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The role of C-reactive protein ratio in predicting mortality in patients with Fournier gangrene

PURPOSE: This study aimed to determine the C-reactive protein (CRP) ratio for the survival of patients with Fournier gangrene (FG). METHODS: Fifty-two patients with FG between January 2011 and September 2018 were retrospectively analyzed. Data on clinical presentation, Fournier Gangrene Severity Ind...

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Autores principales: Eray, Ismail Cem, Dalci, Kubilay, Gumus, Serdar, Yalav, Orcun, Saritas, Ahmet Gokhan, Boz, Asli, Rencuzogullari, Ahmet
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Society of Coloproctology 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10338162/
https://www.ncbi.nlm.nih.gov/pubmed/35109644
http://dx.doi.org/10.3393/ac.2021.00843.0120
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author Eray, Ismail Cem
Dalci, Kubilay
Gumus, Serdar
Yalav, Orcun
Saritas, Ahmet Gokhan
Boz, Asli
Rencuzogullari, Ahmet
author_facet Eray, Ismail Cem
Dalci, Kubilay
Gumus, Serdar
Yalav, Orcun
Saritas, Ahmet Gokhan
Boz, Asli
Rencuzogullari, Ahmet
author_sort Eray, Ismail Cem
collection PubMed
description PURPOSE: This study aimed to determine the C-reactive protein (CRP) ratio for the survival of patients with Fournier gangrene (FG). METHODS: Fifty-two patients with FG between January 2011 and September 2018 were retrospectively analyzed. Data on clinical presentation, Fournier Gangrene Severity Index (FGSI), CRP ratio, management, and outcome were analyzed. The CRP ratio was calculated as preoperative CRP/postoperative CRP value that measured 48 hours after surgical intervention. Possible alternative cutoff points for the FGSI and CRP were determined by receiver operating characteristic (ROC) analyses. The risk factors related to the prognosis were evaluated by univariate and multivariable logistic regression analyses. RESULTS: The mean CRP ratios were 6.7±6.6 in the survivor group and 1.2±0.8 in the nonsurvivor group (P=0.001). FGSI was significantly higher in the non-survivor group compared to survivor group (8.5±2.5 vs. 3.5±2.2, P=0.001). There was a negative correlation between FGSI and CRP ratio (r=–0.51). ROC analysis determined the cutoff value as 1.78 for CRP (sensitivity, 86%; specificity, 82%; area under the ROC curve, 0.90) to predict death. The incidence of death for patients with CRP ratio of ≤1.78 increased 26.7 fold for those with CRP ratio of >1.78 (95% confidence interval [CI], 4.8–146.5; P=0.001). In the multivariable logistic regression model, CRP ratio (odds ratio [OR], 10.3; 95% CI, 1.5–72.2; P=0.019) and FGSI (OR, 17.8; 95% CI, 2.6–121.1; P=0.003) were independent risk factors for death. CONCLUSION: The CRP ratio is a simple method to use to predict mortality in FG.
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spelling pubmed-103381622023-07-13 The role of C-reactive protein ratio in predicting mortality in patients with Fournier gangrene Eray, Ismail Cem Dalci, Kubilay Gumus, Serdar Yalav, Orcun Saritas, Ahmet Gokhan Boz, Asli Rencuzogullari, Ahmet Ann Coloproctol Original Article PURPOSE: This study aimed to determine the C-reactive protein (CRP) ratio for the survival of patients with Fournier gangrene (FG). METHODS: Fifty-two patients with FG between January 2011 and September 2018 were retrospectively analyzed. Data on clinical presentation, Fournier Gangrene Severity Index (FGSI), CRP ratio, management, and outcome were analyzed. The CRP ratio was calculated as preoperative CRP/postoperative CRP value that measured 48 hours after surgical intervention. Possible alternative cutoff points for the FGSI and CRP were determined by receiver operating characteristic (ROC) analyses. The risk factors related to the prognosis were evaluated by univariate and multivariable logistic regression analyses. RESULTS: The mean CRP ratios were 6.7±6.6 in the survivor group and 1.2±0.8 in the nonsurvivor group (P=0.001). FGSI was significantly higher in the non-survivor group compared to survivor group (8.5±2.5 vs. 3.5±2.2, P=0.001). There was a negative correlation between FGSI and CRP ratio (r=–0.51). ROC analysis determined the cutoff value as 1.78 for CRP (sensitivity, 86%; specificity, 82%; area under the ROC curve, 0.90) to predict death. The incidence of death for patients with CRP ratio of ≤1.78 increased 26.7 fold for those with CRP ratio of >1.78 (95% confidence interval [CI], 4.8–146.5; P=0.001). In the multivariable logistic regression model, CRP ratio (odds ratio [OR], 10.3; 95% CI, 1.5–72.2; P=0.019) and FGSI (OR, 17.8; 95% CI, 2.6–121.1; P=0.003) were independent risk factors for death. CONCLUSION: The CRP ratio is a simple method to use to predict mortality in FG. Korean Society of Coloproctology 2023-06 2022-02-03 /pmc/articles/PMC10338162/ /pubmed/35109644 http://dx.doi.org/10.3393/ac.2021.00843.0120 Text en Copyright © 2023 The Korean Society of Coloproctology https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Eray, Ismail Cem
Dalci, Kubilay
Gumus, Serdar
Yalav, Orcun
Saritas, Ahmet Gokhan
Boz, Asli
Rencuzogullari, Ahmet
The role of C-reactive protein ratio in predicting mortality in patients with Fournier gangrene
title The role of C-reactive protein ratio in predicting mortality in patients with Fournier gangrene
title_full The role of C-reactive protein ratio in predicting mortality in patients with Fournier gangrene
title_fullStr The role of C-reactive protein ratio in predicting mortality in patients with Fournier gangrene
title_full_unstemmed The role of C-reactive protein ratio in predicting mortality in patients with Fournier gangrene
title_short The role of C-reactive protein ratio in predicting mortality in patients with Fournier gangrene
title_sort role of c-reactive protein ratio in predicting mortality in patients with fournier gangrene
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10338162/
https://www.ncbi.nlm.nih.gov/pubmed/35109644
http://dx.doi.org/10.3393/ac.2021.00843.0120
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