Key result
Higher beta-blocker dose, but not reduced heart rate, remained significantly associated with reduced all-cause death or hospitalization after adjustment for other predictors.
Why the study?
Does higher beta-blocker dose or lower heart rate have a greater association with improved outcomes in ambulatory heart failure patients with systolic dysfunction?
RCT (n=2,331)
randomized
Yes
Does higher beta-blocker dose or lower heart rate have a greater association with improved outcomes in ambulatory heart failure patients with systolic dysfunction?
Answers are grounded in this paper and cite their sources.
Higher beta-blocker dose, rather than lower heart rate, is independently associated with improved outcomes in patients with HFrEF, suggesting that titrating beta-blockers to target doses is more beneficial than merely reducing heart rate.
OBJECTIVES: This study aimed to compare whether reduced heart rate (HR) or higher beta-blocker (BB) dose affected outcomes to a greater extent in the HF-ACTION (Heart Failure: A Controlled Trial Investigating Outcomes of Exercise Training) trial population. BACKGROUND: Recent data have shown that HR is an important modifiable factor in reducing mortality in heart failure (HF) patients. It has also been shown that titration of doses of BBs improves outcomes of morbidity and mortality in chronic HF patients with reduced ejection fraction. We aimed to compare whether reduced HR or higher BB dose affected outcomes to a greater extent in the HF-ACTION trial population. METHODS: HF-ACTION was a randomized, multicenter trial enrolling 2,331 ambulatory HF patients with systolic dysfunction (New York Heart Association functional class II to IV, left ventricular ejection fraction <0.35) randomized to exercise training versus usual care, with median follow-up of 2.5 years. BB dose at baseline was standardized by use of carvedilol equivalents. BB dose and HR were analyzed by discrete groups (higher/lower dose; higher/lower HR). The relationship of BB dose, HR, and the primary endpoint of all-cause mortality or all-cause hospitalization and other cardiovascular secondary endpoints were determined before and after adjustment for variables found to be significantly associated with outcome in the HF-ACTION cohort. RESULTS: There was a significant inverse relationship between either BB dose (higher was better) or HR (lower was better) and all-cause death or hospitalization in unadjusted analysis; however, only BB dose was significant for improved mortality outcomes. After adjustment for other predictors of outcome, only BB dose remained significant for improving all-cause death or hospitalization. BB dose, but not HR, was associated with improved outcomes of other cardiovascular endpoints in unadjusted analysis but did not remain significant when adjusted for other predictors of outcome in this cohort. CONCLUSIONS: There were more associated improvements in outcomes with higher BB dose than with reduced HR in this well-treated HF cohort with systolic dysfunction, which suggests that titration of BB doses may confer a greater benefit than reduction of HR in such patients. (Heart Failure: A Controlled Trial Investigating Outcomes of Exercise Training [HF-ACTION]; NCT00047437).
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Fiuzat et al. (2015) conducted an RCT in Ambulatory heart failure with systolic dysfunction (n=2,331). Higher beta-blocker dose and reduced heart rate vs. Lower beta-blocker dose and higher heart rate was evaluated on All-cause mortality or all-cause hospitalization. Higher beta-blocker dose, but not reduced heart rate, remained significantly associated with reduced all-cause death or hospitalization after adjustment for other predictors.
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