Heart failure management with β-blockers: can we do better?
Mucio Tavares de Oliveira JuniorRui BaptistaSergio A Chavez-LealMarcely Gimenes BonattoPublished in: Current medical research and opinion (2024)
Heart failure (HF) is associated with disabling symptoms, poor quality of life, and a poor prognosis with substantial excess mortality in the years following diagnosis. Overactivation of the sympathetic nervous system is a key feature of the pathophysiology of HF and is an important driver of the process of adverse remodelling of the left ventricular wall that contributes to cardiac failure. Drugs which suppress the activity of the renin-angiotensin-aldosterone system, including β-blockers, are foundation therapies for the management of heart failure with reduced ejection fraction (HFrEF) and despite a lack of specific outcomes trials, are also widely used by cardiologist in patients with HF with preserved ejection fraction (HFpEF). Today, expert opinion has moved away from recommending that treatment for HF should be guided solely by the LVEF and interventions should rather address signs and symptoms of HF (e.g. oedema and tachycardia), the severity of HF, and concomitant conditions. β-blockers improve HF symptoms and functional status in HF and these agents have demonstrated improved survival, as well as a reduced risk of other important clinical outcomes such as hospitalisation for heart failure, in randomised, placebo-controlled outcomes trials. In HFpEF, β-blockers are anti-ischemic and lower blood pressure and heart rate. Moreover, β-blockers also reduce mortality in the setting of HF occurring alongside common comorbid conditions, such as diabetes, CKD (of any severity), and COPD. Higher doses of β-blockers are associated with better clinical outcomes in populations with HF, so that ensuring adequate titration of therapy to their maximal (or maximally tolerated) doses is important for ensuring optimal outcomes for people with HF. In principle, a patient with HF could have combined treatment with a β-blocker, renin-angiotensin-aldosterone system inhibitor/neprilysin inhibitor, mineralocorticoid receptor antagonist, and a SGLT2 inhibitor, according to tolerability.
Keyphrases
- acute heart failure
- heart failure
- angiotensin converting enzyme
- left ventricular
- heart rate
- angiotensin ii
- blood pressure
- poor prognosis
- ejection fraction
- randomized controlled trial
- risk factors
- squamous cell carcinoma
- clinical trial
- cardiovascular disease
- physical activity
- long non coding rna
- atrial fibrillation
- left atrial
- double blind
- acute myocardial infarction
- machine learning
- ischemia reperfusion injury
- aortic stenosis
- mesenchymal stem cells
- cell therapy
- type diabetes
- heart rate variability
- chronic kidney disease
- mitral valve
- smoking cessation
- subarachnoid hemorrhage
- sleep quality
- lung function
- glycemic control
- blood glucose
- case report
- blood brain barrier
- insulin resistance
- body composition