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Cytomegalovirus reactivation in ICU patients
INTRODUCTION: Approximately 20 years have passed since we reported our results of histologically proven cytomegalovirus (CMV) pneumonia in non-immunocompromised ICU patients. Even if there are more recent reports suggesting that CMV may worsen the outcomes for ICU patients, there is no definite answ...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7095171/ https://www.ncbi.nlm.nih.gov/pubmed/26424680 http://dx.doi.org/10.1007/s00134-015-4066-9 |
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author | Papazian, Laurent Hraiech, Sami Lehingue, Samuel Roch, Antoine Chiche, Laurent Wiramus, Sandrine Forel, Jean-Marie |
author_facet | Papazian, Laurent Hraiech, Sami Lehingue, Samuel Roch, Antoine Chiche, Laurent Wiramus, Sandrine Forel, Jean-Marie |
author_sort | Papazian, Laurent |
collection | PubMed |
description | INTRODUCTION: Approximately 20 years have passed since we reported our results of histologically proven cytomegalovirus (CMV) pneumonia in non-immunocompromised ICU patients. Even if there are more recent reports suggesting that CMV may worsen the outcomes for ICU patients, there is no definite answer to this question: is CMV a potential pathogen for ICU patients or is it simply a bystander? METHODS: We will describe the pathophysiology of active CMV infection and the most recent insights concerning the epidemiological aspects of these reactivations. MAJOR FINDINGS: Cytomegalovirus can be pathogenic by a direct organ insult (such as for the lung), by decreasing host defences against other microorganisms and/or by enhancing the body’s inflammatory response (as in acute respiratory distress syndrome). The incidence of active CMV infection is dependent on the diagnostic method used. Using the most sophisticated available biological tools, the incidence can reach 15–20 % of ICU patients (20–40 % in ICU patients with positive CMV serology). In adequately powered cohorts of patients, active CMV infection appears to be associated with worse outcomes for mechanically ventilated ICU patients. DISCUSSION: There is no absolute direct proof of a negative impact of active CMV infection on the health outcomes of mechanically ventilated patients. Prospective randomized trials are lacking. Future trials should examine the potential benefits for health outcomes of using antiviral treatments. Such treatments could be prophylactic, pre-emptive or used only when there is an end-organ disease. CONCLUSION: Cytomegalovirus infection may affect health outcomes for ICU patients. Additional prospective trials are necessary to confirm this hypothesis. |
format | Online Article Text |
id | pubmed-7095171 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-70951712020-03-26 Cytomegalovirus reactivation in ICU patients Papazian, Laurent Hraiech, Sami Lehingue, Samuel Roch, Antoine Chiche, Laurent Wiramus, Sandrine Forel, Jean-Marie Intensive Care Med My Paper 20 Years Later INTRODUCTION: Approximately 20 years have passed since we reported our results of histologically proven cytomegalovirus (CMV) pneumonia in non-immunocompromised ICU patients. Even if there are more recent reports suggesting that CMV may worsen the outcomes for ICU patients, there is no definite answer to this question: is CMV a potential pathogen for ICU patients or is it simply a bystander? METHODS: We will describe the pathophysiology of active CMV infection and the most recent insights concerning the epidemiological aspects of these reactivations. MAJOR FINDINGS: Cytomegalovirus can be pathogenic by a direct organ insult (such as for the lung), by decreasing host defences against other microorganisms and/or by enhancing the body’s inflammatory response (as in acute respiratory distress syndrome). The incidence of active CMV infection is dependent on the diagnostic method used. Using the most sophisticated available biological tools, the incidence can reach 15–20 % of ICU patients (20–40 % in ICU patients with positive CMV serology). In adequately powered cohorts of patients, active CMV infection appears to be associated with worse outcomes for mechanically ventilated ICU patients. DISCUSSION: There is no absolute direct proof of a negative impact of active CMV infection on the health outcomes of mechanically ventilated patients. Prospective randomized trials are lacking. Future trials should examine the potential benefits for health outcomes of using antiviral treatments. Such treatments could be prophylactic, pre-emptive or used only when there is an end-organ disease. CONCLUSION: Cytomegalovirus infection may affect health outcomes for ICU patients. Additional prospective trials are necessary to confirm this hypothesis. Springer Berlin Heidelberg 2015-09-30 2016 /pmc/articles/PMC7095171/ /pubmed/26424680 http://dx.doi.org/10.1007/s00134-015-4066-9 Text en © Springer-Verlag Berlin Heidelberg and ESICM 2015 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic. |
spellingShingle | My Paper 20 Years Later Papazian, Laurent Hraiech, Sami Lehingue, Samuel Roch, Antoine Chiche, Laurent Wiramus, Sandrine Forel, Jean-Marie Cytomegalovirus reactivation in ICU patients |
title | Cytomegalovirus reactivation in ICU patients |
title_full | Cytomegalovirus reactivation in ICU patients |
title_fullStr | Cytomegalovirus reactivation in ICU patients |
title_full_unstemmed | Cytomegalovirus reactivation in ICU patients |
title_short | Cytomegalovirus reactivation in ICU patients |
title_sort | cytomegalovirus reactivation in icu patients |
topic | My Paper 20 Years Later |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7095171/ https://www.ncbi.nlm.nih.gov/pubmed/26424680 http://dx.doi.org/10.1007/s00134-015-4066-9 |
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