When blood vessels in the lungs become thickened, narrowed, blocked or destroyed, it's harder for blood to flow through the lungs. As a result, blood pressure increases in the lungs, a condition called pulmonary hypertension.
Pulmonary hypertension is a type of high blood pressure that affects the arteries in the lungs and the right side of the heart.
In one form of pulmonary hypertension, called pulmonary arterial hypertension (PAH), blood vessels in the lungs are narrowed, blocked or destroyed. The damage slows blood flow through the lungs, and blood pressure in the lung arteries rises. The heart must work harder to pump blood through the lungs. The extra effort eventually causes the heart muscle to become weak and fail.
In some people, pulmonary hypertension slowly gets worse and can be life-threatening. Although there's no cure for some types of pulmonary hypertension, treatment can help reduce symptoms and improve quality of life.
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The signs and symptoms of pulmonary hypertension develop slowly. You may not notice them for months or even years. Symptoms get worse as the disease progresses.
Pulmonary hypertension signs and symptoms include:
- Blue lips and skin (cyanosis)
- Chest pressure or pain
- Dizziness or fainting spells (syncope)
- Fast pulse or pounding heartbeat (palpitations)
- Shortness of breath (dyspnea), initially while exercising and eventually while at rest
- Swelling (edema) in the ankles, legs and eventually the belly area (abdomen)
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Chambers and valves of the heart
Chambers and valves of the heart
A typical heart has two upper and two lower chambers. The upper chambers, the right and left atria, receive incoming blood. The lower chambers, the more muscular right and left ventricles, pump blood out of the heart. The heart valves, which keep blood flowing in the right direction, are gates at the chamber openings.
The typical heart has two upper chambers (atria) and two lower chambers (ventricles). Each time blood passes through the heart, the lower right chamber (right ventricle) pumps blood to the lungs through a large blood vessel (pulmonary artery).
In the lungs, the blood releases carbon dioxide and picks up oxygen. The blood typically flows easily through blood vessels in the lungs (pulmonary arteries, capillaries and veins) to the left side of the heart.
However, changes in the cells that line the pulmonary arteries can cause the walls of the arteries to become stiff, swollen and thick. These changes may slow down or block blood flow through the lungs, causing pulmonary hypertension.
Pulmonary hypertension is classified into five groups, depending on the cause.
Group 1: Pulmonary arterial hypertension (PAH)
- Unknown cause (idiopathic pulmonary arterial hypertension)
- Changes in a gene passed down through families (heritable pulmonary arterial hypertension)
- Use of certain drugs or illegal substances
- Heart problems present at birth (congenital heart disease)
- Other conditions such as HIV infection, chronic liver disease (cirrhosis) and connective tissue disorders (scleroderma, lupus, others)
Group 2: Pulmonary hypertension caused by left-sided heart disease
- Left-sided heart valve disease such as mitral valve or aortic valve disease
- Failure of the lower left heart chamber (left ventricle)
Group 3: Pulmonary hypertension caused by lung disease
- Chronic obstructive pulmonary disease (COPD)
- Scarring of the tissue between the lung's air sacs (pulmonary fibrosis)
- Obstructive sleep apnea
- Long-term exposure to high altitudes in people who may be at higher risk of pulmonary hypertension
Group 4: Pulmonary hypertension caused by chronic blood clots
- Chronic blood clots in the lungs (pulmonary emboli)
- Other clotting disorders
Group 5: Pulmonary hypertension triggered by other health conditions
- Blood disorders, including polycythemia vera and essential thrombocythemia
- Inflammatory disorders such as sarcoidosis and vasculitis
- Metabolic disorders, including glycogen storage disease
- Kidney disease
- Tumors pressing against pulmonary arteries
Eisenmenger syndrome and pulmonary hypertension
Eisenmenger syndrome is a type of congenital heart disease that causes pulmonary hypertension. It's most commonly caused by a large hole in the heart between the two lower heart chambers (ventricles), called a ventricular septal defect.
This hole in the heart causes blood to flow incorrectly in the heart. Oxygen-carrying blood (red blood) mixes with oxygen-poor blood (blue blood). The blood then returns to the lungs — instead of going to the rest of the body — increasing the pressure in the pulmonary arteries and causing pulmonary hypertension.
Pulmonary hypertension is more often diagnosed in people ages 30 to 60. Growing older can increase the risk of developing Group 1 pulmonary hypertension, called pulmonary arterial hypertension (PAH). However, PAH from an unknown cause (idiopathic PAH) is more common in younger adults.
Other things that can raise the risk of pulmonary hypertension include:
- A family history of the condition
- Being overweight
- Blood-clotting disorders or a family history of blood clots in the lungs
- Exposure to asbestos
- Congenital heart disease
- Living at a high altitude
- Use of certain drugs, including some weight-loss medicines and illegal drugs such as cocaine or methamphetamine
- Use of selective serotonin reuptake inhibitors (SSRIs), used to treat depression and anxiety
Potential complications of pulmonary hypertension include:
Right-sided heart enlargement and heart failure (cor pulmonale). In cor pulmonale, the heart's right lower chamber (ventricle) becomes enlarged. It has to pump harder than usual to move blood through narrowed or blocked pulmonary arteries.
As a result, the heart walls thicken and the right ventricle expands to increase the amount of blood it can hold. But these changes create more strain on the heart, and eventually the right ventricle fails.
- Blood clots. Having pulmonary hypertension increases the risk of blood clots in the small arteries in the lungs.
- Irregular heartbeats (arrhythmias). Certain arrhythmias caused by pulmonary hypertension can be life-threatening.
- Bleeding in the lungs. Pulmonary hypertension can lead to life-threatening bleeding into the lungs and coughing up blood (hemoptysis).
- Pregnancy complications. Pulmonary hypertension can be life-threatening for a developing baby.