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Spirometry
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A spirometer is a device to measure timed expired and inspired volumes, and hence indicate how quickly and effectively the lungs can be emptied and filled.
Spirometry can be used to screen for respiratory disease, diagnose obstructive airways disease and to monitor disease progression and rehabilitation/treatment gains. Vital capacity is a predictor of death from respiratory and cardiac disease and abnormal spirometry is associated with an increase in 'all-cause' mortality.1
It is the gold standard for the diagnosis, assessment and monitoring of chronic obstructive pulmonary disease (COPD) and is now the preferred method in adults for demonstrating airways obstruction in the diagnosis of asthma.2 The recommendation of national evidence-based guidelines for of asthma2 and COPD3 for the use of spirometers in diagnosis and monitoring, together with the their required use in the quality outcome framework of the GMS contract, has led to a large increase in the use of spirometry in primary care (70-80% UK practices in 20054).
Poorly performed spirometry produces misleading results and there have been some concerns regarding the validity of some primary care spirometry but studies incorporating training have found no differences between test results produced in primary care and in pulmonary function laboratories.5 Anyone performing spirometry should be fully trained and undertake regular updates. Quality audits should also be routine.
Many remember the large volume-displacement devices with bellows or water sealed bell beloved of physiology labs but the spirometers most commonly used in primary care are now electronic, flow-sensing devices:
- Small, hand-held devices that provide digital readings. These are the cheapest options (typically about £500) and will fit into a medical bag but do not provide a graphical display (spirogram) and therefore it may be difficult to judge when an expiration is complete. They also need to be used in combination with predicted charts and a calculator to interpret results.
- Portable meters with integrated printers. Typically more expensive than (1) but will provide calculations, spirograms to monitor the blow and a printout including a flow volume loop.
- Systems designed to work with a computer that will display a graph, make calculations of predicted values and reversibility and provide a print-out for records. They also enable tests to be e-mailed for a second opinion and for electronic storage.
Whatever equipment is used, devices should be regularly calibrated, maintained, cleaned and disinfected according to manufacturer's instructions. Disposable 'one-way' valved mouthpieces reduce the risk of cross infection (but prevent inspiratory flow-volume loops). Good practice should be to keep a calibration and maintenance log and list of patients tested with the spirometer (in case of unwitting testing of a patient with TB, for example, to enable contact tracing).
- Prior to testing, the patient's condition should be stable (i.e. at least 6 weeks since the last exacerbation).
- Standing is not mandatory but may provide better results. Sitting is safer for the elderly and infirm - if sitting, sit straight up, and keep head slightly extended.
- Breathe in maximally.
- Hold mouthpiece between teeth, then apply lips for an airtight seal.
- Breath out as hard and fast as possible. The patient should aim for maximal flow at the moment expiration starts. With handheld devices, watch the vane rotating, and make sure it does not start rotating while the spirometer is brought to the lips, thus avoiding artifacts.
- Keep breathing out until the lungs are 'empty'.
- Some get the users to practice just emptying their lungs; i.e. to do a slow vital capacity (SVC) before getting them to repeat the same as quickly as possible. This allows comparison of the SVC with the FVC and allows the user to discard poor attempts where the FVC is below the expiratory volume.
- Limit the total number of attempts (practice and recording) to eight.
Three satisfactory blows should be performed and best values taken for interpretation. Criteria for satisfactory blows are:
- The blow should continue until a volume plateau is reached - this may take more than 12 seconds in severe COPD.
- FVC and FEV1 readings should be within 5% or 100 ml.
- The expiratory volume-time graph should be smooth and free from irregularities.
Reversibility testing
- Perform baseline spirometry first.
- Bronchodilator reversibility testing: before undertaking bronchodilator testing, the patient should stop short acting beta2 agonists for 6 hours, long acting bronchodilators for 12 hours and theophyllines for 24 hours. Administer bronchodilator (at least 400 mcg salbutamol) and repeat spirometry after 15 minutes.
- Steroid reversibility testing: a steroid trial (30 mg prednisolone daily for 2 weeks or 200 mcg beclometasone or equivalent inhaled corticosteroid for 6-8 weeks) is undertaken.
| Reversibility - an increase of >400 ml from baseline in FEV1 is suggestive of asthma. Smaller increases are less discriminatory.2 |
| Measurement | Definition | Interpretation |
| Vital Capacity (VC) | Slow vital capacity (SVC) - maximal amount of air exhaled steadily from full inspiration to maximal expiration. Not time dependent. Forced vital capacity (FVC) - volume of lungs from full inspiration to forced maximal expiration. Expressed as a percentage of the predicted normal for a person. |
SVC should be >80% predicted, reduced in restrictive disease.
