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 makes it hard for blood to move through the lungs. Blood pressure in the lung arteries goes up. 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. It can be life-threatening. There’s no cure for pulmonary hypertension. But treatments are available to help you feel better, live longer and improve your quality of life.

The symptoms of pulmonary hypertension develop slowly. You may not notice them for months or even years. Symptoms get worse as the disease continues.

Pulmonary hypertension symptoms include:

• Shortness of breath. It may first start during exercise and eventually happen at rest.
• Blue or gray skin. Depending on skin color, these changes may be harder or easier to see.
• Chest pressure or pain.
• Dizziness or fainting.
• Fast pulse or pounding heartbeat.
• Fatigue.
• Swelling in the ankles, legs and belly area.

These symptoms may be caused by many other health conditions. See a healthcare professional for an accurate diagnosis.

Pulmonary hypertension is caused by changes in the cells that line the lung arteries. The changes can make the artery walls narrow, stiff, swollen and thick. It gets harder for blood to flow through the lungs.

Pulmonary hypertension is sorted into five groups, depending on the cause.

Group 1: Pulmonary arterial hypertension (PAH)

Causes include:

• Unknown cause, called idiopathic pulmonary arterial hypertension.
• Changes in a gene passed down through families, called heritable pulmonary arterial hypertension.
• Use of some medicines or illicit drugs, including methamphetamine.
• Heart condition present at birth, called a congenital heart defect.
• Other health conditions, including scleroderma, lupus and cirrhosis.

Group 2: Pulmonary hypertension caused by left-sided heart disease

This is the most common form of pulmonary hypertension. Causes include:

• Left heart failure.
• Left-sided heart valve disease, including mitral valve or aortic valve disease.

Group 3: Pulmonary hypertension caused by lung disease

Causes include:

• Scarring of the lungs, called pulmonary fibrosis.
• Chronic obstructive pulmonary disease, also called COPD.
• A sleep disorder in which breathing repeatedly stops and starts, called sleep apnea.
• Being at high altitudes for extended periods of time, if you are at high risk of pulmonary hypertension.

Group 4: Pulmonary hypertension caused by blockages in the pulmonary artery

Causes include:

• Blood clots in the lungs that don’t go away.
• Tumors that block the pulmonary artery.

Group 5: Pulmonary hypertension triggered by other health conditions

Causes include:

• Blood disorders, including polycythemia vera and essential thrombocythemia.
• Inflammatory disorders such as sarcoidosis.
• Conditions that affect the body’s ability to break down certain sugars, including glycogen storage disease.
• Kidney disease.

Eisenmenger syndrome and pulmonary hypertension

Eisenmenger syndrome can lead to pulmonary hypertension.

Eisenmenger syndrome is a long-term complication of an unrepaired heart condition present at birth. An example is a large hole in the heart between the two lower heart chambers called a ventricular septal defect.

The unrepaired hole in the heart causes oxygen-rich blood to mix with oxygen-poor blood. The blood then goes to the lungs instead of going to the rest of the body. This increases pressure in the pulmonary arteries.

Pulmonary hypertension is usually seen in people ages 30 to 60. Growing older can increase the risk of developing Group 1 pulmonary hypertension, called pulmonary arterial hypertension (PAH). PAH from an unknown cause is more common in younger adults.

Other things that can raise the risk of pulmonary hypertension are:

• A family history of the condition.
• Being overweight.
• Smoking.
• Blood-clotting disorders or a family history of blood clots in the lungs.
• A history of being around asbestos.
• A heart condition present at birth, called a congenital heart defect.
• Living at an altitude of 8,000 feet (2,438 meters) or higher.
• Use of some medicines, including those used for weight loss.
• Illicit drugs such as cocaine or methamphetamine.

Potential complications of pulmonary hypertension are:

• Right-sided heart enlargement and heart failure. Also called cor pulmonale, this condition causes the heart’s right lower chamber to get larger. The chamber has to pump harder than usual to move blood through narrowed or blocked lung arteries.

  As a result, the heart walls get thick. The right lower heart chamber stretches to increase the amount of blood it can hold. These changes create more strain on the heart. Eventually the right lower heart chamber fails.

