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This PDF is a print-friendly reproduction of the content included in the Diagnosis Adults section of the
Australian Asthma Handbook at asthmahandbook.org.au/diagnosis/adults
Please note the content of this PDF reflects the Australian Asthma Handbook at publication of Version 1.2
(October 2016). For the most up-to-date content, please visit asthmahandbook.org.au
Please consider the environment if you are printing this PDF to save paper and ink, it has been designed
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CFC chlorofluorocarbon LAMA long-acting muscarinic antagonist
COPD chronic obstructive pulmonary disease LTRA leukotriene receptor antagonist
COX cyclo-oxygenase MBS Medical Benefits Scheme
ED emergency department NIPPV non-invasive positive pressure ventilation
EIB exercise-induced bronchoconstriction NSAIDs nonsteroidal anti-inflammatory drugs
FEV1 forced expiratory volume over one second OCS oral corticosteroids
FVC forced vital capacity OSA obstructive sleep apnoea
FSANZ Food Standards Australia and New Zealand PaCO carbon dioxide partial pressure on blood gas analysis
GORD gastro-oesophageal reflux disease PaO oxygen partial pressure on blood gas analysis
HFA formulated with hydrofluroalkane propellant PBS Pharmaceutical Benefits Scheme
ICS inhaled corticosteroid PEF peak expiratory flow
ICU intensive care unit pMDI pressurised metered-dose inhaler or 'puffer'
IgE Immunoglobulin E SABA short-acting beta2 -adrenergic receptor agonist
IV intravenous LAMA long-acting muscarinic antagonist
LABA long-acting beta2-adrenergic receptor agonist TGA Therapeutic Goods Administration
ABN 61 058 044 634 The Australian Asthma Handbook has been officially
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Tel: 03 9929 4333
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Email: nac@nationalasthma.org.au Association (APNA)
Website: nationalasthma.org.au The Thoracic Society of Australia and New
Zealand (TSANZ)
National Asthma Council Australia. Australian Asthma National Asthma Council Australia would like to
Handbook, Version 1.2. National Asthma Council acknowledge the support of the sponsors of
Australia, Melbourne, 2016. Version 1.2 of the Australian Asthma Handbook:
The Australian Asthma Handbook has been compiled by the The information and treatment protocols contained in the
National Asthma Council Australia for use by general Australian Asthma Handbook are intended as a general guide only
practitioners, pharmacists, asthma educators, nurses and other and are not intended to avoid the necessity for the individual
health professionals and healthcare students. The information examination and assessment of appropriate courses of treatment
and treatment protocols contained in the Australian Asthma on a case-by-case basis. To the maximum extent permitted by law,
Handbook are based on current evidence and medical knowledge acknowledging that provisions of the Australia Consumer Law may
and practice as at the date of publication and to the best of our have application and cannot be excluded, the National Asthma
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preparation of the Australian Asthma Handbook, the National affiliates exclude liability (including but not limited to liability for any
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HOME > DIAGNOSIS > ADULTS
history
physical examination
considering other diagnoses
documenting variable airflow limitation.
In some patients, observing a response to treatment may help confirm the diagnosis, but lack of response to bronchodilators
or to inhaled corticosteroids does not rule out asthma.
In this section
Initial investigations
History, physical examination and lung function testing in the investigation of asthma-like symptoms
https://www.asthmahandbook.org.au/diagnosis/adults/initial-investigations
Alternative diagnoses
Considering features that increase or decrease the probability of asthma
https://www.asthmahandbook.org.au/diagnosis/adults/alternative-diagnoses
Starting treatment
Reviewing the response to treatment to help confirm the diagnosis
https://www.asthmahandbook.org.au/diagnosis/adults/starting-treatment
Further investigations
Conducting further investigations if indicated
https://www.asthmahandbook.org.au/diagnosis/adults/further-investigations
1
Figure. Steps in the diagnosis of asthma in adults
Asset ID: 4
2
HOME > DIAGNOSIS > ADULTS > INITIAL INVESTIGATIONS
History
Taking a history to investigate asthma-like symptoms in adults and adolescents
https://www.asthmahandbook.org.au/diagnosis/adults/initial-investigations/history
Physical examination
Performing a physical examination to investigate asthma-like symptoms in adults and adolescents
https://www.asthmahandbook.org.au/diagnosis/adults/initial-investigations/physical-examination
Lung function
Assessing lung function to investigate asthma-like symptoms in adults and adolescents
https://www.asthmahandbook.org.au/diagnosis/adults/initial-investigations/lung-function
3
HOME > DIAGNOSIS > ADULTS > INITIAL INVESTIGATIONS > HISTORY
episodic breathlessness
wheezing
chest tightness
cough.
