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Inflammatory and perfusion markers as risk factors and predictors of critically ill patient readmission
OBJECTIVE: To assess the performance of central venous oxygen saturation, lactate, base deficit, and C-reactive protein levels and SOFA and SWIFT scores on the day of discharge from the intensive care unit as predictors of patient readmission to the intensive care unit. METHODS: This prospective and...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Associação Brasileira de Medicina intensiva
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4103938/ https://www.ncbi.nlm.nih.gov/pubmed/25028946 http://dx.doi.org/10.5935/0103-507X.20140019 |
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author | dos Santos, Moreno Calcagnotto Boniatti, Márcio Manozzo Lincho, Carla Silva Pellegrini, José Augusto Santos Vidart, Josi Rodrigues, Edison Moraes Vieira, Silvia Regina Rios |
author_facet | dos Santos, Moreno Calcagnotto Boniatti, Márcio Manozzo Lincho, Carla Silva Pellegrini, José Augusto Santos Vidart, Josi Rodrigues, Edison Moraes Vieira, Silvia Regina Rios |
author_sort | dos Santos, Moreno Calcagnotto |
collection | PubMed |
description | OBJECTIVE: To assess the performance of central venous oxygen saturation, lactate, base deficit, and C-reactive protein levels and SOFA and SWIFT scores on the day of discharge from the intensive care unit as predictors of patient readmission to the intensive care unit. METHODS: This prospective and observational study collected data from 1,360 patients who were admitted consecutively to a clinical-surgical intensive care unit from August 2011 to August 2012. The clinical characteristics and laboratory data of readmitted and non-readmitted patients after discharge from the intensive care unit were compared. Using a multivariate analysis, the risk factors independently associated with readmission were identified. RESULTS: The C-reactive protein, central venous oxygen saturation, base deficit, and lactate levels and the SWIFT and SOFA scores did not correlate with the readmission of critically ill patients. Increased age and contact isolation because of multidrug-resistant organisms were identified as risk factors that were independently associated with readmission in this study group. CONCLUSION: Inflammatory and perfusion parameters were not associated with patient readmission. Increased age and contact isolation because of multidrug-resistant organisms were identified as predictors of readmission to the intensive care unit. |
format | Online Article Text |
id | pubmed-4103938 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Associação Brasileira de Medicina intensiva |
record_format | MEDLINE/PubMed |
spelling | pubmed-41039382014-07-22 Inflammatory and perfusion markers as risk factors and predictors of critically ill patient readmission dos Santos, Moreno Calcagnotto Boniatti, Márcio Manozzo Lincho, Carla Silva Pellegrini, José Augusto Santos Vidart, Josi Rodrigues, Edison Moraes Vieira, Silvia Regina Rios Rev Bras Ter Intensiva Original Articles OBJECTIVE: To assess the performance of central venous oxygen saturation, lactate, base deficit, and C-reactive protein levels and SOFA and SWIFT scores on the day of discharge from the intensive care unit as predictors of patient readmission to the intensive care unit. METHODS: This prospective and observational study collected data from 1,360 patients who were admitted consecutively to a clinical-surgical intensive care unit from August 2011 to August 2012. The clinical characteristics and laboratory data of readmitted and non-readmitted patients after discharge from the intensive care unit were compared. Using a multivariate analysis, the risk factors independently associated with readmission were identified. RESULTS: The C-reactive protein, central venous oxygen saturation, base deficit, and lactate levels and the SWIFT and SOFA scores did not correlate with the readmission of critically ill patients. Increased age and contact isolation because of multidrug-resistant organisms were identified as risk factors that were independently associated with readmission in this study group. CONCLUSION: Inflammatory and perfusion parameters were not associated with patient readmission. Increased age and contact isolation because of multidrug-resistant organisms were identified as predictors of readmission to the intensive care unit. Associação Brasileira de Medicina intensiva 2014 /pmc/articles/PMC4103938/ /pubmed/25028946 http://dx.doi.org/10.5935/0103-507X.20140019 Text en http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Articles dos Santos, Moreno Calcagnotto Boniatti, Márcio Manozzo Lincho, Carla Silva Pellegrini, José Augusto Santos Vidart, Josi Rodrigues, Edison Moraes Vieira, Silvia Regina Rios Inflammatory and perfusion markers as risk factors and predictors of critically ill patient readmission |
title | Inflammatory and perfusion markers as risk factors and predictors of
critically ill patient readmission |
title_full | Inflammatory and perfusion markers as risk factors and predictors of
critically ill patient readmission |
title_fullStr | Inflammatory and perfusion markers as risk factors and predictors of
critically ill patient readmission |
title_full_unstemmed | Inflammatory and perfusion markers as risk factors and predictors of
critically ill patient readmission |
title_short | Inflammatory and perfusion markers as risk factors and predictors of
critically ill patient readmission |
title_sort | inflammatory and perfusion markers as risk factors and predictors of
critically ill patient readmission |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4103938/ https://www.ncbi.nlm.nih.gov/pubmed/25028946 http://dx.doi.org/10.5935/0103-507X.20140019 |
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