Key result
Bronchodilator use in patients with heart failure was associated with increased all-cause mortality (HR 1.26; 95% CI 1.09-1.45; P=0.0015) and major adverse cardiovascular events.
Why the study?
Does bronchodilator therapy increase adverse cardiovascular outcomes in patients with symptomatic heart failure?
Cohort (n=7,599)
Yes
Does bronchodilator therapy increase adverse cardiovascular outcomes in patients with symptomatic heart failure?
Effect estimate: HR 1.26 (95% CI 1.09-1.45)
p-value: p=0.0015
Bronchodilator use is an independent predictor of increased mortality and worsening heart failure in patients with symptomatic HF, regardless of ejection fraction.
Warrants caution with bronchodilators in symptomatic HF; hypothesis-generating and requires RCTs to assess causality.
AIMS: Heart failure (HF) and chronic obstructive pulmonary disease are common partners. Bronchodilators are associated with adverse cardiovascular outcomes in patients with pulmonary disease. The outcome of patients with HF prescribed bronchodilators is poorly defined. METHODS AND RESULTS: The Candesartan in Heart failure: Assessment of Reduction in Mortality and morbidity (CHARM) programme randomized 7599 patients with symptomatic HF to receive candesartan or placebo. The relative risk conveyed by bronchodilator therapy was examined using a multivariable Cox proportional hazards model. The prevalence of bronchodilator therapy was similar in patients with reduced and preserved systolic function (respectively, 8.7 vs. 9.2%, P = 0.46). Beta-blocker utilization was markedly lower in patients receiving bronchodilators compared with those without (overall 31.9 vs. 57.6%, P < 0.0001). Bronchodilator use was associated with increased all-cause mortality [HR 1.26 (1.09-1.45), P = 0.0015], cardiovascular death [HR 1.21 (1.03-1.42), P = 0.0216], HF hospitalization [HR 1.49 (1.29-1.72), P < 0.0001], and major adverse cardiovascular events [HR 1.32 (1.17-1.76), P < 0.0001]. The adverse outcomes were consistent in patients with reduced and preserved systolic function. No significant interaction was observed between bronchodilators and beta-blockade with respect to outcomes. CONCLUSION: Bronchodilator use is a powerful independent predictor of worsening HF and increased mortality in a broad spectrum of patients with HF. Whether this relates to a toxic effect of bronchodilators, underlying pulmonary disease, or both is unclear and warrants further investigation.
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Hawkins et al. (2010) conducted a cohort in Heart failure (n=7,599). Bronchodilator therapy vs. No bronchodilator therapy was evaluated on All-cause mortality (HR 1.26, 95% CI 1.09-1.45, p=0.0015). Bronchodilator use in patients with heart failure was associated with increased all-cause mortality (HR 1.26; 95% CI 1.09-1.45; P=0.0015) and major adverse cardiovascular events.
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