Pharmacological treatment options for heart failure with reduced ejection fraction: A 2022 update

• Published in: Expert opinion on pharmacotherapy Vol. 23; no. 6; p. 673
• Main Authors: Hellenkamp, Kristian, Nolte, Kathleen, von Haehling, Stephan
• Format: Journal Article
• Language: English
• Published: England 13.04.2022
• Subjects: Aminobutyrates - therapeutic use; Angiotensin Receptor Antagonists - therapeutic use; Angiotensin-Converting Enzyme Inhibitors - therapeutic use; Biphenyl Compounds - therapeutic use; Drug Combinations; Heart Failure - drug therapy; Humans; Neprilysin - antagonists & inhibitors; Stroke Volume - physiology; Valsartan - therapeutic use; Heart failure; angiotensin receptor-neprilysin inhibitor (ARNI); treatment; sodium glucose co-transporter 2 (SGLT2) inhibitors; vericiguat; drugs
• ISSN: 1744-7666
• DOI: 10.1080/14656566.2022.2047647

Despite considerable advances in the treatment of heart failure with reduced ejection fraction (HFrEF) over the last 60 years, mortality and morbidity remains high. Fortunately, in the last years, further developments expanded the toolbox for HF treatment. The authors provide an overview of recent developments in HF treatment and bring the recommendations in the HF guidelines of the European Society of Cardiology into perspective. Nowadays, basic pharmacological treatment of patients with HFrEF consists of a combination of angiotensin converting enzyme (ACE) inhibitors/angiotensin receptor-neprilysin inhibitor (ARNI), beta-blockers, mineralocorticoid receptor antagonists (MRA), and the SGLT2 inhibitors dapagliflozin or empagliflozin. Treatment initiation of all four drug classes should be fast and simultaneous. In some cases, the ARNI sacubitril/valsartan may be initiated even in ACE inhibitor-naïve patients. Further HF treatment has to be individualized. Another important point is that both SGLT2 inhibitors and vericiguat can be used in patients with severely reduced kidney function. Finally, an important piece in the HF management puzzle is the treatment of its comorbidities. For instance, patients hospitalized for acute HF decompensation should be systematically screened for iron deficiency, since HF patients with proven iron deficiency benefit from intravenous ferric carboxymaltose.