Department of Internal Medicine, Kirk Kerkorian School of Medicine at the University of Nevada Las Vegas (UNLV), 2040 W. Charleston Blvd., Mail Stop: 3070, Las Vegas, NV, 89102-2244, USA.
Department of Medicine, Kirk Kerkorian School of Medicine at UNLV, Las Vegas, Nevada, USA.
Clin Drug Investig. 2022 Sep;42(9):763-774. doi: 10.1007/s40261-022-01187-x. Epub 2022 Aug 17.
Remdesivir is an antiviral drug used to treat coronavirus disease 2019 (COVID-19) with a relatively obscure cardiac effect profile. Previous studies have reported bradycardia associated with remdesivir, but few have examined its clinical characteristics. The objective of this study was to investigate remdesivir associated bradycardia and its associated clinical characteristics and outcomes.
This is a single-institution retrospective study that investigated bradycardia in 600 patients who received remdesivir for treatment of COVID-19. A total of 375 patients were included in the study after screening for other known causes of bradycardia (atrioventricular [AV] nodal blockers). All patients were analyzed for episodes of bradycardia from when remdesivir was initiated up to 5 days after completion, a time frame based on the drug's putative elimination half-life. Univariate and multivariate statistical tests were conducted to analyze the data.
The mean age of the sample was 56.63 ± 13.23 years. Of patients who met inclusion criteria, 49% were found to have bradycardia within 5 days of remdesivir administration. Compared to the cohort without a documented bradycardic episode, patients with bradycardia were significantly more likely to experience inpatient mortality (22% vs 12%, p = 0.01). The patients with bradycardia were found to have marginally higher serum D-dimer levels (5.2 vs 3.4 µg/mL, p = 0.05) and were more likely to undergo endotracheal intubation (28% vs 14%, p = 0.008). Male sex, hyperlipidemia, and bradycardia within 5 days of completing remdesivir were significant predictors of inpatient mortality. No significant differences in length of stay were found.
Bradycardia that occurs during or shortly after remdesivir treatment in COVID-19 patients may be associated with an increased rate of in-hospital mortality. However, COVID-19 and its cardiac complications cannot be excluded as potential contributors of bradycardia in the present study. Future studies are needed to further delineate the cardiac characteristics of COVID-19 and remdesivir.
瑞德西韦是一种用于治疗 2019 年冠状病毒病(COVID-19)的抗病毒药物,其心脏作用谱相对不明确。先前的研究报告瑞德西韦与心动过缓有关,但很少有研究探讨其临床特征。本研究的目的是研究瑞德西韦相关心动过缓及其相关临床特征和结局。
这是一项单中心回顾性研究,调查了 600 例接受瑞德西韦治疗 COVID-19 的患者的心动过缓情况。在筛选出其他已知心动过缓原因(房室结阻滞剂)后,共有 375 例患者纳入研究。所有患者均根据药物假定消除半衰期,分析从开始使用瑞德西韦到完成后 5 天内的心动过缓发作情况。进行单变量和多变量统计检验分析数据。
样本的平均年龄为 56.63 ± 13.23 岁。在符合纳入标准的患者中,49%的患者在使用瑞德西韦后 5 天内出现心动过缓。与未记录心动过缓发作的队列相比,心动过缓患者的住院死亡率显著更高(22% vs 12%,p = 0.01)。心动过缓患者的血清 D-二聚体水平略高(5.2 vs 3.4 µg/mL,p = 0.05),更有可能进行气管插管(28% vs 14%,p = 0.008)。男性、高脂血症和使用瑞德西韦后 5 天内出现心动过缓是住院死亡率的显著预测因素。住院时间无显著差异。
COVID-19 患者在使用瑞德西韦期间或之后不久发生的心动过缓可能与住院死亡率增加有关。然而,在本研究中,不能排除 COVID-19 及其心脏并发症是心动过缓的潜在原因。需要进一步研究来进一步阐明 COVID-19 和瑞德西韦的心脏特征。