Key result
Accelerated HFrEF therapy up-titration and optimized ordering could reduce absolute major event risk by ~5%.
Why the study?
Does accelerated up-titration and optimized alternative ordering of therapies reduce heart failure hospitalization or cardiovascular death in patients with HFrEF?
Does accelerated up-titration and optimized alternative ordering of therapies reduce heart failure hospitalization or cardiovascular death in patients with HFrEF?
Accelerated up-titration and optimized sequencing of HFrEF therapies (starting with SGLT2 inhibitors and MRAs) could substantially reduce mortality and heart failure hospitalizations compared to conventional chronological approaches.
Answers are grounded in this paper and cite their sources.
May support accelerated up-titration in HFrEF; challenges consensus but leaves open benefit pending RCT validation.
AIMS: Previously, guidelines recommended initiating therapy in patients with heart failure and reduced ejection fraction (HFrEF) in a sequence that follows the chronological order in which trials were conducted, with cautious up-titration of each treatment. It remains unclear whether this historical approach is optimal and alternative approaches may improve patient outcomes. METHODS AND RESULTS: The potential reductions in events that might result from (i) more rapid up-titration of therapies used in the conventional order (based on the chronology of the trials), and (ii) accelerated up-titration and using treatments in different orders than is conventional were modelled using data from six pivotal trials in HFrEF. Over the first 12 months from starting therapy, using a rapid up-titration schedule led to 23 fewer patients per 1000 patients experiencing the composite of heart failure hospitalization or cardiovascular death and seven fewer deaths from any cause. In addition to accelerating up-titration of treatments, optimized alternative ordering of the drugs used resulted in a further reduction of 24 patients experiencing the composite outcome and six fewer deaths at 12 months. The optimal alternative sequences included sodium-glucose cotransporter 2 inhibition and a mineralocorticoid receptor antagonist as the first two therapies. CONCLUSION: Modelling of accelerated up-titration schedule and optimized ordering of treatment suggested that at least 14 deaths and 47 patients experiencing the composite outcome per 1000 treated might be prevented over the first 12 months after starting therapy. Standard treatment guidance may not lead to the best patient outcomes in HFrEF, though these findings should be tested in clinical trials.
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Shen et al. (2022) studied Heart failure with reduced ejection fraction (HFrEF). Accelerated up-titration and optimized alternative ordering of therapies vs. Conventional chronological order with cautious up-titration was evaluated on Composite of heart failure hospitalization or cardiovascular death (47 fewer events per 1000 treated). Accelerated up-titration and optimized ordering of HFrEF therapies (starting with SGLT2i and MRA) was modeled to prevent 47 composite events and 14 deaths per 1000 patients over 12 months.
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