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Application of a modified sequential organ failure assessment score to critically ill patients
The purpose of the present study was to explore the usefulness of the Mexican sequential organ failure assessment (MEXSOFA) score for assessing the risk of mortality for critically ill patients in the ICU. A total of 232 consecutive patients admitted to an ICU were included in the study. The MEXSOFA...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Associa¸ão Brasileira de Divulga¸ão Científica
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3854366/ https://www.ncbi.nlm.nih.gov/pubmed/23369978 http://dx.doi.org/10.1590/1414-431X20122308 |
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author | Ñamendys-Silva, S.A. Silva-Medina, M.A. Vásquez-Barahona, G.M. Baltazar-Torres, J.A. Rivero-Sigarroa, E. Fonseca-Lazcano, J.A. Domínguez-Cherit, G. |
author_facet | Ñamendys-Silva, S.A. Silva-Medina, M.A. Vásquez-Barahona, G.M. Baltazar-Torres, J.A. Rivero-Sigarroa, E. Fonseca-Lazcano, J.A. Domínguez-Cherit, G. |
author_sort | Ñamendys-Silva, S.A. |
collection | PubMed |
description | The purpose of the present study was to explore the usefulness of the Mexican sequential organ failure assessment (MEXSOFA) score for assessing the risk of mortality for critically ill patients in the ICU. A total of 232 consecutive patients admitted to an ICU were included in the study. The MEXSOFA was calculated using the original SOFA scoring system with two modifications: the PaO(2)/FiO(2) ratio was replaced with the SpO(2)/FiO(2) ratio, and the evaluation of neurologic dysfunction was excluded. The ICU mortality rate was 20.2%. Patients with an initial MEXSOFA score of 9 points or less calculated during the first 24 h after admission to the ICU had a mortality rate of 14.8%, while those with an initial MEXSOFA score of 10 points or more had a mortality rate of 40%. The MEXSOFA score at 48 h was also associated with mortality: patients with a score of 9 points or less had a mortality rate of 14.1%, while those with a score of 10 points or more had a mortality rate of 50%. In a multivariate analysis, only the MEXSOFA score at 48 h was an independent predictor for in-ICU death with an OR = 1.35 (95%CI = 1.14-1.59, P < 0.001). The SOFA and MEXSOFA scores calculated 24 h after admission to the ICU demonstrated a good level of discrimination for predicting the in-ICU mortality risk in critically ill patients. The MEXSOFA score at 48 h was an independent predictor of death; with each 1-point increase, the odds of death increased by 35%. |
format | Online Article Text |
id | pubmed-3854366 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Associa¸ão Brasileira de Divulga¸ão Científica |
record_format | MEDLINE/PubMed |
spelling | pubmed-38543662013-12-16 Application of a modified sequential organ failure assessment score to critically ill patients Ñamendys-Silva, S.A. Silva-Medina, M.A. Vásquez-Barahona, G.M. Baltazar-Torres, J.A. Rivero-Sigarroa, E. Fonseca-Lazcano, J.A. Domínguez-Cherit, G. Braz J Med Biol Res Clinical Investigation The purpose of the present study was to explore the usefulness of the Mexican sequential organ failure assessment (MEXSOFA) score for assessing the risk of mortality for critically ill patients in the ICU. A total of 232 consecutive patients admitted to an ICU were included in the study. The MEXSOFA was calculated using the original SOFA scoring system with two modifications: the PaO(2)/FiO(2) ratio was replaced with the SpO(2)/FiO(2) ratio, and the evaluation of neurologic dysfunction was excluded. The ICU mortality rate was 20.2%. Patients with an initial MEXSOFA score of 9 points or less calculated during the first 24 h after admission to the ICU had a mortality rate of 14.8%, while those with an initial MEXSOFA score of 10 points or more had a mortality rate of 40%. The MEXSOFA score at 48 h was also associated with mortality: patients with a score of 9 points or less had a mortality rate of 14.1%, while those with a score of 10 points or more had a mortality rate of 50%. In a multivariate analysis, only the MEXSOFA score at 48 h was an independent predictor for in-ICU death with an OR = 1.35 (95%CI = 1.14-1.59, P < 0.001). The SOFA and MEXSOFA scores calculated 24 h after admission to the ICU demonstrated a good level of discrimination for predicting the in-ICU mortality risk in critically ill patients. The MEXSOFA score at 48 h was an independent predictor of death; with each 1-point increase, the odds of death increased by 35%. Associa¸ão Brasileira de Divulga¸ão Científica 2013-02-01 /pmc/articles/PMC3854366/ /pubmed/23369978 http://dx.doi.org/10.1590/1414-431X20122308 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 | Clinical Investigation Ñamendys-Silva, S.A. Silva-Medina, M.A. Vásquez-Barahona, G.M. Baltazar-Torres, J.A. Rivero-Sigarroa, E. Fonseca-Lazcano, J.A. Domínguez-Cherit, G. Application of a modified sequential organ failure assessment score to critically ill patients |
title | Application of a modified sequential organ failure
assessment score to critically ill patients |
title_full | Application of a modified sequential organ failure
assessment score to critically ill patients |
title_fullStr | Application of a modified sequential organ failure
assessment score to critically ill patients |
title_full_unstemmed | Application of a modified sequential organ failure
assessment score to critically ill patients |
title_short | Application of a modified sequential organ failure
assessment score to critically ill patients |
title_sort | application of a modified sequential organ failure
assessment score to critically ill patients |
topic | Clinical Investigation |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3854366/ https://www.ncbi.nlm.nih.gov/pubmed/23369978 http://dx.doi.org/10.1590/1414-431X20122308 |
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