Chronic obstructive pulmonary disease is persistent narrowing (obstruction) of the airways occurring with emphysema, chronic obstructive bronchitis, or both disorders.
In the United States, about 15 million people have chronic obstructive pulmonary disease (COPD). It is the third most common cause of death, accounting for 135,000 deaths in 2010. From 1980 to 2000, the number of deaths due to COPD increased 64%, and more than 97% of all COPD-related deaths occur in people older than age 64. COPD affects women more often than men, but men and women die as a result of COPD at about equal rates. COPD is more often fatal in whites than in nonwhites and in people from lower income groups, probably because people in these groups are also more likely to smoke.
COPD is also increasing worldwide because smoking has increased in many developing countries, people are exposed to toxins in biomass fuels, and deaths due to other causes, such as infectious diseases, have decreased. By 2030, COPD is projected to become the third leading cause of death worldwide.
COPD leads to a persistent decrease in the rate of airflow from the lungs when the person breathes out (exhales), which is called chronic airflow obstruction. In most people, this airflow obstruction is partially reversible, either spontaneously or with treatment. COPD includes the diagnoses of chronic obstructive bronchitis and emphysema. Many people have both disorders.
The small airways (bronchioles) of the lungs contain smooth muscles and are normally held open by their attachments to alveolar walls. In emphysema, the destruction of alveolar wall attachments results in collapse of the bronchioles when a person exhales, causing airflow obstruction that is permanent and irreversible. In chronic bronchitis, the glands lining the larger airways (bronchi) of the lungs enlarge and increase their secretion of mucus. Inflammation of the bronchioles develops and causes smooth muscles in lung tissue to contract (spasm), further obstructing airflow. Inflammation also causes swelling of the airway passages and secretions in them, further limiting airflow. Eventually, the small airways in the lung become narrowed and destroyed. Asthma is also characterized by airflow obstruction (see see Asthma). However, unlike airflow obstruction in COPD, airflow obstruction in asthma is completely reversible in most people, either spontaneously or with treatment.
Airflow obstruction in COPD causes air to become trapped in the lungs after a full exhalation, increasing the effort required to breathe. Also in COPD, the number of capillaries in the walls of the alveoli decreases. These abnormalities impair the exchange of oxygen and carbon dioxide between the alveoli and the blood. In the earlier stages of COPD, oxygen levels in the blood may be decreased, but carbon dioxide levels remain normal. In the later stages, carbon dioxide levels increase and oxygen levels fall.
If low oxygen levels are not treated with supplemental oxygen, complications can occur. Low oxygen levels in the blood, if not treated, stimulate the bone marrow to send more red blood cells into the bloodstream, a condition known as secondary polycythemia (see see Polycythemia Vera). The low oxygen levels in the blood also increases the pressure in the artery through which blood flows from the heart to the lungs (pulmonary artery). As a result of the increased pressure, pulmonary hypertension and cor pulmonale can occur (see see Cor Pulmonale: A Disorder Stemming From Pulmonary Hypertension). People with COPD also have an increased risk of developing heart rhythm abnormalities (arrhythmias). People with COPD who smoke have a higher risk of developing lung cancer than do people who do not have COPD but smoke the same amount. People with COPD seem to have an increased risk of developing osteoporosis, depression, coronary artery disease, muscle wasting (atrophy), and gastroesophageal reflux. However, it is not clear whether the risk is increased because of COPD or other factors.
Cigarette smoking is the most important cause of COPD, although only about 15% of smokers develop the disease. Pipe and cigar smokers develop COPD more often than nonsmokers but not as often as cigarette smokers. With aging, susceptible cigarette smokers lose lung function more rapidly than nonsmokers. Lung function improves only a little if people stop smoking. However, the rate of decline of lung function returns to that of nonsmokers when people stop smoking, thus delaying development and progression of symptoms.
COPD tends to occur more often in some families, so there may be an inherited tendency.
Working in an environment polluted by chemical fumes or dust or by heavy smoke from indoor cooking fires may increase the risk of COPD (see see Overview of Environmental Lung Diseases). Exposure to air pollution and to smoke from nearby cigarette smokers (secondhand or passive smoke exposure) may cause flare-ups in people who have COPD but probably does not cause COPD.
