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Effect of systemic corticosteroid therapy for acute heart failure patients with elevated C‐reactive protein

AIMS: The current study explores whether degree of inflammation, reflected by C‐reactive protein (CRP) level, modifies the effect of intravenous (IV) corticosteroid administered in the emergency department (ED) on clinical outcomes in patients with acute heart failure (AHF). METHODS AND RESULTS: We...

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Autores principales: Miró, Òscar, Takagi, Koji, Davison, Beth A., Edwards, Christopher, Freund, Yonathan, Jacob, Javier, Llorens, Pere, Mebazaa, Alexandre, Cotter, Gad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9288737/
https://www.ncbi.nlm.nih.gov/pubmed/35393762
http://dx.doi.org/10.1002/ehf2.13926
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author Miró, Òscar
Takagi, Koji
Davison, Beth A.
Edwards, Christopher
Freund, Yonathan
Jacob, Javier
Llorens, Pere
Mebazaa, Alexandre
Cotter, Gad
author_facet Miró, Òscar
Takagi, Koji
Davison, Beth A.
Edwards, Christopher
Freund, Yonathan
Jacob, Javier
Llorens, Pere
Mebazaa, Alexandre
Cotter, Gad
author_sort Miró, Òscar
collection PubMed
description AIMS: The current study explores whether degree of inflammation, reflected by C‐reactive protein (CRP) level, modifies the effect of intravenous (IV) corticosteroid administered in the emergency department (ED) on clinical outcomes in patients with acute heart failure (AHF). METHODS AND RESULTS: We selected patients diagnosed with AHF in the ED, with confirmed N‐terminal pro‐B‐type natriuretic peptide > 300 pg/mL and CRP > 5 mg/L in the ED from the Epidemiology of Acute Heart Failure in the Emergency Departments (EAHFE) registry. In these 1109 patients, 121 were treated by corticosteroid. The corticosteroid therapy hazard ratio (HR) for 30 day all‐cause mortality was 1.26 [95% confidence interval (CI) 0.75–2.09, P = 0.38]. Although not statistically significant, HRs tended to decrease with increasing CRP level, with point estimates favouring corticosteroid at CRP levels above 20. In patients with CRP > 40 mg/L, with adjusted HRs of 0.56 (95% CI 0.20–1.55, P = 0.27) for 30 day all‐cause mortality, 0.92 (95% CI 0.52–1.62, P = 0.78) for 30 day post‐discharge ED revisit, hospitalization, or death, and adjusted odds ratio of 0.61 (95% CI 0.17–2.14, P = 0.44) for in‐hospital all‐cause mortality. CONCLUSIONS: The present analysis suggests that corticosteroids might have the potential to improve outcomes in AHF patients with inflammatory activation. Larger, prospective studies of anti‐inflammatory therapy should be considered to assess potential benefit in patients with the highest degree of inflammation.
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spelling pubmed-92887372022-07-19 Effect of systemic corticosteroid therapy for acute heart failure patients with elevated C‐reactive protein Miró, Òscar Takagi, Koji Davison, Beth A. Edwards, Christopher Freund, Yonathan Jacob, Javier Llorens, Pere Mebazaa, Alexandre Cotter, Gad ESC Heart Fail Short Communications AIMS: The current study explores whether degree of inflammation, reflected by C‐reactive protein (CRP) level, modifies the effect of intravenous (IV) corticosteroid administered in the emergency department (ED) on clinical outcomes in patients with acute heart failure (AHF). METHODS AND RESULTS: We selected patients diagnosed with AHF in the ED, with confirmed N‐terminal pro‐B‐type natriuretic peptide > 300 pg/mL and CRP > 5 mg/L in the ED from the Epidemiology of Acute Heart Failure in the Emergency Departments (EAHFE) registry. In these 1109 patients, 121 were treated by corticosteroid. The corticosteroid therapy hazard ratio (HR) for 30 day all‐cause mortality was 1.26 [95% confidence interval (CI) 0.75–2.09, P = 0.38]. Although not statistically significant, HRs tended to decrease with increasing CRP level, with point estimates favouring corticosteroid at CRP levels above 20. In patients with CRP > 40 mg/L, with adjusted HRs of 0.56 (95% CI 0.20–1.55, P = 0.27) for 30 day all‐cause mortality, 0.92 (95% CI 0.52–1.62, P = 0.78) for 30 day post‐discharge ED revisit, hospitalization, or death, and adjusted odds ratio of 0.61 (95% CI 0.17–2.14, P = 0.44) for in‐hospital all‐cause mortality. CONCLUSIONS: The present analysis suggests that corticosteroids might have the potential to improve outcomes in AHF patients with inflammatory activation. Larger, prospective studies of anti‐inflammatory therapy should be considered to assess potential benefit in patients with the highest degree of inflammation. John Wiley and Sons Inc. 2022-04-08 /pmc/articles/PMC9288737/ /pubmed/35393762 http://dx.doi.org/10.1002/ehf2.13926 Text en © 2022 The Authors. ESC Heart Failure published by John Wiley & Sons Ltd on behalf of European Society of Cardiology. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://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 Short Communications
Miró, Òscar
Takagi, Koji
Davison, Beth A.
Edwards, Christopher
Freund, Yonathan
Jacob, Javier
Llorens, Pere
Mebazaa, Alexandre
Cotter, Gad
Effect of systemic corticosteroid therapy for acute heart failure patients with elevated C‐reactive protein
title Effect of systemic corticosteroid therapy for acute heart failure patients with elevated C‐reactive protein
title_full Effect of systemic corticosteroid therapy for acute heart failure patients with elevated C‐reactive protein
title_fullStr Effect of systemic corticosteroid therapy for acute heart failure patients with elevated C‐reactive protein
title_full_unstemmed Effect of systemic corticosteroid therapy for acute heart failure patients with elevated C‐reactive protein
title_short Effect of systemic corticosteroid therapy for acute heart failure patients with elevated C‐reactive protein
title_sort effect of systemic corticosteroid therapy for acute heart failure patients with elevated c‐reactive protein
topic Short Communications
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9288737/
https://www.ncbi.nlm.nih.gov/pubmed/35393762
http://dx.doi.org/10.1002/ehf2.13926
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