Living Well with Heart Failure
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Ischemic Cardiomyopathy: Symptoms, Causes, & Treatment
Ischemic Cardiomyopathy Ischemic cardiomyopathy is a condition that occurs when the heart muscle is weakened due to insufficient blood flow to the heart's muscle. This inhibits the heart's ability to pump blood and can lead to heart failure. What Is Ischemic Cardiomyopathy? Ischemic cardiomyopathy (IC) is a condition that occurs when the heart muscle is weakened. In this condition, the left ventricle, which is the main heart muscle, is usually enlarged and dilated. This condition can be a result of a heart attack or coronary artery disease, a narrowing of the arteries. These narrowed arteries keep blood from reaching portions of your heart. The weakened heart muscle inhibits your heart’s ability to pump blood and can lead to heart failure. Symptoms of IC include shortness of breath, chest pain, and extreme fatigue. If you have IC symptoms, you should seek medical care immediately. Treatment depends on how much damage has been done to your heart. Medications and surgery are often required. You can improve your long-term outlook by making certain lifestyle changes, such as maintaining a healthy diet and avoiding high-risk behaviors, including smoking. Symptoms of Ischemic Cardiomyopathy You can have early-stage heart disease with no symptoms. As the arteries narrow further and blood flow becomes impaired, you may experience a variety of symptoms, including: shortness of breath extreme fatigue dizziness, lightheadedness, or fainting chest pain and pressure (angina) heart palpitations weight gain swelling in the legs and feet (edema) and abdomen difficulty sleeping cough or congestion caused by fluid in the lungs If you have these symptoms, seek emergency medical care or call 9-1-1. -
Myocarditis and Cardiomyopathy
CE: Tripti; HCO/330310; Total nos of Pages: 6; HCO 330310 REVIEW CURRENT OPINION Myocarditis and cardiomyopathy Jonathan Buggey and Chantal A. ElAmm Purpose of review The aim of this study is to summarize the literature describing the pathogenesis, diagnosis and management of cardiomyopathy related to myocarditis. Recent findings Myocarditis has a variety of causes and a heterogeneous clinical presentation with potentially life- threatening complications. About one-third of patients will develop a dilated cardiomyopathy and the pathogenesis is a multiphase, mutlicompartment process that involves immune activation, including innate immune system triggered proinflammatory cytokines and autoantibodies. In recent years, diagnosis has been aided by advancements in cardiac MRI, and in particular T1 and T2 mapping sequences. In certain clinical situations, endomyocardial biopsy (EMB) should be performed, with consideration of left ventricular sampling, for an accurate diagnosis that may aid treatment and prognostication. Summary Although overall myocarditis accounts for a minority of cardiomyopathy and heart failure presentations, the clinical presentation is variable and the pathophysiology of myocardial damage is unique. Cardiac MRI has significantly improved diagnostic abilities, but endomyocardial biopsy remains the gold standard. However, current treatment strategies are still focused on routine heart failure pharmacotherapies and supportive care or cardiac transplantation/mechanical support for those with end-stage heart failure. Keywords cardiac MRI, cardiomyopathy, endomyocardial biopsy, myocarditis INTRODUCTION prevalence seen in children and young adults aged Myocarditis refers to inflammation of the myocar- 20–30 years [1]. dium and may be caused by infectious agents, systemic diseases, drugs and toxins, with viral infec- CAUSE tions remaining the most common cause in the developed countries [1]. -
Non-Coding Rnas in the Cardiac Action Potential and Their Impact on Arrhythmogenic Cardiac Diseases
