File Download

There are no files associated with this item.

  Links for fulltext
     (May Require Subscription)

Article: Effectiveness of nirmatrelvir/ritonavir and molnupiravir in non-hospitalized adults with COVID-19: systematic review and meta-analysis of observational studies

TitleEffectiveness of nirmatrelvir/ritonavir and molnupiravir in non-hospitalized adults with COVID-19: systematic review and meta-analysis of observational studies
Authors
Issue Date31-May-2024
PublisherOxford 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 Identifierhttp://hdl.handle.net/10722/346333
ISSN
2023 Impact Factor: 3.9
2023 SCImago Journal Rankings: 1.271

 

DC FieldValueLanguage
dc.contributor.authorMesfin, YM-
dc.contributor.authorBlais, JE-
dc.contributor.authorKibret, KT-
dc.contributor.authorTegegne, TK-
dc.contributor.authorCowling, BJ-
dc.contributor.authorWu, P-
dc.date.accessioned2024-09-14T00:30:37Z-
dc.date.available2024-09-14T00:30:37Z-
dc.date.issued2024-05-31-
dc.identifier.citationJournal of Antimicrobial Chemotherapy, 2024, v. 79, n. 9, p. 2119-2131-
dc.identifier.issn0305-7453-
dc.identifier.urihttp://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.languageeng-
dc.publisherOxford University Press-
dc.relation.ispartofJournal of Antimicrobial Chemotherapy-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.titleEffectiveness of nirmatrelvir/ritonavir and molnupiravir in non-hospitalized adults with COVID-19: systematic review and meta-analysis of observational studies-
dc.typeArticle-
dc.identifier.doi10.1093/jac/dkae163-
dc.identifier.volume79-
dc.identifier.issue9-
dc.identifier.spage2119-
dc.identifier.epage2131-
dc.identifier.eissn1460-2091-
dc.identifier.issnl0305-7453-

Export via OAI-PMH Interface in XML Formats


OR


Export to Other Non-XML Formats