4 edition of Idiopathic Dilated Cardiomyopathy found in the catalog.
Idiopathic Dilated Cardiomyopathy
H. R. Figulla
April 1993 by Springer-Verlag Telos .
Written in English
|Contributions||B. McManus (Editor)|
|The Physical Object|
|Number of Pages||405|
An introduction to dilated cardiomyopathy (DCM). DCM is a condition where the heart chambers become enlarged, which affects its ability to pump. The left ventricle of the heart becomes enlarged (dilated) and the muscle wall becomes thinner. This gives the heart a . Idiopathic Dilated Cardiomyopathy synonyms, Idiopathic Dilated Cardiomyopathy pronunciation, Idiopathic Dilated Cardiomyopathy translation, English dictionary definition of Idiopathic Dilated Cardiomyopathy. n. pl. cardiomyopathies A disease or disorder of the heart muscle, especially of unknown or obscure cause. n pathol a disease. Hypertrophic cardiomyopathy (HCM) is a familial disease that in fifty percent of the cases is inherited in an autosomal dominant pattern. The disorder shows complete penetrance in most families although it depends on the age and the sex of the patients (Nimura, , Richard, , Richard, ).As the prevalence of HCM is 1: , it can be stated that HCM is undoubtedly the most common Author: Luis Vernengo, Alain Lilienbaum, Onnik Agbulut, Maria-MirtaRodríguez.
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Dilated cardiomyopathy is a disease of the heart muscle, usually starting in your heart's main pumping chamber (left ventricle). The ventricle stretches and thins (dilates) and can't pump blood as well as a healthy heart can. The term "cardiomyopathy" is a general term.
Dilated cardiomyopathy (DCM) is a condition in which the heart becomes enlarged and cannot pump blood effectively. Symptoms vary from none to feeling tired, leg swelling, and shortness of breath. It may also result in chest pain or fainting.
Complications can include heart failure, heart valve disease, or an irregular heartbeat. Causes include genetics, alcohol, cocaine, certain toxins Causes: Genetics, alcohol, cocaine, certain toxins.
Triggers of idiopathic dilated cardiomyopathy. DCM may be the consequence of a wide variety of causes, including virus-mediated disease, immune dysregulation, toxic and metabolic, inherited, and tachycardia-induced conditions (Fig.
1) [2, 3]. We will briefly discuss all the possible triggers of DCM with a special focus on inflammatory- and Cited by: Etiology. The causes of cardiomyopathies are varied (Table 2).
1 Dilated cardiomyopathy in adults is most commonly caused by CAD (ischemic cardiomyopathy) and hypertension, although viral myocarditis, valvular disease, and genetic predisposition may also play a role. 1, 13, 14 In children, idiopathic myocarditis and neuromuscular diseases are the most common etiologies of dilated Cited by: Ventricular Remodeling in Idiopathic Dilated Cardiomyopathies.
Pages Myocardial Oxygen Consumption in Patients with Idiopathic Dilated Cardiomyopathy: Effects of Vasodilating and Inotropic Agents. Pages Idiopathic Dilated Cardiomyopathy Book Subtitle Cellular and Molecular Mechanisms, Clinical Consequences.
Dilated cardiomyopathy (DCM) is traditionally referred to as idiopathic dilated cardiomyopathy (IDC), which includes genetic forms of DCM.
The patients present with a wide range of symptoms like dyspnea, orthopnea, paroxysmal nocturnal dyspnea, arrhythmias or complications associated with DCM.
The Diagnosis and Evaluation of Dilated Cardiomyopathy Alan G. Japp, PHD, aAnkur Gulati, MD, aStuart A. Cook, MD,b c Martin R. Cowie, MD,bSanjay K.
Prasad, MD ABSTRACT Dilated cardiomyopathy (DCM) is best understood as the ﬁnal common response of myocardium to diverse genetic and environmental by: Myocardial Oxygen Consumption in Patients with Idiopathic Dilated Cardiomyopathy: Effects of Vasodilating and Inotropic Agents Ch.
Holubarsch, G. Hasenfuss, H. Just. Cardiomyopathies are heterogeneous diseases of the myocardium associated with abnormal findings of chamber size, wall thickness, and/or functional contractility. In particular, dilated cardiomyopathy (DCM) is mainly characterized by ventricular chamber enlargement with systolic dysfunction and normal left ventricular (LV) wall thickness.
Although DCM is thought to be induced mainly by genetic Author: Santiago Roura, Carolina Gálvez-Montón, Josep Lupón, AntoniBayes-Genis. Dilated cardiomyopathy is defined by the presence of left ventricular dilatation and contractile dysfunction.
