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Cytomegalovirus reactivation in patients diagnosed with severe COVID-19: A point prevalence study in a general hospital

PURPOSE: To determine the prevalence of CMV reactivation in a population admitted for severe COVID-19 to a general hospital. METHODS: Point prevalence study in all hospitalized patients with severe COVID-19 (admitted either to general wards or ICU). Determination of the presence of CMV DNA in circul...

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Autores principales: Pérez-Granda, María Jesús, Catalán, Pilar, Muñoz, Patricia, Aldámiz, Teresa, Barrios, Juan Camilo, Ramírez, Carlos, García-Martínez, Rita, Villalba, María Victoria, Puente, Luis, Bouza, Emilio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sociedad Española de Quimioterapia 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9910675/
https://www.ncbi.nlm.nih.gov/pubmed/36408974
http://dx.doi.org/10.37201/req/068.2022
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author Pérez-Granda, María Jesús
Catalán, Pilar
Muñoz, Patricia
Aldámiz, Teresa
Barrios, Juan Camilo
Ramírez, Carlos
García-Martínez, Rita
Villalba, María Victoria
Puente, Luis
Bouza, Emilio
author_facet Pérez-Granda, María Jesús
Catalán, Pilar
Muñoz, Patricia
Aldámiz, Teresa
Barrios, Juan Camilo
Ramírez, Carlos
García-Martínez, Rita
Villalba, María Victoria
Puente, Luis
Bouza, Emilio
author_sort Pérez-Granda, María Jesús
collection PubMed
description PURPOSE: To determine the prevalence of CMV reactivation in a population admitted for severe COVID-19 to a general hospital. METHODS: Point prevalence study in all hospitalized patients with severe COVID-19 (admitted either to general wards or ICU). Determination of the presence of CMV DNA in circulating blood. COVID-19 was confirmed in patients with compatible clinical manifestations, usually with pneumonia and a positive nasopharyngeal PCR test. RESULTS: We included 140 hospitalized patients with COVID-19 who consented to participate. A total of 16 patients (11.42%), had circulating CMV-DNA in peripheral blood at the time of the study. Patients with positive CMV viral load were mainly ICU patients (11/37 -29,7%) and only 5/103 cases (4,85%) were hospitalized into general wards. The accumulated doses of corticosteroids (prednisone equivalents) in the study day were (median and IQR) 987.50 mg (396.87-2,454.68) and 187.50 mg (75.00-818.12) respectively in CMV positive and negative patients (p < 0.001). A significant proportion of CMV positive patients were discovered because of the study and were clinically unsuspected by their physicians. The coin-fected COVID-CMV positive population had a higher risk of accumulated secondary nosocomially-acquired infections and a worse prognosis. CONCLUSION: CMV reactivation should be systematically searched in patients in COVID-19 cases admitted to the ICU.
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spelling pubmed-99106752023-02-16 Cytomegalovirus reactivation in patients diagnosed with severe COVID-19: A point prevalence study in a general hospital Pérez-Granda, María Jesús Catalán, Pilar Muñoz, Patricia Aldámiz, Teresa Barrios, Juan Camilo Ramírez, Carlos García-Martínez, Rita Villalba, María Victoria Puente, Luis Bouza, Emilio Rev Esp Quimioter Original PURPOSE: To determine the prevalence of CMV reactivation in a population admitted for severe COVID-19 to a general hospital. METHODS: Point prevalence study in all hospitalized patients with severe COVID-19 (admitted either to general wards or ICU). Determination of the presence of CMV DNA in circulating blood. COVID-19 was confirmed in patients with compatible clinical manifestations, usually with pneumonia and a positive nasopharyngeal PCR test. RESULTS: We included 140 hospitalized patients with COVID-19 who consented to participate. A total of 16 patients (11.42%), had circulating CMV-DNA in peripheral blood at the time of the study. Patients with positive CMV viral load were mainly ICU patients (11/37 -29,7%) and only 5/103 cases (4,85%) were hospitalized into general wards. The accumulated doses of corticosteroids (prednisone equivalents) in the study day were (median and IQR) 987.50 mg (396.87-2,454.68) and 187.50 mg (75.00-818.12) respectively in CMV positive and negative patients (p < 0.001). A significant proportion of CMV positive patients were discovered because of the study and were clinically unsuspected by their physicians. The coin-fected COVID-CMV positive population had a higher risk of accumulated secondary nosocomially-acquired infections and a worse prognosis. CONCLUSION: CMV reactivation should be systematically searched in patients in COVID-19 cases admitted to the ICU. Sociedad Española de Quimioterapia 2022-11-22 2023 /pmc/articles/PMC9910675/ /pubmed/36408974 http://dx.doi.org/10.37201/req/068.2022 Text en © The Author 2022 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International (CC BY-NC 4.0)(https://creativecommons.org/licenses/by-nc/4.0/).
spellingShingle Original
Pérez-Granda, María Jesús
Catalán, Pilar
Muñoz, Patricia
Aldámiz, Teresa
Barrios, Juan Camilo
Ramírez, Carlos
García-Martínez, Rita
Villalba, María Victoria
Puente, Luis
Bouza, Emilio
Cytomegalovirus reactivation in patients diagnosed with severe COVID-19: A point prevalence study in a general hospital
title Cytomegalovirus reactivation in patients diagnosed with severe COVID-19: A point prevalence study in a general hospital
title_full Cytomegalovirus reactivation in patients diagnosed with severe COVID-19: A point prevalence study in a general hospital
title_fullStr Cytomegalovirus reactivation in patients diagnosed with severe COVID-19: A point prevalence study in a general hospital
title_full_unstemmed Cytomegalovirus reactivation in patients diagnosed with severe COVID-19: A point prevalence study in a general hospital
title_short Cytomegalovirus reactivation in patients diagnosed with severe COVID-19: A point prevalence study in a general hospital
title_sort cytomegalovirus reactivation in patients diagnosed with severe covid-19: a point prevalence study in a general hospital
topic Original
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9910675/
https://www.ncbi.nlm.nih.gov/pubmed/36408974
http://dx.doi.org/10.37201/req/068.2022
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