2024 update in heart failure

Author:

Beghini Alberto1,Sammartino Antonio Maria1,Papp Zoltán2,von Haehling Stephan34,Biegus Jan5,Ponikowski Piotr5,Adamo Marianna1,Falco Luigi6,Lombardi Carlo Mario1,Pagnesi Matteo1,Savarese Gianluigi78,Metra Marco1,Tomasoni Daniela17

Affiliation:

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

2. Division of Clinical Physiology, Department of Cardiology, Faculty of Medicine University of Debrecen Debrecen Hungary

3. Department of Cardiology and Pneumology University Medical Center Göttingen Göttingen Germany

4. German Centre for Cardiovascular Research (DZHK), partner site Göttingen Göttingen Germany

5. Institute of Heart Diseases Wrocław Medical University Wrocław Poland

6. Heart Failure Unit, Department of Cardiology AORN dei Colli–Monaldi Hospital Naples Naples Italy

7. Cardiology, Department of Medicine, Solna Karolinska Institutet Stockholm Sweden

8. Heart and Vascular and Neuro Theme Karolinska University Hospital Stockholm Sweden

Abstract

AbstractIn the last years, major progress has occurred in heart failure (HF) management. The 2023 ESC focused update of the 2021 HF guidelines introduced new key recommendations based on the results of the last years of science. First, two drugs, sodium–glucose co‐transporter‐2 (SGLT2) inhibitors and finerenone, a novel nonsteroidal, selective mineralocorticoid receptor antagonist (MRA), are recommended for the prevention of HF in patients with diabetic chronic kidney disease (CKD). Second, SGLT2 inhibitors are now recommended for the treatment of HF across the entire left ventricular ejection fraction spectrum. The benefits of quadruple therapy in patients with HF with reduced ejection fraction (HFrEF) are well established. Its rapid and early up‐titration along with a close follow‐up with frequent clinical and laboratory re‐assessment after an episode of acute HF (the so‐called ‘high‐intensity care’ strategy) was associated with better outcomes in the STRONG‐HF trial. Patients experiencing an episode of worsening HF might require a fifth drug, vericiguat. In the STEP‐HFpEF‐DM and STEP‐HFpEF trials, semaglutide 2.4 mg once weekly administered for 1 year decreased body weight and significantly improved quality of life and the 6 min walk distance in obese patients with HF with preserved ejection fraction (HFpEF) with or without a history of diabetes. Further data on safety and efficacy, including also hard endpoints, are needed to support the addition of acetazolamide or hydrochlorothiazide to a standard diuretic regimen in patients hospitalized due to acute HF. In the meantime, PUSH‐AHF supported the use of natriuresis‐guided diuretic therapy. Further options and most recent evidence for the treatment of HF, including specific drugs for cardiomyopathies (i.e., mavacamten in hypertrophic cardiomyopathy and tafamidis in transthyretin cardiac amyloidosis), device therapies, cardiac contractility modulation and percutaneous treatment of valvulopathies, with the recent finding from the TRILUMINATE Pivotal trial, are also reviewed in this article.

Publisher

Wiley

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