Genetic mutations involving genes Idiopathic Dilated Cardiomyopathy book encode cytoskeletal, sarcomere, and nuclear envelope proteins, among others, account for up to 35% of cases. Acquired causes include myocarditis and exposure to alcohol, drugs and toxins, and metabolic and endocrine disturbances.
Abstract. Idiopathic dilated cardiomyopathy is a chronic heart muscle disease characterised by ventricular dilatation and impaired systolic function. 1 The prevalence and incidence of dilated cardiomyopathy is increasing and now represents the commonest indication for cardiac transplantation worldwide.
In recent years the increasing clinical and economic importance of dilated cardiomyopathy. Idiopathic dilated cardiomyopathy is a chronic heart muscle disease characterised by ventricular dilatation and impaired systolic function.1 The prevalence and incidence of dilated cardiomyopathy.
Idiopathic cardiomyopathy: 1. cardiomyopathy of unknown or obscure cause; Synonym(s): idiopathic cardiomyopathy 2.
a disease that affects mainly the heart muscle, sparing other cardiac structures and usually resulting in fibrosis, hypertrophy, or both. But as the name suggests, the specific causes for idiopathic cardiomyopathy can be difficult to identify. Dilated cardiomyopathy is generally considered the primary cause of idiopathic cardiomyopathy and that can occur due to many reasons as well, none of which are definite causes.
Dilated cardiomyopathy can occur due to a damaged myocardium. Müller J, Wallukat G, Dandel M, et al. Immunoglobulin adsorption in patients with idiopathic dilated cardiomyopathy. Circulation ; Wallukat G, Müller J, Hetzer R. Specific removal of beta1-adrenergic autoantibodies from patients with idiopathic dilated.
Dilated cardiomyopathy (DCM) is best understood as the final common response of myocardium to diverse genetic and environmental insults. A rigorous work-up can exclude alternative causes of left ventricular (LV) dilation and dysfunction, identify etiologies that may respond to specific treatments, and guide family screening.
A significant proportion of DCM cases have an underlying Cited by: idiopathic dilated cardiomyopathy: Cardiology ' primary myocardial disease of unknown cause characterized by left ventricular or biventricular dilatation (sic) and impaired myocardial contractility '.
See Actin, Dilated cardiomyopathy. The term nonischemic cardiomyopathy (NICM) encompasses a spectrum of diseases, including dilated idiopathic cardiomyopathy, cardiac sarcoidosis, and other forms of myocarditis as well as Chagas disease, hypertrophic cardiomyopathy, amyloidosis, valvular heart disease, and arrhythmogenic right ventricular cardiomyopathy/dysplasia (ARVC/D).
Most. Dilated Cardiomyopathy. Dilated Cardiomyopathy (DCM), also known as congestive cardiomyopathy, is the most common form of cardiomyopathy in children. About 50 to 60 percent of all pediatric cardiomyopathy cases are diagnosed as DCM, or approximately six out of every million children each year.
DCM is reportedly more common in boys than girls. Dilated cardiomyopathy (DCM) is traditionally referred to as idiopathic dilated cardiomyopathy (IDC), which includes genetic forms of DCM. The patients present with a wide range of symptoms like dyspnea, orthopnea, paroxysmal nocturnal dyspnea, arrhythmias or complications associated with cturer: Elsevier India.
Cardiomyopathy is disease in which the heart muscle becomes weakened, stretched, or has another structural problem. Dilated cardiomyopathy is a condition in which the heart muscle becomes weakened and enlarged.
As a result, the heart cannot pump enough blood to the rest of the body. There are many types of cardiomyopathy. Dilated cardiomyopathy. Dilated cardiomyopathy (DCM) is a disease of the heart muscle which primarily affects the heart's main pumping chamber, the left ventricle.
It is the most common type of cardiomyopathy and typically affects those aged 20 to The left ventricle of affected individuals becomes enlarged (dilated) and cannot pump blood to the body with as much force as a healthy heart can.
Dilated cardiomyopathy (DCM) Dilated cardiomyopathy (DCM) is defined as dilation of one or both ventricles. Dilation of the left ventricle is virtually always accompanied by impaired left ventricular systolic should be noted that several types of cardiomyopathies (e.g ischemic cardiomyopathy, tachycardia-induced cardiomyopathy, diabetic cardiomyopathy, etc.) may ultimately lead to 5/5(3).
Idiopathic dilated cardiomyopathy (IDC) is a primary myocardial disease of unknown cause characterized by left ventricular or biventricular dilatation and impaired myocardial by: Dilated cardiomyopathy (DCM) is a condition in which the heart becomes enlarged and cannot pump blood effectively.
Symptoms vary from none to feeling tired, leg swelling, and shortness of breath. It may also result in chest pain or fainting. Complications can include heart failure, heart valve disease, or an irregular heartbeat.