Review Non-Coding RNAs in the Cardiac Action Potential and Their Impact on Arrhythmogenic Cardiac Diseases Estefania Lozano-Velasco 1,2 , Amelia Aranega 1,2 and Diego Franco 1,2,* 1 Cardiovascular Development Group, Department of Experimental Biology, University of Jaén, 23071 Jaén, Spain; [email protected] (E.L.-V.); [email protected] (A.A.) 2 Fundación Medina, 18016 Granada, Spain * Correspondence: [email protected] Abstract: Cardiac arrhythmias are prevalent among humans across all age ranges, affecting millions of people worldwide. While cardiac arrhythmias vary widely in their clinical presentation, they possess shared complex electrophysiologic properties at cellular level that have not been fully studied. Over the last decade, our current understanding of the functional roles of non-coding RNAs have progressively increased. microRNAs represent the most studied type of small ncRNAs and it has been demonstrated that miRNAs play essential roles in multiple biological contexts, including normal development and diseases. In this review, we provide a comprehensive analysis of the functional contribution of non-coding RNAs, primarily microRNAs, to the normal configuration of the cardiac action potential, as well as their association to distinct types of arrhythmogenic cardiac diseases. Keywords: cardiac arrhythmia; microRNAs; lncRNAs; cardiac action potential Citation: Lozano-Velasco, E.; Aranega, A.; Franco, D. Non-Coding RNAs in the Cardiac Action Potential 1. The Electrical Components of the Adult Heart and Their Impact on Arrhythmogenic The adult heart is a four-chambered organ that propels oxygenated blood to the entire Cardiac Diseases. Hearts 2021, 2, body. It is composed of atrial and ventricular chambers, each of them with distinct left and 307–330. -
Hypertrophic Cardiomyopathy Guide
Hypertrophic Cardiomyopathy Guide HYPERTROPHIC CARDIOMYOPATHY GUIDE What is hypertrophic cardiomyopathy? Hypertrophic cardiomyopathy (HCM) is a complex type of heart disease that affects the heart muscle. It causes thickening of the heart muscle (especially the ventricles, or lower heart chambers), left ventricular stiffness, mitral valve changes and cellular changes. Thickening of the heart muscle (myocardium) occurs most commonly at the septum. The septum is the muscular wall that separates the left and right side of aortic valve narrowed the heart. Problems occur outflow tract when the septum between outflow tract the heart’s lower chambers, leaky mitral mitral valve or ventricles, is thickened. valve septum The thickened septum may thickened cause a narrowing that can septum block or reduce the blood flow from the left ventricle Normal Heart Hypertrophic to the aorta - a condition Cardiomyopathy called “outflow tract obstruction.” The ventricles must pump harder to overcome the narrowing or blockage. This type of hypertrophic cardiomyopathy may be called hypertrophic obstructive cardiomyopathy (HOCM). HCM also may cause thickening in other parts of the heart muscle, such as the bottom of the heart called the apex, right ventricle, or throughout the entire left ventricle. Stiffness in the left ventricle occurs as a result of cellular changes that occur in the heart muscle when it thickens. The left ventricle is unable to relax normally and fill with blood. Since there is less blood at the end of filling, there is less oxygen-rich blood pumped to the organs and muscles. The stiffness in the left ventricle causes pressure to increase inside the heart and may lead to the symptoms described below. -
Atrial Fibrillation in Hypertrophic Cardiomyopathy: Prevalence, Clinical Impact, and Management
Heart Failure Reviews (2019) 24:189–197 https://doi.org/10.1007/s10741-018-9752-6 Atrial fibrillation in hypertrophic cardiomyopathy: prevalence, clinical impact, and management Lohit Garg 1 & Manasvi Gupta2 & Syed Rafay Ali Sabzwari1 & Sahil Agrawal3 & Manyoo Agarwal4 & Talha Nazir1 & Jeffrey Gordon1 & Babak Bozorgnia1 & Matthew W. Martinez1 Published online: 19 November 2018 # Springer Science+Business Media, LLC, part of Springer Nature 2018 Abstract Hypertrophic cardiomyopathy (HCM) is the most common hereditary cardiomyopathy characterized by left ventricular hyper- trophy and spectrum of clinical manifestation. Atrial fibrillation (AF) is a common sustained arrhythmia in HCM patients and is primarily related to left atrial dilatation and remodeling. There are several clinical, electrocardiographic (ECG), and echocardio- graphic (ECHO) features that have been associated with development of AF in HCM patients; strongest predictors are left atrial size, age, and heart failure class. AF can lead to progressive functional decline, worsening heart failure and increased risk for systemic thromboembolism. The management of AF in HCM patient focuses on symptom alleviation (managed with rate and/or rhythm control methods) and prevention of complications such as thromboembolism (prevented with anticoagulation). Finally, recent evidence suggests that early rhythm control strategy may result in more favorable short- and long-term outcomes. Keywords Atrial fibrillation . Hypertrophic cardiomyopathy . Treatment . Antiarrhythmic agents Introduction amyloidosis) [3–5]. The clinical presentation of HCM is het- erogeneous and includes an asymptomatic state, heart failure Hypertrophic cardiomyopathy (HCM) is the most common syndrome due to diastolic dysfunction or left ventricular out- inherited cardiomyopathy due to mutation in one of the sev- flow (LVOT) obstruction, arrhythmias (atrial fibrillation and eral sarcomere genes and transmitted in autosomal dominant embolism), and sudden cardiac death [1, 6]. -
