Accelerated and personalized therapy for heart failure with reduced ejection fraction

Author:

Shen Li12,Jhund Pardeep Singh2,Docherty Kieran Francis2,Vaduganathan Muthiah3ORCID,Petrie Mark Colquhoun2ORCID,Desai Akshay Suvas3,Køber Lars4,Schou Morten5ORCID,Packer Milton67ORCID,Solomon Scott David3,Zhang Xingwei1,McMurray John Joseph Valentine2ORCID

Affiliation:

1. Department of Internal Medicine, School of Clinical Medicine, Hangzhou Normal University , Hangzhou 311121 , China

2. British Heart Foundation Cardiovascular Research Centre, University of Glasgow , 126 University Place, Glasgow G12 8TA , UK

3. Department of Medicine, Division of Cardiovascular Medicine, Brigham and Women’s Hospital , Boston, MA , USA

4. Department of Cardiology, Copenhagen University Hospital, Rigshospitalet , København , Denmark

5. Department of Cardiology, Copenhagen University Hospital Herlev and Gentofte , Herlev , Denmark

6. Cardiovascular Science, Baylor Heart and Vascular Institute, Baylor University Medical Center , Dallas, TX , USA

7. Faculty of Medicine, National Heart and Lung Institute, Imperial College , London , UK

Abstract

Abstract 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.

Funder

National Natural Science Foundation of China

British Heart Foundation

Publisher

Oxford University Press (OUP)

Subject

Cardiology and Cardiovascular Medicine

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