Ask about:
When respiratory symptoms are not typical, do not rule out the possibility of asthma without doing spirometry, because
symptoms of asthma vary widely from person to person.
4
HOME > DIAGNOSIS > ADULTS > INITIAL INVESTIGATIONS > PHYSICAL EXAMINATION
Perform a physical examination, including chest auscultation and inspection of upper respiratory tract for signs of
allergic rhinitis.
Do not rule out the possibility of asthma without doing spirometry, because physical examination may be normal when
symptoms are absent and this does not exclude a diagnosis of asthma.
More information
High-pitched stridor is commonly mistaken for wheezing in people with upper airway dysfunction.2However, careful
2
auscultation will reveal that the sound is localised to theupper airway(not peripheral airway expiratory wheezing).
Crackles on chest auscultation indicate an alternate or concurrent diagnosis.
References
1. Aaron SD, Vandemheen KL, Boulet LP, et al. Overdiagnosis of asthma in obese and nonobese adults. CMAJ. 2008;
179: 1121-1131. Available from: http://www.cmaj.ca/content/179/11/1121.full
2. Morris MJ, Christopher KL. Diagnostic criteria for the classification of vocal cord dysfunction. Chest. 2010; 138:
1213-23. Available from: http://journal.publications.chestnet.org/article.aspx?articleid=1045155
5
HOME > DIAGNOSIS > ADULTS > INITIAL INVESTIGATIONS > LUNG FUNCTION
Measure bronchodilator reversibility by performing spirometry before and after administration of a rapid-onset beta2
agonist bronchodilator (e.g. 4puffs of salbutamol 100mcg/actuation via pressurised metered-dose inhaler and spacer).
Notes
Airflow limitation is defined as reversible (i.e. bronchodilator response is clinically important) if FEV1 increases by 200mL and 12%.
Failure to demonstrate reversible airflow limitation after bronchodilator (bronchodilator reversibility) does not exclude asthma, and
its presence does not prove asthma the pattern of symptoms and other clinical features must also be considered.
Record the ratio of FEV1 to FVC (FEV1/FVC). Before making the diagnosis of asthma, confirm that FEV1/FVC is reduced
(less than the lower limit of normal for age) at a time when FEV1 is lower than predicted.
Note: If the spirometer does not provide lower limit of normal for age, use the follow age-based cut-points to indicate expiratory
airflow limitation in adults and older adolescents:
National Heart Lung and Blood Institute (NHLBI) National Asthma Education and Prevention Program, 20071
Johns and Pierce, 20112
Quanjer et al.20123
6
If a patient shows some improvement in FEV1 after bronchodilator, but does not meet criteria for reversibleairflow
limitation,consider other investigations. If necessary, repeat spirometry after a treatment trial of 46 weeks with
regular low-dose inhaled corticosteroid plus short-acting beta2 agonist as needed, to see if there is a significant
improvement in symptoms and lung function.
Note: Airflow limitation can be transient (e.g. when recorded during a severe acute infection of the respiratory tract) and does not
necessarily mean that the person has chronic asthma. Ideally, airflow limitation should be confirmed when the patient does not have a
respiratory tract infection.
Hand-held lung function-measuring devices (designed to measure FEV1 and/or FEV6, but not FVC) can be used in COPD
case-finding and may also be useful in asthma case-finding, but must not be relied on either for ruling out asthma or
when making a definitive diagnosis of asthma, because there is not enough evidence and validated protocols have not
been developed.
Do not use peak flow meters in place of spirometry for diagnosing asthma.
