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1.
J Med Virol ; 93(1): 506-512, 2021 01.
Artículo en Inglés | MEDLINE | ID: covidwho-1206794

RESUMEN

To investigate the factors associated with the duration of severe acute respiratory syndrome coronavirus 2 RNA shedding in patients with coronavirus disease 2019 (COVID-19). A retrospective cohort of COVID-19 patients admitted to a designated hospital in Beijing was analyzed to study the factors affecting the duration of viral shedding. The median duration of viral shedding was 11 days (IQR, 8-14.3 days) as measured from illness onset. Univariate regression analysis showed that disease severity, corticosteroid therapy, fever (temperature>38.5°C), and time from onset to hospitalization were associated with prolonged duration of viral shedding (P < .05). Multivariate regression analysis showed that fever (temperature>38.5°C) (OR, 5.1, 95%CI: 1.5-18.1), corticosteroid therapy (OR, 6.3, 95%CI: 1.5-27.8), and time from onset to hospitalization (OR, 1.8, 95%CI: 1.19-2.7) were associated with increased odds of prolonged duration of viral shedding. Corticosteroid treatment, fever (temperature>38.5°C), and longer time from onset to hospitalization were associated with prolonged viral shedding in COVID-19 patients.


Asunto(s)
COVID-19/virología , SARS-CoV-2/fisiología , Esparcimiento de Virus/fisiología , Corticoesteroides/uso terapéutico , Adulto , COVID-19/patología , Femenino , Humanos , Masculino , Persona de Mediana Edad , ARN Viral/aislamiento & purificación , Factores de Riesgo , Factores de Tiempo , Tratamiento Farmacológico de COVID-19
2.
Respiration ; 100(2): 116-126, 2021.
Artículo en Inglés | MEDLINE | ID: covidwho-1044350

RESUMEN

BACKGROUND: There is still no clinical evidence available to support or to oppose corticosteroid treatment for coronavirus disease 2019 (COVID-19) pneumonia. OBJECTIVE: To investigate the efficacy and safety of corticosteroid given to the hospitalized patients with COVID-19 pneumonia. METHODS: This was a prospective, multicenter, single-blind, randomized control trial. Adult patients with COVID-19 pneumonia who were admitted to the general ward were randomly assigned to either receive methylprednisolone or not for 7 days. The primary end point was the incidence of clinical deterioration 14 days after randomization. RESULTS: We terminated this trial early because the number of patients with COVID-19 pneumonia in all the centers decreased in late March. Finally, a total of 86 COVID-19 patients underwent randomization. There was no difference of the incidence of clinical deterioration between the methylprednisolone group and control group (4.8 vs. 4.8%, p = 1.000). The duration of throat viral RNA detectability in the methylprednisolone group was 11 days (interquartile range, 6-16 days), which was significantly longer than that in the control group (8 days [2-12 days], p = 0.030). There were no significant differences between the 2 groups in other secondary outcomes. Mass cytometry discovered CD3+ T cells, CD8+ T cells, and NK cells in the methylprednisolone group which were significantly lower than those in the control group after randomization (p < 0.05). CONCLUSIONS: From this prematurely closed trial, we found that the short-term early use of corticosteroid could suppress the immune cells, which may prolong severe acute respiratory syndrome coronavirus 2 shedding in patients with COVID-19 pneumonia. TRIAL REGISTRATION: ClinicalTrials.gov, NCT04273321.


Asunto(s)
Tratamiento Farmacológico de COVID-19 , Glucocorticoides/uso terapéutico , Hospitalización , Metilprednisolona/uso terapéutico , Faringe/química , ARN Viral/aislamiento & purificación , Esparcimiento de Virus , Adulto , Anciano , Antibacterianos/uso terapéutico , Antivirales/uso terapéutico , Complejo CD3 , Linfocitos T CD8-positivos , COVID-19/sangre , COVID-19/terapia , COVID-19/transmisión , Prueba de Ácido Nucleico para COVID-19 , Progresión de la Enfermedad , Intervención Médica Temprana , Oxigenación por Membrana Extracorpórea , Femenino , Humanos , Células Asesinas Naturales , Recuento de Linfocitos , Masculino , Persona de Mediana Edad , Terapia por Inhalación de Oxígeno , Habitaciones de Pacientes , Faringe/virología , Modelos de Riesgos Proporcionales , Respiración Artificial , SARS-CoV-2 , Método Simple Ciego , Subgrupos de Linfocitos T , Linfocitos T , Factores de Tiempo , Resultado del Tratamiento
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