| Hypertrophic Cardiomyopathy
		
			| Hypertrophic CardiomyopathySkip to the navigationTopic OverviewWhat is hypertrophic cardiomyopathy?Hypertrophic
			 cardiomyopathy (say "hy-per-TROH-fik kar-dee-oh-my-AWP-uh-thee") happens when
			 the heart muscle grows too thick, so the heart gets bigger and its
			 chambers get smaller. Many people
				have no symptoms and live a normal life with few problems. But in some people with this condition: The
				heart doesn't get enough blood and oxygen, which can cause chest pain.
				A fast, slow, or uneven heartbeat (arrhythmia) develops. In rare cases, this can cause sudden death. The heart doesn't pump
				blood well, or it doesn't relax between beats as it should. In rare cases,
				this can lead to
				heart failure.
 People who exercise
			 often and hard may have changes in their heart muscle that can
			 be confused with hypertrophic cardiomyopathy. This condition is
			 called athlete's heart syndrome. It is harmless. When an athlete stops
			 training, the heart will return to a normal size.  What causes hypertrophic cardiomyopathy?Certain
			 genes cause the heart to grow more than it should.  Hypertrophic
			 cardiomyopathy is the most common
			 genetic disease  of the heart. This means it runs in families. About 1 in 500 adults has this condition.footnote 1 You are at risk for hypertrophic
			 cardiomyopathy if either of your parents or a brother or sister has it or
			 died suddenly at a young age. Talk to your doctor about
			 getting tested.  What are the symptoms?You may not have any symptoms. Or you might: Feel tired and
				short of breath when you are active.  Have chest
				pain. You may have a heavy, tight feeling in your
				chest. Chest pain is often brought on by exercise, when the heart has to work
				harder. Feel dizzy or faint, often
				after you have been active. Feel like your heart is pounding,
				racing, or beating unevenly (palpitations).
 A rapid or irregular heartbeat or
				fainting spells are signs of an arrhythmia, which makes sudden death more
				likely.  How is hypertrophic cardiomyopathy diagnosed?Your doctor will do a physical exam and ask you about any health problems you've had and about
			 any family history of heart disease or early and sudden death. You may need tests such as:  Your doctor may refer
			 you to a doctor who specializes in heart problems (cardiologist). Based on your
			 symptoms, past health, and family history, the specialist can assess your risk
			 for sudden death. People who are at high risk will need regular checkups. If you are at low risk for sudden death, you may not need to see your doctor often. But you will need a checkup anytime your symptoms change or get worse.  How is it treated?Many people who have hypertrophic
			 cardiomyopathy don't have symptoms and don't need treatment. If you do have symptoms, your  treatment will depend on what your symptoms are and
			 whether you develop heart failure or an abnormal heart rhythm. You may take medicines to treat symptoms such
				as shortness of breath and chest pain.If you get a serious heart rhythm problem such as 
				 atrial fibrillation,  you may take medicines to control your heart rate or rhythm and to prevent blood clots.If you are at high risk for sudden death
			 from an arrhythmia, you may need an
			 implantable cardioverter-defibrillator (ICD). An ICD
			 is a small device like a pacemaker. It can prevent or stop dangerous heart rhythms.If medicines don't work and your heart isn't pumping blood well,  you might have a procedure to reduce the size of the overgrown part of your heart. The overgrown part can be removed with a surgery called myectomy. Or it can be destroyed by injecting alcohol  into the
			 artery that supplies that part of the heart. This procedure is called nonsurgical septal reduction, or alcohol septal ablation.
 What can you do at home for hypertrophic cardiomyopathy?Avoid strenuous activity and intense exercise. Your doctor can tell you  what level
			 of exercise and what kinds of activities are safe for you. Be active at a safe level to help keep your heart and body healthy.  If you smoke, quit. Your doctor can tell you about medicines and counseling that can help you quit for good.Drink plenty of fluids
			 (unless your doctor has told you to limit
			 your fluid intake).Get checkups as often as your doctor recommends.
Frequently Asked Questions| Learning about hypertrophic cardiomyopathy: |  |  | Being diagnosed: |  |  | Getting treatment: |  |  | Living with hypertrophic cardiomyopathy: |  | 
Other Places To Get HelpOrganizationsAmerican Heart Association www.heart.orgNational Heart, Lung, and Blood Institute (U.S.) www.nhlbi.nih.govReferencesCitationsOmmen SR, et al. (2011). Hypertrophic cardiomyopathy. In V Fuster et al., eds., Hurst's The Heart, 13th ed., vol. 1, pp. 817-864. New York: McGraw-Hill.
 Other Works ConsultedFifer MA, Vlahakes GJ (2008). Management of symptoms in hypertrophic cardiomyopathy. Circulation, 117(3): 429-439.Gersh BJ, et al. (2011). 2011 ACCF/AHA guideline for the diagnosis and treatment of hypertrophic cardiomyopathy: A report of the American College of Cardiology Foundation/American Heart Association Task Force on Practice Guidelines. Circulation, 124(24): e783-e831.Ho CY (2012). Hypertrophic cardiomyopathy in 2012. Circulation, 125(11): 1432-1438.Maron BJ, et al. (2015). Eligibility and disqualification recommendations for competitive athletes with cardiovascular abnormalities: Task Force 3: Hypertrophic cardiomyopathy, arrhythmogenic right ventricular cardiomyopathy and other cardiomyopathies, and myocarditis. Circulation, 132(22): e273-e280. DOI: 10.1161/CIR.0000000000000239. Accessed April 7, 2017.Maron BJ, Olivotto I (2015). Hypertrophic cardiomyopathy. In DL Mann et al., eds., Braunwald's Heart Disease: A Textbook of Cardiovascular Medicine, 10th ed., vol. 2, pp. 1574-1588. Philadelphia: Saunders.
CreditsByHealthwise StaffPrimary Medical ReviewerAdam Husney, MD - Family Medicine
 E. Gregory Thompson, MD - Internal Medicine
 Martin J. Gabica, MD - Family Medicine
 Elizabeth T. Russo, MD - Internal Medicine
 Specialist Medical ReviewerGeorge Philippides, MD - Cardiology
Current as ofJune 2, 2017Current as of:
                June 2, 2017Ommen SR, et al. (2011). Hypertrophic cardiomyopathy. In V Fuster et al., eds., Hurst's The Heart, 13th ed., vol. 1, pp. 817-864. New York: McGraw-Hill. Last modified on: 8 September 2017  |  |