Comparison of Gated Myocardial Perfusion SPECT, Echocardiography and Equilibrium Radionuclide Ventriculography in the Evaluation of Left Ventricle Contractility
Türk Kardiyol Dern Arş - Arch Turk Soc Cardiol 2014;42(4):349-357 doi: 10.5543/tkda.2014.74150 349 Comparison of gated myocardial perfusion SPECT, echocardiography and equilibrium radionuclide ventriculography in the evaluation of left ventricle contractility Sol ventrikül kontraktil fonksiyonlarının değerlendirilmesinde equilibrium radyonüklid ventrikülografi, ekokardiyografi ve miyokart perfüzyon gated SPECT görüntülemenin karşılaştırılması Filiz Hatipoğlu, M.D., Zeynep Burak, M.D.,# Özgür Ömür, M.D.# Department of Nuclear Medicine, Afyon Kocatepe University Faculty of Medicine, Afyonkarahisar; #Department of Nuclear Medicine, Ege University Faculty of Medicine, Izmir ABSTRACT ÖZET Objectives: In this study, we investigated the reliability of Amaç: Çalışmamızda, sol ventrikül (SV) fonksiyonlarının gated myocardial perfusion single-photon emission comput- değerlendirilmesinde ‘miyokart perfüzyon gated SPECT’ erized tomography (GSPECT) for the evaluation of left ven- (GSPECT) yönteminin güvenilirliği araştırıldı, GSPECT ile tricle (LV) function. We compared left ventricle ejection frac- hesaplanan sol ventrikül ejeksiyon fraksiyonu (SVEF) orta- tion (LVEF) calculated with GSPECT with the values derived laması planar ‘equilibrium gated radyonüklid ventrikülografi’ from planar equilibrium-gated radionuclide ventriculography (ERVG) ve ekokardiyografi (EKO) ile elde edilen değerlerle (ERVG) and echocardiography (ECHO). karşılaştırıldı. Study design: Forty-eight patients with suspected coronary Çalışma planı: Koroner arter hastalığı (KAH) şüphesi -
Clinical Characteristics and Prognosis Of
Lyu et al. BMC Cardiovascular Disorders (2019) 19:209 https://doi.org/10.1186/s12872-019-1177-1 RESEARCH ARTICLE Open Access Clinical characteristics and prognosis of heart failure with mid-range ejection fraction: insights from a multi-centre registry study in China Lyu Siqi, Yu Litian* , Tan Huiqiong, Liu Shaoshuai, Liu Xiaoning, Guo Xiao and Zhu Jun Abstract Background: Heart failure (HF) with mid-range ejection fraction (EF) (HFmrEF) has attracted increasing attention in recent years. However, the understanding of HFmrEF remains limited, especially among Asian patients. Therefore, analysis of a Chinese HF registry was undertaken to explore the clinical characteristics and prognosis of HFmrEF. Methods: A total of 755 HF patients from a multi-centre registry were classified into three groups based on EF measured by echocardiogram at recruitment: HF with reduced EF (HFrEF) (n = 211), HFmrEF (n = 201), and HF with preserved EF (HFpEF) (n = 343). Clinical data were carefully collected and analyzed at baseline. The primary endpoint was all-cause mortality and cardiovascular mortality while the secondary endpoints included hospitalization due to HF and major adverse cardiac events (MACE) during 1-year follow-up. Cox regression and Logistic regression were performed to identify the association between the three EF strata and 1-year outcomes. Results: The prevalence of HFmrEF was 26.6% in the observed HF patients. Most of the clinical characteristics of HFmrEF were intermediate between HFrEF and HFpEF. But a significantly higher ratio of prior myocardial infarction (p = 0.002), ischemic heart disease etiology (p = 0.004), antiplatelet drug use (p = 0.009), angioplasty or stent implantation (p = 0.003) were observed in patients with HFmrEF patients than those with HFpEF and HFrEF. -
Coronary Microvascular Dysfunction
