| Literature DB >> 33907552 |
Pablo Díez-Villanueva1, César Jiménez-Méndez1, Fernando Alfonso1.
Abstract
Heart failure (HF) is a clinical syndrome caused by structural and/or functional cardiac abnormalities, resulting in a reduced cardiac output and/or elevated intracardiac filling pressures at rest or during stress. HF is a major public health problem with high prevalence and incidence, involving both high morbidity and mortality, but also high economic costs. The incidence of HF progressively increases with age, reaching around 20% among people over 75 years old. Indeed, HF represents the leading cause of hospitalization in patients older than 65 years in Western countries. Hence, some authors even consider HF a geriatric syndrome, entailing worse prognosis and high residual disability, and often associating some complex comorbidities, common in older population, that may further complicate the course of the disease. On the other hand, however, clinical course and prognosis may be often difficult to predict. In this article, main pathophysiological issues related to the aging heart are addressed, together with key aspects related to both diagnosis and prognosis in elderly patients with HF. Besides, main geriatric conditions, common in the elderly population, are reviewed, highlighting the importance of a comprehensive and multidisciplinary approach. Copyright and License information: Journal of Geriatric Cardiology 2021.Entities:
Year: 2021 PMID: 33907552 PMCID: PMC8047189 DOI: 10.11909/j.issn.1671-5411.2021.03.009
Source DB: PubMed Journal: J Geriatr Cardiol ISSN: 1671-5411 Impact factor: 3.327
Physiopathological changes in the heart and cardiovascular system with aging.
| CO: cardiac output; LVEF: left ventricular ejection fraction; RV: right ventricle. | |
| Left ventricle | Left ventricular hypertrophy diastolic dysfunction preservation/modestly enhanced ejection
|
| Right ventricle | Preservation right ventricular ejection fraction
|
| Atria | Atrial dilatation
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| Cardiac function | Decrease in maximal CO
|
| Coronary arteries | Endothelial dysfunction
|
| Chronotropic function | Reduction in maximal heart rate
|
| Myocardial tissue | Myocardial fibrosis due to deleterious effect of chronic neurohumoral activation
|
| Arterial function | Arterial stiffness
|
Heart failure aetiology*.
| *Adapted from ESC Guidelines. ARVC: arrhythmogenic right ventricular cardiomyopathy; DCM: dilated cardiomyopathy; GH: growth hormone; HCM: hypertrophic cardiomyopathy; HIV/AIDS: human immunodeficiency virus/acquired immunodeficiency syndrome; LV non-compaction: left ventricular non-compaction. | ||
| Ischemic heart disease | Myocardial scar
| |
| Toxics | Recreational substance abuse | Alcohol, cocaine, amphetamine, anabolic steroids. |
| Heavy metals | Copper, iron, lead, cobalt. | |
| Medications | Cytostatic drugs (e.g., anthracyclines), immunomodulating drugs (e.g., interferons monoclonal antibodies such as trastuzumab, cetuximab), antidepressant drugs, antiarrhythmics, non-steroidal anti-inflammatory drugs, anaesthetics. | |
| Radiation | ||
| Immune-mediated and inflammatory damage | Infection | Bacteria, spirochaetes, fungi, protozoa, parasites (Chagas disease), |
| Not related to infection | Lymphocytic/giant cell myocarditis, autoimmune diseases (e.g., Graves’ disease, rheumatoid arthritis, connective tissue disorders, mainly systemic lupus erythematosus), hypersensitivity and eosinophilic myocarditis (Churg–Strauss). | |
| Infiltration | Related to malignancy | Direct infiltration or metastases |
| Not related to malignancy | Amyloidosis, sarcoidosis, hemochromatosis, glycogen storage disease, lysosomal storage disease. | |
| Metabolic derangements | Hormonal | Thyroid disease, acromegaly, GH deficiency, hypercortisolaemia, Conn’s disease, Addison disease, diabetes, metabolic syndrome, phaeochromocytoma, pathologies related to pregnancy and peripartum |
| Nutritional | Deficiencies in thiamine, L-carnitine, selenium, iron, phosphates, calcium, obesity. | |
| Genetic | HCM, DCM, LV non-compaction, ARVC, restrictive cardiomyopathy, muscular dystrophies and laminopathies. | |
| Pericardial and endomyocardial pathologies | Pericardial | Constrictive pericarditis
|
| Endomyocardial | Hypereosinophilic syndrome, endomyocardial fibrosis, endomyocardial fibroelastosis. | |
| Hypertension | ||
| Valve and myocardium structural defects | Acquired
| Mitral, aortic, tricuspid and pulmonary valve diseases
|
| High output states | Anaemia, sepsis, Paget’s disease, arteriovenous fistula, pregnancy | |
| Volume overload | Renal failure, iatrogenic | |
| Tachyarrhythmias | Atrial or ventricular arrhythmias | |
| Bradyarrhythmias | Sinus node dysfunctions, conduction disorders | |
Heart failure diagnosis.
| LAVI: left atrial volume index; LVMI: left ventricular mass index; NT-proBNP: N-terminal pro-brain natriuretic peptide. | |
| Breathlessness | Elevated jugular venous pressure |
| Orthopnoea | Third heart sound (gallop rhythm) |
| Paroxysmal nocturnal dyspnoea | Hepatojugular reflux |
| Bendopnea | Laterally displaced apical impulse |
| Reduced exercise tolerance | Weight gain (> 2 kg/week) |
| Fatigue, tiredness, increased time to recover after exercise | Cardiac murmur
|
| Nocturnal cough | Pulmonary crepitation |
| Wheezing | Pleural effusion |
| Bloated feeling | Tachycardia/Tachypnoea |
| Loss of appetite | Hepatomegaly |
| Confusion | Ascites |
| Depression | Cold extremities |
| Palpitations | Oliguria |
| Dizziness | |
| Syncope | |
| < 50 yrs | > 450 pg/mL |
| 50−75 yrs | > 900 pg/mL |
| > 75 yrs | > 1800 pg/mL |
| Left ventricular dysfunction | |
| Diastolic dysfunction | |
| LAVI > 34 mL/m 2 | |
| LVMI ≥ 115 g/m2 (males) and ≥ 95 g/m2 (females) | |
| E/E′ ≥ 13 | |
| Mean E’ septal and lateral wall < 9 cm/s. | |
| Right ventricular dysfunction or increase pulmonary artery pressure | |
Heart failure functional NYHA classification.
| NYHA: New York Heart Association. | |
| Class I | No difficulty with usual physical activities, with no manifestation of dyspnoea, fatigue or palpitations. |
| Class II | Slight limitation for usual physical activities. Patient asymptomatic at rest; in physical activity, expression of fatigue, dyspnoea and palpitations. |
| Class III | Significant limitation of physical activities, although comfortable at rest. Symptoms of dyspnoea, fatigue and palpitations on exertion. |
| Class IV | Symptoms present even at rest, and discomfort with any physical activity. |
Heart failure functional ACC/AHA classification.
| ACC/AHA: American College of Cardiology/American Heart Association. | |
| Stage A | Patients at risk for heart failure who have not yet developed structural heart changes. |
| Stage B | Patients with structural heart disease, but who have not yet developed symptoms of heart failure. |
| Stage C | Patients who have developed clinical heart failure |
| Stage D | Patients with refractory heart failure requiring advanced intervention. |
Figure 1Pharmacological treatment in HFrEF.