Medical College, Wuhan University of Science and Technology, Wuhan, Hubei, China.
Department of Transfusion Medicine; General Hospital of Central Theater Command, Wuhan, Hubei, China.
Front Cell Infect Microbiol. 2024 Nov 7;14:1453234. doi: 10.3389/fcimb.2024.1453234. eCollection 2024.
Azvudine, a repurposed oral small molecule antiviral drug, has potential effects in combating the SARS-CoV-2 virus. However, studies on its clinical efficacy in patients with COVID-19 are still limited and controversial, and further research and validation are necessary.
A retrospective cohort study was conducted on COVID-19 patients who were hospitalized in the General Hospital of Central Theater Command from 1 December 2022 to 31 January 2023. We included 132 patients treated with Azvudine and 132 controls after screening and propensity score matching. The primary outcomes including all-cause mortality and a composite outcome of disease progression such as non-invasive respiratory support, invasive respiratory support, admission to intensive care unit (ICU), and death were compared.
Azvudine recipients had a much lower incidence rate of composite disease progression outcome than controls (13.9075/1000 person-days versus 25.7731/1000 person-days, <0.05). Azvudine recipients also possessed a lower all-cause mortality rate than controls (2.6797/1000 person-days versus 8.5910/1000 person-days, <0.01). Azvudine treatment significantly reduced the risk of composite disease progression (HR: 0.37, 95% CI: 0.16-0.84, =0.017) and all-cause death (HR: 0.25, 95% CI: 0.08-0.81, =0.021) after adjusting potential confounding factors such as age, sex, severity of COVID-19, complications, concomitant therapy, time from symptoms to treatment, and important laboratory indicators. The subgroup analyses of composite disease progression outcome and all-cause death indicated robustness of Azvudine's in treating COVID-19 patients in general.
Our study demonstrates that Azvudine has a significant positive impact on the clinical recovery of hospitalized patients with COVID-19. These findings provide important support for the use of Azvudine as a therapeutic option for COVID-19, given the current divergent views on its therapeutic efficacy and its importance in public health and medical care.
阿兹夫定是一种已被重新用于临床的口服小分子抗病毒药物,具有抗击 SARS-CoV-2 病毒的潜力。然而,关于其在 COVID-19 患者中的临床疗效的研究仍然有限且存在争议,需要进一步的研究和验证。
我们对 2022 年 12 月 1 日至 2023 年 1 月 31 日期间在中部战区总医院住院的 COVID-19 患者进行了回顾性队列研究。我们筛选并进行倾向评分匹配后,纳入了 132 名接受阿兹夫定治疗的患者和 132 名对照。比较了全因死亡率和疾病进展的复合结局,包括非侵入性呼吸支持、侵入性呼吸支持、入住重症监护病房(ICU)和死亡。
阿兹夫定组的复合疾病进展结局发生率明显低于对照组(13.9075/1000 人天比 25.7731/1000 人天,<0.05)。阿兹夫定组的全因死亡率也低于对照组(2.6797/1000 人天比 8.5910/1000 人天,<0.01)。在调整年龄、性别、COVID-19 严重程度、并发症、合并治疗、症状出现到治疗的时间和重要实验室指标等潜在混杂因素后,阿兹夫定治疗显著降低了复合疾病进展(HR:0.37,95%CI:0.16-0.84,=0.017)和全因死亡(HR:0.25,95%CI:0.08-0.81,=0.021)的风险。复合疾病进展结局和全因死亡的亚组分析表明,阿兹夫定对治疗 COVID-19 患者具有稳健的效果。
我们的研究表明,阿兹夫定对住院 COVID-19 患者的临床康复有显著的积极影响。鉴于目前对其治疗效果存在不同意见,以及其在公共卫生和医疗保健方面的重要性,这些发现为将阿兹夫定作为 COVID-19 的治疗选择提供了重要支持。