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Combining C-reactive protein, procalcitonin, and serum albumin to predict long-term mortality in patients with infective endocarditis

OBJECTIVE: To determine the predictive value of C-reactive protein (CRP) plus albumin plus procalcitonin for long-term mortality in patients with infective endocarditis. METHODS: This retrospective study included patients hospitalized with infective endocarditis between February 2008 and December 20...

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Autores principales: Karaca, Banu, Esin, Fatma, Tiryaki, Muhammet Mücahit, Akkan, Gökhun, Kiris, Tuncay
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10612466/
https://www.ncbi.nlm.nih.gov/pubmed/37891466
http://dx.doi.org/10.1177/03000605231208910
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author Karaca, Banu
Esin, Fatma
Tiryaki, Muhammet Mücahit
Akkan, Gökhun
Kiris, Tuncay
author_facet Karaca, Banu
Esin, Fatma
Tiryaki, Muhammet Mücahit
Akkan, Gökhun
Kiris, Tuncay
author_sort Karaca, Banu
collection PubMed
description OBJECTIVE: To determine the predictive value of C-reactive protein (CRP) plus albumin plus procalcitonin for long-term mortality in patients with infective endocarditis. METHODS: This retrospective study included patients hospitalized with infective endocarditis between February 2008 and December 2021. CRP, procalcitonin, and albumin levels were measured within 24 h of admission and dichotomized as high or low. A CRP plus procalcitonin plus albumin points system (range, 3–6) was generated based on high or low CRP, procalcitonin, and albumin concentrations. Patients were divided into two groups: low-risk (≤4 points) and high-risk (>4 points), according to total score. The primary outcome was defined as all-cause mortality rate at long-term follow-up. RESULTS: Out of 204 patients in total, the high-risk group (n = 29) had higher procalcitonin and CRP levels versus the low-risk group (n = 175), but lower albumin level versus the low-risk group (2.7 ± 0.5 versus 3.5 ± 0.6 g/dl). Matching based on propensity scores showed a higher mortality rate in high-risk versus low-risk patients (76% versus 44%, respectively). In multivariate analysis after matching, the high-risk group was associated with increased long-term mortality (adjusted hazard ratio 2.87, 95% confidence interval 1.32, 6.26). Conclusions: A high CRP plus albumin plus procalcitonin score was associated with long-term mortality risk in patients with infective endocarditis.
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spelling pubmed-106124662023-10-29 Combining C-reactive protein, procalcitonin, and serum albumin to predict long-term mortality in patients with infective endocarditis Karaca, Banu Esin, Fatma Tiryaki, Muhammet Mücahit Akkan, Gökhun Kiris, Tuncay J Int Med Res Observational Study OBJECTIVE: To determine the predictive value of C-reactive protein (CRP) plus albumin plus procalcitonin for long-term mortality in patients with infective endocarditis. METHODS: This retrospective study included patients hospitalized with infective endocarditis between February 2008 and December 2021. CRP, procalcitonin, and albumin levels were measured within 24 h of admission and dichotomized as high or low. A CRP plus procalcitonin plus albumin points system (range, 3–6) was generated based on high or low CRP, procalcitonin, and albumin concentrations. Patients were divided into two groups: low-risk (≤4 points) and high-risk (>4 points), according to total score. The primary outcome was defined as all-cause mortality rate at long-term follow-up. RESULTS: Out of 204 patients in total, the high-risk group (n = 29) had higher procalcitonin and CRP levels versus the low-risk group (n = 175), but lower albumin level versus the low-risk group (2.7 ± 0.5 versus 3.5 ± 0.6 g/dl). Matching based on propensity scores showed a higher mortality rate in high-risk versus low-risk patients (76% versus 44%, respectively). In multivariate analysis after matching, the high-risk group was associated with increased long-term mortality (adjusted hazard ratio 2.87, 95% confidence interval 1.32, 6.26). Conclusions: A high CRP plus albumin plus procalcitonin score was associated with long-term mortality risk in patients with infective endocarditis. SAGE Publications 2023-10-27 /pmc/articles/PMC10612466/ /pubmed/37891466 http://dx.doi.org/10.1177/03000605231208910 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by-nc-nd/4.0/Creative Commons NonCommercial-NoDerivs CC BY-NC-ND: This article is distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 License (https://creativecommons.org/licenses/by-nc-nd/4.0/) which permits non-commercial use, reproduction and distribution of the work as published without adaptation or alteration, without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Observational Study
Karaca, Banu
Esin, Fatma
Tiryaki, Muhammet Mücahit
Akkan, Gökhun
Kiris, Tuncay
Combining C-reactive protein, procalcitonin, and serum albumin to predict long-term mortality in patients with infective endocarditis
title Combining C-reactive protein, procalcitonin, and serum albumin to predict long-term mortality in patients with infective endocarditis
title_full Combining C-reactive protein, procalcitonin, and serum albumin to predict long-term mortality in patients with infective endocarditis
title_fullStr Combining C-reactive protein, procalcitonin, and serum albumin to predict long-term mortality in patients with infective endocarditis
title_full_unstemmed Combining C-reactive protein, procalcitonin, and serum albumin to predict long-term mortality in patients with infective endocarditis
title_short Combining C-reactive protein, procalcitonin, and serum albumin to predict long-term mortality in patients with infective endocarditis
title_sort combining c-reactive protein, procalcitonin, and serum albumin to predict long-term mortality in patients with infective endocarditis
topic Observational Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10612466/
https://www.ncbi.nlm.nih.gov/pubmed/37891466
http://dx.doi.org/10.1177/03000605231208910
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