Journal of Clinical Medicine Review Coronary Microvascular Dysfunction Federico Vancheri 1,*, Giovanni Longo 2, Sergio Vancheri 3 and Michael Henein 4,5,6 1 Department of Internal Medicine, S.Elia Hospital, 93100 Caltanissetta, Italy 2 Cardiovascular and Interventional Department, S.Elia Hospital, 93100 Caltanissetta, Italy; [email protected] 3 Radiology Department, I.R.C.C.S. Policlinico San Matteo, 27100 Pavia, Italy; [email protected] 4 Institute of Public Health and Clinical Medicine, Umea University, SE-90187 Umea, Sweden; [email protected] 5 Department of Fluid Mechanics, Brunel University, Middlesex, London UB8 3PH, UK 6 Molecular and Nuclear Research Institute, St George’s University, London SW17 0RE, UK * Correspondence: [email protected] Received: 10 August 2020; Accepted: 2 September 2020; Published: 6 September 2020 Abstract: Many patients with chest pain undergoing coronary angiography do not show significant obstructive coronary lesions. A substantial proportion of these patients have abnormalities in the function and structure of coronary microcirculation due to endothelial and smooth muscle cell dysfunction. The coronary microcirculation has a fundamental role in the regulation of coronary blood flow in response to cardiac oxygen requirements. Impairment of this mechanism, defined as coronary microvascular dysfunction (CMD), carries an increased risk of adverse cardiovascular clinical outcomes. Coronary endothelial dysfunction accounts for approximately two-thirds of clinical conditions presenting with symptoms and signs of myocardial ischemia without obstructive coronary disease, termed “ischemia with non-obstructive coronary artery disease” (INOCA) and for a small proportion of “myocardial infarction with non-obstructive coronary artery disease” (MINOCA). More frequently, the clinical presentation of INOCA is microvascular angina due to CMD, while some patients present vasospastic angina due to epicardial spasm, and mixed epicardial and microvascular forms. -
The Evolution of Heart Failure with Reduced Ejection Fraction Pharmacotherapy: What Do We Have and Where Are We Going?
Pharmacology & Therapeutics 178 (2017) 67–82 Contents lists available at ScienceDirect Pharmacology & Therapeutics journal homepage: www.elsevier.com/locate/pharmthera Associate editor: M. Curtis The evolution of heart failure with reduced ejection fraction pharmacotherapy: What do we have and where are we going? Ahmed Selim, Ronald Zolty, Yiannis S. Chatzizisis ⁎ Division of Cardiovascular Medicine, University of Nebraska Medical Center, Omaha, NE, USA article info abstract Available online 21 March 2017 Cardiovascular diseases represent a leading cause of mortality and increased healthcare expenditure worldwide. Heart failure, which simply describes an inability of the heart to meet the body's needs, is the end point for many Keywords: other cardiovascular conditions. The last three decades have witnessed significant efforts aiming at the discovery Heart failure of treatments to improve the survival and quality of life of patients with heart failure; many were successful, Reduced ejection fraction while others failed. Given that most of the successes in treating heart failure were achieved in patients with re- Pharmacotherapy duced left ventricular ejection fraction (HFrEF), we constructed this review to look at the recent evolution of Novel drugs HFrEF pharmacotherapy. We also explore some of the ongoing clinical trials for new drugs, and investigate poten- tial treatment targets and pathways that might play a role in treating HFrEF in the future. © 2017 Elsevier Inc. All rights reserved. Contents 1. Introduction.............................................. -
Hypertrophic Cardiomyopathy
HYPERTROPHIC CARDIOMYOPATHY Most often diagnosed during infancy or adolescence, hypertrophic cardiomyopathy (HCM) is the second most common form of heart muscle disease, is usually genetically transmitted, and comprises about 35–40% of cardiomyopathies in children. A diagram and echocardiogram comparing a normal heart and a heart with HCM are shown in figures 2a and 2b. Figure 2a- A normal Figure 2b- Multiple heart is shown on echocardiographic the left compared views of a normal to a heart with a heart on the left hypertrophic and a heart with cardiomyopathy on hypertrophic the right. Note the cardiomyopathy increased thickness on the right. Note of the walls of the the increased left ventricle. thickness of the walls of the left ventricle (LV). HCM affects up to 500,000 people in the United States. with children under age 12 accounting for less than 10% of all cases. According to the Pediatric Cardiomyopathy Registry, HCM occurs at a rate of five per 1 million children. “Hypertrophic” refers to an abnormal growth of muscle fibers in the heart. In HCM, the thick heart muscle is stiff, making it difficult for the heart to relax and for blood to fill the heart chambers. While the heart squeezes normally, the limited filling prevents the heart from pumping enough blood, especially during exercise. Although HCM can involve both lower chambers, it usually affects the main pumping chamber (left ventricle) with thickening of the septum (wall separating the pumping chambers), posterior wall or both. With hypertrophic obstructive cardiomyopathy (HOCM), the muscle thickening restricts the flow of blood out of the heart. -
