Table of Contents
- Definition of COPD
- Causes and Risk Factors of COPD
- Epidemiology of COPD
- Etiology of COPD
- Classification of COPD
- Pathogenesis of COPD
- Pathophysiology of COPD
- Signs and Symptoms of COPD
- Diagnosis of COPD
- Differential Diagnosis of COPD
- Acute Exacerbation of COPD
- Therapy of COPD
- Complications of COPD
- Prevention of COPD
- Learn more about COPD
Definition of COPD
The term COPD refers to a chronic obstructive pulmonary disease and thus summarizes chronic respiratory diseases, where an airflow limitation occurs. A distinction must be done between the definition of the WHO and the global initiative for chronic obstructive lung disease (GOLD).
The WHO defines COPD as a lung disease characterized by chronic obstruction of lung airflow that interferes with normal breathing and is not fully reversible. The more familiar terms ‘chronic bronchitis’ and ’emphysema’ are no longer used but are now included within the COPD diagnosis.
According to the global initiative for chronic obstructive lung disease, COPD is a preventable and treatable disease of the airways, which is accompanied by a restriction of the respiratory flow. The disease is progressive and associated with a chronic inflammatory reaction of the lung to noxious particles or gases.
Causes and Risk Factors of COPD
Almost 3 million people suffer from COPD in the United Kingdom. Roughly 900,000 patients among them have a confirmed diagnosis of COPD while about 2 million people have undiagnosed COPD. 90 % of COPD patients are smokers. People above the age of 50 are most affected. Heavy smokers can develop COPD after the age of 35.
The major cause of COPD is smoking, either active or passive. Other causes include long-term inhalation of chemical fumes, dust, and air pollutants. Genetic alpha 1 antitrypsin deficiency can also damage the lungs and lead to COPD. Smoking is a risk factor for these people as well.
Almost all preterm babies need long-term oxygen therapy as their lungs are still underdeveloped. This can lead to lung injury (neonatal chronic lung disease) increasing the risk for COPD later in adult age. Chronic bronchitis is defined on the basis of history as a chronic productive cough for at least 3 months in two consecutive years. Emphysema is defined by the loss of alveoli.
Epidemiology of COPD
The prevalence of COPD in the United States of America is about 5% among individuals over 45 years of age, but due to the unreported cases, a much higher number can be estimated. In the seventh decade of life, the prevalence is the highest. Worldwide, COPD is the third leading cause of death among men and women. Men and women are equally affected.
Etiology of COPD
The causes of COPD include exogenous and endogenous factors. The main exogenous factor is cigarette smoking, which is responsible for COPD in approximately 90 % of cases. However, air pollution by ozone or fine dust is a trigger of COPD. Miners are often affected.
Recurrent bronchopulmonary infections aggravate the progression of COPD. In addition, a disturbed lung maturation in embryogenesis is known as a cause of later COPD. Important endogenous factors are an α1-antitrypsin deficiency and IgA deficiency which may contribute to the development of COPD – especially at younger age.
Classification of COPD
COPD can be divided into different levels of severity. According to the global initiative for chronic obstructive lung disease (GOLD), the following grades can be distinguished:
|GOLD I (easy)||FEV1 ≥ 80 %, FEV1/VC < 70 %|
|GOLD II (medium)||FEV1 50 – 79 %, FEV1/VC < 70 %|
|GOLD III (severe)||FEV1 30 – 49 %, FEV1/VC < 70 %|
|GOLD IV (very severe)||FEV1 < 30 %, FEV1/VC < 70 %|
Spirometry is done every two years after the initial diagnosis. The patient is also evaluated for other associated conditions like anemia, cancer, anxiety/depression, ischemic heart disease, congestive heart failure, metabolic syndrome, peripheral muscle dysfunction, osteopenia, osteoporosis, etc.
