Intended for healthcare professionals

Practice ABC of chronic obstructive pulmonary disease

Diagnosis

BMJ 2006; 332 doi: https://doi.org/10.1136/bmj.332.7552.1261 (Published 25 May 2006) Cite this as: BMJ 2006;332:1261
  1. Graeme P Currie, specialist registrar,
  2. Joe S Legge, consultant
  1. Respiratory Unit, Aberdeen Royal Infirmary, Aberdeen.

    As with most other common medical conditions, the diagnosis of chronic obstructive pulmonary disease (COPD) depends on a consistent history and appropriate examination findings. Confirmatory objective evidence is provided by spirometry. Doctors should consider the possibility of COPD in any patient aged 35 years or older with any relevant respiratory symptom and a history of smoking.

    History

    Consider COPD in any current or former smoker age > 35 years who complains of any combination of breathlessness, chest tightness, wheeze, sputum production, cough, frequent chest infections, and impaired exercise tolerance.

    Differences between COPD and asthma

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    Patients with advanced COPD can develop an increased anteroposterior chest diameter—a barrel shaped chest

    COPD may also be present in the absence of noticeable symptoms, so look for it in individuals who are current or former smokers. Pay particular attention to features in the history or examination that may suggest an alternative or concomitant diagnosis. Since asthma tends to be the main condition in the differential diagnosis of COPD, a careful history should be taken in order to help distinguish between the disorders. Ask about previous and present occupations, particularly with regard to exposure to dusts and chemicals.

    Record the patient's current smoking status and calculate the number of smoking pack years.

    • Number of pack years = (number of cigarettes smoked/day x number of years smoked)/20

    • For example: a patient who has smoked 15 cigarettes a day for 40 years has a (15x40)/20 = 30 pack year smoking history.

    Calculating the number of smoking pack years overcomes the problems of differences in duration and intensity of cigarette smoking. The decline in forced expiratory volume in 1 second (FEV1) is generally related to the extent of cumulative exposure, although there is wide variability between individuals.

    As part of the overall assessment of COPD, find out about symptoms of anxiety and depression, other medical conditions, current drug treatments, frequency of exacerbations, previous hospitalisations, exercise limitation, number of days missed from work and their financial impact, and extent of social and family support. COPD causes systemic effects, with weight loss being an under-recognised symptom in advanced disease.

    Conditions in the differential diagnosis of COPD

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    This is the third in a series of 12 articles

    Examination

    Because of the heterogeneity of COPD, patients may show a range of phenotypic clinical pictures. However, physical examination can be normal especially in patients with mild disease, although it may help suggest an alternative or coexistent diagnosis. Moreover, features of advanced airflow obstruction—peripheral and central cyanosis, hyperinflated chest, pursed lip breathing, accessory muscle use, wheeze, diminished breath sounds, and paradoxical movement of the lower ribs—are found in other chronic respiratory conditions and are therefore of low diagnostic sensitivity and specificity.

    Fig 2
    Fig 2

    The clinical heterogeneity of COPD: a typical “blue bloater” (top) and “pink puffer” (bottom)

    Cor pulmonale is defined as right ventricular hypertrophy due to any chronic lung disorder. Some patients with severe COPD may show signs consistent with cor pulmonale (raised jugular venous pressure, loud P2 heart sounds due to pulmonary hypertension, tricuspid regurgitation, pitting peripheral oedema, and hepatomegaly). Look for skeletal muscle wasting and cachexia, which may be present in those with advanced disease. Finger clubbing is not found in COPD, and its presence should prompt thorough evaluation to exclude a cause such as lung cancer, bronchiectasis, or idiopathic pulmonary fibrosis. At presentation, record the weight and height and calculate the body mass index (weight (kg)/(height (m)2)). It is categorised for both men and women as < 18.5 for underweight, 18.5-24.9 for normal, 25-29.9 for overweight, and ≥ 30 for obese.

    Common causes of obstructive and restrictive spirometry

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    Investigations

    Peak expiratory flow

    Solitary peak expiratory flow readings can seriously underestimate the extent of airflow obstruction, while serial monitoring of peak expiratory flow is not generally useful in the diagnosis of COPD.

    Spirometry

    While history and examination are necessary in the diagnostic work up, showing airflow obstruction is vital in confirming the diagnosis. Spirometry should be arranged in all patients with suspected COPD. It is increasingly performed in primary care and can be carried out with minimal training for both clinician and patient. It measures

    • Forced vital capacity (FVC)—the maximum volume of air forcibly exhaled after full inspiration (that is, from total lung capacity)

    • Forced expiratory volume in one second (FEV1)—the volume of air exhaled during the first second of the FVC manoeuvre

    • The FEV1/FVC ratio.

