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Impact of antiviral treatment on long-term prognosis in non-immunocompromised patients with CMV reactivation

BACKGROUND: Reactivation of human cytomegalovirus (CMV) occurs in non-immunocompromised patients with or without specific organ involvement, but it is still unknown whether it has a clinical implication on long-term prognosis or not. METHODS: A retrospective cohort study evaluating non-immunocomprom...

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Autores principales: Park, Ga Eun, Ki, Hyun Kyun, Ko, Jae-Hoon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8094573/
https://www.ncbi.nlm.nih.gov/pubmed/33947335
http://dx.doi.org/10.1186/s12879-021-06098-4
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author Park, Ga Eun
Ki, Hyun Kyun
Ko, Jae-Hoon
author_facet Park, Ga Eun
Ki, Hyun Kyun
Ko, Jae-Hoon
author_sort Park, Ga Eun
collection PubMed
description BACKGROUND: Reactivation of human cytomegalovirus (CMV) occurs in non-immunocompromised patients with or without specific organ involvement, but it is still unknown whether it has a clinical implication on long-term prognosis or not. METHODS: A retrospective cohort study evaluating non-immunocompromised adult patients with CMV reactivation was conducted during the period between January 2010 and February 2018. Patients were divided into ganciclovir-treated and non-treated groups. Patients who died within 30 days from CMV reactivation were excluded as they died from complex causes of conditions. Survivors were followed for 30-months to evaluate long-term prognosis. RESULTS: A total of 136 patients with CMV reactivation was included, consisting of 66 ganciclovir-treated (48.5%) and 70 non-treated (51.5%) patients. Overall, patients were old-aged (median 70 years old) and most were treated with pneumonia of any cause (91.2%). More patients in ganciclovir-treated group were treated at intensive care unit (43.9% vs 24.3%, respectively) and had higher viral load over 5000 copies/ml (48.5% vs 22.9%) than non-treated group (all P < 0.05). Primary and secondary endpoints including 30-months survival (28.0 vs 38.9%, respectively) and 12-months survival (40.3% vs 49.2%) were not statistically different between the ganciclovir-treated and non-treated groups. In the multivariate analyses, ganciclovir treatment was not associated with 30-months survival (HR 1.307, 95% CI 0.759–2.251) and 12-months survival (HR 1.533, 95% CI 0.895–2.624). CONCLUSION: In a retrospective cohort study evaluating non-immunocompromised patients with CMV reactivation, ganciclovir treatment was not associated with long-term prognosis. Antiviral treatment in this condition would not be necessary unless organ involvement is suspected. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12879-021-06098-4.
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spelling pubmed-80945732021-05-05 Impact of antiviral treatment on long-term prognosis in non-immunocompromised patients with CMV reactivation Park, Ga Eun Ki, Hyun Kyun Ko, Jae-Hoon BMC Infect Dis Research BACKGROUND: Reactivation of human cytomegalovirus (CMV) occurs in non-immunocompromised patients with or without specific organ involvement, but it is still unknown whether it has a clinical implication on long-term prognosis or not. METHODS: A retrospective cohort study evaluating non-immunocompromised adult patients with CMV reactivation was conducted during the period between January 2010 and February 2018. Patients were divided into ganciclovir-treated and non-treated groups. Patients who died within 30 days from CMV reactivation were excluded as they died from complex causes of conditions. Survivors were followed for 30-months to evaluate long-term prognosis. RESULTS: A total of 136 patients with CMV reactivation was included, consisting of 66 ganciclovir-treated (48.5%) and 70 non-treated (51.5%) patients. Overall, patients were old-aged (median 70 years old) and most were treated with pneumonia of any cause (91.2%). More patients in ganciclovir-treated group were treated at intensive care unit (43.9% vs 24.3%, respectively) and had higher viral load over 5000 copies/ml (48.5% vs 22.9%) than non-treated group (all P < 0.05). Primary and secondary endpoints including 30-months survival (28.0 vs 38.9%, respectively) and 12-months survival (40.3% vs 49.2%) were not statistically different between the ganciclovir-treated and non-treated groups. In the multivariate analyses, ganciclovir treatment was not associated with 30-months survival (HR 1.307, 95% CI 0.759–2.251) and 12-months survival (HR 1.533, 95% CI 0.895–2.624). CONCLUSION: In a retrospective cohort study evaluating non-immunocompromised patients with CMV reactivation, ganciclovir treatment was not associated with long-term prognosis. Antiviral treatment in this condition would not be necessary unless organ involvement is suspected. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12879-021-06098-4. BioMed Central 2021-05-04 /pmc/articles/PMC8094573/ /pubmed/33947335 http://dx.doi.org/10.1186/s12879-021-06098-4 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Park, Ga Eun
Ki, Hyun Kyun
Ko, Jae-Hoon
Impact of antiviral treatment on long-term prognosis in non-immunocompromised patients with CMV reactivation
title Impact of antiviral treatment on long-term prognosis in non-immunocompromised patients with CMV reactivation
title_full Impact of antiviral treatment on long-term prognosis in non-immunocompromised patients with CMV reactivation
title_fullStr Impact of antiviral treatment on long-term prognosis in non-immunocompromised patients with CMV reactivation
title_full_unstemmed Impact of antiviral treatment on long-term prognosis in non-immunocompromised patients with CMV reactivation
title_short Impact of antiviral treatment on long-term prognosis in non-immunocompromised patients with CMV reactivation
title_sort impact of antiviral treatment on long-term prognosis in non-immunocompromised patients with cmv reactivation
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8094573/
https://www.ncbi.nlm.nih.gov/pubmed/33947335
http://dx.doi.org/10.1186/s12879-021-06098-4
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