The Medical Research Council (MRC) has proposed a dyspnea scale:
- Grade 1: No breathlessness except with strenuous exercise
- Grade 2: Breathlessness when walking up a slight hill or walking fast on a flat level
- Grade 3: The patient walks relatively slower than normal people on a flat level because of shortness of breath or has to catch for breath while walking at own pace on a flat level.
- Grade 4: The patient stops to catch a breath after roughly 100 yards (90 m) walk or after a few minutes on a flat level.
- Grade 5: The patient is not able to leave his house due to breathlessness or breathless during dressing or undressing.
Pathogenesis of COPD
Airway limitation is the main feature of this disease. Initial stages of COPD are without any significant symptom. People consider a mild cough and shortness of breath on exertion as a normal part of aging. COPD can take years to complicate and produce significant symptoms; however, complications lead to permanent damage to the lungs. Although the damage caused by COPD cannot be undone, it is still possible to prevent further damage and manage the patients.
COPD includes chronic bronchitis and emphysema. Chronic bronchitis is the inflammation of the airways in response to smoking or pollutants leading to narrowing of the airway and increased mucous deposition, which causes excess cough. Narrowed or blocked airways disturb effective respiration, making the patient symptomatic. Emphysema is the breakdown of the air sacs (alveoli) and alveolar membranes. Alveolar walls lose their elastic strength, the air entering the lungs is trapped, occupies space not used in the exchange of gas, leading to dyspnea.
The deficiency of alpha 1 antitrypsin can lead to COPD. Emphysema occurs in these patients after the age of 30. Deficiency of the alpha 1 antitrypsin protein, an antiprotease that controls inflammation in the lungs, leads to the destruction of lung tissue by the WBCs.
Pathophysiology of COPD
After years of damage caused by inhaled toxic material such as cigarette smoke, there is hypertrophy and hyperplasia of goblet cells in the mucosa of the bronchi. This results in an increased production of mucus whose removal can no longer be guaranteed by the ciliated epithelium. The lumen of the bronchi is constricted and therefore promotes a lasting inflammatory reaction.
This inflammation leads to a remodeling process, so the obstruction is both functionally and structurally permanent. Another consequence of chronic inflammation is a non-physiological ratio between proteases and protease inhibitors so that there is a destruction of connective tissue leading to damage to the supporting structures of the lung and development of pulmonary emphysema.
The elasticity of the lung decreases, the residual volume increases. The affected patients have to increase their work of breathing. The obstruction of the respiratory tract causes interference in the distribution of air, which leads to pulmonary vasoconstriction of the hypoxic areas according to the Euler-Liljestrand mechanism. If the total cross-section of all pulmonary vessels continues to decrease, this may cause pulmonary hypertension or even pulmonary heart disease (cor pulmonale).
Additionally, there is a non-specific bronchial hyper-responsiveness. During forced expiration, (for example during physical exertion), a bronchial collapse occurs that contributes to hyperinflation of the lung. This creates a massive performance limitation of patients.
Signs and Symptoms of COPD
COPD produces symptoms, disability and impaired quality of life which may respond to pharmacological and other therapies that have an impact on the airflow obstruction. Symptoms of COPD include:
- Shortness of breath or breathlessness on exertion or at rest (in late stages)
- Chest tightness on exertion or at rest (in late stages)
- Chronic Cough with sputum, a feature of chronic bronchitis
- Wheezing, particularly on expiration
- Other symptoms like weight loss, ankle swelling, low appetite
Signs seen on examination
COPD patients can have the following signs depending upon the severity of the disease:
Barrel-shaped chest due to hyperinflation and labored breathing using accessory muscles of respiration
- Cyanosis of the lips and/or nail beds due to impaired lung function
- Wheeze with breathing, particularly with expiration
- Distant breath sounds on auscultation of the chest
- Scattered rhonchi on auscultation of the chest
- Hyper-resonance of the lungs on percussion
- Pulmonary hypertension can develop and produce signs of cor pulmonale like ankle swelling, orthopnea, chest tightness, raised JVP, etc.
