Impact of Remdesivir on Heart Rate and Bradycardia Incidence Among Hospitalized Adults With COVID-19.

IF 2.3 4区 医学 Q3 PHARMACOLOGY & PHARMACY
Wesley D Kufel, Zoey J Zagoria, Robert W Seabury, Nabil Zeineddine, Stephen J Thomas, Sarah A Spinler, Jeffrey M Steele
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引用次数: 0

Abstract

Background: Bradycardia is not currently described as an adverse effect in prescribing information for remdesivir but has been reported postapproval. Therefore, effects on heart rate (HR) and bradycardia incidence after remdesivir initiation may be underrecognized by clinicians.

Objective: To evaluate HR and bradycardia incidence after remdesivir initiation among patients with COVID-19.

Methods: This was a single-center, retrospective cohort study between May 1, 2020 and December 1, 2021. Hospitalized patients eligible for inclusion were ≥18 years and received > 1 dose of remdesivir. Patients were excluded if they were pregnant, incarcerated, or received new medications associated with bradycardia. The primary outcome was to evaluate differences in median HR among patients preremdesivir (up to 24 hours prior to remdesivir) and postremdesivir (first dose through the treatment duration). Secondary outcomes included bradycardia episodes postremdesivir, nadir HR postremdesivir, and interventions for bradycardia management. Variables to assess postremdesivir bradycardia were considered in multivariate logistic regression if they had a P < 0.1 on univariate analysis.

Results: Among 514 patients, 328 were included. Most were male (53.4%), had severe COVID-19 (59.8%), and median (interquartile range [IQR]) age was 62 (23.7) years. Median (IQR) remdesivir duration was 4.9 (1.5) days. Median (IQR) HR was significantly lower postremdesivir than preremdesivir (74 (15) vs 87 (19), P < 0.001). There were significantly more bradycardia episodes postremdesivir than before (48.8% [160/328] vs (2.4% [8/328]), P < 0.001). Among 48.8% (160/328) of patients with bradycardia postremdesivir, median (IQR) nadir HR was 53 (6.8). Remdesivir was discontinued early in 1 patient (0.6%). In multivariate logistic regression, remdesivir duration (odds ratio [OR] = 1.26, 95% confidence interval [CI] = 1.04 to 1.54, P = 0.019) and median preremdesivir HR (OR = 0.96, 95% CI = 0.94 to 0.97, P < 0.001) were identified as significant predictors for bradycardia.

Conclusion and relevance: Remdesivir was associated with a significantly lower HR and higher incidence of bradycardia among hospitalized patients with COVID-19. These data may help improve recognition and management of these remdesivir-associated effects during COVID-19 treatment.

瑞德西韦对住院成人COVID-19患者心率和心动过缓发生率的影响
背景:目前在瑞德西韦的处方信息中没有将心动过缓描述为不良反应,但在批准后有报道。因此,临床医生可能没有充分认识到瑞德西韦对心率(HR)和心动过缓发生率的影响。目的:评价新冠肺炎患者开始使用瑞德西韦后的心率和心动过缓发生率。方法:这是一项单中心、回顾性队列研究,时间为2020年5月1日至2021年12月1日。符合纳入条件的住院患者年龄≥18岁,接受了bbb1剂量的瑞德西韦。排除怀孕、监禁或接受与心动过缓相关的新药物的患者。主要结果是评估患者在使用remdesivir前(比remdesivir早24小时)和使用remdesivir后(第一次给药到治疗期间)中位HR的差异。次要结局包括瑞姆德西韦后心动过缓发作、瑞姆德西韦后最低HR和心动过缓管理干预。如果单因素分析的P < 0.1,则在多因素logistic回归中考虑评价remdesivir后心动过缓的变量。结果:514例患者中,纳入328例。多数为男性(53.4%),重症(59.8%),年龄中位数(四分位数间距[IQR])为62岁(23.7岁)。瑞德西韦的中位(IQR)持续时间为4.9(1.5)天。中位(IQR) HR在remdesivir后显著低于preremdesivir (74 (15) vs 87 (19), P < 0.001)。使用remdesivir后的心动过缓次数明显多于使用前(48.8% [160/328]vs (2.4% [8/328]), P < 0.001)。在remdesivir后出现心动过缓的48.8%(160/328)患者中,中位(IQR)最低HR为53(6.8)。1例患者(0.6%)早期停用Remdesivir。在多因素logistic回归中,瑞德西韦持续时间(优势比[OR] = 1.26, 95%可信区间[CI] = 1.04 ~ 1.54, P = 0.019)和中位瑞德西韦HR (OR = 0.96, 95% CI = 0.94 ~ 0.97, P < 0.001)被确定为心动缓的重要预测因素。结论及相关性:在COVID-19住院患者中,瑞德西韦与较低的HR和较高的心动过缓发生率相关。这些数据可能有助于在COVID-19治疗期间更好地认识和管理这些瑞德西韦相关效应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
5.70
自引率
0.00%
发文量
166
审稿时长
3-8 weeks
期刊介绍: Annals of Pharmacotherapy (AOP) is a peer-reviewed journal that advances pharmacotherapy throughout the world by publishing high-quality research and review articles to achieve the most desired health outcomes.The articles provide cutting-edge information about the most efficient, safe and cost-effective pharmacotherapy for the treatment and prevention of various illnesses. This journal is a member of the Committee on Publication Ethics (COPE). Average time from submission to first decision: 14 days
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