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Pulmonary cytomegalovirus (CMV) DNA shedding in allogeneic hematopoietic stem cell transplant recipients: Implications for the diagnosis of CMV pneumonia
OBJECTIVES: To date no definitive cut-off value for cytomegalovirus (CMV) DNA load in bronchoalveolar lavage (BAL) fluid specimens has been established to discriminate between CMV pneumonia and pulmonary CMV DNA shedding in allogeneic hematopoietic stem cell transplant (allo-HSCT) recipients. METHOD...
Autores principales: | , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The British Infection Association. Published by Elsevier Ltd.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7126576/ https://www.ncbi.nlm.nih.gov/pubmed/30797790 http://dx.doi.org/10.1016/j.jinf.2019.02.009 |
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author | Piñana, José Luis Giménez, Estela Gómez, María Dolores Pérez, Ariadna González, Eva María Vinuesa, Víctor Hernández-Boluda, Juan Carlos Montoro, Juan Salavert, Miguel Tormo, Mar Amat, Paula Moles, Paula Carretero, Carlos Balaguer-Roselló, Aitana Sanz, Jaime Sanz, Guillermo Solano, Carlos Navarro, David |
author_facet | Piñana, José Luis Giménez, Estela Gómez, María Dolores Pérez, Ariadna González, Eva María Vinuesa, Víctor Hernández-Boluda, Juan Carlos Montoro, Juan Salavert, Miguel Tormo, Mar Amat, Paula Moles, Paula Carretero, Carlos Balaguer-Roselló, Aitana Sanz, Jaime Sanz, Guillermo Solano, Carlos Navarro, David |
author_sort | Piñana, José Luis |
collection | PubMed |
description | OBJECTIVES: To date no definitive cut-off value for cytomegalovirus (CMV) DNA load in bronchoalveolar lavage (BAL) fluid specimens has been established to discriminate between CMV pneumonia and pulmonary CMV DNA shedding in allogeneic hematopoietic stem cell transplant (allo-HSCT) recipients. METHODS: The current retrospective study is aimed at assessing the range of CMV DNA loads quantified in BAL fluid specimens from allo-HSCT patients with pneumonia in which different microorganisms were causally involved. RESULTS: A total of 144 BAL specimens from 123 patients were included. CMV DNA was detected in 56 out of 144 BAL fluid specimens and the median CMV DNA load from patients in whom CMV pneumonia was unlikely or could be tentatively ruled out was 1210 (31–68, 920) IU/ml. The frequency of CMV DNA detection and median CMV DNA loads were comparable, irrespective of the attributable cause of pneumonia. Detection of CMV DNA loads in BAL fluid specimens >500 IU/ml was independently associated with pneumonia-attributable mortality. CONCLUSIONS: The current study highlights the difficulty in establishing universal CMV DNA load thresholds in BAL fluid specimens for distinguishing between CMV pneumonia and pulmonary CMV DNA shedding, and suggests that the presence of CMV DNA in BAL fluid specimens beyond a certain level may have a deleterious impact on patient outcome. |
format | Online Article Text |
id | pubmed-7126576 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | The British Infection Association. Published by Elsevier Ltd. |
record_format | MEDLINE/PubMed |
spelling | pubmed-71265762020-04-08 Pulmonary cytomegalovirus (CMV) DNA shedding in allogeneic hematopoietic stem cell transplant recipients: Implications for the diagnosis of CMV pneumonia Piñana, José Luis Giménez, Estela Gómez, María Dolores Pérez, Ariadna González, Eva María Vinuesa, Víctor Hernández-Boluda, Juan Carlos Montoro, Juan Salavert, Miguel Tormo, Mar Amat, Paula Moles, Paula Carretero, Carlos Balaguer-Roselló, Aitana Sanz, Jaime Sanz, Guillermo Solano, Carlos Navarro, David J Infect Article OBJECTIVES: To date no definitive cut-off value for cytomegalovirus (CMV) DNA load in bronchoalveolar lavage (BAL) fluid specimens has been established to discriminate between CMV pneumonia and pulmonary CMV DNA shedding in allogeneic hematopoietic stem cell transplant (allo-HSCT) recipients. METHODS: The current retrospective study is aimed at assessing the range of CMV DNA loads quantified in BAL fluid specimens from allo-HSCT patients with pneumonia in which different microorganisms were causally involved. RESULTS: A total of 144 BAL specimens from 123 patients were included. CMV DNA was detected in 56 out of 144 BAL fluid specimens and the median CMV DNA load from patients in whom CMV pneumonia was unlikely or could be tentatively ruled out was 1210 (31–68, 920) IU/ml. The frequency of CMV DNA detection and median CMV DNA loads were comparable, irrespective of the attributable cause of pneumonia. Detection of CMV DNA loads in BAL fluid specimens >500 IU/ml was independently associated with pneumonia-attributable mortality. CONCLUSIONS: The current study highlights the difficulty in establishing universal CMV DNA load thresholds in BAL fluid specimens for distinguishing between CMV pneumonia and pulmonary CMV DNA shedding, and suggests that the presence of CMV DNA in BAL fluid specimens beyond a certain level may have a deleterious impact on patient outcome. The British Infection Association. Published by Elsevier Ltd. 2019-05 2019-02-21 /pmc/articles/PMC7126576/ /pubmed/30797790 http://dx.doi.org/10.1016/j.jinf.2019.02.009 Text en © 2019 The British Infection Association. Published by Elsevier Ltd. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Article Piñana, José Luis Giménez, Estela Gómez, María Dolores Pérez, Ariadna González, Eva María Vinuesa, Víctor Hernández-Boluda, Juan Carlos Montoro, Juan Salavert, Miguel Tormo, Mar Amat, Paula Moles, Paula Carretero, Carlos Balaguer-Roselló, Aitana Sanz, Jaime Sanz, Guillermo Solano, Carlos Navarro, David Pulmonary cytomegalovirus (CMV) DNA shedding in allogeneic hematopoietic stem cell transplant recipients: Implications for the diagnosis of CMV pneumonia |
title | Pulmonary cytomegalovirus (CMV) DNA shedding in allogeneic hematopoietic stem cell transplant recipients: Implications for the diagnosis of CMV pneumonia |
title_full | Pulmonary cytomegalovirus (CMV) DNA shedding in allogeneic hematopoietic stem cell transplant recipients: Implications for the diagnosis of CMV pneumonia |
title_fullStr | Pulmonary cytomegalovirus (CMV) DNA shedding in allogeneic hematopoietic stem cell transplant recipients: Implications for the diagnosis of CMV pneumonia |
title_full_unstemmed | Pulmonary cytomegalovirus (CMV) DNA shedding in allogeneic hematopoietic stem cell transplant recipients: Implications for the diagnosis of CMV pneumonia |
title_short | Pulmonary cytomegalovirus (CMV) DNA shedding in allogeneic hematopoietic stem cell transplant recipients: Implications for the diagnosis of CMV pneumonia |
title_sort | pulmonary cytomegalovirus (cmv) dna shedding in allogeneic hematopoietic stem cell transplant recipients: implications for the diagnosis of cmv pneumonia |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7126576/ https://www.ncbi.nlm.nih.gov/pubmed/30797790 http://dx.doi.org/10.1016/j.jinf.2019.02.009 |
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