FVC is reduced in restrictive disease and also in obstructive disease if air-trapping occurs. |
| Forced expiratory volume in one second (FEV1) | Volume of air expelled in the first second of a forced expiration. | Reduced in both obstructive and restrictive disease. |
| Forced expiratory ratio (FER) % | (FEV1/FVC)x100 Percentage of FVC expelled in the first second of a forced expiration. |
Remains normal (or even elevated) in restrictive disease, reduced in obstructive disease. |
| Forced expiratory flow between 25-75%(FEF 25-75%) Also known as MMEF (maximum midexpiratory flow) |
Average expiratory flow rate in the middle part of a forced expiration. Is a sensitive indicator of what is happening in the middle and lower airways but is not as reproducible as FEV1. | Normal in restrictive disease. |
Abnormal spirometry is divided into restrictive and obstructive ventilatory patterns:
|
Always repeat a series of readings on another occasion before basing a diagnosis on spirometry. For a full assessment you need to:
- Consider the spirometry derived values: FEV1, FVC.
- Calculate the FEV1/FVC ratio.
- Compare these with the individual's predicted values (based on age, sex, race and height).
FEV1
FEV1 is strongly recommended as the measurement of choice in COPD as:
- It is reproducible and objective with well defined normal ranges.
- It can be measured quickly and easily at all stages of disease. In very advanced COPD, forced expiration may result in closing of airways and trapping of air, so relaxed vital capacity (SVC) may be a better measure of lung function.
- Variation on different occasions on the same patient is low (<170 ml).
- FEV1 is a good predictor of future morbidity and mortality, better than FEV1/VC.
- Serial measurements provide evidence of disease progression.
- Peak flow measurements do not distinguish between obstruction and restriction of airflow, and may seriously underestimate the degree of airway obstruction in COPD.
- In mild asthma, FEV1 is likely to show up the lesser degrees of airflow obstruction occurring later in the expiratory effort.
FVC
- There is likely to be a reduction in FVC in patients with moderate to severe COPD, which is caused by the alveolar damage and coalescence, together with loss of elasticity of the lung tissue.
- Patients with chronic asthma may have a reduction in FVC.
FEV1/FVC ratio
- A ratio of <70% implies obstructive disease.
- In the elderly, the FEV1/FVC may fall to <70% in the absence of airways obstruction so use tables to compare to predicted values, but in everyone, if the value is >70%, obstruction is effectively excluded.
- The hallmark of an obstructive defect is slowing of expiratory flow, so that a low proportion of the FVC is expired in the first second and the FEV1/FVC ratio is reduced.
- If the patient has a restrictive ventilatory defect the FEV1 and FVC are both reduced, but in proportion, so the FEV1/FVC ratio remains normal (greater than 75%).
- Restrictive ventilatory defects can be due to various intrapulmonary diseases, e.g. pulmonary fibrosis, pulmonary oedema, collapse or consolidation of the lung, but also importantly with extra-pulmonary conditions, e.g. large pleural effusion, rib cage deformity (scoliosis), after lung surgery and with weakness of the respiratory muscles. Clearly the measurements need to be interpreted in the clinical context and if a restrictive abnormality is discovered a chest x-ray is usually essential for interpretation.
Restrictive vs obstructive patterns - summary
Restrictive ventilatory pattern:
|
Flow volume loops
Flow volume loops show flow rate as the lung empties - the shape of the loop depends on the mechanical properties of the lung and different diagnoses provide different shaped loops:
- Normal - on exhalation there is a rapid rise to the maximal expiratory flow followed by a steady uniform decline until exhalation is complete.
- Asthma - typically the curve is a smooth concave shape as airway obstruction is relatively constant throughout expiration.
- COPD - typically the curve is angled or 'kinked' as COPD lungs collapse with forced expiration.
- Restrictive disease - the curve is typically a normal height but with a very steep gradient as the lung volume is diminished.
All patients with either suspected asthma or COPD should ideally have spirometry performed to aid initial diagnosis.