Angina: Contemporary Diagnosis and Management Thomas Joseph Ford ,1,2,3 Colin Berry 1
Education in Heart CHRONIC ISCHAEMIC HEART DISEASE Heart: first published as 10.1136/heartjnl-2018-314661 on 12 February 2020. Downloaded from Angina: contemporary diagnosis and management Thomas Joseph Ford ,1,2,3 Colin Berry 1 1BHF Cardiovascular Research INTRODUCTION Learning objectives Centre, University of Glasgow Ischaemic heart disease (IHD) remains the leading College of Medical Veterinary global cause of death and lost life years in adults, and Life Sciences, Glasgow, UK ► Around one half of angina patients have no 2 notably in younger (<55 years) women.1 Angina Department of Cardiology, obstructive coronary disease; many of these Gosford Hospital, Gosford, New pectoris (derived from the Latin verb ‘angere’ to patients have microvascular and/or vasospastic South Wales, Australia strangle) is chest discomfort of cardiac origin. It is a 3 angina. Faculty of Health and Medicine, common clinical manifestation of IHD with an esti- The University of Newcastle, ► Tests of coronary artery function empower mated prevalence of 3%–4% in UK adults. There Newcastle, NSW, Australia clinicians to make a correct diagnosis (rule- in/ are over 250 000 invasive coronary angiograms rule- out), complementing coronary angiography. Correspondence to performed each year with over 20 000 new cases of ► Physician and patient education, lifestyle, Dr Thomas Joseph Ford, BHF angina. The healthcare resource utilisation is appre- medications and revascularisation are key Cardiovascular Research Centre, ciable with over 110 000 inpatient episodes each aspects of management. University of Glasgow College year leading to substantial associated morbidity.2 In of Medical Veterinary and Life Sciences, Glasgow G128QQ, UK; 1809, Allen Burns (Lecturer in Anatomy, Univer- tom. -
Calcium-Activated Ion Currents in Heart Failure and Ischemia: Point Counter Point
Open Access Full Text Article Journal of Cardiovascular Disorders A Austin Publishing Group Review Article Calcium-activated Ion Currents in Heart Failure and Ischemia: Point Counter Point William T Clusin* Division of Cardiology, Stanford University School of Abstract Medicine, USA A fundamental principle of cellular electrophysiology is that certain ionic *Corresponding author: William T Clusin, Division currents are activated (i.e. controlled) by the rise in and fall of cytosolic free of Cardiology, Stanford University School of Medicine, calcium at the inner surface of the cell membrane during action potentials and Stanford, CA, 94305, USA, Email: [email protected] the intervals between them. Knowledge about calcium-activated currents has developed in parallel with, and has been incorporated into emerging ideas Received: August 14, 2014; Accepted: September 17, about the mechanisms of cardiac arrhythmias and sudden death in patients with 2014; Published: September 19, 2014 heart disease. Among the earliest discoveries in this field was the recognition that calcium- activated inward current through the sodium calcium exchanger can lead to early or late after-depolarization’s (EAD’s and DAD’s) that trigger premature beats. More recently it has been found that calcium activated outward currents are more important in the heart than initially recognized because a group of calcium activated potassium channels known as SK channels is up-regulated in the ventricles during heart failure. Finally the idea that action potential shortening, which accompanies acute myocardial infarction, is a consequence of impaired calcium sequestration during ischemia, leading to increased outward potassium current, is supported by very recent research. The manner in which these different calcium activated ion currents in the heart regulate membrane potential and can cause – or in some cases prevent – arrhythmias is reconsidered in light of new evidence.