A rare cause of COPD is a hereditary condition in which the body does not produce enough of the protein alpha1-antitrypsin. The main role of this protein is to prevent neutrophil elastase (an enzyme in certain white blood cells) from damaging the alveoli. Consequently, emphysema develops by early middle age in people with severe alpha1-antitrypsin deficiency (also called alpha1-antiprotease inhibitor deficiency), especially in those who also smoke.
COPD takes years to develop and progress.
In people with COPD, a mild cough that produces clear sputum develops during a person's 40s or 50s. The cough usually occurs when the person first gets out of bed in the morning. Cough and sputum production persist. Shortness of breath may occur during exertion. People often think at first that aging or being in poor physical condition is the cause, and they tend to decrease their physical activity in response. Sometimes, shortness of breath first occurs only when the person has a lung infection (usually bronchitis), during which time the person coughs more and has an increased amount of sputum. The color of the sputum changes from clear or white to yellow or green.
By the time people with COPD reach their middle to late 60s, especially if they continue smoking, shortness of breath during exertion becomes more troublesome. Pneumonia and other lung infections occur more often. Infections may result in severe shortness of breath even when the person is at rest and may require hospitalization. Shortness of breath during activities of daily living, such as toileting, washing, dressing, and sexual activity, may persist after the person has recovered from the lung infection.
About one third of people with severe COPD experience severe weight loss. The cause of weight loss is not clear, and causes may differ among different people. Possible causes include shortness of breath that makes eating difficult and increased levels in the blood of a substance called tumor necrosis factor. Swelling of the legs often develops, which may be due to cor pulmonale. People with COPD may intermittently cough up blood, which is usually due to inflammation of the bronchi, but which always raises the concern of lung cancer. Morning headaches may occur because breathing decreases during sleep, which causes increased retention of carbon dioxide and decreased levels of oxygen in the blood.
As COPD progresses, some people, especially those who have emphysema, develop unusual breathing patterns. Some people breathe out through pursed lips. Others find it more comfortable to stand over a table with their arms outstretched and weight on their palms or elbows, a maneuver that improves the function of the respiratory muscles. Over time, many people develop a barrel chest as the size of the lungs increases because of trapped air. Low oxygen levels in the blood can give a blue tint to the skin (cyanosis). Clubbing of the fingers is rare (see see Clubbing) and raises the suspicion of lung cancer or other lung disorders.
Fragile areas in the lungs may rupture, permitting air to leak from the lungs into the pleural space, a condition called pneumothorax (see see Pneumothorax). This condition often causes sudden pain and shortness of breath and requires immediate intervention by a doctor to remove the air from the pleural space.
A flare-up (or exacerbation) of COPD is a worsening of symptoms, usually cough, increased sputum, and shortness of breath. Sputum color often changes to yellow or green, and fever and body aches sometimes occur. Shortness of breath may be present when the person is at rest and may be severe enough to require hospitalization. Severe air pollution, common allergens, and viral or bacterial infections may cause flare-ups. During severe flare-ups, people may develop a life-threatening condition called acute respiratory failure. Among the possible symptoms are severe shortness of breath (a feeling likened to being drowned), severe anxiety, sweating, cyanosis, and confusion.
Chronic bronchitis is diagnosed by the history of a prolonged productive cough. People with chronic obstructive bronchitis have chronic bronchitis, plus evidence of airflow obstruction on pulmonary function tests.
Emphysema is diagnosed on the basis of findings observed during a physical examination and on pulmonary function test results. However, by the time the doctor notices these abnormalities, emphysema is moderately severe. Findings on a chest x-ray or computed tomography (CT) of the chest may also help in diagnosis of emphysema and sometimes chronic bronchitis. It is not important for doctors to differentiate between chronic obstructive bronchitis and emphysema. The most important determinant of how the person feels and functions is the severity of the airflow obstruction.
