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Signals of Significantly Increased Vaccine Breakthrough, Decreased Hospitalization Rates, and Less Severe Disease in Patients with Coronavirus Disease 2019 Caused by the Omicron Variant of Severe Acute Respiratory Syndrome Coronavirus 2 in Houston, Texas

Genetic variants of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) continue to dramatically alter the landscape of the coronavirus disease 2019 (COVID-19) pandemic. The recently described variant of concern designated Omicron (B.1.1.529) has rapidly spread worldwide and is now responsi...

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Autores principales: Christensen, Paul A., Olsen, Randall J., Long, S. Wesley, Snehal, Richard, Davis, James J., Ojeda Saavedra, Matthew, Reppond, Kristina, Shyer, Madison N., Cambric, Jessica, Gadd, Ryan, Thakur, Rashi M., Batajoo, Akanksha, Mangham, Regan, Pena, Sindy, Trinh, Trina, Kinskey, Jacob C., Williams, Guy, Olson, Robert, Gollihar, Jimmy, Musser, James M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Investigative Pathology 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8812084/
https://www.ncbi.nlm.nih.gov/pubmed/35123975
http://dx.doi.org/10.1016/j.ajpath.2022.01.007
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author Christensen, Paul A.
Olsen, Randall J.
Long, S. Wesley
Snehal, Richard
Davis, James J.
Ojeda Saavedra, Matthew
Reppond, Kristina
Shyer, Madison N.
Cambric, Jessica
Gadd, Ryan
Thakur, Rashi M.
Batajoo, Akanksha
Mangham, Regan
Pena, Sindy
Trinh, Trina
Kinskey, Jacob C.
Williams, Guy
Olson, Robert
Gollihar, Jimmy
Musser, James M.
author_facet Christensen, Paul A.
Olsen, Randall J.
Long, S. Wesley
Snehal, Richard
Davis, James J.
Ojeda Saavedra, Matthew
Reppond, Kristina
Shyer, Madison N.
Cambric, Jessica
Gadd, Ryan
Thakur, Rashi M.
Batajoo, Akanksha
Mangham, Regan
Pena, Sindy
Trinh, Trina
Kinskey, Jacob C.
Williams, Guy
Olson, Robert
Gollihar, Jimmy
Musser, James M.
author_sort Christensen, Paul A.
collection PubMed
description Genetic variants of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) continue to dramatically alter the landscape of the coronavirus disease 2019 (COVID-19) pandemic. The recently described variant of concern designated Omicron (B.1.1.529) has rapidly spread worldwide and is now responsible for the majority of COVID-19 cases in many countries. Because Omicron was recognized recently, many knowledge gaps exist about its epidemiology, clinical severity, and disease course. A genome sequencing study of SARS-CoV-2 in the Houston Methodist health care system identified 4468 symptomatic patients with infections caused by Omicron from late November 2021 through January 5, 2022. Omicron rapidly increased in only 3 weeks to cause 90% of all new COVID-19 cases, and at the end of the study period caused 98% of new cases. Compared with patients infected with either Alpha or Delta variants in our health care system, Omicron patients were significantly younger, had significantly increased vaccine breakthrough rates, and were significantly less likely to be hospitalized. Omicron patients required less intense respiratory support and had a shorter length of hospital stay, consistent with on average decreased disease severity. Two patients with Omicron stealth sublineage BA.2 also were identified. The data document the unusually rapid spread and increased occurrence of COVID-19 caused by the Omicron variant in metropolitan Houston, Texas, and address the lack of information about disease character among US patients.
