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Patient information: Chronic obstructive pulmonary disease (COPD)

COPD OVERVIEW

COPD, or chronic obstructive pulmonary disease, is a condition in which the airways in the lungs become broken down and narrowed, often due to smoking cigarettes. Sometimes the air sacs are also damaged. As the lungs become more damaged over time, it becomes increasingly difficult to breathe through the narrowed airways (also known as bronchial tubes). When the damage is severe, it may also become difficult to get enough oxygen into the blood and to get rid of excess carbon dioxide. These changes all lead to shortness of breath and other symptoms. Unfortunately, the symptoms of COPD cannot be completely eliminated with treatment and the condition usually worsens over time.

The term COPD is often used interchangeably with the terms chronic bronchitis and/or emphysema because chronic bronchitis and emphysema are the most common forms of COPD. Also, the current treatments for COPD, chronic bronchitis, and emphysema are similar. In the discussion that follows, chronic bronchitis and emphysema are referred to collectively as COPD.

This article reviews the risk factors, symptoms, and tests used to diagnose COPD. An article that discusses treatment of COPD is available separately. (See "Patient information: Chronic obstructive pulmonary disease (COPD) treatments".)

COPD CAUSES

To understand why COPD develops, it is important to understand how the lungs work. Normally, air that we breathe passes from the nose and mouth through the airways to the tiny air sacs of the lung, called alveoli. In the air sacs, oxygen that we breathe passes through the walls of air sacs into the bloodstream (figure 1). Carbon dioxide passes in the reverse direction, out of the bloodstream, back into the alveoli, and is then eliminated by breathing out (figure 2). Carbon dioxide is a waste product of the body's metabolism, and must be regularly removed.

In people who develop COPD, irritating gases and particles are inhaled while smoking or breathing smoke filled air (secondhand smoke) or other fumes or particles. These gases and particles can injure the airways and lungs and cause swelling (inflammation). Over time, the inflammation becomes chronic, damages the lung tissue, and may cause scarring (figure 3). This lung damage makes it more difficult to breathe in and out and makes it harder for oxygen and carbon dioxide to pass across the air sac walls in and out of the blood. (See "Chronic obstructive pulmonary disease: Definition, clinical manifestations, diagnosis, and staging".)

Reasons for airflow blockage — Any disease that interferes with airflow out of the lungs can cause COPD. Most people with COPD have chronic bronchitis and emphysema, and some also have asthma.

Chronic bronchitis — Chronic bronchitis is the term used to describe people who have a chronic cough that produces sputum. Chronic bronchitis can scar the airways and reduce airflow.

Emphysema — Emphysema is the term used to describe damage to the air sacs in the lung. This damage can also restrict airflow.

Asthma — Asthma is a chronic inflammatory disorder of the airways. The chronic inflammation leads to recurrent episodes of wheezing, breathlessness, chest tightness, and coughing, particularly at night or in the early morning. Treatment is usually successful in reversing inflammation and airway narrowing. In a minority of people with asthma, the chronic inflammation permanently restricts airflow. When this airway narrowing cannot be completely reversed with treatment, the person is said to have COPD.

COPD RISK FACTORS

Smoking cigarettes significantly increases the risk of developing COPD. However, approximately 20 percent of people who develop COPD have never smoked.

Other factors that increase the risk of developing COPD include an abnormal sensitivity and exaggerated response to inhaled substances (called airway responsiveness), other exposures, such as secondhand exposure to smoke and workplace exposure to environmental dust or organic materials, or exposure to air pollution. COPD can run in families. (See "Chronic obstructive pulmonary disease: Risk factors and risk reduction".)

Genetic risk factors for COPD include severe deficiency of alpha-1 antitrypsin, a protein that protects the lungs. (See 'Alpha-1 antitrypsin deficiency' below.)

COPD SYMPTOMS

COPD usually causes no or mild symptoms at first. As the disease progresses, symptoms usually worsen. The most common symptoms include:

  • Coughing and spitting up phlegm (mucus)
  • Wheezing (a whistling or squeaking noise as you breathe)
  • Shortness of breath with activity or even at rest
  • Fatigue
  • Morning headaches

COPD DIAGNOSIS

If you have shortness of breath, a chronic cough, or cough up phlegm, your healthcare provider may recommend testing for COPD. The test used to diagnose COPD is a type of a pulmonary (lung) function test (PFT). (See "Chronic obstructive pulmonary disease: Definition, clinical manifestations, diagnosis, and staging".)

Pulmonary function tests (PFTs) — The pulmonary function test (PFT) that measures airway obstruction is called spirometry, and is the best test for diagnosing COPD. Spirometry can detect COPD even in people who do not yet have symptoms.

During spirometry, you take a deep breath in and then blow out as hard and as fast as you can into a tube connected to a machine called a spirometer. The spirometer measures how fast and how much air you can blow out of your lungs. If the measurement is abnormal, the next step is to repeat the test after you use an inhaler (which should improve the measurement). In people with asthma, the test measurements usually return to normal, but in people with COPD, the test measurements may only partially improve.

After the diagnosis of COPD is confirmed, spirometry is repeated over time to monitor the status of the disease and the effectiveness of treatment.

In some cases, additional pulmonary function tests are performed. These tests include measurements of lung volume, oxygenation, and carbon dioxide. The results of these tests are used to evaluate for lung diseases other than COPD that may be contributing to shortness of breath and to guide treatment.

