A Real-World Retrospective Study on the Efficacy and Safety of Four Antiviral Drugs for Hospitalized COVID-19 Patients: Nirmatrelvir/Ritonavir, Simnotrelvir/Ritonavir, Molnupiravir and Azvudine

IF 2.9 3区 医学 Q2 INFECTIOUS DISEASES Infection and Drug Resistance Pub Date : 2024-09-14 DOI:10.2147/idr.s477083
Ximiao Yu, Ruiqi Luo, Guijuan Xie, Jiali Ji, Jiehong Wang, Xiyue Li, Xiaojun Qian, Xun Wang
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Abstract

Purpose: This retrospective study aims to compare the effectiveness and safety of four oral antiviral drugs including Simnotrelvir/Ritonavir, Nirmatrelvir/Ritonavir, Azvudine and Molnupiravir in hospitalized patients with Coronavirus Disease 2019 (COVID-19) in a real-world setting, providing evidence to guide clinical practice against COVID-19.
Patients and Methods: Patients with mild or moderate COVID-19 hospitalized at Wuxi City’s Second People’s Hospital during December 2022 to June 2023 were included in this study. Patients were grouped by the antiviral drug received. The primary endpoint was the length of hospital stay. Patients were further divided into subgroups for stratified analysis, considering age, timing of medication, and drug mechanisms, to explore whether these factors could influence the treatment efficacy.
Results: Of the enrolled 195 patients receiving any treatment, 42 received Nirmatrelvir/Ritonavir, 33 received Molnupiravir, 81 received Simnotrelvir/Ritonavir, and 39 received Azvudine. Patients in Nirmatrelvir/Ritonavir and Simnotrelvir/Ritonavir groups had significantly shorter hospital stays compared to those in Azvudine group (P < 0.05). No significant difference was observed in hospital stays between those initiating antiviral therapy within or more than five days after symptom onset (P = 0.1109). Among patients with comorbidities, the Nirmatrelvir/Ritonavir and Simnotrelvir/Ritonavir group showed shorter hospital stays than the Azvudine group (P < 0.05). No serious treatment-related adverse events were observed across the groups.
Conclusion: In this retrospective study, Nirmatrelvir/Ritonavir and Simnotrelvir/Ritonavir exerts stronger potency on reducing duration of hospital stays in hospitalized patient with COVID-19, suggestive of a better choice for antiviral therapy. Patients who fail to take antiviral drugs in time after symptom onset would still benefit from these antiviral regimens. Additional well-designed clinical trials with large sample size are still needed to further confirm the effectiveness of these antivirals.

Keywords: antivirals, COVID-19, molnupiravir, simnotrelvir/ritonavir, azvudine, nirmatrelvir/ritonavir
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关于四种抗病毒药物对 COVID-19 住院患者疗效和安全性的真实世界回顾性研究:尼马瑞韦/利托那韦、西诺瑞韦/利托那韦、莫鲁吡拉韦和阿唑夫定
目的:本回顾性研究旨在比较四种口服抗病毒药物(包括辛诺雷韦/利托那韦、尼尔马特雷韦/利托那韦、阿孜夫定和莫鲁吡拉韦)在实际环境中对住院的2019年冠状病毒病(COVID-19)患者的有效性和安全性,为指导COVID-19的临床实践提供证据:本研究纳入了2022年12月至2023年6月期间在无锡市第二人民医院住院治疗的轻度或中度COVID-19患者。患者按接受的抗病毒药物分组。主要终点是住院时间。考虑到年龄、用药时间和药物机制等因素,将患者进一步分为亚组进行分层分析,以探讨这些因素是否会影响治疗效果:在接受任何治疗的 195 名患者中,42 人接受了 Nirmatrelvir/Ritonavir,33 人接受了 Molnupiravir,81 人接受了 Simnotrelvir/Ritonavir,39 人接受了阿兹夫定。与阿兹夫定组相比,Nirmatrelvir/Ritonavir 组和 Simnotrelvir/Ritonavir 组患者的住院时间明显更短(P < 0.05)。在症状出现后五天内或五天以上开始接受抗病毒治疗的患者之间,住院时间没有明显差异(P = 0.1109)。在合并症患者中,Nirmatrelvir/Ritonavir 组和 Simnotrelvir/Ritonavir 组的住院时间短于阿兹夫定组(P < 0.05)。各组均未观察到与治疗相关的严重不良事件:在这项回顾性研究中,Nirmatrelvir/Ritonavir和Simnotrelvir/Ritonavir在缩短COVID-19住院患者的住院时间方面发挥了更强的作用,表明抗病毒治疗是更好的选择。症状出现后未能及时服用抗病毒药物的患者仍可从这些抗病毒治疗方案中获益。关键词:抗病毒药物;COVID-19;莫鲁吡拉韦;辛诺雷韦/利托那韦;阿孜夫定;尼麦雷韦/利托那韦
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来源期刊
Infection and Drug Resistance
Infection and Drug Resistance Medicine-Pharmacology (medical)
CiteScore
5.60
自引率
7.70%
发文量
826
审稿时长
16 weeks
期刊介绍: About Journal Editors Peer Reviewers Articles Article Publishing Charges Aims and Scope Call For Papers ISSN: 1178-6973 Editor-in-Chief: Professor Suresh Antony An international, peer-reviewed, open access journal that focuses on the optimal treatment of infection (bacterial, fungal and viral) and the development and institution of preventative strategies to minimize the development and spread of resistance.
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