» Articles » PMID: 36472873

Incidence of Viral Rebound After Treatment With Nirmatrelvir-Ritonavir and Molnupiravir

Overview
Journal JAMA Netw Open
Specialty General Medicine
Date 2022 Dec 6
PMID 36472873
Authors
Affiliations
Soon will be listed here.
Abstract

Importance: Some patients treated with nirmatrelvir-ritonavir have experienced rebound of COVID-19 infections and symptoms; however, data are scarce on whether viral rebound also occurs in patients with COVID-19 receiving or not receiving molnupiravir.

Objective: To examine the incidence of viral rebound in patients with COVID-19 who were treated with the oral antiviral agents nirmatrelvir-ritonavir and molnupiravir.

Design, Setting, And Participants: This cohort study identified 41 255 patients with COVID-19 who were hospitalized from January 1, 2022, to March 31, 2022, in Hong Kong and assessed 12 629 patients with serial cycle threshold (Ct) values measured. Patients were followed up until the occurrence of the clinical end point of interest, death, date of data retrieval (July 31, 2022), or up to 30 days of follow-up, whichever came first.

Exposures: Molnupiravir or nirmatrelvir-ritonavir treatment.

Main Outcomes And Measures: Viral rebound, defined as a Ct value greater than 40 that decreased to 40 or less.

Results: Of 12 629 patients (mean [SD] age, 65.4 [20.9] years; 6624 [52.5%] male), 11 688 (92.5%) were oral antiviral nonusers, 746 (5.9%) were molnupiravir users, and 195 (1.5%) were nirmatrelvir-ritonavir users. Compared with nonusers, oral antiviral users were older, had more comorbidities, and had lower complete vaccination rates. The mean (SD) baseline Ct value was slightly higher in nirmatrelvir-ritonavir users (22.2 [6.0]) than nonusers (21.0 [5.4]) and molnupiravir users (20.9 [5.4]) (P = .04). Viral rebound occurred in 68 nonusers (0.6%), 2 nirmatrelvir-ritonavir users (1.0%), and 6 molnupiravir users (0.8%). Among 76 patients with viral rebound, 12 of 68 nonusers, 1 of 6 molnupiravir users, and neither of the nirmatrelvir-ritonavir users died of COVID-19.

Conclusions And Relevance: In this cohort study, viral rebound was uncommon in patients taking molnupiravir or nirmatrelvir-ritonavir and was not associated with increased risk of mortality. Given these findings, novel oral antivirals should be considered as a treatment for more patients with COVID-19 in the early phase of the infection.

Citing Articles

Cardiac Arrhythmias and Autonomic Dysfunction Associated With COVID-19: A Scientific Statement From the American Heart Association.

Gopinathannair R, Olshansky B, Chung M, Gordon S, Joglar J, Marcus G Circulation. 2024; 150(21):e449-e465.

PMID: 39397661 PMC: 11734731. DOI: 10.1161/CIR.0000000000001290.


Modeling suggests SARS-CoV-2 rebound after nirmatrelvir-ritonavir treatment is driven by target cell preservation coupled with incomplete viral clearance.

Phan T, Ribeiro R, Edelstein G, Boucau J, Uddin R, Marino C bioRxiv. 2024; .

PMID: 39345409 PMC: 11429690. DOI: 10.1101/2024.09.13.613000.


Persistence of an Infectious Form of SARS-CoV-2 After Protease Inhibitor Treatment of Permissive Cells In Vitro.

Nair M, Luck M, Huang Y, Sabo Y, Ho D J Infect Dis. 2024; 231(1):e68-e76.

PMID: 39132824 PMC: 11793057. DOI: 10.1093/infdis/jiae385.


Comprehensive Review of COVID-19: Epidemiology, Pathogenesis, Advancement in Diagnostic and Detection Techniques, and Post-Pandemic Treatment Strategies.

Chung Y, Lam C, Tan P, Tsang H, Wong S Int J Mol Sci. 2024; 25(15).

PMID: 39125722 PMC: 11312261. DOI: 10.3390/ijms25158155.


Viral SARS-CoV-2 Rebound Rates in Linked Commercial Pharmacy-Based Testing and Health Care Claims.

Kelly S, McEwen L, Isaksson M, Murphy S, White S, Levy M Open Forum Infect Dis. 2024; 11(6):ofae243.

PMID: 38854397 PMC: 11161861. DOI: 10.1093/ofid/ofae243.


References
1.
Yip T, Wong V, Lui G, Chow V, Tse Y, Hui V . Current and Past Infections of HBV Do Not Increase Mortality in Patients With COVID-19. Hepatology. 2021; 74(4):1750-1765. PMC: 8239872. DOI: 10.1002/hep.31890. View

2.
Jayk Bernal A, Gomes da Silva M, Musungaie D, Kovalchuk E, Gonzalez A, Delos Reyes V . Molnupiravir for Oral Treatment of Covid-19 in Nonhospitalized Patients. N Engl J Med. 2021; 386(6):509-520. PMC: 8693688. DOI: 10.1056/NEJMoa2116044. View

3.
Boucau J, Uddin R, Marino C, Regan J, Flynn J, Choudhary M . Characterization of Virologic Rebound Following Nirmatrelvir-Ritonavir Treatment for Coronavirus Disease 2019 (COVID-19). Clin Infect Dis. 2022; 76(3):e526-e529. PMC: 9384370. DOI: 10.1093/cid/ciac512. View

4.
S K S, P A A, B S, Kalala K, Pm A, Sabarathinam S . Drug interaction risk between cardioprotective drugs and drugs used in treatment of COVID-19: A evidence-based review from six databases. Diabetes Metab Syndr. 2022; 16(3):102451. PMC: 8898923. DOI: 10.1016/j.dsx.2022.102451. View

5.
Yip T, Lui G, Lai M, Wong V, Tse Y, Ma B . Impact of the Use of Oral Antiviral Agents on the Risk of Hospitalization in Community Coronavirus Disease 2019 Patients (COVID-19). Clin Infect Dis. 2022; 76(3):e26-e33. PMC: 9452147. DOI: 10.1093/cid/ciac687. View