• Blood clots. Pulmonary hypertension increases the risk of blood clots in the small arteries in the lungs.
• Irregular heartbeats, also called arrhythmias. Pulmonary hypertension can cause changes in the heartbeat, which can be life-threatening.
• Bleeding in the lungs. Pulmonary hypertension can lead to life-threatening bleeding in the lungs and coughing up blood.
• Pregnancy complications. Pulmonary hypertension can be life-threatening for the mother and the developing baby.

Pulmonary hypertension is hard to diagnose early. It’s not often found during a routine physical exam. Even when pulmonary hypertension is more advanced, its symptoms are similar to those of other heart and lung conditions.

To diagnose pulmonary hypertension, a healthcare professional examines you and asks about your symptoms. You are usually asked questions about your medical and family history.

Tests

Tests to diagnose pulmonary hypertension may include:

• Blood tests. Blood tests can help find the cause of pulmonary hypertension. The test also may help find complications of the disease.
• Chest X-ray. A chest X-ray is a picture of the heart, lungs and chest. It may be used to check for other lung conditions that can cause pulmonary hypertension.
• Electrocardiogram (ECG or EKG). This simple test records the electrical activity of the heart. It shows how the heart is beating.

• Echocardiogram. Sound waves create pictures of the beating heart. An echocardiogram shows how blood flows through the heart and heart valves. This test may be done to help diagnose pulmonary hypertension or to learn how treatments are working.

  Sometimes, an echocardiogram is done while exercising on a stationary bike or treadmill to learn how activity affects the heart. If you have this test, you may be asked to wear a mask that checks how well the heart and lungs use oxygen and carbon dioxide.

• Right heart catheterization. If an echocardiogram shows pulmonary hypertension, this test may be done to confirm the diagnosis.

  During this procedure, a doctor places a thin, flexible tube called a catheter into a blood vessel, usually in the neck. The tube is gently guided into the lower right heart chamber and the pulmonary artery. The doctor can then measure blood pressure in the main pulmonary arteries and the right ventricle.

Other tests may be done to check the condition of the lungs and pulmonary arteries. The following tests may give more information about the cause of pulmonary hypertension:

• Exercise stress tests. These tests often involve walking on a treadmill or riding a stationary bike while the heartbeat is watched. They can show how the heart reacts to exercise.

• Computerized tomography (CT) scan. This test uses X-rays to make pictures of specific parts of the body. Dye called contrast may be given into a vein to help the blood vessels show up more clearly on the images.

  A heart CT scan, called a cardiac CT scan, can show the size of the heart and any blockages in the pulmonary arteries. It can help diagnose lung diseases that might lead to pulmonary hypertension. Examples are COPD or pulmonary fibrosis.

• Magnetic resonance imaging (MRI). This test uses magnetic fields and radio waves to make detailed pictures of the heart. It can show blood flow in the pulmonary arteries. The test may be done to learn how well the right lower heart chamber is working.
• Lung function test. For this test, you blow into a special device. The device measures how much air the lungs can hold. It shows how air flows in and out of the lungs.
• Sleep study. A sleep study measures brain activity, heart rate, blood pressure, oxygen levels and other things as you sleep. The test can help diagnose sleep apnea, which can cause pulmonary hypertension.
• Ventilation/perfusion (V/Q) scan. In this test, a radioactive tracer is given through a vein (IV). The tracer shows how blood flows. You also may breathe in a tracer that shows airflow to the lungs. A V/Q scan can tell whether blood clots are causing symptoms of pulmonary hypertension.
• Lung biopsy. Rarely, a sample of tissue may be taken from the lung to check for a possible cause of pulmonary hypertension.

Genetic testing

Screening for gene changes that cause pulmonary hypertension may be recommended. If you have these gene changes, other family members may need to be screened too.

Pulmonary hypertension functional classification

Once a diagnosis of pulmonary hypertension is confirmed, the condition is classified according to how the symptoms affect you and your ability to do everyday tasks.