More information
Sit upright with legs uncrossed and feet flat on the floor and do not lean forward.
Breathe in rapidly until lungs feel absolutely full. (Coaching is essential to do this properly.)
Do not pause formorethan 1 second.
Place mouthpiece in mouth and close lips to form a tight seal.
Blast air out as hard and fast as possible and for as long as possible, until the lungs are completely empty or you are
unable to blow out any longer.
Remove mouthpiece.
Go to: National Asthma Council Australia'sspirometry technique video, Performing spirometry inprimary care
Repeat the test until you obtain three acceptable tests and these meet repeatability criteria.
7
Acceptability of test
A test is acceptable if all the following apply:
Record the highest FEV1 and FVC result from the three acceptable tests, even if they come from separate blows.2
Repeatability criteria
Repeatability criteria for a set of acceptable tests are met if both of the following apply:4
the difference between the highest and second-highest values for FEV1 is less than 150 mL
the difference between the highest and second-highest values for FVC is less than 150 mL.
For most people, it is not practical to make more than eight attempts to meet acceptability and repeatability criteria.2
Testing bronchodilator response (reversibility of airflow limitation)
Repeat spirometry 10-15 minutes after giving 4 separate puffs of salbutamol (100 mcg/actuation) via a pressurised
metered-dose inhaler and spacer.2 (For patients who have reported unacceptable side-effects with 400 mcg, 2 puffs can
be used.)
For adults and adolescents, record a clinically important bronchodilator response if FEV1 increases by 200 mL and
12%.2
For children, record a clinically important bronchodilator response if FEV1 increases by
12%.2
improvement in peak expiratory flow rate of at least 60 mL/min (or at least 20%) after inhaling a short-acting beta2
agonist bronchodilator, compared with baseline measure
diurnal variation in peak expiratory flow rate of more than 10% with twice-daily readings.
8
Most of the tests for variable expiratory airflow limitation are based on showing variability in FEV1. While reduced FEV1
may be seen with many other lung diseases (or due to poor spirometric technique), a reduced ratio of FEV1 to FVC
indicates airflow limitation.8Normal FEV1/FVC values derived from population studies vary,1,3but are usually greater
than:1
In children, it is less useful to define expiratory airflow limitation according to a specific cut-off for FEV1/FVC ratio,
because normal values in children change considerably with age.3
Some spirometers provide predicted normal values specific to age group. If these are available, a FEV1/FVC ratio less than
the lower limit of normal (i.e. less than the 5th percentile of normal population) indicates airflow limitation.
Variableexpiratory airflow limitation (beyond the range seen in healthy populations) can be documented if any of the
following are recorded:
a clinically important increase in FEV1 (change in FEV1 of at least 200mL and 12% from baseline for adults, or at least
12% from baseline for children) 1015 minutes after administration of bronchodilator
clinically important variation in lung function (at least 20% change in FEV1) when measured repeatedly over time (e.g.
spirometry on separate visits)
a clinically important reduction in lung function (decrease in FEV1 of at least 200mL and 12% from baseline on
spirometry, or decrease in peak expiratory flow rate by at least 20%) after exercise(formal laboratory-based exercise
challenge testing uses different criteria for exercise-induced bronchoconstriction)
a clinically important increase in lung function (at least 200mL and 12% from baseline) after a trial of 4 or moreweeks
of treatment with an inhaled corticosteroid
clinically importantvariation in peak expiratory flow (diurnal variability of more than 10%)
a clinically important reduction in lung function (1520%, depending on the test)during a test for airway
hyperresponsiveness (exercise challenge test or bronchial provocation test) measured by a respiratory function
laboratory.
Notes
Patients referred to a respiratory function laboratory may be asked not to take certain medicines within a few hours to days before a
spirometry visit.
A clinically important increase or decrease in lung function is defined as a change in FEV1of at least 200mL and 12% from baseline for
adults, or at least 12% from baseline for children, or a change in peak expiratory flow rate of at least 20% on the same meter.5,8 A
clinically important increase in FVC after administering bronchodilator may also indicate reversible airflow limitation, but FVC is a less
reliable measure in primary care because FVC may varydue to factors such as variation in inspiratory volume or expiratory time.
