What Is Cor Pulmonale?

Right-Sided Heart Failure Associated With Advanced COPD

chest wall pain
kupicoo/Getty Images

Cor pulmonale is a complication of chronic obstructive pulmonary disease (COPD) and emphysema. It is sometimes called right-sided heart failure.

Cor pulmonale is caused by an increase in blood pressure in the vessel, known as the pulmonary artery, which carries blood from the heart to the lungs. The increased blood pressure leads to the enlargement and subsequent failure of the right side of the heart.

Under normal circumstances, the left side of the heart is responsible for pumping blood to the entire body and requires a higher pressure. The right side, by contrast, assumes the role of pumping blood through the lungs and requires a much lower pressure.

However, when a condition leads to increased pressure in the arteries and right side of the heart, we refer to that as pulmonary hypertension. The term pulmonary relates specifically to the lungs.

Causes and Symptoms of Cor Pulmonale

Any condition that leads to pulmonary hypertension can put a strain on the right ventricle and atrium of the heart. The right ventricle pumps blood to the lungs; the right atrium receives blood return from the heart. When these two chambers fail or are unable to work against the abnormally high pressures within the lungs, this condition called cor pulmonale.

While COPD is a common cause of cor pulmonale, other causes include cystic fibrosis, sleep apnea, scleroderma of the lungs, blot clots in the lungs, or lung tissue damage.

The symptoms are normally related to the underlying lung disease and can include:

  • shortness of breath (dyspnea)
  • wheezing and coughing
  • swelling of the feet and/or ankles
  • chest pains
  • bluish tinge to your skin, nail bed, lips, or gums (cyanosis)
  • pronounced neck veins
  • inability to tolerate exercise

Pulmonary hypertension and cor pulmonale can lead to severe fluid retention which, in turn, can cause life-threatening dyspnea, shock, and even death.

Diagnosing Cor Pulmonale

The initial diagnosis for cor pulmonale is usually made the doctor’s office. A physical exam would typically pick up any abnormal heartbeats, fluid retention, or protruding neck veins indicative of pulmonary hypertension.

Blood tests would also be performed to check for, among other things, an amino acid made in the heart called brain natriuretic peptide (BNP). If BNP levels are high, it indicates that the heart is being stressed and, in severe cases, can be an early indication of heart failure.

To provide a definitive diagnosis, the doctor may also perform the following tests:

  • echocardiogram, which uses sound waves to visualize the heart
  • chest x-ray
  • computerized tomography (CT) scan of the chest
  • arterial blood gases
  • pulmonary artery catheterization (the insertion a catheter into the pulmonary artery to check for heart failure
  • ventilation/perfusion scan (the use of radioactive materials to examine the airflow and blood flow into the lung)

Treatment of  Cor Pulmonale

Treatment for cor pulmonale is focused on treating the underlying illness. With regards to COPD and other lung disorders, the options may include:

  • calcium channel blockers which prevent calcium from entering cells of the heart and blood vessel walls, thereby lowering blood pressure
  • anticoagulants (blood thinners) which are known to decrease mortality in persons with pulmonary hypertension
  • possibly a heart or lung transplant in very advanced cases

Treatment with oxygen, medications, and/or surgery can result in an improvement of symptoms, greater energy, and oftentimes a longer survival time.

Since COPD is a leading cause of cor pulmonale, quitting smoking can help slow the progression of COPD and may prevent cor pulmonale from ever happening.

Source:

U.S. National Library of Medicine: National Institutes of Health. "Cor pulmonale." Bethesda, Maryland; updated January 30, 2016.

Continue Reading