Cardiomegaly · What Is It, Causes, Treatment, and More

Published: Sep 29, 2025
Author: Ashley Mauldin, MSN, APRN, FNP-BC
Editor: Alyssa Haag, MD
Editor: Ian Mannarino, MD, MBA
Editor: Kelsey LaFayette, DNP, ARNP, FNP-C
Editor: Emily Miao, MD, PharmD
Illustrator: Jillian Dunbar
Copyeditor: Joy Mapes
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What is cardiomegaly?

Cardiomegaly refers to the enlargement of the heart. The heart, which sits slightly behind and left of the sternum, is responsible for pumping blood throughout the body. It is made up of two atria, the chambers at the base, and two ventricles in the apex. The septum, a dividing wall of tissue, separates the heart into left and right halves.  

In cardiomegaly, enlargement of the heart can include the entire heart, one side of the heart (i.e., the right or left), or a specific area (i.e., the atria or ventricles).  

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What causes cardiomegaly?

Cardiomegaly can develop from a variety of conditions that affect how the heart functions. Certain conditions, such as high blood pressure, can make the heart work harder to pump blood throughout the body. On the other hand, conditions like coronary artery disease and cardiomyopathy can lead to damage of the heart muscle. Regardless, all of these conditions can reduce the heart’s ability to pump bloodefficiently and consequently cause the heart muscle to enlarge, resulting in cardiomegaly.    

In the case of high blood pressure, the heart muscle enlarges because the heart muscle must work harder to overcome the higher pressure and maintain cardiac output. Similarly, pulmonary hypertension, which occurs when there is increased pressure in the pulmonary artery that connects the right side of the heart to the lungs, can also force the heart to pump harder in order to push blood forward, through the lungs, and into the left side of the heart. As a result of the increased exertion, the right side of the heart may enlarge.  

Coronary artery disease, which results from the build-up of plaque in the arteries supplying blood flow to the heart, can result in poor blood flow or blockages, leading to poor tissue perfusion and subsequently ischemia. Prolonged ischemia to these areas can lead to heart muscledamage. In order to compensate for the damaged muscle, the rest of the heart muscle will enlarge so it can continue pumping blood throughout the body. 

Cardiomyopathy, a group of heart conditions that directly affect the heart muscle, also lead to cardiomegaly. The most common types of cardiomyopathy are dilated, restrictive, and hypertrophic cardiomyopathy. In addition, pericarditis, or inflammation of the heart’s pericardium (i.e., the fibrous sac surrounding the heart), can make the heart enlarge.  

Moreover, conditions that do not directly affect the heart can also lead to cardiomegaly. Anemia, which is characterized by low red blood cell counts, may require the heart to pump harder in order to circulate enough oxygen throughout the body. An underactive thyroid (i.e., hypothyroidism) or an overactive thyroid (i.e., hyperthyroidism) can change the heart rate and blood pressure in ways that enlarge the heart. Additionally, excessive iron in the body, or hemochromatosis, can cause cardiomegaly as a result of iron deposition and accumulation in the heart.  

Other risk factors for the development of cardiomegaly include heart valve disease, congenital heart conditions, rare diseases (e.g., amyloidosis), and having a family history of cardiomegaly.  

What are the signs and symptoms of cardiomegaly?

People who have an enlarged heart usually show signs or symptoms that may include shortness of breath, abnormal heart rhythms, fatigue, chest pain, dizziness or lightheadedness, and swollen feet. 

How is cardiomegaly diagnosed?

To diagnose cardiomegaly, a healthcare provider will start by reviewing the individual’s medical history and performing a physical exam. A chest X-ray is often conducted in order to visualize the heart. Once cardiomegaly has been confirmed, additional tests will be performed to determine the cause of the enlargement. These tests can include an electrocardiogram, which looks at the electrical activity of the heart; an echocardiogram, to assess the heart’s ejection fraction, or how effectively the heart is able to pump blood forward to the rest of the body; and cardiac magnetic resonance imaging (MRI), which can assess the size and shape of the heart. Blood tests (e.g., complete blood count, complete metabolic panel, brain natriuretic peptide test, troponins, lipid panel, hemoglobin A1c, thyroid stimulating hormone ) may also be recommended to help determine the underlying cause and for further risk stratification.  

How is cardiomegaly treated?

Treatment of cardiomegaly often begins with lifestyle modifications to address modifiable risk factors. These may include losing weight, increasing exercise, decreasing alcohol consumption, and eating a variety of fruits, vegetables, whole grains, nuts, poultry, and fish, while limiting intake of sodium, red meats, and saturated fats.  