Asthma and COPD have a different pathogenesis. Asthma is triggered by allergens in the environment and airway inflammation is caused by CD4+ T cells, lymphocytes, eosinophil, and ILs-4. However, the symptoms of asthma are completely reversible, while COPD develops in response to noxious agents. Airway inflammation in COPD is caused by CD8+ T-lymphocytes and CD68+ macrophages/PMNS but airway obstruction is permanent and irreversible.
The typical presentation of COPD is a chronic cough with whitish or purulent sputum to expectoration and dyspnea. Frequently COPD follows simple chronic bronchitis. Two types can be distinguished in their clinical picture:
- Pink puffer: emphysemic COPD type with strong dyspnoea and late pulmonary heart disease
- Blue bloater: bronchial COPD type with low dyspnea, cyanosis, and pronounced edema
Diagnosis of COPD
History and physical examination
History is essential for existing risk factors, particularly asking about smoking behavior and already known respiratory diseases such as asthma. You can determine the severity of the disease from history by asking about the degree of distress with daily activities.
At physical examination, evidence of COPD (for example cyanosis or barrel chest) can already be found by inspection. A reduced vocal fremitus may be detected upon palpation, and during percussion, a hyper-resonant sound can be heard due to the hyperinfiltration of the lungs.
During auscultation, a prolonged expiratory phase can be heard, which is accompanied by whistling and also by wheezing and humming. Reduced breathing sounds can be heard in the hyperinflated lungs. Fine rales can also be heard accompanying pneumonia.
Pulmonary functions tests
A patient presenting with shortness of breath, cough with sputum and chest tightness should be thoroughly evaluated and tests for COPD should be performed.
Initially, clinical history and physical examination should be done. Baseline blood chemistry and hematology investigations should be sent to the laboratory and an ECG with a chest x-ray is advised to rule out other causes like lung cancer or cardiac disease. Pulmonary function tests are performed using a spirometer.
Spirometry is the most important test to diagnose obstructive and restrictive lung disease. FEV1 and FVC are calculated using spirometry. FEV1 is the forced expiratory volume of the air in one sec while FVC is the forced vital capacity. FEV1 measures the rate at which air moves out of the lungs. Arterial blood gases are done to measure the content of oxygen, carbon dioxide, and H+ ions. Oxygen saturation is also monitored regularly for COPD patients.
An alpha 1 antitrypsin test is done rarely to rule out the inherited cause of COPD. A CT scan, plain or HRCT (High-Resolution CT) of the chest is done to see a detailed picture of the lungs.
After inhalation of salbutamol, only slight reversibility of less than 200 ml/or less than 15 % appears in the post-bronchodilation test. A reduced transfer coefficient (DLCO/VA) sheds light on the severity of existing emphysema. A decreased MEF25-75 shows obstruction of the small airways.In smokers, the CO content in the exhaled air may be determined, which increases with cigarette consumption (> 50 ppm). In addition, the HbCO in blood gas analysis is increased in smokers. The arterial blood gas analysis also gives information about whether there is a partial respiratory insufficiency counteracted with hyperventilation (pCO2 decreased) or a generalized respiratory insufficiency (pO2 decreased and pCO2 increased).
Type of respiratory failure:
- Pco2 increased → if the patient is hypercapnic only: type 1 respiratory failure.
- Po2 decreased and pco2 decreased → if the patient is hypoxic and hypercapnic: it´s type 2 respiratory failure.
Arterial blood gases and oximetry may demonstrate resting exertional hypoxemia. Arterial blood gases provide additional information about alveolar ventilation and acid-base status by measuring arterial Pco2 and pH.
In addition, certain patterns can be identified in spirometry, which are typical of COPD. Typical in the flow-volume graph is the emphysema bend and in the resistance loop the image of a golf club shown below.
