TY - JOUR
T1 - 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
AU - Christensen, Paul A.
AU - Olsen, Randall J.
AU - Long, S. Wesley
AU - Snehal, Richard
AU - Davis, James J.
AU - Ojeda Saavedra, Matthew
AU - Reppond, Kristina
AU - Shyer, Madison N.
AU - Cambric, Jessica
AU - Gadd, Ryan
AU - Thakur, Rashi M.
AU - Batajoo, Akanksha
AU - Mangham, Regan
AU - Pena, Sindy
AU - Trinh, Trina
AU - Kinskey, Jacob C.
AU - Williams, Guy
AU - Olson, Robert
AU - Gollihar, Jimmy
AU - Musser, James M.
N1 - Funding Information:
Supported by the Houston Methodist Academic Institute Infectious Diseases Fund ; and in part with funds from the National Institute of Allergy and Infectious Diseases , NIH, Department of Health and Human Services , under contract 75N93019C00076 (J.J.D.).
Publisher Copyright:
© 2022 American Society for Investigative Pathology
PY - 2022/4
Y1 - 2022/4
N2 - 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.
AB - 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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U2 - 10.1016/j.ajpath.2022.01.007
DO - 10.1016/j.ajpath.2022.01.007
M3 - Article
C2 - 35123975
AN - SCOPUS:85126385569
VL - 192
SP - 642
EP - 652
JO - American Journal of Pathology
JF - American Journal of Pathology
SN - 0002-9440
IS - 4
ER -