Accelerated and personalized therapy for heart failure with reduced ejection fraction
Li Shen1,2, Pardeep Singh Jhund2, Kieran Francis Docherty2
1Department of Internal Medicine, School of Clinical Medicine, Hangzhou Normal University, Hangzhou 311121, China.
Insights
Accelerating treatment up-titration and optimizing drug sequencing in heart failure with reduced ejection fraction (HFrEF) may prevent deaths and hospitalizations. Standard guidelines may not be optimal for HFrEF patient outcomes.
Area of Science:
- Cardiology
- Pharmacology
- Clinical Trials
Background:
- Current guidelines for heart failure with reduced ejection fraction (HFrEF) recommend sequential therapy initiation based on historical trial timelines.
- The optimal timing and sequence for initiating HFrEF therapies remain subjects of ongoing investigation.
Purpose of the Study:
- To model the potential benefits of accelerated up-titration and alternative sequencing of HFrEF therapies.
- To compare outcomes of conventional versus optimized treatment initiation strategies.
Main Methods:
- Utilized data from six pivotal HFrEF trials to simulate different treatment initiation strategies.
- Modeled rapid up-titration and optimized alternative sequences, including sodium-glucose cotransporter 2 inhibitors and mineralocorticoid receptor antagonists.
Main Results:
- Rapid up-titration reduced composite events (HFrEF hospitalization or cardiovascular death) by 23 per 1000 patients and all-cause deaths by seven per 1000 within 12 months.
- Optimized sequencing further reduced composite outcomes by 24 per 1000 and deaths by six per 1000 at 12 months.
- The optimal sequences prioritized sodium-glucose cotransporter 2 inhibition and mineralocorticoid receptor antagonist initiation.
Conclusions:
- Accelerated up-titration and optimized sequencing of HFrEF therapies show potential to significantly improve patient outcomes.
- Modeling suggests substantial reductions in mortality and hospitalizations compared to standard treatment approaches.
- Further clinical trials are warranted to validate these findings in practice.
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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