In the laboratory diagnosis, it is necessary to investigate the α1-antitrypsin deficiency, especially in younger patients who do not smoke. A complete blood count may show an elevated hematocrit, which suggests the presence of chronic hypoxemia.
In cases of recurrent severe exacerbations or treatment failure, sputum culture should be obtained. A morning expectoration should be collected, but obtaining endobronchial secretions as part of bronchoscopy is even better. Potential pathogens are frequently Haemophilus influenza, pneumococcus or Moraxella catarrhalis and different virus types.
Characteristic radiographic findings:
- Hyperinflation with → 1- flattened hemidiaphragms 2- increased anteroposterior chest diameter
- Parenchymal destruction produces attenuated peripheral vascular markings.
- Pulmonary hypertension produces proximal pulmonary artery dilation .
- Cardiac size may be increased, suggesting the right heart volume overload.
- Cystic or bullous changes.
On chest X-ray, small opacities may suggest inflammatory infiltrates or restricted ventilation. Changes due to emphysema or cor pulmonale can be detected, and other diseases such as lung cancer or pneumonia are excluded. Since chronic bronchitis is a diagnosis of exclusion, an X-ray image is always needed before a diagnosis is made.
In addition, bronchoscopy should be entertained to exclude various differential diagnoses that result in symptoms similar to COPD such as haemoptysis and dyspnoea. During bronchoscopy, biopsies may be obtained for histological examination.
There is no single diagnostic test for COPD. Physicians rely on clinical judgment based on a combination of history, physical examination, and confirmation of the presence of airflow obstruction using spirometry. COPD is characterized by airflow obstruction that is not fully reversible. Airflow obstruction is defined as a reduced FEV1/FVC ratio such that the diagnosis of COPD is made when the FEV1/FVC ratio is less than 0.7 and the FEV1 is less than 80% of predicted. Additionally, a diagnosis of COPD should only be made in the presence of respiratory symptoms, for example, breathlessness or cough.
Differential Diagnosis of COPD
Differential diagnosis of COPD is bronchial asthma. Unlike COPD, asthma is prevalent mostly in childhood or adolescence, and is accompanied by paroxysmal dyspnoea, allergies and a good response to corticosteroids and is completely reversible in the post-bronchodilation test.
Other lung diseases must be excluded. To exclude bronchiectasis a greater amount of sputum is necessary as well as a High-Resolution CT scan. Tracheal or laryngeal stenosis may be differentiated by laryngoscopy or bronchoscopy. An otolaryngologist may establish the diagnosis of a sinobronchial syndrome, a combination of sinusitis and the resulting lower respiratory tract symptoms such as chronic bronchitis or asthma.
To exclude a left ventricular failure that occurs especially with nocturnal cough and cardiac asthma, cardiac diagnostics are necessary. Cystic fibrosis can be diagnosed through a sweat test. The detection of bronchial carcinoma is important, therefore X-rays and CT scans with a bronchoscopy-guided biopsy may be necessary. In addition, a pulmonary embolism and the presence of gastroesophageal reflux disease should be excluded.
- Cardiovascular or pulmonary vascular disease
- Severe exercise deconditioning
- Interstitial lung disease
- Neuromuscular disease
Acute Exacerbation of COPD
A sudden attack of shortness of breath, wheezing and cyanosis with signs of respiratory distress in a patient with diagnosed COPD is called acute exacerbation of COPD. Infections caused by bacteria or viruses, or body response to environmental pollutants can be the triggers of an acute attack. Management includes systemic and inhaled corticosteroids with oxygen therapy and regular monitoring with antibiotic cover if required.
Therapy of COPD
The treatment of COPD is divided into a medical and conservative approach. The basis of conservative therapy is the absolute nicotine abstention and the elimination of other inhaled noxious agents. Patient training and breathing exercises combined with training to improve cardiopulmonary capacity are also necessary.