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spelling pubmed-88120842022-02-04 Signals of Significantly Increased Vaccine Breakthrough, Decreased Hospitalization Rates, and Less Severe Disease in Patients with Coronavirus Disease 2019 Caused by the Omicron Variant of Severe Acute Respiratory Syndrome Coronavirus 2 in Houston, Texas Christensen, Paul A. Olsen, Randall J. Long, S. Wesley Snehal, Richard Davis, James J. Ojeda Saavedra, Matthew Reppond, Kristina Shyer, Madison N. Cambric, Jessica Gadd, Ryan Thakur, Rashi M. Batajoo, Akanksha Mangham, Regan Pena, Sindy Trinh, Trina Kinskey, Jacob C. Williams, Guy Olson, Robert Gollihar, Jimmy Musser, James M. Am J Pathol Regular Article Genetic variants of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) continue to dramatically alter the landscape of the coronavirus disease 2019 (COVID-19) pandemic. The recently described variant of concern designated Omicron (B.1.1.529) has rapidly spread worldwide and is now responsible for the majority of COVID-19 cases in many countries. Because Omicron was recognized recently, many knowledge gaps exist about its epidemiology, clinical severity, and disease course. A genome sequencing study of SARS-CoV-2 in the Houston Methodist health care system identified 4468 symptomatic patients with infections caused by Omicron from late November 2021 through January 5, 2022. Omicron rapidly increased in only 3 weeks to cause 90% of all new COVID-19 cases, and at the end of the study period caused 98% of new cases. Compared with patients infected with either Alpha or Delta variants in our health care system, Omicron patients were significantly younger, had significantly increased vaccine breakthrough rates, and were significantly less likely to be hospitalized. Omicron patients required less intense respiratory support and had a shorter length of hospital stay, consistent with on average decreased disease severity. Two patients with Omicron stealth sublineage BA.2 also were identified. The data document the unusually rapid spread and increased occurrence of COVID-19 caused by the Omicron variant in metropolitan Houston, Texas, and address the lack of information about disease character among US patients. American Society for Investigative Pathology 2022-04 /pmc/articles/PMC8812084/ /pubmed/35123975 http://dx.doi.org/10.1016/j.ajpath.2022.01.007 Text en © 2022 American Society for Investigative Pathology. Published by Elsevier Inc. All rights reserved.
spellingShingle Regular Article
Christensen, Paul A.
Olsen, Randall J.
Long, S. Wesley
Snehal, Richard
Davis, James J.
Ojeda Saavedra, Matthew
Reppond, Kristina
Shyer, Madison N.
Cambric, Jessica
Gadd, Ryan
Thakur, Rashi M.
Batajoo, Akanksha
Mangham, Regan
Pena, Sindy
Trinh, Trina
Kinskey, Jacob C.
Williams, Guy
Olson, Robert
Gollihar, Jimmy
Musser, James M.
Signals of Significantly Increased Vaccine Breakthrough, Decreased Hospitalization Rates, and Less Severe Disease in Patients with Coronavirus Disease 2019 Caused by the Omicron Variant of Severe Acute Respiratory Syndrome Coronavirus 2 in Houston, Texas
title Signals of Significantly Increased Vaccine Breakthrough, Decreased Hospitalization Rates, and Less Severe Disease in Patients with Coronavirus Disease 2019 Caused by the Omicron Variant of Severe Acute Respiratory Syndrome Coronavirus 2 in Houston, Texas
title_full Signals of Significantly Increased Vaccine Breakthrough, Decreased Hospitalization Rates, and Less Severe Disease in Patients with Coronavirus Disease 2019 Caused by the Omicron Variant of Severe Acute Respiratory Syndrome Coronavirus 2 in Houston, Texas
title_fullStr Signals of Significantly Increased Vaccine Breakthrough, Decreased Hospitalization Rates, and Less Severe Disease in Patients with Coronavirus Disease 2019 Caused by the Omicron Variant of Severe Acute Respiratory Syndrome Coronavirus 2 in Houston, Texas
title_full_unstemmed Signals of Significantly Increased Vaccine Breakthrough, Decreased Hospitalization Rates, and Less Severe Disease in Patients with Coronavirus Disease 2019 Caused by the Omicron Variant of Severe Acute Respiratory Syndrome Coronavirus 2 in Houston, Texas
title_short Signals of Significantly Increased Vaccine Breakthrough, Decreased Hospitalization Rates, and Less Severe Disease in Patients with Coronavirus Disease 2019 Caused by the Omicron Variant of Severe Acute Respiratory Syndrome Coronavirus 2 in Houston, Texas
title_sort signals of significantly increased vaccine breakthrough, decreased hospitalization rates, and less severe disease in patients with coronavirus disease 2019 caused by the omicron variant of severe acute respiratory syndrome coronavirus 2 in houston, texas
topic Regular Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8812084/
https://www.ncbi.nlm.nih.gov/pubmed/35123975
http://dx.doi.org/10.1016/j.ajpath.2022.01.007
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