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Time to vasopressor initiation and organ failure progression in early septic shock

OBJECTIVE: Research evaluating the relationship between vasopressor initiation timing and clinical outcomes is limited and conflicting. We investigated the association between time to vasopressors, worsening organ failure, and mortality in patients with septic shock. METHODS: This was a retrospectiv...

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Autores principales: Black, Lauren Page, Puskarich, Michael A., Smotherman, Carmen, Miller, Taylor, Fernandez, Rosemarie, Guirgis, Faheem W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7493499/
https://www.ncbi.nlm.nih.gov/pubmed/33000037
http://dx.doi.org/10.1002/emp2.12060
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author Black, Lauren Page
Puskarich, Michael A.
Smotherman, Carmen
Miller, Taylor
Fernandez, Rosemarie
Guirgis, Faheem W.
author_facet Black, Lauren Page
Puskarich, Michael A.
Smotherman, Carmen
Miller, Taylor
Fernandez, Rosemarie
Guirgis, Faheem W.
author_sort Black, Lauren Page
collection PubMed
description OBJECTIVE: Research evaluating the relationship between vasopressor initiation timing and clinical outcomes is limited and conflicting. We investigated the association between time to vasopressors, worsening organ failure, and mortality in patients with septic shock. METHODS: This was a retrospective study of patients with septic shock (2013–2016) within 24 hours of emergency department (ED) presentation. The primary outcome was worsening organ failure, defined as an increase in Sequential Organ Failure Assessment (SOFA) score ≥2 at 48 hours compared to baseline, or death within 48 hours. The secondary outcome was 28‐day mortality. Time to vasopressor initiation was categorized into 6, 4‐hour intervals from time of ED triage. Multiple logistic regression was used to identify predictors of worsening organ failure. RESULTS: We analyzed data from 428 patients with septic shock. There were 152 patients with the composite primary outcome (SOFA increase ≥2 or death at 48 hours). Of these, 77 patients died in the first 48 hours and 75 patients had a SOFA increase ≥2. Compared to the patients who received vasopressors in the first 4 hours, those with the longest time to vasopressors (20–24 hours) had increased odds of developing worsening organ failure (odds ratios [OR] = 4.34, 95% confidence intervals [CI] = 1.47–12.79, P = 0.008). For all others, the association between vasopressor timing and worsening organ failure was non‐significant. There was no association between time to vasopressor initiation and 28‐day mortality. CONCLUSIONS: Increased time to vasopressor initiation is an independent predictor of worsening organ failure for patients with vasopressor initiation delays >20 hours.
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spelling pubmed-74934992020-09-29 Time to vasopressor initiation and organ failure progression in early septic shock Black, Lauren Page Puskarich, Michael A. Smotherman, Carmen Miller, Taylor Fernandez, Rosemarie Guirgis, Faheem W. J Am Coll Emerg Physicians Open Infectious Disease OBJECTIVE: Research evaluating the relationship between vasopressor initiation timing and clinical outcomes is limited and conflicting. We investigated the association between time to vasopressors, worsening organ failure, and mortality in patients with septic shock. METHODS: This was a retrospective study of patients with septic shock (2013–2016) within 24 hours of emergency department (ED) presentation. The primary outcome was worsening organ failure, defined as an increase in Sequential Organ Failure Assessment (SOFA) score ≥2 at 48 hours compared to baseline, or death within 48 hours. The secondary outcome was 28‐day mortality. Time to vasopressor initiation was categorized into 6, 4‐hour intervals from time of ED triage. Multiple logistic regression was used to identify predictors of worsening organ failure. RESULTS: We analyzed data from 428 patients with septic shock. There were 152 patients with the composite primary outcome (SOFA increase ≥2 or death at 48 hours). Of these, 77 patients died in the first 48 hours and 75 patients had a SOFA increase ≥2. Compared to the patients who received vasopressors in the first 4 hours, those with the longest time to vasopressors (20–24 hours) had increased odds of developing worsening organ failure (odds ratios [OR] = 4.34, 95% confidence intervals [CI] = 1.47–12.79, P = 0.008). For all others, the association between vasopressor timing and worsening organ failure was non‐significant. There was no association between time to vasopressor initiation and 28‐day mortality. CONCLUSIONS: Increased time to vasopressor initiation is an independent predictor of worsening organ failure for patients with vasopressor initiation delays >20 hours. John Wiley and Sons Inc. 2020-05-02 /pmc/articles/PMC7493499/ /pubmed/33000037 http://dx.doi.org/10.1002/emp2.12060 Text en © 2020 The Authors. JACEP Open published by Wiley Periodicals LLC on behalf of the American College of Emergency Physicians. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Infectious Disease
Black, Lauren Page
Puskarich, Michael A.
Smotherman, Carmen
Miller, Taylor
Fernandez, Rosemarie
Guirgis, Faheem W.
Time to vasopressor initiation and organ failure progression in early septic shock
title Time to vasopressor initiation and organ failure progression in early septic shock
title_full Time to vasopressor initiation and organ failure progression in early septic shock
title_fullStr Time to vasopressor initiation and organ failure progression in early septic shock
title_full_unstemmed Time to vasopressor initiation and organ failure progression in early septic shock
title_short Time to vasopressor initiation and organ failure progression in early septic shock
title_sort time to vasopressor initiation and organ failure progression in early septic shock
topic Infectious Disease
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7493499/
https://www.ncbi.nlm.nih.gov/pubmed/33000037
http://dx.doi.org/10.1002/emp2.12060
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