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Oxford University Press - PMC COVID-19 Collection logoLink to Oxford University Press - PMC COVID-19 Collection
. 2022 Aug 29:ciac687. doi: 10.1093/cid/ciac687

Impact of the use of oral antiviral agents on the risk of hospitalization in community COVID-19 patients

Terry Cheuk Fung Yip 1,2,3,#, Grace Chung Yan Lui 4,5,6,#, Mandy Sze Man Lai 7,8, Vincent Wai Sun Wong 9,10,11, Yee Kit Tse 12,13,14, Bosco Hon Ming Ma 15, Elsie Hui 16, Maria KW Leung 17, Henry Lik Yuen Chan 18,19,20, David Shu Cheong Hui 21,22,23,, Grace Lai Hung Wong 24,25,26,
PMCID: PMC9452147  PMID: 36031408

ABSTRACT

Background

We examined the effectiveness of molnupiravir and nirmatrelvir/ritonavir in reducing hospitalization and deaths in a real-world cohort of non-hospitalized COVID-19 patients.

Methods

This was a territory-wide retrospective cohort study in Hong Kong. Non-hospitalized COVID-19 patients who attended designated outpatient clinics between 16 February and 31 March 2022 were identified. Patients hospitalized on the day of the first clinic appointment or used both oral antivirals were excluded. The primary endpoint was hospitalization. The secondary endpoint was a composite of intensive care unit admission, invasive mechanical ventilation use, and/or death.

Results

Of 93,883 patients, 83,154 (88.6%), 5,808 (6.2%), and 4,921 (5.2%) were oral antiviral non-users, molnupiravir users, and nirmatrelvir/ritonavir users respectively. Compared to non-users, oral antiviral users were older and had more comorbidities, lower complete vaccination rate, and more hospitalizations in the previous year. Molnupiravir users were older, and had more comorbidities, lower complete vaccination rate, and more hospitalizations in the previous year than nirmatrelvir/ritonavir users. At a median follow-up of 30 days, 1,931 (2.1%) patients were hospitalized and 225 (0.2%) patients developed the secondary endpoint. After propensity score weighting, nirmatrelvir/ritonavir use (weighted hazard ratio 0.79, 95%CI 0.65-0.95, P = 0.011) but not molnupiravir use (weighted hazard ratio 1.17, 95%CI 0.99-1.39, P = 0.062) was associated with a reduced risk of hospitalization than non-users. The use of molnupiravir or nirmatrelvir/ritonavir was not associated with a lower risk of the secondary endpoint as compared to non-users.

Conclusion

Use of nirmatrelvir/ritonavir but not molnupiravir was associated with a reduced risk of hospitalization in real-world non-hospitalized COVID-19 patients.

Keywords: SARS-CoV-2, hospital admission, death, molnupiravir, nirmatrelvir/ritonavir

Contributor Information

Terry Cheuk Fung Yip, Department of Medicine and Therapeutics; Medical Data Analytics Centre (MDAC); Institute of Digestive Disease.

Grace Chung Yan Lui, Department of Medicine and Therapeutics; Medical Data Analytics Centre (MDAC); Stanley Ho Centre for Emerging Infectious Diseases, Jockey Club School of Public Health & Primary Care.

Mandy Sze Man Lai, Department of Medicine and Therapeutics; Medical Data Analytics Centre (MDAC).

Vincent Wai Sun Wong, Department of Medicine and Therapeutics; Medical Data Analytics Centre (MDAC); Stanley Ho Centre for Emerging Infectious Diseases, Jockey Club School of Public Health & Primary Care.

Yee Kit Tse, Department of Medicine and Therapeutics; Medical Data Analytics Centre (MDAC); Institute of Digestive Disease.

Bosco Hon Ming Ma, Department of Medicine and Therapeutics.

Elsie Hui, Department of Medicine and Therapeutics.

Maria KW Leung, Department of Family Medicine, Prince of Wales Hospital, Hospital Authority, Hong Kong.

Henry Lik Yuen Chan, Medical Data Analytics Centre (MDAC); Faculty of Medicine, The Chinese University of Hong Kong; Hong Kong; Department of Internal Medicine, Union Hospital, Hong Kong.

David Shu Cheong Hui, Department of Medicine and Therapeutics; Medical Data Analytics Centre (MDAC); Stanley Ho Centre for Emerging Infectious Diseases, Jockey Club School of Public Health & Primary Care.

Grace Lai Hung Wong, Department of Medicine and Therapeutics; Medical Data Analytics Centre (MDAC); Institute of Digestive Disease.

Supplementary Material

ciac687_Supplementary_Data

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Supplementary Materials

ciac687_Supplementary_Data

Articles from Clinical Infectious Diseases: An Official Publication of the Infectious Diseases Society of America are provided here courtesy of Oxford University Press

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