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Clinical and inflammatory response to bloodstream infections in octogenarians

BACKGROUND: Given the increasing incidence of bacteraemia causing significant morbidity and mortality in older patients, this study aimed to compare the clinical features, laboratory findings and mortality of patients over the age of 80 to younger adults. METHODS: This study was a retrospective, obs...

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Autores principales: Green, Jessica Emily, Ariathianto, Yohanes, Wong, Si Mun, Aboltins, Craig, Lim, Kwang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4000140/
https://www.ncbi.nlm.nih.gov/pubmed/24754903
http://dx.doi.org/10.1186/1471-2318-14-55
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author Green, Jessica Emily
Ariathianto, Yohanes
Wong, Si Mun
Aboltins, Craig
Lim, Kwang
author_facet Green, Jessica Emily
Ariathianto, Yohanes
Wong, Si Mun
Aboltins, Craig
Lim, Kwang
author_sort Green, Jessica Emily
collection PubMed
description BACKGROUND: Given the increasing incidence of bacteraemia causing significant morbidity and mortality in older patients, this study aimed to compare the clinical features, laboratory findings and mortality of patients over the age of 80 to younger adults. METHODS: This study was a retrospective, observational study. Participants were taken to be all patients aged 18 and above with confirmed culture positive sepsis, admitted to a large metropolitan hospital in the year 2010. Measurements taken included patient demographics (accommodation, age, sex, comorbidities), laboratory investigations (white cell count, neutrophil count, C-reactive protein, microbiology results), clinical features (vital signs, presence of localising symptoms, complications, place of acquisition). RESULTS: A total of 1367 patient episodes were screened and 155 met study inclusion criteria. There was no statistically significant difference between likelihood of fever or systolic blood pressure between younger and older populations (p-values of 0.81 and 0.64 respectively). Neutrophil count was higher in the older cohort (p = 0.05). Higher Charlson (J Chronic Dis40(5):373–383, 1987) comorbidity index, greater age and lower systolic blood pressure were found to be statistically significant predictors of mortality (p-values of 0.01, 0.02 and 0.03 respectively). CONCLUSION: The findings of this study indicate older patients are more likely to present without localising features. However, importantly, there is no significant difference in the likelihood of fever or inflammatory markers. This study also demonstrates the importance of the Charlson Index of Comorbidities (J Chronic Dis40(5):373–383, 1987) as a predictive factor for mortality, with age and hypotension being less important but statistically significant predictive factors of mortality.
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spelling pubmed-40001402014-04-26 Clinical and inflammatory response to bloodstream infections in octogenarians Green, Jessica Emily Ariathianto, Yohanes Wong, Si Mun Aboltins, Craig Lim, Kwang BMC Geriatr Research Article BACKGROUND: Given the increasing incidence of bacteraemia causing significant morbidity and mortality in older patients, this study aimed to compare the clinical features, laboratory findings and mortality of patients over the age of 80 to younger adults. METHODS: This study was a retrospective, observational study. Participants were taken to be all patients aged 18 and above with confirmed culture positive sepsis, admitted to a large metropolitan hospital in the year 2010. Measurements taken included patient demographics (accommodation, age, sex, comorbidities), laboratory investigations (white cell count, neutrophil count, C-reactive protein, microbiology results), clinical features (vital signs, presence of localising symptoms, complications, place of acquisition). RESULTS: A total of 1367 patient episodes were screened and 155 met study inclusion criteria. There was no statistically significant difference between likelihood of fever or systolic blood pressure between younger and older populations (p-values of 0.81 and 0.64 respectively). Neutrophil count was higher in the older cohort (p = 0.05). Higher Charlson (J Chronic Dis40(5):373–383, 1987) comorbidity index, greater age and lower systolic blood pressure were found to be statistically significant predictors of mortality (p-values of 0.01, 0.02 and 0.03 respectively). CONCLUSION: The findings of this study indicate older patients are more likely to present without localising features. However, importantly, there is no significant difference in the likelihood of fever or inflammatory markers. This study also demonstrates the importance of the Charlson Index of Comorbidities (J Chronic Dis40(5):373–383, 1987) as a predictive factor for mortality, with age and hypotension being less important but statistically significant predictive factors of mortality. BioMed Central 2014-04-23 /pmc/articles/PMC4000140/ /pubmed/24754903 http://dx.doi.org/10.1186/1471-2318-14-55 Text en Copyright © 2014 Green 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 credited.
spellingShingle Research Article
Green, Jessica Emily
Ariathianto, Yohanes
Wong, Si Mun
Aboltins, Craig
Lim, Kwang
Clinical and inflammatory response to bloodstream infections in octogenarians
title Clinical and inflammatory response to bloodstream infections in octogenarians
title_full Clinical and inflammatory response to bloodstream infections in octogenarians
title_fullStr Clinical and inflammatory response to bloodstream infections in octogenarians
title_full_unstemmed Clinical and inflammatory response to bloodstream infections in octogenarians
title_short Clinical and inflammatory response to bloodstream infections in octogenarians
title_sort clinical and inflammatory response to bloodstream infections in octogenarians
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4000140/
https://www.ncbi.nlm.nih.gov/pubmed/24754903
http://dx.doi.org/10.1186/1471-2318-14-55
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