    Compare the FEV1 and FVC with predicted normal values for age, height, and sex. These measures are often expressed as the percentage predicted as well as in absolute values in litres. Airflow obstruction is present if the FEV1/FVC ratio is < 0.7 and the FEV1 is < 80% of the predicted value. A ratio of ≥ 0.7 is either normal or suggestive of a restrictive ventilatory defect.

    Fig 3
    Fig 3

    Volume time curves showing typical features of obstructive, restrictive, and mixed obstructive-restrictive ventilatory disorders

    Spirometry also allows patients with COPD to be categorised according to severity, and enables monitoring of changes in lung function over time and the response to treatment. If spirometric values return to normal after treatment then clinically significant COPD is not present.

    Categorisation of COPD severity by different guidelines

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    Reversibility testing

    Patients with COPD used to be categorised by their response to a therapeutic trial of corticosteroids. However, it is now known that an improvement in lung function after a short course of oral corticosteroids usually fails to predict future benefit from long term inhaled corticosteroids. Reversibility testing to oral corticosteroids or inhaled bronchodilator is not always necessary, but it should be performed if asthma is thought likely or if the response to treatment (β2 agonists or corticosteroids) is surprisingly good. However, asthma can often be distinguished from COPD by the history, examination, and baseline spirometry.

    More detailed lung function measurements such as lung volumes (total lung capacity and residual volume), gas transfer coefficient, and walking distance in six minutes can be done if diagnostic doubt persists or more thorough evaluation is required.

    Changes in lung function consistent with a diagnosis of asthma

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    Chest radiograph showing typical changes of COPD (hyperinflated lung fields, flat diaphragms, prominent pulmonary arteries, increased translucency of lung fields and “squared off” lung apices)

    Imaging

    At the time of diagnosis, arrange a chest radiograph in all patients. This is useful in excluding other conditions as a cause of respiratory symptoms and may show typical features of COPD. When there is diagnostic doubt or a surgical procedure is contemplated (such as lung volume reduction surgery or bullectomy) computed tomography of the chest is required.

    Other tests

    A full blood count should be arranged. This may show secondary polycythaemia, which can result from chronic hypoxaemia, and it is important to exclude anaemia as a cause of breathlessness. A raised eosinophil count suggests the possibility of an alternative diagnosis such as asthma.


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    Electrocardiogram showing typical changes in a patient with cor pulmonale secondary to advanced COPD (p-pulmonale, right axis deviation, partial right bundle branch block, dominant R wave in lead V1)

    In patients with signs of cor pulmonale, electrocardiography may show typical changes of chronic right sided heart strain. However, echocardiography is more sensitive in detecting tricuspid valve incompetence, as well as right atrial and ventricular hypertrophy, and may indirectly assess pulmonary artery pressure. It is also useful in determining whether left ventricular dysfunction is present, especially when the spirometric impairment is disproportional to the extent of breathlessness. Ischaemic heart disease may be the sole or contributory cause of breathlessness even in the absence of chest pain, and investigations should be tailored accordingly. Indeed, dyspnoea due to causes other than COPD should be considered when the extent of physical limitation seems disproportionate to the degree of airflow obstruction, or in patients with normal oxygen saturation who have little or no fall in levels during a six minute walk.

    Patients with a family history of COPD or in whom it presents at a young age (especially when smoking pack years are negligible) should have their α1 antitrypsin concentrations measured. If α1 antitrypsin deficiency is discovered, appropriate family screening and counselling is advised.

    Pulse oximetry is useful in most patients, especially those with advanced disease (such as FEV1 < 50% predicted) or polycythaemia, in order to check for significant hypoxaemia. Patients with a resting oxygen saturation of < 92% should have measurement of arterial blood gases and, where necessary and appropriate, be assessed for long term domiciliary or ambulatory oxygen therapy.

    Further reading

    The ABC of chronic obstructive pulmonary disease is edited by Graeme P Currie. The series will be published as a book by Blackwell Publishing in autumn 2006.

    Footnotes

    • Competing interests GPC has received funding for attending international conferences and honorariums for giving talks from pharmaceutical companies GlaxoSmithKline, Pfizer, and AstraZeneca.

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