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Residual rates of mortality in patients with severe sepsis: a fatality or a new challenge?

Phase III clinical trials on severe sepsis and septic shock published during the past decade have failed to reveal the superiority of any therapeutic intervention on mortality compared with evolving standards of care, with the exception of the Early-Goal Directed Therapy reported in 2001. This viewp...

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Autores principales: Asfar, Pierre, Claessens, Yann-Erick, Duranteau, Jacques, Kipnis, Eric, Leone, Marc, Lévy, Bruno, Mira, Jean-Paul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3846490/
https://www.ncbi.nlm.nih.gov/pubmed/23958052
http://dx.doi.org/10.1186/2110-5820-3-27
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author Asfar, Pierre
Claessens, Yann-Erick
Duranteau, Jacques
Kipnis, Eric
Leone, Marc
Lévy, Bruno
Mira, Jean-Paul
author_facet Asfar, Pierre
Claessens, Yann-Erick
Duranteau, Jacques
Kipnis, Eric
Leone, Marc
Lévy, Bruno
Mira, Jean-Paul
author_sort Asfar, Pierre
collection PubMed
description Phase III clinical trials on severe sepsis and septic shock published during the past decade have failed to reveal the superiority of any therapeutic intervention on mortality compared with evolving standards of care, with the exception of the Early-Goal Directed Therapy reported in 2001. This viewpoint paper presents an analysis of these studies in order to understand what lessons can be learned and proposes perspectives for future study designs. A total of 102 studies were selected among clinical trials published in the field of severe sepsis and septic shock from 2001 to 2013, based on the assessment of a therapeutic intervention and mortality as an outcome. Studies were further selected according to randomized, controlled trial (RCT) quality criteria and analysed according to reported data. Most (n = 61) were excluded because they did not comply with RCT quality criteria or did not report inclusion criteria or patient severity (n = 22). The 19 remaining studies were categorized into three groups depending on whether the intervention assessed led to better, worse, or equivalent outcomes. It appears that the mortality rate in the control arm, ranging from 17% to 61%, impacted the results, with a benefit reported in the studies with the highest rates. Both heterogeneous studied populations and uncontrolled diversity of care among participating centres probably contributed to discrepancies between studies assessing the same intervention. The new challenge to enhance the probability of decreasing mortality rates should include a more appropriate definition of sepsis based on more specific criteria involving biomarker use and accurate patient phenotypes.
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spelling pubmed-38464902013-12-06 Residual rates of mortality in patients with severe sepsis: a fatality or a new challenge? Asfar, Pierre Claessens, Yann-Erick Duranteau, Jacques Kipnis, Eric Leone, Marc Lévy, Bruno Mira, Jean-Paul Ann Intensive Care Review Phase III clinical trials on severe sepsis and septic shock published during the past decade have failed to reveal the superiority of any therapeutic intervention on mortality compared with evolving standards of care, with the exception of the Early-Goal Directed Therapy reported in 2001. This viewpoint paper presents an analysis of these studies in order to understand what lessons can be learned and proposes perspectives for future study designs. A total of 102 studies were selected among clinical trials published in the field of severe sepsis and septic shock from 2001 to 2013, based on the assessment of a therapeutic intervention and mortality as an outcome. Studies were further selected according to randomized, controlled trial (RCT) quality criteria and analysed according to reported data. Most (n = 61) were excluded because they did not comply with RCT quality criteria or did not report inclusion criteria or patient severity (n = 22). The 19 remaining studies were categorized into three groups depending on whether the intervention assessed led to better, worse, or equivalent outcomes. It appears that the mortality rate in the control arm, ranging from 17% to 61%, impacted the results, with a benefit reported in the studies with the highest rates. Both heterogeneous studied populations and uncontrolled diversity of care among participating centres probably contributed to discrepancies between studies assessing the same intervention. The new challenge to enhance the probability of decreasing mortality rates should include a more appropriate definition of sepsis based on more specific criteria involving biomarker use and accurate patient phenotypes. Springer 2013-08-19 /pmc/articles/PMC3846490/ /pubmed/23958052 http://dx.doi.org/10.1186/2110-5820-3-27 Text en Copyright © 2013 Asfar et al.; licensee Springer. 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 Review
Asfar, Pierre
Claessens, Yann-Erick
Duranteau, Jacques
Kipnis, Eric
Leone, Marc
Lévy, Bruno
Mira, Jean-Paul
Residual rates of mortality in patients with severe sepsis: a fatality or a new challenge?
title Residual rates of mortality in patients with severe sepsis: a fatality or a new challenge?
title_full Residual rates of mortality in patients with severe sepsis: a fatality or a new challenge?
title_fullStr Residual rates of mortality in patients with severe sepsis: a fatality or a new challenge?
title_full_unstemmed Residual rates of mortality in patients with severe sepsis: a fatality or a new challenge?
title_short Residual rates of mortality in patients with severe sepsis: a fatality or a new challenge?
title_sort residual rates of mortality in patients with severe sepsis: a fatality or a new challenge?
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3846490/
https://www.ncbi.nlm.nih.gov/pubmed/23958052
http://dx.doi.org/10.1186/2110-5820-3-27
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