Patient-Reported Adverse Events Among Elderly Patients Receiving Novel Oral COVID-19 Antivirals: A Nationwide Sampled Survey in Korea.

IF 3 3区 医学 Q1 MEDICINE, GENERAL & INTERNAL
Hyunah Jung, Ji Yeon Park, Dongwon Yoon, Dong Yoon Kang, Jaehun Jung, Ju Hwan Kim, Ju-Young Shin
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引用次数: 0

Abstract

Background: There is a dearth of research on the factors linked with adverse events (AEs) associated with nirmatrelvir/ritonavir (NMVr) and molnupiravir (MOL), particularly in the elderly. Therefore, this study aimed to investigate self-reported AEs and identify factors associated with the occurrence of AEs following NMVr or MOL treatment among survey participants aged 60 years or older in South Korea.

Methods: This nationwide survey was conducted through in-person interviews using structured questionnaires, from July 24 to August 31, 2023. Eligible participants included individuals aged 60 years or older who had been diagnosed with coronavirus disease 2019 (COVID-19) and received NMVr or MOL. The study outcomes included self-reported demographic, lifestyle, and health characteristics associated with the occurrence of AEs. Multivariate logistic regression analysis was used to estimate the adjusted odds ratio (aOR) and 95% confidence interval (CI) of each characteristic in participants with and without AEs.

Results: Of the 520 participants, 123 (23.7%) experienced at least one AE with oral COVID-19 treatment: 21.0% (96/458) for NMVr and 43.5% (27/62) for MOL. None of the participants reported any serious AEs. Increased odds of AE occurrence were observed in participants treated with MOL compared to those treated with NMVr (aOR, 3.05; 95% CI, 1.67-5.57), a history of two or more compared to one COVID-19 diagnosis (1.93; 1.03-3.62), and self-reported health status as "Unhealthy" compared to "Healthy" (2.65; 1.31-5.36).

Conclusion: No AEs required further evaluation to change treatment strategies in elderly patients on NMVr or MOL. Several factors, including the use of MOL, history of COVID-19, and reported health status, were associated with an increased incidence of AEs. Both treatments may still be useful choices for patients with non-severe COVID-19 aged 60 years or older. However, close monitoring of unidentified potential harm and further investigation of the factors associated with the occurrence of AEs are needed.

接受新型口服 COVID-19 抗病毒药物治疗的老年患者报告的不良事件:韩国全国抽样调查。
背景:关于与尼马瑞韦/利托那韦(NMVr)和莫鲁吡拉韦(MOL)相关的不良事件(AEs)有关的因素,尤其是老年人的不良事件,目前还缺乏相关研究。因此,本研究旨在调查韩国 60 岁或以上的调查对象在接受 NMVr 或 MOL 治疗后自我报告的 AEs,并确定与 AEs 发生相关的因素:这项全国性调查于 2023 年 7 月 24 日至 8 月 31 日通过结构化问卷进行面谈。符合条件的参与者包括被诊断患有冠状病毒病 2019(COVID-19)并接受过 NMVr 或 MOL 治疗的 60 岁或以上的人。研究结果包括与AEs发生相关的自我报告的人口统计学、生活方式和健康特征。研究采用多变量逻辑回归分析来估算出现和未出现AEs的参与者中每个特征的调整赔率(aOR)和95%置信区间(CI):在520名参与者中,123人(23.7%)在口服COVID-19治疗过程中至少出现过一次AE:NMVr为21.0%(96/458),MOL为43.5%(27/62)。所有参与者均未报告任何严重的不良反应。与接受 NMVr 治疗的参与者相比,接受 MOL 治疗的参与者发生 AE 的几率更高(aOR,3.05;95% CI,1.67-5.57);与接受一次 COVID-19 诊断的参与者相比,接受过两次或两次以上 COVID-19 诊断的参与者发生 AE 的几率更高(1.93;1.03-3.62);自我报告健康状况为 "不健康 "的参与者发生 AE 的几率更高(2.65;1.31-5.36):对于使用 NMVr 或 MOL 的老年患者,没有任何 AEs 需要进一步评估以改变治疗策略。一些因素(包括使用 MOL、COVID-19 病史和报告的健康状况)与 AEs 发生率增加有关。对于 60 岁或以上的非重度 COVID-19 患者来说,这两种治疗方法可能仍然是有用的选择。但是,需要密切监测未发现的潜在危害,并进一步调查与发生 AEs 相关的因素。
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
Journal of Korean Medical Science
Journal of Korean Medical Science 医学-医学:内科
CiteScore
7.80
自引率
8.90%
发文量
320
审稿时长
3-6 weeks
期刊介绍: The Journal of Korean Medical Science (JKMS) is an international, peer-reviewed Open Access journal of medicine published weekly in English. The Journal’s publisher is the Korean Academy of Medical Sciences (KAMS), Korean Medical Association (KMA). JKMS aims to publish evidence-based, scientific research articles from various disciplines of the medical sciences. The Journal welcomes articles of general interest to medical researchers especially when they contain original information. Articles on the clinical evaluation of drugs and other therapies, epidemiologic studies of the general population, studies on pathogenic organisms and toxic materials, and the toxicities and adverse effects of therapeutics are welcome.
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