The finding of normal lung function during symptoms reduces the probability that a patient has asthma, but a clinically important
improvement in response to bronchodilator or inhaled corticosteroid can occur in patients whose baseline value is within the predicted
normal range.
The greater the variation in lung function, the more certain is the diagnosis of asthma. However, people with longstanding asthma may
develop fixed airflow limitation.
Reversibility in airflow limitation may not be detected if the person is already taking a long-acting beta2agonist or inhaled
corticosteroid.
Airflow limitation can be transient and does not necessarily mean that the person has asthma (e.g. when recorded during a severe
acuteinfection of the respiratory tract). Ideally, airflow limitation should be confirmed when the patient does not have a respiratory
tract infection. Reduction in lung function during a respiratory tract infection with improvement in lung function after its resolution,
commonly occurs in people with asthma, but can also be seen in patients with COPD or in healthy people without either asthma or
COPD.9,10
References
1. National Heart Lung and Blood Institute (NHLBI) National Asthma Education and Prevention Program. Expert Panel
Report 3: guidelines for the diagnosis and management of asthma. Full report 2007. US Department of Health and Human
Services National Institutes of Health, Bethesda, 2007. Available from: http://www.nhlbi.nih.gov/health-
pro/guidelines/current/asthma-guidelines/full-report
9
2. Johns DP, Pierce R. Pocket guide to spirometry. 3rd edn. McGraw Hill, North Ryde, 2011.
3. Quanjer PH, Stanojevic S, Cole TJ, et al. Multi-ethnic reference values for spirometry for the 3-95-yr age range: the
global lung function 2012 equations. Eur Respir J. 2012; 40: 1324-43. Available from:
http://www.ncbi.nlm.nih.gov/pubmed/22743675
4. Miller MR, Hankinson J, Brusasco V, et al. Standardisation of spirometry. Eur Respir J. 2005; 26: 319-338. Available
from: http://erj.ersjournals.com/content/26/2/319
5. Levy ML, Quanjer PH, Booker R, et al. Diagnostic Spirometry in Primary Care: Proposed standards for general
practice compliant with American Thoracic Society and European Respiratory Society recommendations. Prim Care
Respir J. 2009; 18: 130-147. Available from: http://www.ncbi.nlm.nih.gov/pubmed/19684995
6. National Asthma Council Australia. Asthma and lung function tests. An information paper for health professionals.
National Asthma Council Australia, Melbourne, 2012. Available from:
http://www.nationalasthma.org.au/publication/asthma-lung-function-tests-hp
7. Global Initiative for Asthma (GINA). Global strategy for asthma management and prevention. GINA, 2012. Available
from: http://www.ginasthma.org
8. Pellegrino R, Viegi G, Brusasco V, et al. Interpretative strategies for lung function tests. Eur Respir J. 2005; 26: 948-
968. Available from: http://erj.ersjournals.com/content/26/5/948
9. Collier AM, Pimmel RL, Hasselblad V, et al. Spirometric changes in normal children with upper respiratory infections.
Am Rev Respir Dis. 1978; 117: 47-53. Available from: http://www.ncbi.nlm.nih.gov/pubmed/619724
10. Melbye H, Kongerud J, Vorland L. Reversible airflow limitation in adults with respiratory infection. Eur Respir J. 1994;
7: 1239-1245. Available from: http://www.ncbi.nlm.nih.gov/pubmed/7925901
10
HOME > DIAGNOSIS > ADULTS > ALTERNATIVE DIAGNOSES
Asthma is more likely to explain the symptoms if Asthma is less likely to explain the symptoms if any
any of these apply of these apply
Symptoms worse at night or in the early morning Symptoms only present during upper respiratory
tract infections
History of allergies (e.g. allergic rhinitis, atopic
dermatitis) Heavy smoker (now or in past)
11
Adapted from:
Respiratory Expert Group, Therapeutic Guidelines Limited. Therapeutic Guidelines: Respiratory, Version 4. Therapeutic
Guidelines Limited, Melbourne,2009.
