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Cytomegalovirus infection in immunocompetent adults: Is observation still the best strategy?

Cytomegalovirus (CMV) infection in immunocompetent patients generally resolves with few sequelae. However, it can cause severe and relapsing symptoms that can last for several weeks. Due to the self-limiting nature of CMV disease in immunocompetent individuals, criteria for specific antiviral therap...

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Detalles Bibliográficos
Autores principales: Nangle, Sarah, Mitra, Subhashis, Roskos, Steven, Havlichek, Daniel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6129681/
https://www.ncbi.nlm.nih.gov/pubmed/30202727
http://dx.doi.org/10.1016/j.idcr.2018.e00442
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author Nangle, Sarah
Mitra, Subhashis
Roskos, Steven
Havlichek, Daniel
author_facet Nangle, Sarah
Mitra, Subhashis
Roskos, Steven
Havlichek, Daniel
author_sort Nangle, Sarah
collection PubMed
description Cytomegalovirus (CMV) infection in immunocompetent patients generally resolves with few sequelae. However, it can cause severe and relapsing symptoms that can last for several weeks. Due to the self-limiting nature of CMV disease in immunocompetent individuals, criteria for specific antiviral therapy in this cohort are not well established. Additionally the adverse effect profile of currently available anti-CMV therapy limits its use in specific patient populations .We describe 3 immunocompetent adults who developed symptomatic CMV infection and were ill for several weeks. All patients had positive CMV viral assays and ultimately received anti-CMV therapy with significant improvement in symptoms within a few days of starting therapy. Choosing appropriate candidates for anti-CMV therapy, among mmunocompetent individuals, requires further research.
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spelling pubmed-61296812018-09-10 Cytomegalovirus infection in immunocompetent adults: Is observation still the best strategy? Nangle, Sarah Mitra, Subhashis Roskos, Steven Havlichek, Daniel IDCases Article Cytomegalovirus (CMV) infection in immunocompetent patients generally resolves with few sequelae. However, it can cause severe and relapsing symptoms that can last for several weeks. Due to the self-limiting nature of CMV disease in immunocompetent individuals, criteria for specific antiviral therapy in this cohort are not well established. Additionally the adverse effect profile of currently available anti-CMV therapy limits its use in specific patient populations .We describe 3 immunocompetent adults who developed symptomatic CMV infection and were ill for several weeks. All patients had positive CMV viral assays and ultimately received anti-CMV therapy with significant improvement in symptoms within a few days of starting therapy. Choosing appropriate candidates for anti-CMV therapy, among mmunocompetent individuals, requires further research. Elsevier 2018-08-28 /pmc/articles/PMC6129681/ /pubmed/30202727 http://dx.doi.org/10.1016/j.idcr.2018.e00442 Text en © 2018 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Nangle, Sarah
Mitra, Subhashis
Roskos, Steven
Havlichek, Daniel
Cytomegalovirus infection in immunocompetent adults: Is observation still the best strategy?
title Cytomegalovirus infection in immunocompetent adults: Is observation still the best strategy?
title_full Cytomegalovirus infection in immunocompetent adults: Is observation still the best strategy?
title_fullStr Cytomegalovirus infection in immunocompetent adults: Is observation still the best strategy?
title_full_unstemmed Cytomegalovirus infection in immunocompetent adults: Is observation still the best strategy?
title_short Cytomegalovirus infection in immunocompetent adults: Is observation still the best strategy?
title_sort cytomegalovirus infection in immunocompetent adults: is observation still the best strategy?
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6129681/
https://www.ncbi.nlm.nih.gov/pubmed/30202727
http://dx.doi.org/10.1016/j.idcr.2018.e00442
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