Why the study?
Chronic heart failure is a major risk factor for mortality in COVID-19, but its role in critically ill older intensive care patients required investigation.
Does pre-existing chronic heart failure increase mortality in critically ill older intensive care patients with COVID-19?
Cohort (n=3,917)
Yes
Does pre-existing chronic heart failure increase mortality in critically ill older intensive care patients with COVID-19?
Odds Ratio: 1.2 (95% CI 0.5–1.5)
Absolute Event Rate: 60% vs 48%
p-value: p=0.137
In critically ill older COVID-19 patients, pre-existing chronic heart failure is associated with higher crude mortality but is not an independent risk factor after adjusting for age, frailty, and disease severity.
AIMS: Chronic heart failure (CHF) is a major risk factor for mortality in coronavirus disease 2019 (COVID-19). This prospective international multicentre study investigates the role of pre-existing CHF on clinical outcomes of critically ill old (≥70 years) intensive care patients with COVID-19. METHODS AND RESULTS: Patients with pre-existing CHF were subclassified as having ischaemic or non-ischaemic cardiac disease; patients with a documented ejection fraction (EF) were subclassified according to heart failure EF: reduced (HFrEF, n = 132), mild (HFmrEF, n = 91), or preserved (HFpEF, n = 103). Associations of heart failure characteristics with the 30 day mortality were analysed in univariate and multivariate logistic regression analyses. Pre-existing CHF was reported in 566 of 3917 patients (14%). Patients with CHF were older, frailer, and had significantly higher SOFA scores on admission. CHF patients showed significantly higher crude 30 day mortality [60% vs. 48%, P < 0.001; odds ratio 1.87, 95% confidence interval (CI) 1.5-2.3] and 3 month mortality (69% vs. 56%, P < 0.001). After multivariate adjustment for confounders (SOFA, age, sex, and frailty), no independent association of CHF with mortality remained [adjusted odds ratio (aOR) 1.2, 95% CI 0.5-1.5; P = 0.137]. More patients suffered from pre-existing ischaemic than from non-ischaemic disease [233 vs. 328 patients (n = 5 unknown aetiology)]. There were no differences in baseline characteristics between ischaemic and non-ischaemic disease or between HFrEF, HFmrEF, and HFpEF. Crude 30 day mortality was significantly higher in HFrEF compared with HFpEF (64% vs. 48%, P = 0.042). EF as a continuous variable was not independently associated with 30 day mortality (aOR 0.98, 95% CI 0.9-1.0; P = 0.128). CONCLUSIONS: In critically ill older COVID-19 patients, pre-existing CHF was not independently associated with 30 day mortality. TRIAL REGISTRATION NUMBER: NCT04321265.
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Bruno et al. (2022) conducted a cohort in COVID-19 (n=3,917). Pre-existing chronic heart failure vs. No pre-existing chronic heart failure was evaluated on 30-day mortality (aOR 1.2, 95% CI 0.5-1.5, p=0.137).
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