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c19early.org COVID-19 treatment researchAzvudineAzvudine (more..)
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Effectiveness of azvudine in reducing mortality of COVID-19 patients: a systematic review and meta-analysis

Wang et al., Virology Journal, doi:10.1186/s12985-024-02316-y
Feb 2024  
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Azvudine for COVID-19
44th treatment shown to reduce risk in July 2023, now with p = 0.0000013 from 28 studies.
Lower risk for mortality, progression, and viral clearance.
No treatment is 100% effective. Protocols combine treatments.
5,300+ studies for 115 treatments. c19early.org
Systematic review and meta-analysis of 17 studies showing significantly lower mortality with azvudine compared to no antiviral treatment in COVID-19 patients. The mortality benefit was seen in both mild/moderate and severe disease, as well as in patients over 65 years old. There was no significant difference found between azvudine and control groups for ICU admission, invasive ventilation, or adverse events.
4 meta analyses show significant improvements with azvudine for mortality1-4, mechanical ventilation1, improvement1, and viral clearance1,3,4.
Currently there are 28 azvudine for COVID-19 studies, showing 31% lower mortality [20‑40%], 20% lower ventilation [-50‑57%], 20% lower ICU admission [-16‑45%], and 6% lower hospitalization [-3‑15%].
Wang et al., 23 Feb 2024, peer-reviewed, 13 authors. Contact: tianxl@pumch.cn.
This PaperAzvudineAll
Effectiveness of azvudine in reducing mortality of COVID-19 patients: a systematic review and meta-analysis
Yaqi Wang, Huaiya Xie, Luo Wang, Junping Fan, Ying Zhang, Siqi Pan, Wangji Zhou, Qiaoling Chen, Xueqi Liu, Aohua Wu, Hong Zhang, Jinglan Wang, Xinlun Tian
Virology Journal, doi:10.1186/s12985-024-02316-y
Background Azvudine has been approved for the treatment of coronavirus disease 2019 patients in China, and this meta-analysis aims to illustrate the safety of azvudine and its effectiveness in reducing mortality. Methods PubMed, Embase, Web of science, Cochrane Library and the Epistemonikos COVID-19 Living Overview of Evidence database (L.OVE) were searched to aggregate currently published studies. Cochrane risk of bias tool and ROBINS-I tool were used to assess the risk of bias of randomized controlled study and cohort study respectively. Odds radios (ORs) with 95% confidence interval (CIs) were combined for dichotomous variables. Publication bias was assessed by Egger's test and funnel plots. Results A total of 184 articles were retrieved from the included databases and 17 studies were included into the final analysis. Pooled analysis showed that azvudine significantly reduced mortality risk in COVID-19 patients compared with controls (OR: 0.41, 95%CI 0.31-0.54, p < 0.001). Besides, either mild to moderate or severe COVID-19 patients could benefit from azvudine administration. There was no significant difference in the incidence of ICU admission (OR: 0.90, 95%CI 0.47-1.72, p = 0.74) and invasive ventilation (OR: 0.94, 95%CI 0.54-1.62, p = 0.82) between azvudine and control group. The incidence of adverse events was similar between azvudine and control (OR: 1.26, 95%CI 0.59-2.70, p = 0.56). Conclusions This meta-analysis suggests that azvudine could reduce the mortality risk of COVID-19 patients, and the safety of administration is acceptable.
Abbreviations Supplementary Information The online version contains supplementary material available at https://doi. org/10.1186/s12985-024-02316-y. Supplementary Material 1: Supplementary Declarations Ethics approval and consent to participate Not applicable. Consent for publication Not applicable. Competing interests The authors declare no competing interests. Publisher's Note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
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DOI record: { "DOI": "10.1186/s12985-024-02316-y", "ISSN": [ "1743-422X" ], "URL": "http://dx.doi.org/10.1186/s12985-024-02316-y", "abstract": "<jats:title>Abstract</jats:title><jats:sec>\n <jats:title>Background</jats:title>\n <jats:p>Azvudine has been approved for the treatment of coronavirus disease 2019 (COVID-19) patients in China, and this meta-analysis aims to illustrate the safety of azvudine and its effectiveness in reducing mortality.</jats:p>\n </jats:sec><jats:sec>\n <jats:title>Methods</jats:title>\n <jats:p>PubMed, Embase, Web of science, Cochrane Library and the Epistemonikos COVID-19 Living Overview of Evidence database (L.OVE) were searched to aggregate currently published studies. Cochrane risk of bias tool and ROBINS-I tool were used to assess the risk of bias of randomized controlled study and cohort study respectively. Odds radios (ORs) with 95% confidence interval (CIs) were combined for dichotomous variables. Publication bias was assessed by Egger’s test and funnel plots.</jats:p>\n </jats:sec><jats:sec>\n <jats:title>Results</jats:title>\n <jats:p>A total of 184 articles were retrieved from the included databases and 17 studies were included into the final analysis. Pooled analysis showed that azvudine significantly reduced mortality risk in COVID-19 patients compared with controls (OR: 0.41, 95%CI 0.31–0.54, <jats:italic>p</jats:italic> &lt; 0.001). Besides, either mild to moderate or severe COVID-19 patients could benefit from azvudine administration. There was no significant difference in the incidence of ICU admission (OR: 0.90, 95%CI 0.47–1.72, <jats:italic>p</jats:italic> = 0.74) and invasive ventilation (OR: 0.94, 95%CI 0.54–1.62, <jats:italic>p</jats:italic> = 0.82) between azvudine and control group. 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Please send us corrections, updates, or comments. c19early involves the extraction of 100,000+ datapoints from thousands of papers. Community updates help ensure high accuracy. Treatments and other interventions are complementary. All practical, effective, and safe means should be used based on risk/benefit analysis. No treatment or intervention is 100% available and effective for all current and future variants. We do not provide medical advice. Before taking any medication, consult a qualified physician who can provide personalized advice and details of risks and benefits based on your medical history and situation. FLCCC and WCH provide treatment protocols.
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