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Early initiation of low-dose corticosteroid therapy in the management of septic shock: a retrospective observational study
INTRODUCTION: The use of low-dose steroid therapy in the management of septic shock has been extensively studied. However, the association between the timing of low-dose steroid therapy and the outcome has not been evaluated. Therefore, we evaluated whether early initiation of low-dose steroid thera...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3396228/ https://www.ncbi.nlm.nih.gov/pubmed/22226237 http://dx.doi.org/10.1186/cc10601 |
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author | Park, Hye Yun Suh, Gee Young Song, Jae-Uk Yoo, Hongseok Jo, Ik Joon Shin, Tae Gun Lim, So Yeon Woo, Sookyoung Jeon, Kyeongman |
author_facet | Park, Hye Yun Suh, Gee Young Song, Jae-Uk Yoo, Hongseok Jo, Ik Joon Shin, Tae Gun Lim, So Yeon Woo, Sookyoung Jeon, Kyeongman |
author_sort | Park, Hye Yun |
collection | PubMed |
description | INTRODUCTION: The use of low-dose steroid therapy in the management of septic shock has been extensively studied. However, the association between the timing of low-dose steroid therapy and the outcome has not been evaluated. Therefore, we evaluated whether early initiation of low-dose steroid therapy is associated with mortality in patients with septic shock. METHODS: We retrospectively analyzed the clinical data of 178 patients who received low-dose corticosteroid therapy for septic shock between January 2008 and December 2009. Time-dependent Cox regression models were used to adjust for potential confounding factors in the association between the time to initiation of low-dose corticosteroid therapy and in-hospital mortality. RESULTS: The study population consisted of 107 men and 71 women with a median age of 66 (interquartile range, 54 to 71) years. The 28-day mortality was 44% and low-dose corticosteroid therapy was initiated within a median of 8.5 (3.8 to 19.1) hours after onset of septic shock-related hypotension. Median time to initiation of low-dose corticosteroid therapy was significantly shorter in survivors than in non-survivors (6.5 hours versus 10.4 hours; P = 0.0135). The mortality rates increased significantly with increasing quintiles of time to initiation of low-dose corticosteroid therapy (P = 0.0107 for trend). Other factors associated with 28-day mortality were higher Simplified Acute Physiology Score (SAPS) 3 (P < 0.0001) and Sequential Organ Failure Assessment (SOFA) scores (P = 0.0007), dose of vasopressor at the time of initiation of low-dose corticosteroid therapy (P < 0.0001), need for mechanical ventilation (P = 0.0001) and renal replacement therapy (P < 0.0001), while the impaired adrenal reserve did not affect 28-day mortality (81% versus 82%; P = 0.8679). After adjusting for potential confounding factors, the time to initiation of low-dose corticosteroid therapy was still significantly associated with 28-day mortality (adjusted odds ratio (OR) 1.025, 95% confidence interval (CI) 1.007 to 1.044, P = 0.0075). The early therapy group (administered within 6 hours after the onset of septic shock, n = 66) had a 37% lower mortality rate than the late therapy group (administered more than 6 hours after the onset of septic shock, n = 112) (32% versus 51%, P = 0.0132). CONCLUSIONS: Early initiation of low-dose corticosteroid therapy was significantly associated with decreased mortality. |
format | Online Article Text |
id | pubmed-3396228 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-33962282012-07-13 Early initiation of low-dose corticosteroid therapy in the management of septic shock: a retrospective observational study Park, Hye Yun Suh, Gee Young Song, Jae-Uk Yoo, Hongseok Jo, Ik Joon Shin, Tae Gun Lim, So Yeon Woo, Sookyoung Jeon, Kyeongman Crit Care Research INTRODUCTION: The use of low-dose steroid therapy in the management of septic shock has been extensively studied. However, the association between the timing of low-dose steroid therapy and the outcome has not been evaluated. Therefore, we evaluated whether early initiation of low-dose steroid therapy is associated with mortality in patients with septic shock. METHODS: We retrospectively analyzed the clinical data of 178 patients who received low-dose corticosteroid therapy for septic shock between January 2008 and December 2009. Time-dependent Cox regression models were used to adjust for potential confounding factors in the association between the time to initiation of low-dose corticosteroid therapy and in-hospital mortality. RESULTS: The study population consisted of 107 men and 71 women with a median age of 66 (interquartile range, 54 to 71) years. The 28-day mortality was 44% and low-dose corticosteroid therapy was initiated within a median of 8.5 (3.8 to 19.1) hours after onset of septic shock-related hypotension. Median time to initiation of low-dose corticosteroid therapy was significantly shorter in survivors than in non-survivors (6.5 hours versus 10.4 hours; P = 0.0135). The mortality rates increased significantly with increasing quintiles of time to initiation of low-dose corticosteroid therapy (P = 0.0107 for trend). Other factors associated with 28-day mortality were higher Simplified Acute Physiology Score (SAPS) 3 (P < 0.0001) and Sequential Organ Failure Assessment (SOFA) scores (P = 0.0007), dose of vasopressor at the time of initiation of low-dose corticosteroid therapy (P < 0.0001), need for mechanical ventilation (P = 0.0001) and renal replacement therapy (P < 0.0001), while the impaired adrenal reserve did not affect 28-day mortality (81% versus 82%; P = 0.8679). After adjusting for potential confounding factors, the time to initiation of low-dose corticosteroid therapy was still significantly associated with 28-day mortality (adjusted odds ratio (OR) 1.025, 95% confidence interval (CI) 1.007 to 1.044, P = 0.0075). The early therapy group (administered within 6 hours after the onset of septic shock, n = 66) had a 37% lower mortality rate than the late therapy group (administered more than 6 hours after the onset of septic shock, n = 112) (32% versus 51%, P = 0.0132). CONCLUSIONS: Early initiation of low-dose corticosteroid therapy was significantly associated with decreased mortality. BioMed Central 2012 2012-01-07 /pmc/articles/PMC3396228/ /pubmed/22226237 http://dx.doi.org/10.1186/cc10601 Text en Copyright ©2012 Park et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Park, Hye Yun Suh, Gee Young Song, Jae-Uk Yoo, Hongseok Jo, Ik Joon Shin, Tae Gun Lim, So Yeon Woo, Sookyoung Jeon, Kyeongman Early initiation of low-dose corticosteroid therapy in the management of septic shock: a retrospective observational study |
title | Early initiation of low-dose corticosteroid therapy in the management of septic shock: a retrospective observational study |
title_full | Early initiation of low-dose corticosteroid therapy in the management of septic shock: a retrospective observational study |
title_fullStr | Early initiation of low-dose corticosteroid therapy in the management of septic shock: a retrospective observational study |
title_full_unstemmed | Early initiation of low-dose corticosteroid therapy in the management of septic shock: a retrospective observational study |
title_short | Early initiation of low-dose corticosteroid therapy in the management of septic shock: a retrospective observational study |
title_sort | early initiation of low-dose corticosteroid therapy in the management of septic shock: a retrospective observational study |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3396228/ https://www.ncbi.nlm.nih.gov/pubmed/22226237 http://dx.doi.org/10.1186/cc10601 |
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