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Sequential Organ Failure Assessment (SOFA) scores differ between genders in a sepsis cohort: Cause or effect?
BACKGROUND. Controversy exists regarding the influence of gender on sepsis events and outcome. Epidemiological data from other countries may not always apply to local circumstances. The aim of this study was to identify gender differences in patient characteristics, treatment, and outcome related to...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Informa Healthcare
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3497227/ https://www.ncbi.nlm.nih.gov/pubmed/22793786 http://dx.doi.org/10.3109/03009734.2012.703255 |
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author | Jacobson, Sofie Liedgren, Eva Johansson, Göran Ferm, Martin Winsö, Ola |
author_facet | Jacobson, Sofie Liedgren, Eva Johansson, Göran Ferm, Martin Winsö, Ola |
author_sort | Jacobson, Sofie |
collection | PubMed |
description | BACKGROUND. Controversy exists regarding the influence of gender on sepsis events and outcome. Epidemiological data from other countries may not always apply to local circumstances. The aim of this study was to identify gender differences in patient characteristics, treatment, and outcome related to the occurrence of sepsis at admission to the ICU. METHODS. A prospective observational cohort study on patients admitted to the ICU over a 3-year period fulfilling sepsis criteria during the first 24 hours. Demographic data, APACHE II score, SOFA score, TISS 76, aetiology, length of stay (LOS), mortality rate, and aspects of treatment were collected and then analysed with respect to gender differences. RESULTS. There were no gender-related differences in mortality or length of stay. Early organ dysfunction assessed as SOFA score at admission was a stronger risk factor for hospital mortality for women than for men. This discrepancy was mainly associated with the coagulation sub-score. CRP levels differed between genders in relation to hospital mortality. Infection from the abdominopelvic region was more common among women, whereas infection from skin or skin structures were more common in men. CONCLUSION. In this cohort, gender was not associated with increased mortality during a 2-year follow-up period. SOFA score at ICU admission was a stronger risk factor for hospital mortality for women than for men. The discrepancy was mainly related to the coagulation SOFA sub-score. Together with differences in CRP levels this may suggest differences in inflammatory response patterns between genders. |
format | Online Article Text |
id | pubmed-3497227 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Informa Healthcare |
record_format | MEDLINE/PubMed |
spelling | pubmed-34972272012-11-14 Sequential Organ Failure Assessment (SOFA) scores differ between genders in a sepsis cohort: Cause or effect? Jacobson, Sofie Liedgren, Eva Johansson, Göran Ferm, Martin Winsö, Ola Ups J Med Sci Original Articles BACKGROUND. Controversy exists regarding the influence of gender on sepsis events and outcome. Epidemiological data from other countries may not always apply to local circumstances. The aim of this study was to identify gender differences in patient characteristics, treatment, and outcome related to the occurrence of sepsis at admission to the ICU. METHODS. A prospective observational cohort study on patients admitted to the ICU over a 3-year period fulfilling sepsis criteria during the first 24 hours. Demographic data, APACHE II score, SOFA score, TISS 76, aetiology, length of stay (LOS), mortality rate, and aspects of treatment were collected and then analysed with respect to gender differences. RESULTS. There were no gender-related differences in mortality or length of stay. Early organ dysfunction assessed as SOFA score at admission was a stronger risk factor for hospital mortality for women than for men. This discrepancy was mainly associated with the coagulation sub-score. CRP levels differed between genders in relation to hospital mortality. Infection from the abdominopelvic region was more common among women, whereas infection from skin or skin structures were more common in men. CONCLUSION. In this cohort, gender was not associated with increased mortality during a 2-year follow-up period. SOFA score at ICU admission was a stronger risk factor for hospital mortality for women than for men. The discrepancy was mainly related to the coagulation SOFA sub-score. Together with differences in CRP levels this may suggest differences in inflammatory response patterns between genders. Informa Healthcare 2012-11 2012-10-30 /pmc/articles/PMC3497227/ /pubmed/22793786 http://dx.doi.org/10.3109/03009734.2012.703255 Text en © Informa Healthcare http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the source is credited. |
spellingShingle | Original Articles Jacobson, Sofie Liedgren, Eva Johansson, Göran Ferm, Martin Winsö, Ola Sequential Organ Failure Assessment (SOFA) scores differ between genders in a sepsis cohort: Cause or effect? |
title | Sequential Organ Failure Assessment (SOFA) scores differ between genders in a sepsis cohort: Cause or effect? |
title_full | Sequential Organ Failure Assessment (SOFA) scores differ between genders in a sepsis cohort: Cause or effect? |
title_fullStr | Sequential Organ Failure Assessment (SOFA) scores differ between genders in a sepsis cohort: Cause or effect? |
title_full_unstemmed | Sequential Organ Failure Assessment (SOFA) scores differ between genders in a sepsis cohort: Cause or effect? |
title_short | Sequential Organ Failure Assessment (SOFA) scores differ between genders in a sepsis cohort: Cause or effect? |
title_sort | sequential organ failure assessment (sofa) scores differ between genders in a sepsis cohort: cause or effect? |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3497227/ https://www.ncbi.nlm.nih.gov/pubmed/22793786 http://dx.doi.org/10.3109/03009734.2012.703255 |
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