Effect of sacubitril/valsartan vs. enalapril on changes in heart failure therapies over time: the PARADIGM-HF trial.

Guideline-directed medical therapy Heart failure with reduced ejection fraction Mineralocorticoid receptor antagonists Sacubitril/valsartan β-blockers

Journal

European journal of heart failure
ISSN: 1879-0844
Titre abrégé: Eur J Heart Fail
Pays: England
ID NLM: 100887595

Informations de publication

Date de publication:
09 2021
Historique:
revised: 28 04 2021
received: 13 03 2021
accepted: 30 05 2021
pubmed: 9 6 2021
medline: 26 10 2021
entrez: 8 6 2021
Statut: ppublish

Résumé

Sacubitril/valsartan improves morbidity and mortality in patients with heart failure and reduced ejection fraction (HFrEF). Whether initiation of sacubitril/valsartan limits the use and dosing of other elements of guideline-directed medical therapy for HFrEF is unknown. We examined the effects of sacubitril/valsartan, compared with enalapril, on β-blocker and mineralocorticoid receptor antagonist (MRA) use and dosing in a large randomized clinical trial. Patients with full data on medication use were included. We examined β-blocker and MRA use in patients randomized to sacubitril/valsartan vs. enalapril through 12-month follow-up. New initiations and discontinuations of β-blocker and MRA were compared between treatment groups. Overall, 8398 (99.9%) had full medication and dose data at baseline. Baseline use of β-blocker and MRA at any dose was 87% and 56%, respectively. Mean doses of β-blocker and MRA were similar between treatment groups at baseline and at 6-month and 12-month follow-up. New initiations through 12-month follow-up were infrequent and similar in the sacubitril/valsartan and enalapril groups for β-blockers [37 (9.0%) vs. 42 (10.2%), P = 0.56] and MRA [127 (7.6%) vs. 143 (9.2%), P = 0.10]. Among patients on MRA therapy at baseline, there were fewer MRA discontinuations in patients on sacubitril/valsartan as compared with enalapril at 12 months [125 (6.2%) vs. 187 (9.0%), P = 0.001]. Discontinuations of β-blockers were not significantly different between groups in follow-up (2.2% vs. 2.6%, P = 0.26). Initiation of sacubitril/valsartan, even when titrated to target dose, did not appear to lead to greater discontinuation or dose down-titration of other key guideline-directed medical therapies, and was associated with fewer discontinuations of MRA. Use of sacubitril/valsartan (when compared with enalapril) may promote sustained MRA use in follow-up.

Identifiants

pubmed: 34101308
doi: 10.1002/ejhf.2259
pmc: PMC9291580
doi:

Substances chimiques

Aminobutyrates 0
Angiotensin Receptor Antagonists 0
Biphenyl Compounds 0
Drug Combinations 0
Tetrazoles 0
Enalapril 69PN84IO1A
Valsartan 80M03YXJ7I
sacubitril and valsartan sodium hydrate drug combination WB8FT61183

Types de publication

Journal Article Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1518-1524

Commentaires et corrections

Type : CommentIn

Informations de copyright

© 2021 The Authors. European Journal of Heart Failure published by John Wiley & Sons Ltd on behalf of European Society of Cardiology.

Références

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Auteurs

Ankeet S Bhatt (AS)

Division of Cardiology, Brigham and Women's Hospital, Boston, MA, USA.

Muthiah Vaduganathan (M)

Division of Cardiology, Brigham and Women's Hospital, Boston, MA, USA.

Brian L Claggett (BL)

Division of Cardiology, Brigham and Women's Hospital, Boston, MA, USA.

Jiankang Liu (J)

Division of Cardiology, Brigham and Women's Hospital, Boston, MA, USA.

Milton Packer (M)

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

Akshay S Desai (AS)

Division of Cardiology, Brigham and Women's Hospital, Boston, MA, USA.

Martin P Lefkowitz (MP)

Novartis Pharmaceuticals Corporation, East Hanover, NJ, USA.

Jean L Rouleau (JL)

Montreal Heart Institute, Université de Montréal, Montréal, QC, Canada.

Victor C Shi (VC)

Novartis Pharmaceuticals Corporation, East Hanover, NJ, USA.

Michael R Zile (MR)

Medical University of South Carolina, Charleston and Ralph H. Johnston Veterans Administration Medical Center, Charleston, SC, USA.

Karl Swedberg (K)

Department of Molecular and Clinical Medicine, University of Gothenburg, Gothenburg, Sweden.

Orly Vardeny (O)

Center for Care Delivery and Outcomes Research, Minneapolis VA Health Care System, and University of Minnesota, Minneapolis, MN, USA.

John J V McMurray (JJV)

British Heart Foundation Cardiovascular Research Centre, University of Glasgow, Glasgow, UK.

Scott D Solomon (SD)

Division of Cardiology, Brigham and Women's Hospital, Boston, MA, USA.

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Classifications MeSH