Key result
Intravenous corticosteroid therapy did not significantly reduce 30-day all-cause mortality compared to no corticosteroid therapy in acute heart failure patients with elevated C-reactive protein (HR 1.26).
Why the study?
It was unknown whether the degree of inflammation, reflected by CRP levels, modifies the effect of IV corticosteroids given in the ED on clinical outcomes in acute heart failure.
Does intravenous corticosteroid therapy reduce 30-day all-cause mortality in acute heart failure patients with elevated C-reactive protein?
Cohort (n=1,109)
Yes
Does intravenous corticosteroid therapy reduce 30-day all-cause mortality in acute heart failure patients with elevated C-reactive protein?
Answers are grounded in this paper and cite their sources.
Intravenous corticosteroid therapy in the ED did not significantly reduce 30-day mortality in acute heart failure patients with elevated CRP, though there was a non-significant trend toward benefit in those with the highest inflammation (CRP > 40 mg/L).
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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Miró et al. (2022) conducted a cohort in Acute heart failure with elevated C-reactive protein (n=1,109). Intravenous corticosteroids vs. No corticosteroids was evaluated on 30-day all-cause mortality (HR 1.26, 95% CI 0.75-2.09, p=0.38). Intravenous corticosteroid therapy did not significantly reduce 30-day all-cause mortality compared to no corticosteroid therapy in acute heart failure patients with elevated C-reactive protein (HR 1.26).
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