British Thoracic Society (BTS) Scottish Intercollegiate Guidelines Network (SIGN). British Guideline on the Management
of Asthma. A national clinical guideline. BTS/SIGN, Edinburgh; 2012. Available from: https://www.brit-
thoracic.org.uk/guidelines-and-quality-standards/asthma-guideline/.
Asset ID: 2
Consider the possibility of upper airway dysfunction when FEV1/FVC ratio on spirometry is normal or when symptoms
of breathlessness or wheeze do not improve after taking short acting beta2 agonist.
Benningeret al.2011 1
2
Deckert and Deckert, 2010
Weinberger and Abu-Hasan, 20073
Morris and Christopher, 20104
Kenn and Balkissoon, 20115
Investigate cough thoroughly if there are findings that might indicate a serious alternative or comorbid diagnosis.
Gibson et al.20106
If airflow limitation is not completely reversible, consider the possibility of COPD as an alternative diagnosis or a
coexisting diagnosis (including asthma-COPD overlap), especially in smokers and ex-smokers over 35 years old and in
people over 65 years old.
Abramsonet al.20127
Consider the possibility of adult-onset asthma in people with dyspnoea, wheeze or cough, even if they have no previous
diagnosis of asthma.
12
More information
Upper airway dysfunction can coexist with asthma.1 People with asthma who also have upper airway dysfunction
experience more symptoms than those with asthma alone and this can result in over-treatment if vocal cord dysfunction
is not identified and managed appropriately.1
Upper airway dysfunction probably has multiple causes.1 In some people it is probably due to hyperresponsiveness of the
larynx in response to intrinsic and extrinsic triggers.1,8 Triggers can include exercise, psychological conditions, airborne
irritants, rhinosinusitis, gastro-esophageal reflux disease, and medicines.2,4
Upper airway dysfunction should be considered when spirometry shows normal FEV1/FVC ratio ina patient with
suspected asthma4 or symptoms do not respond to short-acting beta2 agonist reliever. The shape of the maximal
respiratory flow loop obtained by spirometry may suggest the diagnosis.3 Direct observation of the vocal cordsis the best
method to confirm the diagnosis of upper airway dysfunction.1
For information on diagnosis and management of COPD, refer to the COPD-X Concise Guide for Primary Care.10
The Global Initiative for Asthma (GINA) and Global Initiative Obstructive Lung Disease (GOLD) recommend the following
stepwise approach for adults presenting with respiratory symptoms:11
1. Identify whether the patient has clinical features of, or is at risk of, chronic airway disease. This may be suggested
by the clinical history and physical examination.
2. Identify features that favour a diagnosis of typical asthma or typical COPD. If several features of both are present,
asthma-COPD overlap is likely.
3. Perform spirometry to confirm airflow limitation.
4. Start treatment, selected according to whether the assessment favoured the single diagnosis of asthma, the single
diagnosis of COPD, or asthma-COPD overlap.
5. Refer for specialist assessment and other investigations, if necessary.
cough is episodic
cough with exercise is associated with other symptoms that suggest airflow limitation(expiratory wheeze or
breathlessness)
spirometry confirms reversible airflow limitation.
13
If cough is due to asthma, it should respond to treatment with an inhaled corticosteroid preventer taken regularly and
reliever as needed).6
Findings that suggest a serious alternative or comorbid diagnosis that requires further investigationinclude:6
haemoptysis
smoker with > 20 packyear smoking history
smoker aged over 45 years with a new cough, altered cough, or cough with voice disturbance
prominent dyspnoea, especially at rest or at night
substantial sputum production
hoarseness
fever
weight loss
complicated gastro-oesophageal reflux disease
swallowing disorders with choking or vomiting
recurrent pneumonia
abnormal clinical respiratory examination.
Sit upright with legs uncrossed and feet flat on the floor and do not lean forward.
Breathe in rapidly until lungs feel absolutely full. (Coaching is essential to do this properly.)
Do not pause formorethan 1 second.
Place mouthpiece in mouth and close lips to form a tight seal.
Blast air out as hard and fast as possible and for as long as possible, until the lungs are completely empty or you are
unable to blow out any longer.
Remove mouthpiece.