Beyond lifestyle modifications, treatment often involves medication to address the underlying cause. In cases of coronary artery disease, medication may be prescribed to reduce cholesterol levels in the body (e.g., statins, niacin) and keep blood flowing through the arteries (e.g., aspirin). Other prescription medications, like angiotensin-converting enzyme (ACE) inhibitors, can help regulate high blood pressure and help cardiac remodeling in congestive heart failure. Hypertrophic cardiomyopathy treatment usually consists of medications (e.g., beta blockers, calcium channel blockers) that aim to decrease heart rate so the heart can fill and pump blood more effectively. 

If left untreated, cardiomegaly can lead to the development of blood clots, life-threatening arrhythmias, and heart failure. Cardiomegaly can be life-threatening, so diagnosis and treatment is critical.  

What are the most important facts to know about cardiomegaly?

Cardiomegaly refers to the enlargement of the heart. Cardiomegaly is caused by any condition that  either make the heart work harder to pump blood throughout the body or damages the heart muscle, so the heart enlarges to compensate for the extra exertion. Coronary artery disease, high blood pressure, cardiomyopathy, pulmonary hypertension, pericarditis, anemia, thyroid disease, hemochromatosis, heart valve disease, congenital heart conditions, pregnancy, and a family history of cardiomegaly can all increase the risk of cardiomegaly. People who have an enlarged heart usually show signs or symptoms that may include shortness of breath, abnormal heart rhythms, fatigue, chest pain, and swollen feet. Treatment of cardiomegaly often involves lifestyle changes to address modifiable risk factors and medication to treat the underlying cause. If the cause of cardiomegaly is left untreated, blood clots, arrhythmias, cardiac arrest, heart failure, and death can occur.  

Key Takeaways

Definition 

Cardiomegaly is an abnormal enlargement of the heart, which may involve the entire heart, one side (right or left), or a specific area (atrium or ventricle).  

Causes 

- High blood pressure 

- Pulmonary hypertension  

- Coronary artery disease  

- Cardiomyopathy   

- Pericarditis  

- Anemia 

- Hypo- or hyperthyroidism  

- Hemochromatosis  

- Other risk factors:  

     - Heart valve disease 

     - Congenital heart conditions  

     - Rare diseases (e.g., amyloidosis) 

     - Family history of cardiomegaly  

Signs and Symptoms 

- Shortness of breath  

- Abnormal heart rhythm  

- Fatigue  

- Chest pain  

- Dizziness  

- Lightheadedness  

- Swollen feet  

Diagnosis 

- Medical history  

- Physical examination  

- Chest X-ray  

- Tests to determine the cause:  

     - Electrocardiogram  

     - Echocardiogram  

     - Cardiac MRI  

     - Blood tests 

Treatment 

- Lifestyle modifications (address modifiable risk factors): 

     - Weight loss 

     - Regular exercise 

     - Reduced alcohol intake 

     - Healthy diet: fruits, vegetables, whole grains, nuts, poultry, fish; limited sodium, red meat, and saturated fats  

- Medications (target underlying cause): 

     - Coronary artery diseasestatins, aspirin 

     - Hypertension / heart failureACE inhibitors, other antihypertensives 

     - Hypertrophic cardiomyopathy → beta blockers, calcium channel blockers (slow heart rate, improve filling/pumping) 

-  If untreated: 

     - Blood clots, life-threatening arrhythmias, heart failure 

References


American Heart Association. (2017, August 15). The American Heart Association diet and lifestyle recommendations. [Online]. Available from: https://www.heart.org/en/healthy-living/healthy-eating/eat-smart/nutrition-basics/aha-diet-and-lifestyle-recommendations. Accessed March 31, 2021. 


American Heart Association. (n.d.). How the healthy heart works. In American Heart Association: Health topics; Congenital heart defects. [Online]. Available from: https://www.heart.org/en/health-topics/congenital-heart-defects/about-congenital-heart-defects/how-the-healthy-heart-works. Accessed March 15, 2021. 


American Heart Association. (2017, May 31). What is heart failure? In American Heart Association: Health topics; Heart failure. [Online].Available from: https://www.heart.org/en/health-topics/heart-failure/what-is-heart-failure. Accessed March 20, 2021. 


2024 AHA/ACC/AMSSM/HRS/PACES/SCMR Guideline for the Management of Hypertrophic Cardiomyopathy: A Report of the American Heart Association/American College of Cardiology Joint Committee on Clinical Practice Guidelines https://www.ahajournals.org/doi/10.1161/CIR.0000000000001250. Accessed April 15, 2025.  


Felker GM, Thompson RE, Hare JM, et al. Underlying causes and long-term survival in patients with initially unexplained cardiomyopathy. N Engl J Med. 2000;342(15):1077-1084. doi:10.1056/NEJM200004133421502 


Sethi T, Singh AP, Singla V, Singh Y. Biatrial enlargement: An unusual cause of massive cardiomegaly. BMJ Case Rep. 2013;2013:bcr2012008320. Published 2013 Jan 31. doi:10.1136/bcr-2012-008320