Pulmonary hypertension may fall into one of the following groups:

• Class I. Pulmonary hypertension is diagnosed, but there are no symptoms during rest or exercise.
• Class II. There are no symptoms at rest. Everyday chores or activities such as going to work or the grocery store may cause some shortness of breath or mild chest pain. There’s a slight limitation of physical activity.
• Class III. It’s comfortable at rest, but doing simple tasks such as bathing, dressing or preparing meals causes fatigue, shortness of breath and chest pain. The ability to do physical activity becomes very limited.
• Class IV. Symptoms occur at rest and during physical activity. Any type of activity causes increasing discomfort.

Your healthcare team may use a risk calculator that looks at symptoms and test results to understand what type of treatment is needed. This is called pulmonary hypertension risk stratification.

There’s no cure for pulmonary hypertension. But treatments can improve symptoms and help you live longer. Treatment also can help keep the disease from getting worse.

It often takes some time to find the best pulmonary hypertension treatment. The treatments are often complex. You usually need a lot of health checkups.

Medications

If you have pulmonary hypertension, you may get medicines to treat your symptoms and help you feel better. Medicines also may be used to treat or prevent complications. Treatment may include:

• Medicines to relax blood vessels, called vasodilators. These medicines open narrowed blood vessels and improve blood flow. The medicine may be breathed in, taken by mouth or given through a vein. Sometimes, it’s given continuously through a small pump attached to the body.

  Examples of vasodilators to treat pulmonary hypertension include epoprostenol (Flolan, Veletri), treprostinil (Remodulin, Tyvaso, others), iloprost and selexipag (Uptravi).

• Soluble guanylate cyclase (sGC) stimulators. This type of medicine relaxes the pulmonary arteries and lowers pressure in the lungs. An example is riociguat (Adempas). Do not take these medicines if you’re pregnant.
• Medicines to widen blood vessels. Medicines called endothelin receptor antagonists reverse the effect of a substance in the walls of blood vessels that causes them to narrow. Such medicines include bosentan (Tracleer), macitentan (Opsumit) and ambrisentan (Letairis). They may improve energy level and symptoms. Do not take these medicines if you’re pregnant.
• Medicines to increase blood flow. Medicines called phosphodiesterase 5 (PDE5) inhibitors may be used to increase blood flow through the lungs. These medicines also are used to treat erectile dysfunction. They include sildenafil (Revatio, Viagra) and tadalafil (Adcirca, Alyq, Cialis).
• High-dose calcium channel blockers. These medicines help relax the muscles in the walls of blood vessels. They include amlodipine (Norvasc), diltiazem (Cardizem, Tiazac, others) and nifedipine (Procardia). Although calcium channel blockers can be effective, only a small number of people with pulmonary hypertension improve while taking them.
• Blood thinners. Also called anticoagulants, these medicines help prevent blood clots. One example is warfarin (Jantoven). The medicines can increase the risk of bleeding. This is especially true if you’re having surgery or a treatment that enters the body or creates an opening in the skin. Talk to your healthcare team about your risk.
• Digoxin (Lanoxin). This medicine helps the heart beat stronger and pump more blood. It can help control irregular heartbeats.
• Water pills, also called diuretics. These medicines help the kidneys remove excess fluid from the body. This reduces the amount of work the heart has to do. Diuretics also may be used to reduce fluid buildup in the lungs, legs and belly area.
• Oxygen therapy. Breathing pure oxygen may be suggested if you live at a high altitude or have sleep apnea. Some people with pulmonary hypertension need oxygen therapy all the time.

Surgery or other procedures

If medicines do not help control the symptoms of pulmonary hypertension, surgery may be recommended. Surgeries and procedures to treat pulmonary hypertension may include:

• Atrial septostomy. This treatment may be done if medicines don’t control pulmonary hypertension symptoms. In an atrial septostomy, a doctor creates an opening between the upper left and right chambers of the heart. The opening reduces the pressure on the right side of the heart. Potential complications include irregular heartbeats called arrhythmias.
• Lung or heart-lung transplant. Sometimes, a lung or heart-lung transplant may be needed, especially for younger people who have idiopathic pulmonary arterial hypertension. After a transplant, medicine must be taken for life to prevent the body from rejecting the new organ.