Go to: National Asthma Council Australia'sspirometry technique video, Performing spirometry inprimary care
Repeat the test until you obtain three acceptable tests and these meet repeatability criteria.
Acceptability of test
A test is acceptable if all the following apply:
Record the highest FEV1 and FVC result from the three acceptable tests, even if they come from separate blows.14
Repeatability criteria
Repeatability criteria for a set of acceptable tests are met if both of the following apply:12
the difference between the highest and second-highest values for FEV1 is less than 150 mL
the difference between the highest and second-highest values for FVC is less than 150 mL.
14
For most people, it is not practical to make more than eight attempts to meet acceptability and repeatability criteria.14
Testing bronchodilator response (reversibility of airflow limitation)
Repeat spirometry 10-15 minutes after giving 4 separate puffs of salbutamol (100 mcg/actuation) via a pressurised
metered-dose inhaler and spacer.14 (For patients who have reported unacceptable side-effects with 400 mcg, 2 puffs can
be used.)
For adults and adolescents, record a clinically important bronchodilator response if FEV1 increases by 200 mL and
12%.14
For children, record a clinically important bronchodilator response if FEV1 increases by
12%.14
References
1. Benninger C, Parsons JP, Mastronarde JG. Vocal cord dysfunction and asthma. Curr Opin Pulm Med. 2011; 17: 45-49.
Available from: http://www.ncbi.nlm.nih.gov/pubmed/21330824
2. Deckert J, Deckert L. Vocal cord dysfunction. Am Fam Physician. 2010; 81: 156-159. Available from:
http://www.aafp.org/afp/2010/0115/p156.html
3. Weinberger M, Abu-Hasan M. Pseudo-asthma: when cough, wheezing, and dyspnea are not asthma. Pediatrics. 2007;
120: 855-864. Available from: http://pediatrics.aappublications.org/content/120/4/855.full
4. Morris MJ, Christopher KL. Diagnostic criteria for the classification of vocal cord dysfunction. Chest. 2010; 138:
1213-23. Available from: http://journal.publications.chestnet.org/article.aspx?articleid=1045155
5. Kenn K, Balkissoon R. Vocal cord dysfunction: what do we know?. Eur Respir J. 2011; 37: 194-200. Available from:
http://erj.ersjournals.com/content/37/1/194.long
6. Gibson PG, Chang AB, Glasgow NJ, et al. CICADA: cough in children and adults: diagnosis and assessment. Australian
cough guidelines summary statement. Med J Aust. 2010; 192: 265-271. Available from:
http://www.lungfoundation.com.au/professional-resources/guidelines/cough-guidelines
7. Abramson MJ, Crockett AJ, Dabscheck E, et al. The COPD-X Plan: Australian and New Zealand guidelines for the
management of chronic obstructive pulmonary disease. Version 2.34. The Australian Lung Foundation and The Thoracic
Society of Australia and New Zealand, 2012. Available from: http://www.copdx.org.au/
8. Gimenez LM, Zafra H. Vocal cord dysfunction: an update. Ann Allergy Asthma Immunol. 2011; 106: 267-274. Available
from: http://www.ncbi.nlm.nih.gov/pubmed/21457874
9. Gibson PG, McDonald VM, Marks GB. Asthma in older adults. Lancet. 2010; 376: 803-813. Available from:
http://www.ncbi.nlm.nih.gov/pubmed/20816547
10. Abramson M, Frith P, Yang I, et al. COPD-X Concise Guide for Primary Care. Lung Foundation Australia, Brisbane, 2016.
Available from: http://lungfoundation.com.au/health-professionals/guidelines/copd/copd-x-concise-guide-for-
primary-care/
11. Global Initiative for Asthma (GINA). Global strategy for asthma management and prevention. GINA, 2016. Available
from: http://ginasthma.org/
12. Miller MR, Hankinson J, Brusasco V, et al. Standardisation of spirometry. Eur Respir J. 2005; 26: 319-338. Available
from: http://erj.ersjournals.com/content/26/2/319
13. Levy ML, Quanjer PH, Booker R, et al. Diagnostic Spirometry in Primary Care: Proposed standards for general
practice compliant with American Thoracic Society and European Respiratory Society recommendations. Prim Care
Respir J. 2009; 18: 130-147. Available from: http://www.ncbi.nlm.nih.gov/pubmed/19684995
