Nirmatrelvir Plus Ritonavir for Early COVID-19 in a Large U.S. Health System : A Population-Based Cohort Study.


Journal

Annals of internal medicine
ISSN: 1539-3704
Titre abrégé: Ann Intern Med
Pays: United States
ID NLM: 0372351

Informations de publication

Date de publication:
01 2023
Historique:
pubmed: 13 12 2022
medline: 19 1 2023
entrez: 12 12 2022
Statut: ppublish

Résumé

In the EPIC-HR (Evaluation of Protease Inhibition for Covid-19 in High-Risk Patients) trial, nirmatrelvir plus ritonavir led to an 89% reduction in hospitalization or death among unvaccinated outpatients with early COVID-19. The clinical impact of nirmatrelvir plus ritonavir among vaccinated populations is uncertain. To assess whether nirmatrelvir plus ritonavir reduces risk for hospitalization or death among outpatients with early COVID-19 in the setting of prevalent SARS-CoV-2 immunity and immune-evasive SARS-CoV-2 lineages. Population-based cohort study analyzed to emulate a clinical trial using inverse probability-weighted models to account for anticipated bias in treatment. A large health care system providing care for 1.5 million patients in Massachusetts and New Hampshire during the Omicron wave (1 January to 17 July 2022). 44 551 nonhospitalized adults (90.3% with ≥3 vaccine doses) aged 50 years or older with COVID-19 and no contraindications for nirmatrelvir plus ritonavir. The primary outcome was a composite of hospitalization within 14 days or death within 28 days of a COVID-19 diagnosis. During the study period, 12 541 (28.1%) patients were prescribed nirmatrelvir plus ritonavir, and 32 010 (71.9%) were not. Patients prescribed nirmatrelvir plus ritonavir were more likely to be older, have more comorbidities, and be vaccinated. The composite outcome of hospitalization or death occurred in 69 (0.55%) patients who were prescribed nirmatrelvir plus ritonavir and 310 (0.97%) who were not (adjusted risk ratio, 0.56 [95% CI, 0.42 to 0.75]). Recipients of nirmatrelvir plus ritonavir had lower risk for hospitalization (adjusted risk ratio, 0.60 [CI, 0.44 to 0.81]) and death (adjusted risk ratio, 0.29 [CI, 0.12 to 0.71]). Potential residual confounding due to differential access to COVID-19 vaccines, diagnostic tests, and treatment. The overall risk for hospitalization or death was already low (1%) after an outpatient diagnosis of COVID-19, but nirmatrelvir plus ritonavir reduced this risk further. National Institutes of Health.

Sections du résumé

BACKGROUND
In the EPIC-HR (Evaluation of Protease Inhibition for Covid-19 in High-Risk Patients) trial, nirmatrelvir plus ritonavir led to an 89% reduction in hospitalization or death among unvaccinated outpatients with early COVID-19. The clinical impact of nirmatrelvir plus ritonavir among vaccinated populations is uncertain.
OBJECTIVE
To assess whether nirmatrelvir plus ritonavir reduces risk for hospitalization or death among outpatients with early COVID-19 in the setting of prevalent SARS-CoV-2 immunity and immune-evasive SARS-CoV-2 lineages.
DESIGN
Population-based cohort study analyzed to emulate a clinical trial using inverse probability-weighted models to account for anticipated bias in treatment.
SETTING
A large health care system providing care for 1.5 million patients in Massachusetts and New Hampshire during the Omicron wave (1 January to 17 July 2022).
PATIENTS
44 551 nonhospitalized adults (90.3% with ≥3 vaccine doses) aged 50 years or older with COVID-19 and no contraindications for nirmatrelvir plus ritonavir.
MEASUREMENTS
The primary outcome was a composite of hospitalization within 14 days or death within 28 days of a COVID-19 diagnosis.
RESULTS
During the study period, 12 541 (28.1%) patients were prescribed nirmatrelvir plus ritonavir, and 32 010 (71.9%) were not. Patients prescribed nirmatrelvir plus ritonavir were more likely to be older, have more comorbidities, and be vaccinated. The composite outcome of hospitalization or death occurred in 69 (0.55%) patients who were prescribed nirmatrelvir plus ritonavir and 310 (0.97%) who were not (adjusted risk ratio, 0.56 [95% CI, 0.42 to 0.75]). Recipients of nirmatrelvir plus ritonavir had lower risk for hospitalization (adjusted risk ratio, 0.60 [CI, 0.44 to 0.81]) and death (adjusted risk ratio, 0.29 [CI, 0.12 to 0.71]).
LIMITATION
Potential residual confounding due to differential access to COVID-19 vaccines, diagnostic tests, and treatment.
CONCLUSION
The overall risk for hospitalization or death was already low (1%) after an outpatient diagnosis of COVID-19, but nirmatrelvir plus ritonavir reduced this risk further.
PRIMARY FUNDING SOURCE
National Institutes of Health.

Identifiants

pubmed: 36508742
doi: 10.7326/M22-2141
pmc: PMC9753458
doi:

Substances chimiques

Antiviral Agents 0
COVID-19 Vaccines 0
Ritonavir O3J8G9O825

Types de publication

Clinical Trial Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

77-84

Subventions

Organisme : NICHD NIH HHS
ID : K01 HD100222
Pays : United States
Organisme : NCI NIH HHS
ID : R01 CA236546
Pays : United States

Commentaires et corrections

Type : UpdateOf
Type : CommentIn

Auteurs

Scott Dryden-Peterson (S)

Brigham and Women's Hospital and Harvard T.H. Chan School of Public Health, Boston, Massachusetts, and Botswana Harvard AIDS Institute, Gaborone, Botswana (S.D.).

Andy Kim (A)

Brigham and Women's Hospital, Boston, Massachusetts (A.K., L.D., E.D., L.R.B., A.E.W.).

Arthur Y Kim (AY)

Massachusetts General Hospital, Boston, Massachusetts (A.Y.K., I.T.L., R.T.G.).

Ellen C Caniglia (EC)

Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania (E.C.C.).

Inga T Lennes (IT)

Massachusetts General Hospital, Boston, Massachusetts (A.Y.K., I.T.L., R.T.G.).

Rajesh Patel (R)

Beth Israel Lahey Health, Cambridge, Massachusetts (R.P.).

Lindsay Gainer (L)

Mass General Brigham Integrated Care, Somerville, Massachusetts (L.G.).

Lisa Dutton (L)

Brigham and Women's Hospital, Boston, Massachusetts (A.K., L.D., E.D., L.R.B., A.E.W.).

Elizabeth Donahue (E)

Brigham and Women's Hospital, Boston, Massachusetts (A.K., L.D., E.D., L.R.B., A.E.W.).

Rajesh T Gandhi (RT)

Massachusetts General Hospital, Boston, Massachusetts (A.Y.K., I.T.L., R.T.G.).

Lindsey R Baden (LR)

Brigham and Women's Hospital, Boston, Massachusetts (A.K., L.D., E.D., L.R.B., A.E.W.).

Ann E Woolley (AE)

Brigham and Women's Hospital, Boston, Massachusetts (A.K., L.D., E.D., L.R.B., A.E.W.).

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