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C-reactive protein for simple prediction of mortality in patients with acute non-variceal upper gastrointestinal bleeding: A retrospective analysis

In upper gastrointestinal bleeding (UGIB), scoring systems using multiple variables were developed to predict patient outcomes. We evaluated serum C-reactive protein (CRP) for simple prediction of patient mortality after acute non-variceal UGIB. The associated factors for 30-day mortality was invest...

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Autores principales: Park, Se Hwan, Mun, Yoon Gwon, Lim, Chul-Hyun, Cho, Yu Kyung, Park, Jae Myung
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7748191/
https://www.ncbi.nlm.nih.gov/pubmed/33371112
http://dx.doi.org/10.1097/MD.0000000000023689
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author Park, Se Hwan
Mun, Yoon Gwon
Lim, Chul-Hyun
Cho, Yu Kyung
Park, Jae Myung
author_facet Park, Se Hwan
Mun, Yoon Gwon
Lim, Chul-Hyun
Cho, Yu Kyung
Park, Jae Myung
author_sort Park, Se Hwan
collection PubMed
description In upper gastrointestinal bleeding (UGIB), scoring systems using multiple variables were developed to predict patient outcomes. We evaluated serum C-reactive protein (CRP) for simple prediction of patient mortality after acute non-variceal UGIB. The associated factors for 30-day mortality was investigated by regression analysis in patients with acute non-variceal UGIB (N = 1232). The area under the receiver operating characteristics (AUROC) curve was analyzed with serum CRP in these patients and a prospective cohort (N = 435). The discriminant validity of serum CRP was compared to other prognostic scoring systems by means of AUROC curve analysis. Serum CRP was significantly higher in the expired than survived patients (median, 4.53 vs 0.49; P < .001). The odds ratio of serum CRP was 4.18 (2.10–9.27) in multivariate analysis. The odds ratio of high serum CRP was higher than Rockall score (4.15 vs 1.29), AIMS65 (3.55 vs 1.71) and Glasgow-Blatchford score (4.32 vs 1.08) in multivariate analyses. The AUROC of serum CRP at bleeding was 0.78 for 30-day mortality (P < .001). In the validation set, serum CRP was also significantly higher in the expired than survived patients, of which AUROC was 0.73 (P < .001). In predicting 30-day mortality, the AUROC with serum CRP was not inferior to that of other scoring systems. Serum CRP at bleeding can be simply used to identify the patients with high mortality after acute non-variceal UGIB.
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spelling pubmed-77481912020-12-21 C-reactive protein for simple prediction of mortality in patients with acute non-variceal upper gastrointestinal bleeding: A retrospective analysis Park, Se Hwan Mun, Yoon Gwon Lim, Chul-Hyun Cho, Yu Kyung Park, Jae Myung Medicine (Baltimore) 4500 In upper gastrointestinal bleeding (UGIB), scoring systems using multiple variables were developed to predict patient outcomes. We evaluated serum C-reactive protein (CRP) for simple prediction of patient mortality after acute non-variceal UGIB. The associated factors for 30-day mortality was investigated by regression analysis in patients with acute non-variceal UGIB (N = 1232). The area under the receiver operating characteristics (AUROC) curve was analyzed with serum CRP in these patients and a prospective cohort (N = 435). The discriminant validity of serum CRP was compared to other prognostic scoring systems by means of AUROC curve analysis. Serum CRP was significantly higher in the expired than survived patients (median, 4.53 vs 0.49; P < .001). The odds ratio of serum CRP was 4.18 (2.10–9.27) in multivariate analysis. The odds ratio of high serum CRP was higher than Rockall score (4.15 vs 1.29), AIMS65 (3.55 vs 1.71) and Glasgow-Blatchford score (4.32 vs 1.08) in multivariate analyses. The AUROC of serum CRP at bleeding was 0.78 for 30-day mortality (P < .001). In the validation set, serum CRP was also significantly higher in the expired than survived patients, of which AUROC was 0.73 (P < .001). In predicting 30-day mortality, the AUROC with serum CRP was not inferior to that of other scoring systems. Serum CRP at bleeding can be simply used to identify the patients with high mortality after acute non-variceal UGIB. Lippincott Williams & Wilkins 2020-12-18 /pmc/articles/PMC7748191/ /pubmed/33371112 http://dx.doi.org/10.1097/MD.0000000000023689 Text en Copyright © 2020 the Author(s). Published by Wolters Kluwer Health, Inc. http://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 4.0 (CCBY-NC), where it is permissible to download, share, remix, transform, and buildup the work provided it is properly cited. The work cannot be used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc/4.0
spellingShingle 4500
Park, Se Hwan
Mun, Yoon Gwon
Lim, Chul-Hyun
Cho, Yu Kyung
Park, Jae Myung
C-reactive protein for simple prediction of mortality in patients with acute non-variceal upper gastrointestinal bleeding: A retrospective analysis
title C-reactive protein for simple prediction of mortality in patients with acute non-variceal upper gastrointestinal bleeding: A retrospective analysis
title_full C-reactive protein for simple prediction of mortality in patients with acute non-variceal upper gastrointestinal bleeding: A retrospective analysis
title_fullStr C-reactive protein for simple prediction of mortality in patients with acute non-variceal upper gastrointestinal bleeding: A retrospective analysis
title_full_unstemmed C-reactive protein for simple prediction of mortality in patients with acute non-variceal upper gastrointestinal bleeding: A retrospective analysis
title_short C-reactive protein for simple prediction of mortality in patients with acute non-variceal upper gastrointestinal bleeding: A retrospective analysis
title_sort c-reactive protein for simple prediction of mortality in patients with acute non-variceal upper gastrointestinal bleeding: a retrospective analysis
topic 4500
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7748191/
https://www.ncbi.nlm.nih.gov/pubmed/33371112
http://dx.doi.org/10.1097/MD.0000000000023689
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