Article Contents ::
- 1 Details Descriptions About :: Cardiomyopathy
- 2 Cardiomyopathy is classified as dilated, hypertrophic, or restrictive. Dilated cardiomyopathy results from damage to cardiac muscle fibers; loss of muscle tone grossly dilates all four chambers of the heart, giving the heart a globular shape. Hypertrophic cardiomyopathy is characterized by disproportionate, asymmetrical thickening of the interventricular septum and left ventricular hypertrophy. Restrictive cardiomyopathy is characterized by restricted ventricular filling due to decreased ventricular compliance and endocardial fibrosis and thickening. If severe, it’s irreversible.
- 3 Causes for Cardiomyopathy
- 4 Pathophysiology Cardiomyopathy
- 5 Signs and symptoms Cardiomyopathy
- 6 Diagnostic Lab Test results
- 7 Treatment for Cardiomyopathy
- 8 Disclaimer ::
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Details Descriptions About :: Cardiomyopathy
Cardiomyopathy is classified as dilated, hypertrophic, or restrictive. Dilated cardiomyopathy results from damage to cardiac muscle fibers; loss of muscle tone grossly dilates all four chambers of the heart, giving the heart a globular shape. Hypertrophic cardiomyopathy is characterized by disproportionate, asymmetrical thickening of the interventricular septum and left ventricular hypertrophy. Restrictive cardiomyopathy is characterized by restricted ventricular filling due to decreased ventricular compliance and endocardial fibrosis and thickening. If severe, it’s irreversible.
Causes for Cardiomyopathy
Causes Most patients with cardiomyopathy have idiopathic disease, but some are secondary to these possible causes: Dilated cardiomyopathy Viral or bacterial infection Hypertension Peripartum syndrome (related to toxemia) Ischemic heart disease or valvular disease Drug hypersensitivity or chemotherapy Cardiotoxic effects of drugs or alcohol Hypertrophic cardiomyopathy Autosomal dominant inheritance Hypertension Obstructive valvular disease Thyroid disease Restrictive cardiomyopathy Amyloidosis or sarcoidosis Hemochromatosis Infiltrative neoplastic disease
Pathophysiology In dilated cardiomyopathy, extensive damage to cardiac muscle fibers reduces contractility in the left ventricle. As systolic function declines, stroke volume, ejection fraction, and cardiac output fall. In hypertrophic cardiomyopathy, hypertrophy of the left ventricle and interventricular septum obstruct left ventricular outflow. The heart compensates for the decreased cardiac output (caused by obstructed outflow) by increasing the rate and force of contractions. The hypertrophied ventricle becomes stiff and unable to relax and fill during diastole. As left ventricular volume diminishes and filling pressure rises, pulmonary venous pressure also rises, leading to venous congestion and dyspnea. In restrictive cardiomyopathy, left ventricular hypertrophy and endocardial fibrosis limit myocardial contraction and emptying during systole as well as ventricular relaxation and filling during diastole. As a result, cardiac output falls.
Signs and symptoms Cardiomyopathy
Signs and symptoms Dilated cardiomyopathy Shortness of breath, orthopnea, dyspnea on exertion, paroxysmal nocturnal dyspnea, fatigue, and dry cough at night Peripheral edema, hepatomegaly, jugular vein distention, and weight gain Peripheral cyanosis Tachycardia Pansystolic murmur or S3 and S4 gallop rhythms Irregular pulse, if atrial fibrillation is present Hypertrophic cardiomyopathy Angina, syncope, dyspnea, or fatigue Systolic ejection murmur along the left sternal border and at the apex Pulsus biferiens or abrupt arterial pulse Irregular pulse, if atrial fibrillation is present Restrictive cardiomyopathy Fatigue, dyspnea, orthopnea, chest pain, peripheral edema, liver engorgement, ascites, and jugular vein distention Peripheral cyanosis, pallor S3 or S4 gallop rhythms or systolic murmurs
Diagnostic Lab Test results
Diagnostic test results Chest X-rays show cardiomegaly and increased in heart size. Echocardiography reveals left ventricular dilation and dysfunction or left ventricular hypertrophy and a thick, asymmetrical intraventricular septum. Cardiac catheterization shows left ventricular dilation and dysfunction, elevated left ventricular and, commonly, right ventricular filling pressures, and diminished cardiac output. Thallium scan usually reveals myocardial perfusion defects. Cardiac catheterization reveals elevated left ventricular end-diastolic pressure and, possibly, mitral insufficiency. Electrocardiography usually shows left ventricular hypertrophy, ST-segment and T-wave abnormalities, Q waves in leads II, III, aVF, and in V4 to V6, left anterior hemiblock, left axis deviation, and ventricular and atrial arrhythmias.
Treatment for Cardiomyopathy
Treatment Dilated cardiomyopathy Treatment of underlying cause Angiotensin-converting enzyme inhibitors, diuretics, digoxin, hydralazine, isosorbide dinitrate, beta-adrenergic blockers, antiarrhythmics, and anticoagulants Cardioversion or pacemaker insertion Revascularization Implantable cardioverter-defibrillator (ICD) Valve repair or replacement Heart transplantation Lifestyle modifications, such as quitting smoking; avoiding alcohol; eating a low-fat, low-salt diet; and restricting fluids Hypertrophic cardiomyopathy Beta-adrenergic blockers, antiarrhythmics, anticoagulants Cardioversion Ablation and implantation of a dual-chamber pacemaker ICD Ventricular myotomy or myectomy Mitral valve repair or replacement Heart transplantation Restrictive cardiomyopathy Treatment of underlying cause Beta-adrenergic blockers, digoxin, diuretics, and oral vasodilators Restricted-sodium diet (may ease symptoms of heart failure)