Many disorders can cause pulmonary hypertension.
People usually have shortness of breath with even mild exercise and loss of energy, and some people feel light-headed or fatigued with even mild exercise.
Chest x-rays, electrocardiography (ECG), and echocardiography give clues to the diagnosis, but measurement of blood pressure in the right ventricle and the pulmonary artery is needed for confirmation.
Treatment of the cause and use of drugs that improve blood flow through the lungs are helpful.
Blood travels from the right side of the heart through the pulmonary arteries into the small blood vessels of the lungs (the capillaries) where carbon dioxide is removed from the blood and oxygen is added. Normally, the pressure in the pulmonary arteries is low, allowing the right side of the heart to be less muscular than the left side (because relatively little muscle and effort are needed to push the blood through the lungs via the pulmonary arteries). In contrast, the left side of the heart is more muscular because it has to push blood through the entire body against a much higher pressure.
If the pressure of the blood in the pulmonary arteries increases to a sufficiently high level, the condition is called pulmonary hypertension. In pulmonary hypertension, the right side of the heart must work harder to push the blood through the pulmonary arteries. Over time, the right ventricle becomes thickened and enlarged and cor pulmonale Cor Pulmonale Cor pulmonale is enlargement and thickening of the ventricle on the right side of the heart resulting from an underlying lung disorder that causes pulmonary hypertension (high pressures in the... read more develops, resulting in right-sided heart failure Pulmonary Hypertension .
Causes of Pulmonary Hypertension
Pulmonary hypertension is currently classified into the following 5 groups based on the cause of the disease:
Pulmonary arterial hypertension
Left-sided heart failure
Lung disorders or low blood oxygen levels
Chronic disorders that cause blood clots
Pulmonary arterial hypertension can be caused by numerous different disorders. It sometimes occurs without a clear cause (idiopathic). Women are affected by idiopathic pulmonary hypertension twice as often as men, and the average age at which the diagnosis is made is about 35 years. A number of genetic mutations have been identified in families with this disorder (heritable). The actual mechanism by which these inherited genetic mutations cause pulmonary hypertension is not yet known. A number of drugs and toxins have been identified as risk factors for pulmonary arterial hypertension such as fenfluramine (and other related weight-loss drugs), amphetamines, cocaine, and selective serotonin reuptake inhibitors (SSRIs). If SSRIs are taken by pregnant women after 20 weeks of pregnancy, risk of pulmonary hypertension in the newborn is higher than normal. Pulmonary arterial hypertension can also develop in people who have certain disorders, such as portal hypertension Portal Hypertension Portal hypertension is abnormally high blood pressure in the portal vein (the large vein that brings blood from the intestine to the liver) and its branches. Cirrhosis (scarring that distorts... read more , HIV infection Human Immunodeficiency Virus (HIV) Infection Human immunodeficiency virus (HIV) infection is a viral infection that progressively destroys certain white blood cells and can cause acquired immunodeficiency syndrome (AIDS). HIV is transmitted... read more , congenital heart diseases Birth Defects of the Heart , schistosomiasis Schistosomiasis Schistosomiasis is infection caused by certain flatworms (flukes), called schistosomes. People acquire schistosomiasis by swimming or bathing in fresh water that is contaminated with the flukes... read more , and systemic sclerosis Systemic Sclerosis Systemic sclerosis is a rare, chronic autoimmune rheumatic disorder characterized by degenerative changes and scarring in the skin, joints, and internal organs and by blood vessel abnormalities... read more (scleroderma).
Left-sided heart failure Pulmonary Hypertension is one of the most common causes of pulmonary hypertension. Left-sided heart failure can occur in people who have longstanding high blood pressure High Blood Pressure High blood pressure (hypertension) is persistently high pressure in the arteries. Often no cause for high blood pressure can be identified, but sometimes it occurs as a result of an underlying... read more or coronary artery disease Overview of Coronary Artery Disease (CAD) Coronary artery disease is a condition in which the blood supply to the heart muscle is partially or completely blocked. The heart muscle needs a constant supply of oxygen-rich blood. The coronary... read more . When the left side of the heart cannot pump blood out to the body normally, blood backs up in the lungs and increases blood pressure there. Inability of the heart to relax appropriately can also cause blood to back up into the lungs, which contributes to pulmonary hypertension.
