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Article: Effectiveness of nirmatrelvir/ritonavir and molnupiravir in non-hospitalized adults with COVID-19: systematic review and meta-analysis of observational studies
Title | Effectiveness of nirmatrelvir/ritonavir and molnupiravir in non-hospitalized adults with COVID-19: systematic review and meta-analysis of observational studies |
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Authors | |
Issue Date | 31-May-2024 |
Publisher | Oxford University Press |
Citation | Journal of Antimicrobial Chemotherapy, 2024, v. 79, n. 9, p. 2119-2131 How to Cite? |
Abstract | Objective To determine the effectiveness of nirmatrelvir/ritonavir and molnupiravir among vaccinated and unvaccinated non-hospitalized adults with COVID-19. Methods Observational studies of nirmatrelvir/ritonavir or molnupiravir compared to no antiviral drug treatment for COVID-19 in non-hospitalized adults with data on vaccination status were included. We searched MEDLINE, EMBASE, Scopus, Web of Science, WHO COVID-19 Research Database and medRxiv for reports published between 1 January 2022 and 8 November 2023. The primary outcome was a composite of hospitalization or mortality up to 35 days after COVID-19 diagnosis. Risk of bias was assessed with ROBINS-I. Risk ratios (RR), hazard ratios (HR) and risk differences (RD) were separately estimated using random-effects models. Results We included 30 cohort studies on adults treated with nirmatrelvir/ritonavir (n = 462 279) and molnupiravir (n = 48 008). Nirmatrelvir/ritonavir probably reduced the composite outcome (RR 0.62, 95%CI 0.55–0.70; I2 = 0%; moderate certainty) with no evidence of effect modification by vaccination status (RR Psubgroup = 0.47). In five studies, RD estimates against the composite outcome for nirmatrelvir/ritonavir were 1.21% (95%CI 0.57% to 1.84%) in vaccinated and 1.72% (95%CI 0.59% to 2.85%) in unvaccinated subgroups. Molnupiravir may slightly reduce the composite outcome (RR 0.75, 95%CI 0.67–0.85; I2 = 32%; low certainty). Evidence of effect modification by vaccination status was inconsistent among studies reporting different effect measures (RR Psubgroup = 0.78; HR Psubgroup = 0.08). In two studies, RD against the composite outcome for molnupiravir were −0.01% (95%CI −1.13% to 1.10%) in vaccinated and 1.73% (95%CI −2.08% to 5.53%) in unvaccinated subgroups. Conclusions Among cohort studies of non-hospitalized adults with COVID-19, nirmatrelvir/ritonavir is effective against the composite outcome of severe COVID-19 independent of vaccination status. Further research and a reassessment of molnupiravir use among vaccinated adults are warranted. |
Persistent Identifier | http://hdl.handle.net/10722/346333 |
ISSN | 2023 Impact Factor: 3.9 2023 SCImago Journal Rankings: 1.271 |
DC Field | Value | Language |
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dc.contributor.author | Mesfin, YM | - |
dc.contributor.author | Blais, JE | - |
dc.contributor.author | Kibret, KT | - |
dc.contributor.author | Tegegne, TK | - |
dc.contributor.author | Cowling, BJ | - |
dc.contributor.author | Wu, P | - |
dc.date.accessioned | 2024-09-14T00:30:37Z | - |
dc.date.available | 2024-09-14T00:30:37Z | - |
dc.date.issued | 2024-05-31 | - |
dc.identifier.citation | Journal of Antimicrobial Chemotherapy, 2024, v. 79, n. 9, p. 2119-2131 | - |
dc.identifier.issn | 0305-7453 | - |
dc.identifier.uri | http://hdl.handle.net/10722/346333 | - |
dc.description.abstract | <p>Objective</p><p>To determine the effectiveness of nirmatrelvir/ritonavir and molnupiravir among vaccinated and unvaccinated non-hospitalized adults with COVID-19.</p><p>Methods</p><p>Observational studies of nirmatrelvir/ritonavir or molnupiravir compared to no antiviral drug treatment for COVID-19 in non-hospitalized adults with data on vaccination status were included. We searched MEDLINE, EMBASE, Scopus, Web of Science, WHO COVID-19 Research Database and <em>medRxiv</em> for reports published between 1 January 2022 and 8 November 2023. The primary outcome was a composite of hospitalization or mortality up to 35 days after COVID-19 diagnosis. Risk of bias was assessed with ROBINS-I. Risk ratios (RR), hazard ratios (HR) and risk differences (RD) were separately estimated using random-effects models.</p><p>Results</p><p>We included 30 cohort studies on adults treated with nirmatrelvir/ritonavir (<em>n</em> = 462 279) and molnupiravir (<em>n</em> = 48 008). Nirmatrelvir/ritonavir probably reduced the composite outcome (RR 0.62, 95%CI 0.55–0.70; <em>I</em><sup>2 </sup>= 0%; moderate certainty) with no evidence of effect modification by vaccination status (RR <em>P</em><sub>subgroup </sub>= 0.47). In five studies, RD estimates against the composite outcome for nirmatrelvir/ritonavir were 1.21% (95%CI 0.57% to 1.84%) in vaccinated and 1.72% (95%CI 0.59% to 2.85%) in unvaccinated subgroups.</p><p>Molnupiravir may slightly reduce the composite outcome (RR 0.75, 95%CI 0.67–0.85; <em>I</em><sup>2 </sup>= 32%; low certainty). Evidence of effect modification by vaccination status was inconsistent among studies reporting different effect measures (RR <em>P</em><sub>subgroup </sub>= 0.78; HR <em>P</em><sub>subgroup </sub>= 0.08). In two studies, RD against the composite outcome for molnupiravir were −0.01% (95%CI −1.13% to 1.10%) in vaccinated and 1.73% (95%CI −2.08% to 5.53%) in unvaccinated subgroups.</p><p>Conclusions</p><p>Among cohort studies of non-hospitalized adults with COVID-19, nirmatrelvir/ritonavir is effective against the composite outcome of severe COVID-19 independent of vaccination status. Further research and a reassessment of molnupiravir use among vaccinated adults are warranted.</p> | - |
dc.language | eng | - |
dc.publisher | Oxford University Press | - |
dc.relation.ispartof | Journal of Antimicrobial Chemotherapy | - |
dc.rights | This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. | - |
dc.title | Effectiveness of nirmatrelvir/ritonavir and molnupiravir in non-hospitalized adults with COVID-19: systematic review and meta-analysis of observational studies | - |
dc.type | Article | - |
dc.identifier.doi | 10.1093/jac/dkae163 | - |
dc.identifier.volume | 79 | - |
dc.identifier.issue | 9 | - |
dc.identifier.spage | 2119 | - |
dc.identifier.epage | 2131 | - |
dc.identifier.eissn | 1460-2091 | - |
dc.identifier.issnl | 0305-7453 | - |