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1.
PLoS One ; 18(2): e0274470, 2023.
Artículo en Inglés | MEDLINE | ID: covidwho-2224441

RESUMEN

We derive a simple asymptotic approximation for the long-run case fatality rate of COVID-19 (alpha and delta variants) and show that these estimations are highly correlated to the interaction between US State median age and projected US unemployment rate (Adj. r2 = 60%). We contrast this to the high level of correlation between point (instantaneous) estimates of per state case fatality rates and the interaction of median age, population density and current unemployment rates (Adj. r2 = 50.2%). To determine whether this is caused by a "race effect," we then analyze unemployment, race, median age and population density across US states and show that adding the interaction of African American population and unemployment explains 53.5% of the variance in COVID case fatality rates for the alpha and delta variants when considering instantaneous case fatality rate. Interestingly, when the asymptotic case fatality rate is used, the dependence on the African American population disappears, which is consistent with the fact that in the long-run COVID does not discriminate on race, but may discriminate on access to medical care which is highly correlated to employment in the US. The results provide further evidence of the impact inequality can have on case fatality rates in COVID-19 and the impact complex social, health and economic factors can have on patient survival.


Asunto(s)
COVID-19 , Humanos , COVID-19/epidemiología , SARS-CoV-2 , Pandemias , Empleo
2.
Science ; 372(6538)2021 04 09.
Artículo en Inglés | MEDLINE | ID: covidwho-1476375

RESUMEN

A severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) variant, VOC 202012/01 (lineage B.1.1.7), emerged in southeast England in September 2020 and is rapidly spreading toward fixation. Using a variety of statistical and dynamic modeling approaches, we estimate that this variant has a 43 to 90% (range of 95% credible intervals, 38 to 130%) higher reproduction number than preexisting variants. A fitted two-strain dynamic transmission model shows that VOC 202012/01 will lead to large resurgences of COVID-19 cases. Without stringent control measures, including limited closure of educational institutions and a greatly accelerated vaccine rollout, COVID-19 hospitalizations and deaths across England in the first 6 months of 2021 were projected to exceed those in 2020. VOC 202012/01 has spread globally and exhibits a similar transmission increase (59 to 74%) in Denmark, Switzerland, and the United States.


Asunto(s)
COVID-19/transmisión , COVID-19/virología , SARS-CoV-2 , Adolescente , Adulto , Anciano , Anciano de 80 o más Años , Número Básico de Reproducción , COVID-19/epidemiología , COVID-19/mortalidad , Vacunas contra la COVID-19 , Niño , Preescolar , Control de Enfermedades Transmisibles , Inglaterra/epidemiología , Europa (Continente)/epidemiología , Femenino , Humanos , Lactante , Masculino , Persona de Mediana Edad , Modelos Teóricos , Mutación , SARS-CoV-2/genética , SARS-CoV-2/crecimiento & desarrollo , SARS-CoV-2/patogenicidad , Índice de Severidad de la Enfermedad , Factores Socioeconómicos , Estados Unidos/epidemiología , Carga Viral , Adulto Joven
3.
Science ; 371(6538):149-149, 2021.
Artículo en Inglés | Academic Search Complete | ID: covidwho-1181922

RESUMEN

The article discusses about the novel variants of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) that caused COVID-19. One of these variant of concern was B.1.1.7 which was first detected in southeast England and spread to become the dominant lineage in the United Kingdom in just a few months.

4.
Sci Transl Med ; 12(554)2020 07 29.
Artículo en Inglés | MEDLINE | ID: covidwho-610874

RESUMEN

Detection of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infections to date has relied heavily on reverse transcription polymerase chain reaction testing. However, limited test availability, high false-negative rates, and the existence of asymptomatic or subclinical infections have resulted in an undercounting of the true prevalence of SARS-CoV-2. Here, we show how influenza-like illness (ILI) outpatient surveillance data can be used to estimate the prevalence of SARS-CoV-2. We found a surge of non-influenza ILI above the seasonal average in March 2020 and showed that this surge correlated with coronavirus disease 2019 (COVID-19) case counts across states. If one-third of patients infected with SARS-CoV-2 in the United States sought care, this ILI surge would have corresponded to more than 8.7 million new SARS-CoV-2 infections across the United States during the 3-week period from 8 to 28 March 2020. Combining excess ILI counts with the date of onset of community transmission in the United States, we also show that the early epidemic in the United States was unlikely to have been doubling slower than every 4 days. Together, these results suggest a conceptual model for the COVID-19 epidemic in the United States characterized by rapid spread across the United States with more than 80% infected individuals remaining undetected. We emphasize the importance of testing these findings with seroprevalence data and discuss the broader potential to use syndromic surveillance for early detection and understanding of emerging infectious diseases.


Asunto(s)
Betacoronavirus/fisiología , Infecciones por Coronavirus/epidemiología , Gripe Humana/epidemiología , Neumonía Viral/epidemiología , Vigilancia de la Población , COVID-19 , Infecciones por Coronavirus/mortalidad , Humanos , Pandemias , Aceptación de la Atención de Salud , Neumonía Viral/mortalidad , Prevalencia , SARS-CoV-2 , Síndrome , Estados Unidos/epidemiología
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