Causes include genetics, alcohol, cocaine, certain toxins Complications: Heart failure, heart valve disease. Idiopathic cardiomyopathy (DCM) is a condition of the heart that starts in the ventricle and causes the heart chamber to enlarge and weaken.
DCM presents itself similarly to other cardiac diseases. ISBN: OCLC Number: Notes: "[Papers presented] at an International Symposium on Idiopathic Dilated Cardiomyopathy in Baden-Baden, Federal Republic of Germany, January February 1, "--Preface.
Doctors usually treat dilated cardiomyopathy with a combination of medications. Depending on your symptoms, you might need two or more of these drugs.
Drugs that have proved useful in the treatment of heart failure and dilated cardiomyopathy include: Angiotensin-converting enzyme (ACE) inhibitors. ACE inhibitors are a type of drug that widens. Determining the etiology of dilated cardiomyopathy is a key element in the management and prognosis of a patient with heart failure (HF).
The same etiology may not only damage the myocardium. Objective Dilated cardiomyopathy (DCM) is characterised by left ventricular dilation and dysfunction not caused by coronary disease, valvular disease or hypertension.
Owing to the considerable aetiological and prognostic heterogeneity in DCM, an extensive diagnostic work-up is recommended. We aimed to assess the value of diagnostic testing beyond careful physical examination, blood tests Cited by: 3. Dilated cardiomyopathy has many known and probably many unidentified causes (see table Causes of Dilated Cardiomyopathy).
More than 20 viruses can cause dilated cardiomyopathy; in temperate zones, coxsackievirus B is most common. In Central and South America, Chagas disease due to Trypanosoma cruzi is the most common infectious cause.
Dilated cardiomyopathy (DCM) can be caused by a variety of disorders. In more than 50 percent of cases, however, no cause can be found, and the cardiomyopathy is called "idiopathic." Some causes of DCM are reversible and the condition improves once the cause is. Dilated cardiomyopathy (DCM) is a disease of your heart muscle where it becomes stretched and thin.
This means that it’s unable to pump blood around your body efficiently. Inherited DCM is caused by a change or mutation in one or more genes. If you have DCM, there is a 50 per cent chance that your child will inherit the condition.
To the Editor: Dec and Fuster (Dec. 8 issue)1 categorized the use of beta-blockers in patients with idiopathic dilated cardiomyopathy as investigational.
There is now sufficient evidence to support. Idiopathic Dilated Cardiomyopathy: Cellular and Molecular Mechanisms, Clinical Consequences [Hans-Reiner Figulla, Reinhard Kandolf, Bruce McManus] on *FREE* shipping on qualifying offers.
of progressive disease is unclear. Prevalence and etiology of idiopathic dilated cardiomyopathy (summary of National Heart, Lung, and Blood Institute Workshop). Am J Cardiol. ; – Crossref Medline Google Scholar; 4 Dilated cardiomyopathy and enteroviruses.
Lancet. ; – Crossref Medline Google ScholarCited by: In idiopathic dilated cardiomyopathy, by definition an etiology has not been determined, although genetic, autoimmune, viral, and metabolic causes have been implicated. A common feature of DCM regardless of the underlying cause is a propensity to ventricular arrhythmias and sudden death.
Inflammatory dilated cardiomyopathy (DCMI) is a late and serious consequence of the complex interplay of the infectious agent, most often a virus, and the (auto)-immunologic response, which primarily develops in susceptible individuals (according to a genetic factor) (17).
Although the DCMI phenotype is indistinguishable from the typical DCM. Idiopathic Dilated Cardiomyopathy Cardiomyopathy (HCM). Book Maron, Barry and Salberg, Lisa. Hypertrophic Cardiomyopathy for Patients, Their Families and Interested Physician.
(2nd Ed.). Hibernia NJ: Hypertrophic Cardiomyopathy Association, Web ResourcesFile Size: KB. Idiopathic dilated cardiomyopathy is a subtype of dilated cardiomyopathy. It is a type of non-ischemic cardiomyopathy where no underlying cause can be found. Epidemiology This form of cardiomyopathy may account for up to 50% of all dilated card.
DCM i.e. dilated cardiomyopathy problem comes with survival rate equal to 50percent. However, if patients manage their symptoms properly based on the necessary precautions and regular checkups as well as recommendations from doctors, they can increase to up to 10 years period.Cardiomyopathies () Definition (MEDLINEPLUS) Cardiomyopathy is the name for diseases of the heart muscle.
These diseases enlarge your heart muscle or make it thicker and more rigid than normal. Dilated cardiomyopathy with implantable cardiovascular defibrillator (Live demonstration) - Duration: Woochon Cardio-Neuro-Vascular Research Foundation views