Key result
Up-titration of beta-blockers after CRT (n=191) was associated with lower cardiovascular mortality, heart failure hospitalizations, and arrhythmic events compared to no dose increase (n=289).
Why the study?
The extent to which beta-blockers are utilized and whether their doses can be increased in patients receiving cardiac resynchronization therapy is not well known.
Does up-titration of beta-blockers reduce cardiovascular mortality, heart failure hospitalizations, and arrhythmic events in patients with HFrEF after CRT-D implantation?
Cohort (n=480)
No
Does up-titration of beta-blockers reduce cardiovascular mortality, heart failure hospitalizations, and arrhythmic events in patients with HFrEF after CRT-D implantation?
Up-titration of beta-blockers after CRT-D implantation in HFrEF patients is associated with reduced cardiovascular mortality, heart failure hospitalizations, and arrhythmic events.
May support beta-blocker up-titration after CRT in HFrEF; leaves open confirmation in randomized trials.
Clinical trials have shown the benefits of β-blockers therapy in patients with heart failure reduced ejection fraction. These benefits include improved survival and a reduced need for hospitalization. Cardiac resynchronization therapy has emerged as an essential device-based therapy for symptomatic patients with heart failure reduced ejection fraction despite optimal pharmacologic treatment. The extent to which β-blockers are being utilized in patients receiving cardiac resynchronization therapy is not well known. In this study, we evaluate the possibility of increasing β-blockers doses in an unselected cohort of heart failure reduced ejection patients after cardiac resynchronization therapy capable defibrillator system implantation and the correlation between β-blockers treatments and clinical outcome. Methods and results: Patients with heart failure reduced ejection fraction in β-blockers therapy that underwent cardiac resynchronization therapy capable defibrillator system implantation between July 2008, and December 2016 were enrolled in the study. The β-blockers dose was determined at the time of discharge and during follow-up. Cardiovascular mortality, hospitalization for worsening heart failure or arrhythmic storm and appropriate intervention of the device, were recorded. The study cohort included 480 patients, 289 patients (60.3%) had β-blockers doses equal to the dose before CRT (Group 1), 191 patients (39.7%) had higher β-blockers doses than those before the CRT implant (Group 2). Comparing the two groups, Group 2 have lower cardiovascular mortality, heart failure-related hospitalization, and arrhythmic events than Group 1. Conclusion: After initiating CRT, β-blockers could be safely up-titrated at higher doses with the reduction in mortality, heart failure-related hospitalization, and arrhythmic events.
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Masarone et al. (2019) conducted a cohort in Heart failure with reduced ejection fraction (HFrEF) (n=480). Beta-blocker up-titration vs. Beta-blocker dose equal to the dose before CRT was evaluated on Cardiovascular mortality, hospitalization for worsening heart failure or arrhythmic storm and appropriate intervention of the device. Up-titration of beta-blockers after CRT (n=191) was associated with lower cardiovascular mortality, heart failure hospitalizations, and arrhythmic events compared to no dose increase (n=289).
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