In mild COPD, doctors may find nothing unusual during the physical examination. As the disease progresses, doctors may hear wheezing or notice a decrease in the normal sounds of breathing (decreased breath sounds) when they listen to the lungs with a stethoscope. Doctors may note that it takes a long time for the person to exhale air that has been inhaled (prolonged expiration). Chest movement diminishes during breathing, and the person may use the neck and shoulder muscles to breathe.
In mild COPD, the chest x-ray is usually normal. As COPD worsens, the chest x-ray shows that the lungs contain excess air (over-inflation of the lungs). Over-inflation, thinning of blood vessels, or the presence of cysts in the lungs (called bullae) suggests the presence of emphysema.
Doctors can evaluate airflow obstruction with forced expiratory spirometry (tests that measure how much and how quickly air can be exhaled from the lungs—see see Pulmonary Function Testing (PFT)). Decreases in the maximum amount of air a person can exhale in one second (forced expiratory volume in 1 second, or FEV1) and the ratio of the FEV1 to the amount of air that a person can force out of the lungs after taking the deepest breath possible (forced vital capacity, or FVC) are required to demonstrate airflow obstruction and to make the diagnosis.
Doctors may measure the amount of oxygen in the blood by using a sensor placed on a finger or an earlobe (pulse oximetry) or by taking a sample of blood from an artery. Oxygen levels tend to be low in people with COPD. High levels of carbon dioxide in the arteries occur late in the course of the disease.
In people who develop COPD at a young age, especially when there is a family history of COPD, the level of alpha1-antitrypsin in the blood is measured to determine whether alpha1-antitrypsin deficiency is present. This genetic disorder is also suspected when COPD develops in people who have never smoked.
Sometimes doctors also test heart function with electrocardiography (ECG) or examine the heart with echocardiography to ensure that a heart disorder is not causing shortness of breath. They may do other tests to detect other disorders that could be causing the person's symptoms.
The most important treatment for COPD is to stop smoking (see Smoking Cessation). Stopping smoking when the airflow obstruction is mild or moderate often lessens cough, reduces the amount of sputum, and slows the development of shortness of breath. Stopping smoking at any point in the disease process provides some benefit. Trying several strategies at once is most likely to be effective. Among these strategies are committing to a specific date for quitting, using behavioral modification techniques (for example, making cigarettes difficult to obtain or rewarding oneself for abstaining for increasingly long periods of time), group counseling and support sessions, and nicotine replacement (for example, by chewing nicotine gum, wearing a nicotine skin patch, or using a nicotine inhaler, nicotine lozenge, or nicotine nasal spray). The drugs varenicline and bupropion may also help decrease tobacco craving. However, even with the most effective methods, less than half of people have quit smoking after one year.
People should also try to avoid exposure to other airborne irritants, including secondhand smoke and air pollution.
Contracting influenza or developing pneumonia may worsen COPD markedly. Therefore, all people with COPD should receive an influenza vaccination every year. Pneumococcal vaccination every 5 or 6 years also probably helps.
Treatment of symptoms:
Wheezing and shortness of breath are relieved when airflow obstruction decreases. Although airflow obstruction due to emphysema is not reversible, bronchial smooth muscle spasm, inflammation, and increased secretions are all potentially reversible.
Inhaled bronchodilators are given with a device that allows the user to spray a specific and consistent dose of a drug into the airways via the mouth and throat (inhalers, including metered-dose inhalers and dry powder inhalers). Inhaled bronchodilators include anticholinergic and beta-adrenergic drugs. Both relax muscles around the bronchioles. Anticholinergic drugs include ipratropium, aclidinium, and tiotropium. Ipratropium is given about 4 times daily, aclidinium is given twice per day, and tiotropium is given once per day. Inhaled short-acting beta-adrenergic drugs, such as albuterol, more rapidly relieve shortness of breath than anticholinergic drugs and so can be most useful during flare-ups. Salmeterol, formoterol, arformoterol, and indacaterol are long-acting beta-adrenergic drugs. Salmeterol, arformoterol, and formoterol are given every 12 hours. Indacaterol is given once a day. Long-acting beta-adrenergic drugs are useful for prolonged relief of symptoms in some people, especially at night, but they should not be used for rapid relief of symptoms.
