Evaluating the Real-World Safety of Icosapent Ethyl Versus Omega-3 Polyunsaturated Fatty Acid in Nationwide US Veterans Cohort: Examining Atrial Fibrillation and Bleeding Endpoints.

IF 2.9 3区 医学 Q2 PHARMACOLOGY & PHARMACY Clinical Drug Investigation Pub Date : 2025-01-11 DOI:10.1007/s40261-024-01417-4
Tanvi Patil, Michael Gregory, Natalie Savona, Nabil Jarmukli, Charles E Leonard
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Abstract

Purpose: The REDUCE-IT randomized trial demonstrated a cardiovascular benefit of icosapent ethyl (IPE) but also raised potential safety signals for atrial fibrillation (AF) and serious bleeding. We aimed to evaluate the real-world safety of IPE versus mixed omega-3 polyunsaturated fatty acid (OM-3) formulations.

Methods: This retrospective active comparator new-user cohort study compared rates of new-onset AF and major bleeding (MB) among adult new users of IPE versus OM-3 in 2020-2024 US Veterans Affairs data. Daily drug exposure was determined via prescription dispensing dates. AF and MB outcomes were identified via validated algorithms based on the International Statistical Classification of Diseases and Related Health Problems, 10th revision, clinical modification. Confounding was accounted for via nearest-neighbor pairwise propensity score (PS) matching. The PS, constructed via logistic regression, was informed by expert-identified variables meeting the disjunctive cause criterion. Cox regression was used to estimate adjusted hazard ratios (aHRs), interpretable as average treatment effects for the treated.

Results: Cohorts for analyses of AF and MB endpoints included 1927 and 2015 people, respectively, in each of the IPE and OM-3 exposure groups. The median age was 70 years, and the groups exhibited a predominance of white (80%) males (93%). The median follow-up time was 1.29 years per person. Baseline covariates were well balanced by treatment arm after PS matching. Incidence rates for AF were 7.29 versus 7.48 per 100 person-years among new users of IPE versus OM-3. The aHR for AF was 1.15 (95% confidence interval 0.82-1.63). Incidence rates for MB were 3.27 versus 3.35 per 100 person-years among new users of IPE versus OM-3. The aHR for MB was 1.22 (95% confidence interval 0.87-3.02).

Conclusions: Our measures of association were consistent with the null, but we were unable to rule out harms from IPE (vs. OM-3) more modest than a 63% increased rate of AF and threefold increased rate of MB.

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在美国退伍军人队列中评估二碳戊二酯与Omega-3多不饱和脂肪酸的实际安全性:检查心房颤动和出血终点
目的:REDUCE-IT随机试验证明了乙基戊二醇(IPE)对心血管的益处,但也提高了心房颤动(AF)和严重出血的潜在安全信号。我们的目的是评估IPE与混合omega-3多不饱和脂肪酸(OM-3)制剂的实际安全性。方法:这项回顾性的主动比较新用户队列研究比较了2020-2024年美国退伍军人事务部数据中成年IPE新用户与OM-3新用户的新发房颤和大出血(MB)发生率。每日药物暴露量通过处方配药日期确定。AF和MB的结果通过基于国际疾病和相关健康问题统计分类,第10版,临床修改的验证算法确定。通过最近邻两两倾向评分(PS)匹配来解释混淆。PS通过逻辑回归构建,由专家确定的变量满足析取原因标准。Cox回归用于估计校正风险比(aHRs),可解释为被治疗者的平均治疗效果。结果:在IPE和OM-3暴露组中,AF和MB终点分析的队列分别包括1927人和2015人。中位年龄为70岁,各组以白人(80%)和男性(93%)为主。平均随访时间为每人1.29年。PS匹配后,各治疗组的基线协变量平衡良好。新使用IPE和OM-3的AF发病率分别为7.29和7.48 / 100人年。AF的aHR为1.15(95%可信区间0.82-1.63)。在IPE和OM-3的新使用者中,MB的发病率分别为3.27 / 100人-年和3.35 / 100人-年。MB的aHR为1.22(95%可信区间0.87-3.02)。结论:我们的关联测量值与零值一致,但我们无法排除IPE的危害(相对于OM-3),其危害比房颤发生率增加63%和MB发生率增加三倍更为温和。
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来源期刊
CiteScore
5.90
自引率
3.10%
发文量
108
审稿时长
6-12 weeks
期刊介绍: Clinical Drug Investigation provides rapid publication of original research covering all phases of clinical drug development and therapeutic use of drugs. The Journal includes: -Clinical trials, outcomes research, clinical pharmacoeconomic studies and pharmacoepidemiology studies with a strong link to optimum prescribing practice for a drug or group of drugs. -Clinical pharmacodynamic and clinical pharmacokinetic studies with a strong link to clinical practice. -Pharmacodynamic and pharmacokinetic studies in healthy volunteers in which significant implications for clinical prescribing are discussed. -Studies focusing on the application of drug delivery technology in healthcare. -Short communications and case study reports that meet the above criteria will also be considered. Additional digital features (including animated abstracts, video abstracts, slide decks, audio slides, instructional videos, infographics, podcasts and animations) can be published with articles; these are designed to increase the visibility, readership and educational value of the journal’s content. In addition, articles published in Clinical Drug Investigation may be accompanied by plain language summaries to assist readers who have some knowledge, but non in-depth expertise in, the area to understand important medical advances.
期刊最新文献
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