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Viral and Symptom Rebound in Untreated COVID-19 Infection

BACKGROUND: There are reports of viral RNA and symptom rebound in people with COVID-19 treated with nirmatrelvir/ritonavir. Since the natural course of viral and symptom trajectories of COVID-19 has not been well described, we evaluated the incidence of viral and symptom rebound in untreated outpati...

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Autores principales: Deo, Rinki, Choudhary, Manish C., Moser, Carlee, Ritz, Justin, Daar, Eric S., Wohl, David A., Greninger, Alexander L., Eron, Joseph J., Currier, Judith S., Hughes, Michael D., Smith, Davey M., Chew, Kara W., Li, Jonathan Z.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9387151/
https://www.ncbi.nlm.nih.gov/pubmed/35982660
http://dx.doi.org/10.1101/2022.08.01.22278278
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author Deo, Rinki
Choudhary, Manish C.
Moser, Carlee
Ritz, Justin
Daar, Eric S.
Wohl, David A.
Greninger, Alexander L.
Eron, Joseph J.
Currier, Judith S.
Hughes, Michael D.
Smith, Davey M.
Chew, Kara W.
Li, Jonathan Z.
author_facet Deo, Rinki
Choudhary, Manish C.
Moser, Carlee
Ritz, Justin
Daar, Eric S.
Wohl, David A.
Greninger, Alexander L.
Eron, Joseph J.
Currier, Judith S.
Hughes, Michael D.
Smith, Davey M.
Chew, Kara W.
Li, Jonathan Z.
author_sort Deo, Rinki
collection PubMed
description BACKGROUND: There are reports of viral RNA and symptom rebound in people with COVID-19 treated with nirmatrelvir/ritonavir. Since the natural course of viral and symptom trajectories of COVID-19 has not been well described, we evaluated the incidence of viral and symptom rebound in untreated outpatients with mild-moderate COVID-19. METHODS: The study population included 568 participants enrolled in the ACTIV-2/A5401 platform trial who received placebo. Anterior nasal swabs were collected for SARS-CoV-2 RNA testing on days 0–14, 21 and 28. Participants recorded the severity of 13 targeted symptoms daily from day 0 to 28. Viral rebound was defined as ≥0.5 log(10) viral RNA copies/mL increase and symptom rebound was defined as a 4-point total symptom score increase from baseline. Baseline was defined as study day 4 (primary analysis) or 8 days from symptom onset (secondary analysis). FINDINGS: In both the primary and secondary analyses, 12% of participants had viral rebound. Viral rebounders were older than non-rebounders (median 54 vs 47 years, P=0.04). Symptom rebound occurred in 27% of participants after initial symptom improvement and in 10% of participants after initial symptom resolution. The combination of high-level viral rebound to ≥5.0 log(10) RNA copies/mL and symptom rebound after initial improvement was observed in 1–2% of participants. INTERPRETATION: Viral RNA rebound or symptom relapse in the absence of antiviral treatment is common, but the combination of high-level viral and symptom rebound is rare.
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spelling pubmed-93871512022-08-19 Viral and Symptom Rebound in Untreated COVID-19 Infection Deo, Rinki Choudhary, Manish C. Moser, Carlee Ritz, Justin Daar, Eric S. Wohl, David A. Greninger, Alexander L. Eron, Joseph J. Currier, Judith S. Hughes, Michael D. Smith, Davey M. Chew, Kara W. Li, Jonathan Z. medRxiv Article BACKGROUND: There are reports of viral RNA and symptom rebound in people with COVID-19 treated with nirmatrelvir/ritonavir. Since the natural course of viral and symptom trajectories of COVID-19 has not been well described, we evaluated the incidence of viral and symptom rebound in untreated outpatients with mild-moderate COVID-19. METHODS: The study population included 568 participants enrolled in the ACTIV-2/A5401 platform trial who received placebo. Anterior nasal swabs were collected for SARS-CoV-2 RNA testing on days 0–14, 21 and 28. Participants recorded the severity of 13 targeted symptoms daily from day 0 to 28. Viral rebound was defined as ≥0.5 log(10) viral RNA copies/mL increase and symptom rebound was defined as a 4-point total symptom score increase from baseline. Baseline was defined as study day 4 (primary analysis) or 8 days from symptom onset (secondary analysis). FINDINGS: In both the primary and secondary analyses, 12% of participants had viral rebound. Viral rebounders were older than non-rebounders (median 54 vs 47 years, P=0.04). Symptom rebound occurred in 27% of participants after initial symptom improvement and in 10% of participants after initial symptom resolution. The combination of high-level viral rebound to ≥5.0 log(10) RNA copies/mL and symptom rebound after initial improvement was observed in 1–2% of participants. INTERPRETATION: Viral RNA rebound or symptom relapse in the absence of antiviral treatment is common, but the combination of high-level viral and symptom rebound is rare. Cold Spring Harbor Laboratory 2022-08-02 /pmc/articles/PMC9387151/ /pubmed/35982660 http://dx.doi.org/10.1101/2022.08.01.22278278 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which allows reusers to copy and distribute the material in any medium or format in unadapted form only, for noncommercial purposes only, and only so long as attribution is given to the creator.
spellingShingle Article
Deo, Rinki
Choudhary, Manish C.
Moser, Carlee
Ritz, Justin
Daar, Eric S.
Wohl, David A.
Greninger, Alexander L.
Eron, Joseph J.
Currier, Judith S.
Hughes, Michael D.
Smith, Davey M.
Chew, Kara W.
Li, Jonathan Z.
Viral and Symptom Rebound in Untreated COVID-19 Infection
title Viral and Symptom Rebound in Untreated COVID-19 Infection
title_full Viral and Symptom Rebound in Untreated COVID-19 Infection
title_fullStr Viral and Symptom Rebound in Untreated COVID-19 Infection
title_full_unstemmed Viral and Symptom Rebound in Untreated COVID-19 Infection
title_short Viral and Symptom Rebound in Untreated COVID-19 Infection
title_sort viral and symptom rebound in untreated covid-19 infection
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9387151/
https://www.ncbi.nlm.nih.gov/pubmed/35982660
http://dx.doi.org/10.1101/2022.08.01.22278278
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