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Dilated cardiomyopathyDefinitionDilated cardiomyopathy is a condition in which the heart becomes weakened and enlarged, and it cannot pump blood efficiently. The decreased heart function can affect the lungs, liver, and other body systems. There are several different types of cardiomyopathy. Dilated cardiomyopathy is the most common form. See also: Alternative NamesCardiomyopathy - dilated CausesThere are many causes of dilated cardiomyopathy. Some of these are:
This condition can affect anyone at any age. However, it is most common in adult men. The most common causes of dilated cardiomyopathy in children are:
SymptomsSymptoms of heart failure are most common. Usually, they develop slowly over time. However, sometimes symptoms start very suddenly and are severe. Common symptoms are:
Other symptoms may include:
Exams and TestsCardiomyopathy is usually discovered when the doctor is examining and testing you for the cause of heart failure.
A number of laboratory tests may be done to determine the cause:
Children will have:
Heart enlargement, congestion of the lungs, decreased movement/functioning of the heart, or heart failure may show on these tests:
Other tests may include: Lab tests vary depending on the suspected cause. TreatmentThis version of the Encyclopedia has no treatment information. Please discuss any and all treatment options for your condition with your healthcare professional. Outlook (Prognosis)The outcome varies. Some people remain in a stable condition for long periods of time, some continue to gradually get sicker, and others quickly get worse. Cardiomyopathy can only be corrected if the disease that caused it can be cured. About one-third of children recover completely, one-third recover but continue to have some heart problems, and one-third die. Possible Complications
When to Contact a Medical ProfessionalCall your health care provider if you have symptoms of cardiomyopathy. If chest pain, palpitations, or faintness develop seek emergency medical treatment immediately. Prevention
ReferencesHare JM. The dilated, restrictive, and infiltrative cardiomyopathies. Zipes DP, Libby P, Bonow RO, Braunwald E, eds. Braunwald's Heart Disease: A Textbook of Cardiovascular Medicine. 8th ed. Philadelphia, Pa: Saunders Elsevier; 2007: chap 64. Hunt SA, Abraham WT, Chin MH, Fedlman AM, Francis GS, Ganiats TG, et al. ACC/AHA 2005 Guideline Update for the Diagnosis and Management of Chronic Heart Failure in the Adult: a report of the American College of Cardiology/American Heart Association Task Force on Practice Guidelines (Writing Committee to Update the 2001 Guidelines for the Evaluation and Management of Heart Failure): developed in collaboration with the American College of Chest Physicians and the International Society for Heart and Lung Transplantation: endorsed by the Heart Rhythm Society. Circulation. 2005;112:1825-1852. Dickstein K, Cohen-Solal A, Filippatos, G, McMurray JJV, Ponikowski P, Poole-Wilson PA, et al. ESC Guidelines for the diagnosis and treatment of acute and chronic heart failure 2008: the Task Force for the Diagnosis and Treatment of Acute and Chronic Heart Failure 2008 of the European Society of Cardiology, Developed in collaboration with the Heart Failure Association of the ESC (HFA) and endorsed by the European Society of Intensive Care Medicine (ESICM). Eur Heart J. 2008;29:2388-2442.
Review Date:
4/23/2009 Reviewed By: Alan Berger, MD, Assistant Professor, Divisions of Cardiology and Epidemiology, University of Minnesota, Minneapolis, MN. Review provided by VeriMed Healthcare Network. Also reviewed by David Zieve, MD, MHA, Medical Director, A.D.A.M., Inc. The information provided herein should not be used during any medical emergency or for the diagnosis or treatment of any medical condition. A licensed medical professional should be consulted for diagnosis and treatment of any and all medical conditions. Call 911 for all medical emergencies. Links to other sites are provided for information only -- they do not constitute endorsements of those other sites. © 1997-
A.D.A.M., Inc. Any duplication or distribution of the information contained herein is strictly prohibited.
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