Real‐world effectiveness of Azvudine versus nirmatrelvir–ritonavir in hospitalized patients with COVID‐19: A retrospective cohort study

Author:

Deng Guangtong12345ORCID,Li Daishi12345,Sun Yuming6,Jin Liping12345,Zhou Qian12345,Xiao Chenggen7,Wu Qingrong12345,Sun Huiyan12345,Dian Yating12345,Zeng Furong8ORCID,Pan Pinhua9ORCID,Shen Minxue12345

Affiliation:

1. Department of Dermatology, Xiangya Hospital Central South University Changsha China

2. National Engineering Research Center of Personalized Diagnostic and Therapeutic Technology Changsha China

3. Furong Laboratory Changsha Hunan China

4. Hunan Key Laboratory of Skin Cancer and Psoriasis, Hunan Engineering Research Center of Skin Health and Disease, Xiangya Hospital Central South University Changsha China

5. National Clinical Research Center for Geriatric Disorders Xiangya Hospital Changsha China

6. Department of Plastic and Cosmetic Surgery, Xiangya Hospital Central South University Changsha Hunan China

7. Department of Emergency, Xiangya Hospital Central South University Changsha Hunan China

8. Department of Oncology, Xiangya Hospital Central South University Changsha Hunan China

9. Department of Respiratory Medicine, Xiangya Hospital Central South University Changsha Hunan China

Abstract

AbstractChinese guidelines prioritize the use of Azvudine and nirmatrelvir–ritonavir in COVID‐19 patients. Nevertheless, the real‐world effectiveness of Azvudine versus nirmatrelvir–ritonavir is still lacking, despite clinical trials showing their effectiveness compared with matched controls. To compare the effectiveness of Azvudine versus nirmatrelvir–ritonavir treatments in real‐world clinical practice, we identified 2118 hospitalized COVID‐19 patients, with a follow‐up of up to 38 days. After exclusions and propensity score matching, we included 281 Azvudine recipients and 281 nirmatrelvir–ritonavir recipients who did not receive oxygen therapy at admission. The lower crude incidence rate of composite disease progression outcome (7.83 vs. 14.83 per 1000 person‐days, p = 0.026) and all‐cause death (2.05 vs. 5.78 per 1000 person‐days, p = 0.052) were observed among Azvudine recipients. Azvudine was associated with lower risks of composite disease progression outcome (hazard ratio [HR]: 0.55; 95% confidence interval [CI]: 0.32–0.94) and all‐cause death (HR: 0.40; 95% CI: 0.16–1.04). In subgroup analyses, the results of composite outcome retained significance among patients aged <65 years, those having a history of disease, those with severe COVID‐19 at admission, and those receiving antibiotics. These findings suggest that Azvudine treatment showed effectiveness in hospitalized COVID‐19 patients compared with nirmatrelvir–ritonavir in terms of composite disease progression outcome.

Funder

National Natural Science Foundation of China

Publisher

Wiley

Subject

Infectious Diseases,Virology

Reference18 articles.

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5. Azvudine is a thymus-homing anti-SARS-CoV-2 drug effective in treating COVID-19 patients

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