Vaccination against pneumococcal and influenza viruses is indicated for the prevention of infections. Furthermore, prophylaxis of osteoporosis with calcium and vitamin D3 is useful as is counteracts glucocorticoid-induced osteoporosis. Existing infection sources have to be eliminated and comorbidities need to be treated.
Drug therapy is structured according to a graduate scheme.
The first group of patients with GOLD 1 to 2, 0 to 1 exacerbations per year and a few symptoms can be treated with a short-acting anticholinergic or short-acting β2-sympathomimetic as needed. Alternative or adjunctive to this regime is therapy with theophylline.
The second group of patients with GOLD 1 to 2, from 0 to 1 exacerbations per year but with stronger symptoms is treated with a long-acting anticholinergic or a long-acting β2-sympathomimetic. Supplementary in this stage is therapy with short-acting anticholinergics and/or short-acting β2-sympathomimetics and theophylline.
The third group of patients with GOLD 3 to 4, with two or more exacerbations per year and few symptoms, is treated with an inhaled glucocorticosteroids and a long-acting anticholinergic, or a long-acting β2-sympathomimetic. Alternative or supplement to this stage is therapy with short-acting anticholinergics and/or short-acting β2-sympathomimetic and theophylline.
The fourth group of patients with GOLD 3 to 4, two or more exacerbations per years and stronger symptoms get inhaled glucocorticosteroids and a long-effective β2-sympathomimetic and/or a long-acting anticholinergic. Alternative or supplement to this stage is therapy with short-acting anticholinergics and/or short-acting β2-sympathomimetic and theophylline and carbocisteine.
Therapy of acute recurrent exacerbations
In this case, hospitalization is often sought, especially if strong dyspnoea and/or tachypnoea or older age of the patients occur. In infection-related exacerbations, antibiotic therapy is indicated based on antibiotic susceptibility of the suspected pathogens as well as the patient’s clinical condition. Patients with mild exacerbations can be treated as outpatients with aminopenicillin (alternatively doxycycline, macrolides).
Patients with moderate to severe exacerbations need hospital admission and treatment with aminopenicillin with beta-lactamase inhibitor or parenteral cephalosporin of the 2nd or 3rd generation (alternatively anti-pneumococcal fluoroquinolones). In patients with suspected P. aeruginosa infections or in patients in intensive care, pseudomonas effective carbapenems, cephalosporin or fluoroquinolones should be used.
The bronchodilator therapy may be temporarily intensified and combined with intravenous glucocorticoids. There are also aerosol treatments, an apparatus inhalation therapy with 0.9 % NaCl, β2-sympathomimetics such as salbutamol, and an oxygen treatment so that the pO2 is maintained above 60 mmHg.
Complications of COPD
Acute recurrent exacerbations are complications of COPD that require an adjustment of therapy. Viral or bacterial infections may cause a more severe deterioration that may last longer than 24 hours. Also, co-morbidities such as cardiovascular disease or metabolic syndrome, lung carcinoma, muscle weakness and osteoporosis (due to catabolic mechanisms requiring an increased work of breathing) and depression are complications of COPD.
Weight loss with increased work of breathing is typical. Among the late complications, respiratory failure is common and cor pulmonale is due to the Euler-Liljestrand mechanism and direct vascular loss. Pulmonary hypertension may lead to right heart failure with hepatomegaly and ascites.
Prevention of COPD
The most effective preventive method is risk factors avoidance. It has been shown that middle-aged smokers who were able to successfully stop smoking experienced a significant improvement in their prognosis with a slower progression of the disease. For this purpose, the detailed medical reconnaissance and surveillance are essential as well as assisting with substitution drugs and anti-depressants in order to facilitate the cessation.
In occupational COPD, immediate avoidance of inhaled noxious substances is crucial. Also, vaccines against pneumococcal and influenza are indexed to avoid acute exacerbations due to these infections.
Learn more about COPD
To learn more about this topic you may test the course “Respiratory Medicine” by Prof. Jermey Brown for free! An extra lecture about COPD is included!