Many people can use metered dose inhalers more effectively when they inhale the drug through a delivery device called a spacer (see see How to Use a Metered-Dose Inhaler). Inhaled bronchodilators may also be given using nebulizers. This mode of therapy should be reserved for people who have severe disease or for those who cannot use a metered-dose inhaler properly. A nebulizer creates a mist of drug, and the timing of its inhalation does not have to be coordinated with breathing. Nebulizers are portable, and some units can even be plugged into the cigarette lighter in a car.
Corticosteroids are helpful for many people with moderate and severe COPD whose symptoms cannot be controlled by the other drugs or for those who get frequent flare-ups despite the use of other drugs. Inhaled corticosteroids do not prevent decline of lung function over time. However, their use decreases symptoms and the frequency of COPD flare-ups. Because the drug is delivered to the lungs, typical doses of inhaled corticosteroids cause fewer side effects than corticosteroid treatment given by mouth. However, high doses of inhaled corticosteroids can have effects throughout the body, such as worsening of osteoporosis, particularly in older people. Corticosteroids given by mouth are largely restricted to treatment of COPD flare-ups or are given to people who continue to have symptoms due to airflow obstruction and who are not responding to a simpler regimen.
Theophylline is given infrequently, only to people who do not respond to other drugs. The dose must be carefully controlled by the doctor, and, in some people, levels of the drug in the blood must be measured periodically. A long-acting form of the drug permits once-daily or twice-daily dosing in many people and helps to control shortness of breath at night.
Phosphodiesterase 4 inhibitors, such as roflumilast, reduce inflammation and widen the airways. Phosphodiesterase 4 inhibitors can be used together with other bronchodilators to reduce the risk of COPD flare-ups. Common side effects include nausea, headache, and weight loss, but these effects may decline with continued use of the drugs.
Doctors used to give drugs (expectorants) to help thin secretions and make them easier to cough up. However, there is no good evidence that these drugs work. However, avoiding dehydration may prevent thickening of secretions. A rule of thumb is to drink enough fluids to keep the urine pale except for that passed first in the morning. In severe COPD, respiratory therapy may help loosen secretions in the chest.
Spirometry and pulse oximetry are often used to monitor symptoms. Taking a sample of blood from an artery and measuring the amount of oxygen and carbon dioxide in the blood provide additional information that is useful in monitoring severe disease.
Treatment of flare-ups:
Flare-ups should be treated as soon as possible. When bacterial infection is suspected, a 7- to 10-day course of antibiotic treatment is usually prescribed. Many doctors give people who have COPD a supply of an antibiotic to be kept on hand and taken early in a flare-up. A number of antibiotics can be taken by mouth, including trimethoprim-sulfamethoxazole, doxycycline, amoxicillin-clavulanate, and ampicillin. Many doctors reserve newer antibiotics, such as azithromycin, clarithromycin, and levofloxacin, for people with more severe lung infections, people in whom treatment with the older drugs has not worked, people who have severe symptoms, and people at risk of infection with organisms that are not likely to be eliminated by the older drugs (resistant bacteria). People whose immune system is suppressed or those who live in nursing homes are most likely to be infected with resistant bacteria.
People with severe flare-ups require hospitalization and treatment with short-acting beta-adrenergic drugs and ipratropium, corticosteroids given by mouth or by vein, and oxygen. They may require machine-assistance with breathing (mechanical ventilation) and sometimes placement of an endotracheal (breathing) tube.
Some people with severe disease or frequent flare-ups benefit from taking antibiotics long-term. Commonly given antibiotics include azithromycin, clarithromycin, or erythromycin. However, long-term antibiotic use may not be possible or recommended because of troublesome side effects or because bacteria that people have in their bodies tend to become resistant to the drugs, making flare-ups difficult to treat.
