根据两个项目集之间的相关性,Lift值用于识别最常见的ade和升高的INR。此外,本研究试图确定INR风险增加是否受性别、年龄、时间分布和地理分布的影响,并以报告优势比(RORs)进行报告。结果:与华法林患者INR升高最相关的前5个不良事件分别是血红蛋白降低(lift = 2.31)、药物相互作用(lift = 1.88)、血尿(lift = 1.58)、乏力(lift = 1.44)和跌倒(lift = 1.32)。INR风险随着年龄的增长而增加,80岁以上的人与50岁以下的人相比,INR升高的可能性高63%。男性报告INR增加作为ADE的可能性比女性高9%。同时服用华法林和至少一种其他药物的个体报告INR增加的可能性要高出43%。在服用华法林并出现INR升高的患者中,最常见的5种ddi分别是对乙酰氨基酚(lift = 1.81)、雷米普利(lift = 1.71)、呋塞米(lift = 1.64)、比索洛尔(lift = 1.58)和辛伐他汀(lift = 1.58)。结论:INR升高的风险随着患者年龄的增加而增加,特别是在80岁以上的患者中。在服用华法林的患者中,INR升高常伴有血红蛋白降低、药物相互作用、血尿、虚弱和跌倒。由于雌激素信号的促凝作用,这种作用在女性中可能不太明显。确定了多种可能的ddi,包括对乙酰氨基酚、雷米普利和速尿。
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The association between warfarin usage and international normalized ratio increase: systematic analysis of FDA Adverse Event Reporting System (FAERS)
Introduction: Elevated international normalized ratio (INR) has been commonly reported as an adverse drug event (ADE) for patients taking warfarin for anticoagulant therapy. Aim: The purpose of this study was to determine the association between increased INR and the usage of warfarin by using the pharmacovigilance data from the FDA Adverse Event Reporting System (FAERS). Methods: The ADEs in patients who took warfarin (N = 77,010) were analyzed using FAERS data. Association rule mining was applied to identify warfarin-related ADEs that were most associated with elevated INR (n = 15,091) as well as possible drug-drug interactions (DDIs) associated with increased INR. Lift values were used to identify ADEs that were most commonly reported alongside elevated INR based on the correlation between both item sets. In addition, this study sought to determine if the increased INR risk was influenced by sex, age, temporal distribution, and geographic distribution and were reported as reporting odds ratios (RORs). Results: The top 5 ADEs most associated with increased INR in patients taking warfarin were decreased hemoglobin (lift = 2.31), drug interactions (lift = 1.88), hematuria (lift = 1.58), asthenia (lift = 1.44), and fall (lift = 1.32). INR risk increased as age increased, with individuals older than 80 having a 63% greater likelihood of elevated INR compared to those younger than 50. Males were 9% more likely to report increased INR as an ADE compared to females. Individuals taking warfarin concomitantly with at least one other drug were 43% more likely to report increased INR. The top 5 most frequently identified DDIs in patients taking warfarin and presenting with elevated INR were acetaminophen (lift = 1.81), ramipril (lift = 1.71), furosemide (lift = 1.64), bisoprolol (lift = 1.58), and simvastatin (lift = 1.58). Conclusion: The risk of elevated INR increased as patient age increased, particularly among those older than 80. Elevated INR frequently co-presented with decreased hemoglobin, drug interactions, hematuria, asthenia, and fall in patients taking warfarin. This effect may be less pronounced in women due to the procoagulatory effects of estrogen signaling. Multiple possible DDIs were identified, including acetaminophen, ramipril, and furosemide.
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