Lung disorders or low blood oxygen levels can also lead to pulmonary hypertension. When the lungs are impaired by a disorder, more effort is needed to pump blood through them. One of the most common conditions is chronic obstructive pulmonary disease (COPD Chronic Obstructive Pulmonary Disease (COPD) ). Over time, COPD destroys the small air sacs (alveoli) together with their small blood vessels (capillaries) in the lungs. The single most important cause of pulmonary hypertension in COPD is the narrowing (constriction) of the pulmonary arteries that occurs as a result of low blood oxygen levels. Other conditions that lower blood oxygen levels, such as having sleep apnea Sleep Apnea Sleep apnea is a serious disorder in which breathing repeatedly stops long enough to disrupt sleep and often temporarily decrease the amount of oxygen and increase the amount of carbon dioxide... read more , or living in or prolonged visiting in places that are at high altitudes can also cause pulmonary hypertension. Other lung disorders that may cause pulmonary hypertension include pulmonary fibrosis Idiopathic Pulmonary Fibrosis Idiopathic pulmonary fibrosis is the most common form of idiopathic interstitial pneumonia. Idiopathic pulmonary fibrosis affects mostly people over the age of 50, usually former smokers. People... read more , cystic fibrosis Cystic Fibrosis (CF) Cystic fibrosis is a hereditary disease that causes certain glands to produce abnormally thick secretions, resulting in tissue and organ damage, especially in the lungs and the digestive tract... read more , sarcoidosis Sarcoidosis Sarcoidosis is a disease in which abnormal collections of inflammatory cells (granulomas) form in many organs of the body. Sarcoidosis usually develops in people aged 20 to 40, most often people... read more , pulmonary Langerhans cell histiocytosis Pulmonary Langerhans Cell Histiocytosis Pulmonary Langerhans cell histiocytosis is a disorder in which cells called histiocytes and eosinophils (types of white blood cells) proliferate in the lungs, often causing scarring. People... read more (granulomatosis), and extensive loss of lung tissue as a result of surgery or injury.
Certain chronic disorders can cause repeated (chronic) blood clots, typically blood clots in the deep leg veins (called deep vein thrombosis Deep Vein Thrombosis (DVT) Deep vein thrombosis is the formation of blood clots (thrombi) in the deep veins, usually in the legs. Blood clots may form in veins if the vein is injured, a disorder causes the blood to clot... read more ). Blood clots in the leg may dislodge and travel through the venous system and the right side of the heart to lodge in the pulmonary arteries or the smaller branches of these arteries in the lungs, causing pulmonary embolism Pulmonary Embolism (PE) Pulmonary embolism is the blocking of an artery of the lung (pulmonary artery) by a collection of solid material brought through the bloodstream (embolus)—usually a blood clot (thrombus) or... read more . If these clots do not resolve properly, the pulmonary arteries can become narrower and stiffer. This results in a type of pulmonary hypertension called chronic thromboembolic pulmonary hypertension.
Disorders that cause pulmonary hypertension by other mechanisms include blood (hematologic) disorders (such as chronic hemolytic anemia, myeloproliferative disorders Overview of Myeloproliferative Neoplasms In myeloproliferative neoplasms (myelo = bone marrow; proliferative = rapid multiplication; and neoplasm = new abnormal growth), the blood-producing cells in the bone marrow (precursor cells... read more , and splenectomy), systemic disorders (such as sarcoidosis Sarcoidosis Sarcoidosis is a disease in which abnormal collections of inflammatory cells (granulomas) form in many organs of the body. Sarcoidosis usually develops in people aged 20 to 40, most often people... read more , pulmonary Langerhans cell histiocytosis, and lymphangioleiomyomatosis Lymphangioleiomyomatosis Lymphangioleiomyomatosis (LAM) is a rare, slowly progressive growth of smooth muscle cells throughout the lungs. (See also Overview of Interstitial Lung Diseases.) Lymphangioleiomyomatosis ... read more ), and some other disorders.
Symptoms of Pulmonary Hypertension
Shortness of breath during exertion is the most common symptom of pulmonary hypertension, and virtually everyone who has the condition develops it. Some people feel light-headed or fatigued during exertion. The person is likely to feel weak because body tissues are not receiving enough oxygen. Other symptoms, such as coughing (rarely, coughing up blood) and wheezing, are usually caused by the underlying lung disorder. Swelling (edema), particularly of the legs, may occur because fluid may leak out of the blood vessels and into the tissues. Swelling is usually a sign that right-sided heart failure has developed. Rarely, people with pulmonary hypertension become hoarse.