Some people with COPD need to receive extra oxygen to maintain sufficient oxygen in the blood. Some people need oxygen therapy for only a short time, for example when they are released from a hospital after a COPD flare-up. Long-term oxygen therapy (see Oxygen Therapy) prolongs the life of people who have advanced COPD and severely reduced oxygen levels in their blood. Although round-the-clock therapy is best, using oxygen 12 hours a day also has some benefits. This therapy reduces the excess of red blood cells caused by low blood oxygen levels and helps to relieve cor pulmonale caused by COPD. Oxygen therapy may also decrease shortness of breath during exercise.
Different devices are available for oxygen therapy. Electrically driven oxygen concentrators are used when electrical outlets are available. Compressed oxygen is available in small tanks that permit people to travel outside of their homes for 2 to 6 hours. Liquid oxygen systems are more expensive but are preferable for active people as they permit several hours away from the source reservoir. Battery-driven portable oxygen concentrators are another option and can be used while travelling on commercial airplanes. People must never use oxygen therapy near open flames or while smoking.
Pulmonary rehabilitation can help people who have COPD (see see Overview of Pulmonary Rehabilitation), but it does not improve lung function. Programs encompass education about the disease, exercise, and nutritional and psychosocial counseling. These programs can improve independence and quality of life, decrease the frequency and length of hospital stays, and improve the ability to exercise. Exercise programs can be carried out in an outpatient treatment facility or at home. Walking (sometimes on a treadmill) is usually used to exercise the legs. Sometimes stationary bicycling and stair climbing are also used. Weight lifting is used for the arms. Often, oxygen is recommended during exercise. As with any exercise program, gains in conditioning are quickly lost if the person stops exercising. Special techniques are taught for decreasing shortness of breath during activities, such as cooking, engaging in hobbies, and sexual activity.
Over-the-counter cough suppressants usually help little and are not recommended. Opioids are sometimes used to relieve severe coughing spells or pain but should be avoided when possible because they can cause drowsiness and constipation, suppress cough (which can cause or worsen infection) and, if used regularly, can cause dependence or addiction. For people with a severe alpha1-antitrypsin deficiency, the missing protein can be replaced. The treatment requires weekly intravenous infusions of the protein (see see Treatment).
Lung transplantation, of either one lung or two, may be used in certain people who are usually younger than 65 and have severe airflow obstruction. The goal of lung transplantation is to improve quality of life, because survival time is not necessarily increased. Lifelong immunosuppression is required, placing people at risk of infections.
Lung volume reduction surgery can be carried out in people with severe emphysema in the upper portions of their lungs. The goal is to improve exercise ability and quality of life. In this operation, the most severely diseased portions of the lungs are removed, thus permitting the remaining portions of the lungs and the diaphragm to function better. The improvement lasts for at least several years. People are required to stop smoking for at least 6 months before surgery. They should undergo an intense rehabilitation program to determine whether overall function can be improved significantly without surgery before undertaking this operation, which carries a risk of death of about 5%.
Prognosis and End-of-Life Issues
COPD itself usually does not cause death or severe symptoms if the person stops smoking at a time when airflow is only mildly obstructed. Continued smoking, however, virtually assures that symptoms will worsen. With moderate and severe airflow obstruction, the prognosis becomes progressively worse. People in advanced stages of COPD are likely to need considerable help with medical care and with activities of daily living. They may, for example, arrange to live on a single floor of their house, eat several small meals rather than one large meal, and avoid wearing shoes that must be tied. Death may result from respiratory failure, lung cancer, heart disorders (for example, heart failure or heart rhythm abnormalities), pneumonia, pneumothorax, or blockage of the arteries leading to the lungs (pulmonary embolism).
People with end-stage disease who develop flare-ups may need a breathing tube and mechanical ventilation. The duration of mechanical ventilation may be prolonged, and some people remain ventilator-dependent until death. It is important for people to consider with their doctors and loved ones whether or not they wish this kind of supportive therapy and to do so before a flare-up occurs. An alternative to this supportive therapy is treatment aimed at comfort (and not at prolonging life), such as opioids (see Pain). The best way to ensure that the person's wishes regarding prolonged mechanical ventilation are carried out is to prepare an advance directive (see see Advance Directives) and appoint a health care proxy (see see Default Surrogate Decision Making).
Last full review/revision July 2013 by Robert A. Wise, MD