Guideline‐directed medical therapy in severe heart failure with reduced ejection fraction: an analysis from the HELP‐HF registry

Author:

Tomasoni Daniela12,Pagnesi Matteo1,Colombo Giada1,Chiarito Mauro34,Stolfo Davide5,Baldetti Luca6,Lombardi Carlo Mario1,Adamo Marianna1,Maggi Giuseppe1,Inciardi Riccardo Maria1,Loiacono Ferdinando3,Maccallini Marta34,Villaschi Alessandro34,Gasparini Gaia34,Montella Marco34,Contessi Stefano5,Cocianni Daniele5,Perotto Maria5,Barone Giuseppe6,Merlo Marco5,Cappelletti Alberto Maria6,Rosano Giuseppe7,Sinagra Gianfranco5,Pini Daniela3,Savarese Gianluigi2,Metra Marco1ORCID

Affiliation:

1. Institute of Cardiology, ASST Spedali Civili, Department of Medical and Surgical specialties, Radiological Sciences and Public Health University of Brescia Brescia Italy

2. Division of Cardiology, Department of Medicine, Karolinska Institutet, and Heart and Vascular and Neuro Theme Karolinska University Hospital Stockholm Sweden

3. Humanitas Research Hospital IRCCS Rozzano Italy

4. Department of Biomedical Sciences Humanitas University Pieve Emanuele Italy

5. Cardiovascular Department Azienda Sanitaria Universitaria Giuliano Isontina (ASUGI), University of Trieste Trieste Italy

6. Cardiac Intensive Care Unit IRCCS San Raffaele Scientific Institute Milan Italy

7. Department of Medical Sciences, Centre for Clinical and Basic Research IRCCS San Raffaele Pisana Rome Italy

Abstract

AbstractAimPersistent symptoms despite guideline‐directed medical therapy (GDMT) and poor tolerance of GDMT are hallmarks of patients with advanced heart failure (HF) with reduced ejection fraction (HFrEF). However, real‐world data on GDMT use, dose, and prognostic implications are lacking.Methods and resultsWe included 699 consecutive patients with HFrEF and at least one ‘I NEED HELP’ marker for advanced HF enrolled in a multicentre registry. Beta‐blockers (BB) were administered to 574 (82%) patients, angiotensin‐converting enzyme inhibitors, angiotensin receptor blockers or angiotensin receptor–neprilysin inhibitors (ACEi/ARB/ARNI) were administered to 381 (55%) patients and 416 (60%) received mineralocorticoid receptor antagonists (MRA). Overall, ≥50% of target doses were reached in 41%, 22%, and 56% of the patients on BB, ACEi/ARB/ARNI and MRA, respectively. Hypotension, bradycardia, kidney dysfunction and hyperkalaemia were the main causes of underprescription and/or underdosing, but up to a half of the patients did not receive target doses for unknown causes (51%, 41%, and 55% for BB, ACEi/ARB/ARNI and MRA, respectively). The proportions of patients receiving BB and ACEi/ARB/ARNI were lower among those fulfilling the 2018 HFA‐ESC criteria for advanced HF. Treatment with BB and ACEi/ARB/ARNI were associated with a lower risk of death or HF hospitalizations (adjusted hazard ratio [HR] 0.63, 95% confidence interval [CI] 0.48–0.84, and HR 0.74, 95% CI 0.58–0.95, respectively).ConclusionsIn a large, real‐world, contemporary cohort of patients with severe HFrEF, with at least one marker for advanced HF, prescription and uptitration of GDMT remained limited. A significant proportion of patients were undertreated due to unknown reasons suggesting a potential role of clinical inertia either by the prescribing healthcare professional or by the patient. Treatment with BB and ACEi/ARB/ARNI was associated with lower mortality/morbidity.

Publisher

Wiley

Subject

Cardiology and Cardiovascular Medicine

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