Lifestyle changes may help improve pulmonary hypertension symptoms. Try these tips:

• Eat healthy. Eat a healthy diet rich in whole grains, fruits and vegetables, lean meats, and low-fat dairy products. Try to stay away from saturated fat, trans fat and cholesterol. Use less salt.
• Stay as active as possible and manage weight. Even mild forms of activity might be too exhausting for some people who have pulmonary hypertension. For others, moderate exercise, such as walking, might be helpful — especially when done during oxygen therapy. Your healthcare team can help you plan an appropriate exercise program.
• Don’t smoke. If you smoke, quit. If you need help, ask your healthcare team for treatment that can help. Avoid secondhand smoke too, if possible.
• Get plenty of rest. Resting can reduce tiredness related to pulmonary hypertension.
• Avoid high altitudes. High altitudes can make pulmonary hypertension worse. If you live at an altitude of 8,000 feet (2,438 meters) or higher, you might be told to consider moving to a lower altitude.
• Avoid activities that can lower blood pressure a lot. These include sitting in a hot tub or sauna or taking long hot baths or showers. Such activities lower blood pressure and can cause fainting. Also, do not do activities that cause a lot of straining, such as lifting heavy objects or weights.
• Tell your healthcare team about the medicines you take. Some medicines can make pulmonary hypertension worse or affect its treatment.
• Get regular health checkups. Tell your healthcare team about any new or worsening symptoms or medicine side effects. If pulmonary hypertension affects your quality of life, ask about treatments that could help.
• Get recommended vaccines. Respiratory infections can cause serious health concerns for people with pulmonary hypertension. Ask your healthcare team which vaccines you need to prevent common viral infections.
• Talk to a healthcare professional before becoming pregnant. Pulmonary hypertension can cause serious complications for the pregnant person and unborn baby, also called a fetus. Birth control pills can increase the risk of blood clots. Talk to your healthcare team about other birth control options.

You may find that talking with other people who have pulmonary hypertension brings you comfort and encouragement. Ask your healthcare team if there are any support groups in your area.

If you think that you are at risk of or that you might have pulmonary hypertension, make an appointment for a health checkup.

There’s often a lot to discuss at your appointment, so it’s a good idea to be prepared. Here’s some information to help you get ready for your appointment.

What you can do

• Be aware of any preappointment restrictions. When you make your appointment, ask if there is anything you need to do before your checkup. For example, you might be told not to eat or drink before some medical tests.
• Write down any symptoms you’re having, including any that might not seem related to pulmonary hypertension. Try to remember when they began. Be specific, such as days, weeks and months.
• Make a list of important personal information. Include any family history of pulmonary hypertension, lung disease, heart disease, stroke, high blood pressure or diabetes. Also list any major stresses or recent life changes.
• Make a list of all medicines that you take. Also include vitamins, herbal products, supplements and any medicines bought without a prescription.
• Take someone with you, if possible. Someone who goes with you can help you remember information you’re given.
• Be prepared to discuss your diet and exercise habits. If you don’t already follow a diet or exercise routine, talk to your healthcare team about any challenges you might face in getting started.
• Make a list of questions to ask your healthcare team. List your questions from most important to least important in case time runs out.

For pulmonary hypertension, some questions to ask your healthcare team are:

• What is the likely cause of my symptoms or condition?
• What are other possible causes?
• What tests do I need?
• What treatment do you recommend?
• What are the other treatment options?
• Is there a generic form of the medicine you’re prescribing?
• What’s an appropriate level of physical activity?
• Are there any restrictions that I need to follow?
• How often do I need health checkups?
• I have other health conditions. How can I best manage them together?
• Should I see a specialist?
• Is there any information that I can take home? What websites do you suggest?

Don’t hesitate to ask other questions.

What to expect from your doctor

Your healthcare team may ask you many questions. Being ready to answer them might give you more time to discuss any concerns. You may be asked:

• When did you first begin having symptoms?
• Do you always have symptoms, or do they come and go?
• On a scale of 1 to 10, with 10 being the worst, how bad are your symptoms?
• What, if anything, seems to make your symptoms better?
• What, if anything, seems to make your symptoms worse?

What you can do in the meantime

It’s never too late to make healthy lifestyle changes. Do not smoke, eat less salt, and choose nutritious foods. These changes may help prevent pulmonary hypertension from getting worse.