Diagnosis of Pulmonary Hypertension
A doctor's evaluation
Chest x-ray, echocardiography, and electrocardiography
Based on the symptoms, doctors may suspect pulmonary hypertension, particularly in people who have an underlying lung disorder or other known cause of pulmonary hypertension. Tests, including a chest x-ray X-Rays of the Chest Anyone thought to have a heart disorder has chest x-rays taken from the front and the side. Typically, the person is standing upright, but chest x-rays can be done with people lying in bed if... read more , echocardiography Echocardiography and Other Ultrasound Procedures Ultrasonography uses high-frequency (ultrasound) waves bounced off internal structures to produce a moving image. It uses no x-rays. Ultrasonography of the heart (echocardiography) is one of... read more , and electrocardiography Electrocardiography Electrocardiography (ECG) is a quick, simple, painless procedure in which the heart’s electrical impulses are amplified and recorded. This record, the electrocardiogram (also known as an ECG)... read more , are done. A chest x-ray may show that the pulmonary arteries are enlarged. Electrocardiography (ECG) and echocardiography enable doctors to look for certain problems with the right side of the heart before cor pulmonale develops. For example, thickening of the right ventricle or a partial reversal (back flow) of blood through the tricuspid valve between the right ventricle and the right atrium may be detected on an echocardiogram.
Pulmonary function tests help doctors assess the extent of lung damage. A sample of blood may be taken from an artery in an arm to measure the level of oxygen in the blood.
A definite diagnosis of pulmonary hypertension usually requires passing a tube through a vein in an arm or a leg into the right side of the heart to measure the blood pressure in the right ventricle and the pulmonary artery (right heart catheterization Cardiac Catheterization and Coronary Angiography Cardiac catheterization and coronary angiography are minimally invasive methods of studying the heart and the blood vessels that supply the heart (coronary arteries) without doing surgery. These... read more ).
Other tests may be done to help determine the cause of pulmonary hypertension and to measure its severity. For example, testing may include high-resolution computed tomography (CT) of the chest (for detailed information about lung disorders), blood tests to identify autoimmune disorders, and CT angiography to look for blood clots in the lungs. Testing for gene mutations may be done to look for causes of hereditary pulmonary arterial hypertension.
Treatment of Pulmonary Hypertension
Treatment of the cause of pulmonary hypertension
Often treatments to relieve symptoms, such as drugs that dilate blood vessels and supplemental oxygen
Sometimes treatments to prevent or treat complications, such as anticoagulants and lung transplantation
Treatment of pulmonary hypertension is best directed at the cause when the cause has been identified.
Vasodilators (drugs to dilate blood vessels) work by reducing blood pressure in the pulmonary arteries. Vasodilators may improve quality of life, prolong survival, and prolong the time until lung transplantation needs to be considered. Before administering vasodilators, however, doctors may first test the effectiveness of these drugs while the person is in a cardiac catheterization laboratory because use of these drugs may be dangerous in some people. Vasodilators have not proved effective for people with pulmonary hypertension due to an underlying lung disorder. In contrast, vasodilators are often helpful for pulmonary hypertension that occurs in people with the following:
Idiopathic or inherited pulmonary hypertension
Chronic liver disease
Some congenital heart disorders
Pulmonary hypertension caused by drugs or toxins
Chronic thromboembolic pulmonary hypertension
Vasodilators include drugs related to prostacyclin (which dilates the pulmonary artery), such as epoprostenol given intravenously, iloprost or treprostinil given via inhalation, treprostinil injected under the skin, or selexipag given orally. Vasodilators can also be given by mouth, including phosphodiesterase-5 inhibitors (for example, sildenafil and tadalafil), endothelin-receptor antagonists (bosentan, ambrisentan, and macitentan), and a guanylate cyclase stimulator (riociguat). Endothelin is a substance in the blood that causes constriction of the blood vessels. Phosphodiesterase inhibitors and the guanylate cyclase stimulator increase the ability of nitric oxide, a substance normally present in the body, to widen (dilate) the pulmonary artery.
In people with pulmonary hypertension who have a low level of oxygen in the blood, the continuous use of oxygen through nasal prongs or an oxygen mask may reduce blood pressure in the pulmonary arteries and may relieve shortness of breath. A diuretic drug is usually given to assist the right ventricle in maintaining a normal volume for effective beating and to reduce leg swelling. An anticoagulant may also be given to reduce the risk of blood clots and subsequent pulmonary embolism Pulmonary Embolism (PE) Pulmonary embolism is the blocking of an artery of the lung (pulmonary artery) by a collection of solid material brought through the bloodstream (embolus)—usually a blood clot (thrombus) or... read more .
Lung transplantation Lung and Heart-Lung Transplantation Lung transplantation is the surgical removal of a healthy lung or part of a lung from a living person and then its transfer into someone whose lungs no longer function. Heart-lung transplantation... read more is an established procedure for treating people with pulmonary hypertension. Lung transplantation can be used only in people with severe disease who are healthy enough to withstand the potential consequences and difficulties with the procedure.