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Biomarkers and clinical scoring systems in community-acquired pneumonia

Community-acquired pneumonia (CAP) is the third most common cause of death globally. Due to the complexity of CAP, it is widely accepted that, currently, clinical prognosis and diagnosis is inadequate for the assessment of the severity of the disease. With the aim to determining the initial treatmen...

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Autores principales: Karakioulaki, Meropi, Stolz, Daiana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6611198/
https://www.ncbi.nlm.nih.gov/pubmed/31333765
http://dx.doi.org/10.4103/atm.ATM_305_18
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author Karakioulaki, Meropi
Stolz, Daiana
author_facet Karakioulaki, Meropi
Stolz, Daiana
author_sort Karakioulaki, Meropi
collection PubMed
description Community-acquired pneumonia (CAP) is the third most common cause of death globally. Due to the complexity of CAP, it is widely accepted that, currently, clinical prognosis and diagnosis is inadequate for the assessment of the severity of the disease. With the aim to determining the initial treatment and the appropriate level of intervention, several clinical scores of severity and biomarkers have been developed. Both biomarkers and clinical scoring systems are expected to determine the different aspects of the host factor and the response to therapy, in order for physicians to be able to make an accurate benefit/risk assessment that will lead to proper diagnosis and correct prescription of antibiotics. This review aims to highlight the prognostic and diagnostic accuracy of various laboratory and clinical parameters in CAP and discuss the perspectives for the reduction of CAP mortality.
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spelling pubmed-66111982019-07-22 Biomarkers and clinical scoring systems in community-acquired pneumonia Karakioulaki, Meropi Stolz, Daiana Ann Thorac Med Review Article Community-acquired pneumonia (CAP) is the third most common cause of death globally. Due to the complexity of CAP, it is widely accepted that, currently, clinical prognosis and diagnosis is inadequate for the assessment of the severity of the disease. With the aim to determining the initial treatment and the appropriate level of intervention, several clinical scores of severity and biomarkers have been developed. Both biomarkers and clinical scoring systems are expected to determine the different aspects of the host factor and the response to therapy, in order for physicians to be able to make an accurate benefit/risk assessment that will lead to proper diagnosis and correct prescription of antibiotics. This review aims to highlight the prognostic and diagnostic accuracy of various laboratory and clinical parameters in CAP and discuss the perspectives for the reduction of CAP mortality. Wolters Kluwer - Medknow 2019 /pmc/articles/PMC6611198/ /pubmed/31333765 http://dx.doi.org/10.4103/atm.ATM_305_18 Text en Copyright: © 2019 Annals of Thoracic Medicine http://creativecommons.org/licenses/by-nc-sa/4.0 This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Review Article
Karakioulaki, Meropi
Stolz, Daiana
Biomarkers and clinical scoring systems in community-acquired pneumonia
title Biomarkers and clinical scoring systems in community-acquired pneumonia
title_full Biomarkers and clinical scoring systems in community-acquired pneumonia
title_fullStr Biomarkers and clinical scoring systems in community-acquired pneumonia
title_full_unstemmed Biomarkers and clinical scoring systems in community-acquired pneumonia
title_short Biomarkers and clinical scoring systems in community-acquired pneumonia
title_sort biomarkers and clinical scoring systems in community-acquired pneumonia
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6611198/
https://www.ncbi.nlm.nih.gov/pubmed/31333765
http://dx.doi.org/10.4103/atm.ATM_305_18
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