COPD 3
- A diagnosis of COPD should be considered in all patients over 35 years who smoke or have smoked and have chronic symptoms of breathlessness, cough and sputum.
- Symptoms may be accepted as a consequence of smoking and therefore medical help not sought or not apparent until significant airways obstruction is present (up to half of respiratory reserve may be lost prior to developing chronic symptoms).
- Early diagnosis with spirometry is vital - enabling the identification of susceptible patients, improve smoking cessation rates and prevent deterioration of patients identified with early COPD.
The grade of COPD is important in deciding on appropriate treatment for COPD patients:
- If patients have mild symptoms but their spirometry result confirms mild or moderate COPD then they might be more persuaded to stop smoking. Smoking cessation is the single most important intervention in controlling progression of COPD.
- All patients with COPD should have their FEV1 monitored annually to assess progression of their disease as the level of FEV1is related to complications such as development of respiratory failure or pulmonary hypertension. Serial measurements over a few years allow assessment of rate of decline of FEV 1, an indicator of mortality risk in COPD.
Grading of COPD
| COPD unlikely - FEV1 >80 % of predicted Mild airflow obstruction - FEV1 50-80% of predicted Moderate airflow obstruction - FEV1 30-49% of predicted Severe airflow obstruction FEV1 - <30% of predicted |
Asthma2
- Spirometry is now preferred over peak expiratory flow (PEF) measurement for confirmation of airways obstruction in the diagnosis of asthma in adults and children with an intermediate probability of asthma able to undertake it (children under 5 years are unsuitable for this form of testing and there is great variation in the 5-12 year range). It is felt to offer clearer identification of airways obstruction and to be less effort dependent.2 Spirometry may be normal in individuals currently asymptomatic and does not exclude asthma and should be repeated, ideally when symptomatic. However, a normal spirogram when symptomatic does make asthma an unlikely diagnosis.
- In those with evidence of airways obstruction and an intermediate probability of asthma, arrange reversibility testing and/or a treatment trial for a defined period.2 NICE guidance3 suggests that reversibility testing should not be routine if clinical features and spirometry are strongly suggestive of COPD.
- Slowly progressive respiratory symptoms in a middle-aged or elderly smoker are most likely due to COPD but it is not uncommon for patients to have both conditions - more likely if symptoms have onset prior to age of 35 years and have symptoms that vary in severity.
Document references
- Hole DJ, Watt GC, Davey-Smith G, et al; Impaired lung function and mortality risk in men and women: findings from the Renfrew and Paisley prospective population study. BMJ. 1996 Sep 21;313(7059):711-5; discussion 715-6. [abstract]
- British Guideline on the Management of Asthma, British Thoracic Society and SIGN (May 2008)
- Chronic obstructive pulmonary disease, NICE Clinical Guideline (2004); Management of chronic obstructive pulmonary disease in adults in primary and secondary care
- BTS COPD Consortium; Spirometry in practice (2nd edition). Practical guide to using spirometry in primary care. April 2005.; Very useful booklet guiding those new to the use of spirometry. Has training contact details.
- Schermer TR, Jacobs JE, Chavannes NH, et al; Validity of spirometric testing in a general practice population of patients with chronic obstructive pulmonary disease (COPD). Thorax. 2003 Oct;58(10):861-6. [abstract]
- GPIAG Opinion: Spirometry; Kaplan A, Pinnock H. Spirometry. Sept 2004. GPIAG Opinion 1(2); useful diagrams to guide interpretation
Internet and further reading
- Barreiro TJ, Perillo I An Approach to Interpreting Spirometry American Family Physician March 2004; (Contains Spirograms, Flow Volume Curves, FEV Values etc.)
- General Practice Airways Group; Home Page.
- Spirometry Handbook National Asthma Council, Australia. Revised 2004
- Global Initiative for chronic lung disease; collaboration of US National Heart, Lung and Blood Institute and WHO
- British Lung foundation
- Pierce R; Spirometry: an essential clinical measurement. Aust Fam Physician. 2005 Jul;34(7):535-9. [abstract]
DocID: 1322
Document Version: 22
DocRef: bgp25305
Last Updated: 23 Jul 2008
Review Date: 23 Jul 2010
The authors and editors of this article are employed to create accurate and up to date content reflecting reliable research evidence, guidance and best clinical practice. They are free from any commercial conflicts of interest. Find out more about updating.
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