  • Measurements of lung volume are usually performed in a box that looks like an old fashioned phone booth. People with more severe COPD may have an increase in lung volume. The same machine can also measure the ability of the lungs to transfer gases like oxygen and carbon dioxide. With emphysema, the ability to transfer gases is typically reduced.
  • Oximetry measures the amount of oxygen in the blood using a device called a finger oximeter, which clips onto the finger like a clip-on earring. Oximetry may also be checked during exercise, such as walking on level ground or climbing stairs. When the oxygen saturation drops to 88 percent or below, supplemental oxygen is usually prescribed. (See "Patient information: Chronic obstructive pulmonary disease (COPD) treatments".)

  • An arterial blood gas sample may be obtained to determine if you have problems clearing carbon dioxide from the blood. Arterial blood gas is usually obtained by taking a blood sample from the artery in your wrist.

Alpha-1 antitrypsin deficiency — Alpha-1 antitrypsin deficiency is a genetic disorder which causes 2 to 3 percent of the cases of emphysema in the United States. All adults who have symptoms of COPD should be tested for alpha-1 antitrypsin deficiency. (See "Clinical manifestations, diagnosis, and natural history of alpha-1 antitrypsin deficiency" and "Treatment of alpha-1 antitrypsin deficiency".)

COPD TREATMENT

The first and most important part of any treatment plan for COPD is for smokers to stop smoking. This is true regardless of how long ago you were diagnosed with COPD and how severe your disease is. Studies of people with COPD show that worsening of the disease is slowed in people who stop smoking. (See "Patient information: Smoking cessation".)

Currently, there is no cure for COPD; however, many treatments are available for the symptoms and complications of this disorder. Most patients require ongoing treatment to keep symptoms under control.

A separate topic discusses the treatment of COPD. (See "Patient information: Chronic obstructive pulmonary disease (COPD) treatments".)

WHERE TO GET MORE INFORMATION

Your healthcare provider is the best source of information for questions and concerns related to your medical problem. Because no two people are exactly alike and recommendations can vary from one person to another, it is important to seek guidance from a provider who is familiar with your individual situation.

This discussion will be updated as needed every four months on our web site (www.uptodate.com/patients). Additional topics as well as selected discussions written for healthcare professionals are also available for those who would like more detailed information.

Some of the most pertinent include:

Patient Level Information:
Patient information: Chronic obstructive pulmonary disease (COPD) treatments
Patient information: Smoking cessation

Professional Level Information:
Arrhythmias in COPD
Chronic obstructive pulmonary disease: Definition, clinical manifestations, diagnosis, and staging
Chronic obstructive pulmonary disease: Risk factors and risk reduction
Delivery of inhaled medication in adults
Diagnosis and treatment of infection in acute exacerbations of chronic obstructive pulmonary disease
Dynamic hyperinflation in patients with COPD
Lung volume reduction and bullectomy in COPD
Management of acute exacerbations of chronic obstructive pulmonary disease
Management of stable chronic obstructive pulmonary disease
Management of the patient with severe COPD and coronary artery disease
Mechanical ventilation in acute respiratory failure complicating COPD
Natural history and prognosis of COPD
Nocturnal ventilatory support in COPD
Nutritional support in advanced lung disease
Oxygen conserving devices
Pulmonary rehabilitation in COPD
Role of anticholinergic therapy in COPD
Role of inhaled glucocorticoid therapy in stable COPD
Role of methylxanthines in the treatment of COPD
Role of mucoactive agents in the treatment of COPD
Role of systemic glucocorticoid therapy in COPD
Use of oxygen in patients with hypercapnia
Clinical manifestations, diagnosis, and natural history of alpha-1 antitrypsin deficiency
Treatment of alpha-1 antitrypsin deficiency

A number of web sites have information about medical problems and treatments, although it can be difficult to know which sites are reputable. Information provided by the National Institutes of Health, national medical societies and some other well-established organizations are often reliable sources of information, although the frequency with which they are updated is variable.

  • National Library of Medicine

  (www.nlm.nih.gov/medlineplus/copdchronicobstructivepulmonarydisease.html, available in Spanish)

  • National Heart, Lung, and Blood Institute

      (www.nhlbi.nih.gov/health/dci/Diseases/Copd/Copd_WhatIs.html)

  • National Lung Health Education Program

      (www.nlhep.org)

  • American Lung Association

      (www.lungusa.org)

  • Alpha-1 Foundation

      (www.alphaone.org)

Patient Support — There are a number of online forums where patients can find information and support from other people with similar conditions.

      (http://copd.about.com/forum)

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Last literature review version 17.3: September 2009
This topic last updated: June 9, 2009
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References Top
  1. Global strategy for the diagnosis, management, and prevention of chronic obstructive pulmonary disease: Executive summary 2006. Global Initiative for Chronic Obstructive Lung Disease (GOLD). Available from http://www.goldcopd.org. (Accessed April 17, 2009).
  2. Celli, BR, MacNee, W. Standards for the diagnosis and treatment of patients with COPD: a summary of the ATS/ERS position paper. Eur Respir J 2004; 23:932.
  3. Qaseem, A, Snow, V, Shekelle, P, et al. Diagnosis and management of stable chronic obstructive pulmonary disease: a clinical practice guideline from the American College of Physicians. Ann Intern Med 2007; 147:633.
  4. Screening for chronic obstructive pulmonary disease using spirometry: U.S. Preventive Services Task Force recommendation statement. Ann Intern Med 2008; 148:529.

UpToDate performs a continuous review of over 430 journals and other resources. Updates are added as important new information is published. The literature review for version 17.3 is current through September 2009; this topic was last changed on June 9, 2009. The next version of UpToDate (18.1) will be released in March 2010.

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