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Immune risk phenotype is associated with nosocomial lung infections in elderly in-patients

BACKGROUND: Nosocomial infections are extremely common in the elderly and may be related to ageing of the immune system. The Immune Risk Phenotype (IRP), which predicts shorter survival in elderly patients, has not been evaluated as a possible risk factor for nosocomial infection. Our aim was to ass...

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Autores principales: Plonquet, A, Bastuji-Garin, S, Tahmasebi, F, Brisacier, C, Ledudal, K, Farcet, JP, Paillaud, E
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3203033/
https://www.ncbi.nlm.nih.gov/pubmed/21961997
http://dx.doi.org/10.1186/1742-4933-8-8
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author Plonquet, A
Bastuji-Garin, S
Tahmasebi, F
Brisacier, C
Ledudal, K
Farcet, JP
Paillaud, E
author_facet Plonquet, A
Bastuji-Garin, S
Tahmasebi, F
Brisacier, C
Ledudal, K
Farcet, JP
Paillaud, E
author_sort Plonquet, A
collection PubMed
description BACKGROUND: Nosocomial infections are extremely common in the elderly and may be related to ageing of the immune system. The Immune Risk Phenotype (IRP), which predicts shorter survival in elderly patients, has not been evaluated as a possible risk factor for nosocomial infection. Our aim was to assess the prevalence of nosocomial infections in elderly in-patients and to investigate potential relationships between nosocomial infections and the immunophenotype, including IRP parameters. RESULTS: We included 252 consecutive in-patients aged 70 years or over (mean age, 85 ± 6.2 years), between 2006 and 2008. Among them, 97 experienced nosocomial infections, yielding a prevalence rate of 38.5% (95% confidence interval, 32.5-44.5). The main infection sites were the respiratory tract (21%) and urinary tract (17.1%) When we compared immunological parameters including cell counts determined by flow cytometry in the groups with and without nosocomial infections, we found that the group with nosocomial infections had significantly lower values for the CD4/CD8 ratio and naive CD8 and CD4 T-cell counts and higher counts of memory CD8 T-cells with a significant increase in CD28-negative CD8-T cells. Neither cytomegalovirus status (positive in 193/246 patients) nor presence of the IRP was associated with nosocomial infections. However, nosocomial pneumonia was significantly more common among IRP-positive patients than IRP-negative patients (17/60 versus 28/180; p = 0.036). CONCLUSION: Immunological parameters that are easy to determine in everyday practice and known to be associated with immune system ageing and shorter survival in the elderly are also associated with an elevated risk of nosocomial pneumonia in the relatively short term.
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spelling pubmed-32030332011-10-28 Immune risk phenotype is associated with nosocomial lung infections in elderly in-patients Plonquet, A Bastuji-Garin, S Tahmasebi, F Brisacier, C Ledudal, K Farcet, JP Paillaud, E Immun Ageing Research BACKGROUND: Nosocomial infections are extremely common in the elderly and may be related to ageing of the immune system. The Immune Risk Phenotype (IRP), which predicts shorter survival in elderly patients, has not been evaluated as a possible risk factor for nosocomial infection. Our aim was to assess the prevalence of nosocomial infections in elderly in-patients and to investigate potential relationships between nosocomial infections and the immunophenotype, including IRP parameters. RESULTS: We included 252 consecutive in-patients aged 70 years or over (mean age, 85 ± 6.2 years), between 2006 and 2008. Among them, 97 experienced nosocomial infections, yielding a prevalence rate of 38.5% (95% confidence interval, 32.5-44.5). The main infection sites were the respiratory tract (21%) and urinary tract (17.1%) When we compared immunological parameters including cell counts determined by flow cytometry in the groups with and without nosocomial infections, we found that the group with nosocomial infections had significantly lower values for the CD4/CD8 ratio and naive CD8 and CD4 T-cell counts and higher counts of memory CD8 T-cells with a significant increase in CD28-negative CD8-T cells. Neither cytomegalovirus status (positive in 193/246 patients) nor presence of the IRP was associated with nosocomial infections. However, nosocomial pneumonia was significantly more common among IRP-positive patients than IRP-negative patients (17/60 versus 28/180; p = 0.036). CONCLUSION: Immunological parameters that are easy to determine in everyday practice and known to be associated with immune system ageing and shorter survival in the elderly are also associated with an elevated risk of nosocomial pneumonia in the relatively short term. BioMed Central 2011-10-01 /pmc/articles/PMC3203033/ /pubmed/21961997 http://dx.doi.org/10.1186/1742-4933-8-8 Text en Copyright ©2011 Plonquet et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Plonquet, A
Bastuji-Garin, S
Tahmasebi, F
Brisacier, C
Ledudal, K
Farcet, JP
Paillaud, E
Immune risk phenotype is associated with nosocomial lung infections in elderly in-patients
title Immune risk phenotype is associated with nosocomial lung infections in elderly in-patients
title_full Immune risk phenotype is associated with nosocomial lung infections in elderly in-patients
title_fullStr Immune risk phenotype is associated with nosocomial lung infections in elderly in-patients
title_full_unstemmed Immune risk phenotype is associated with nosocomial lung infections in elderly in-patients
title_short Immune risk phenotype is associated with nosocomial lung infections in elderly in-patients
title_sort immune risk phenotype is associated with nosocomial lung infections in elderly in-patients
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3203033/
https://www.ncbi.nlm.nih.gov/pubmed/21961997
http://dx.doi.org/10.1186/1742-4933-8-8
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