14. Johns DP, Pierce R. Pocket guide to spirometry. 3rd edn. McGraw Hill, North Ryde, 2011.
15
HOME > DIAGNOSIS > ADULTS > MAKING THE DIAGNOSIS
Asthma is more likely to explain the symptoms if Asthma is less likely to explain the symptoms if any
any of these apply of these apply
Symptoms worse at night or in the early morning Symptoms only present during upper respiratory
Adapted from:
Respiratory Expert Group, Therapeutic Guidelines Limited. Therapeutic Guidelines: Respiratory, Version 4. Therapeutic
Guidelines Limited, Melbourne,2009.
British Thoracic Society (BTS) Scottish Intercollegiate Guidelines Network (SIGN). British Guideline on the Management
of Asthma. A national clinical guideline. BTS/SIGN, Edinburgh; 2012. Available from: https://www.brit-
thoracic.org.uk/guidelines-and-quality-standards/asthma-guideline/.
16
Asset ID: 2
The person has a history of variable symptoms (especially cough, chest tightness, wheeze and shortness of breath).
Expiratory airflow limitation has been demonstrated (FEV1/FVC less thanlower limit of normal for age).
Expiratory airflow limitation has been shown to be variable.
There are no findings that suggest an alternative diagnosis.
Note: If the spirometer does not provide lower limit of normal for age, use the follow age-based cut-points to indicate expiratory
airflow limitation in adults and older adolescents:
If a patients asthma has been diagnosed elsewhere (e.g. in a new patient reporting the diagnosis of asthma), try to
confirm the diagnosis whether or not the person has current symptoms, and whether or not the person is taking
asthma medicines.
More information
17
In children, it is less useful to define expiratory airflow limitation according to a specific cut-off for FEV1/FVC ratio,
because normal values in children change considerably with age.5
Some spirometers provide predicted normal values specific to age group. If these are available, a FEV1/FVC ratio less than
the lower limit of normal (i.e. less than the 5th percentile of normal population) indicates airflow limitation.
Variableexpiratory airflow limitation (beyond the range seen in healthy populations) can be documented if any of the
following are recorded:
a clinically important increase in FEV1 (change in FEV1 of at least 200mL and 12% from baseline for adults, or at least
12% from baseline for children) 1015 minutes after administration of bronchodilator
clinically important variation in lung function (at least 20% change in FEV1) when measured repeatedly over time (e.g.
spirometry on separate visits)
a clinically important reduction in lung function (decrease in FEV1 of at least 200mL and 12% from baseline on
spirometry, or decrease in peak expiratory flow rate by at least 20%) after exercise(formal laboratory-based exercise
challenge testing uses different criteria for exercise-induced bronchoconstriction)
a clinically important increase in lung function (at least 200mL and 12% from baseline) after a trial of 4 or moreweeks
of treatment with an inhaled corticosteroid
clinically importantvariation in peak expiratory flow (diurnal variability of more than 10%)
a clinically important reduction in lung function (1520%, depending on the test)during a test for airway
hyperresponsiveness (exercise challenge test or bronchial provocation test) measured by a respiratory function
laboratory.
Notes
Patients referred to a respiratory function laboratory may be asked not to take certain medicines within a few hours to days before a
spirometry visit.
A clinically important increase or decrease in lung function is defined as a change in FEV1of at least 200mL and 12% from baseline for
6,3
adults, or at least 12% from baseline for children, or a change in peak expiratory flow rate of at least 20% on the same meter. A
clinically important increase in FVC after administering bronchodilator may also indicate reversible airflow limitation, but FVC is a less
reliable measure in primary care because FVC may varydue to factors such as variation in inspiratory volume or expiratory time.
The finding of normal lung function during symptoms reduces the probability that a patient has asthma, but a clinically important
improvement in response to bronchodilator or inhaled corticosteroid can occur in patients whose baseline value is within the predicted
normal range.
The greater the variation in lung function, the more certain is the diagnosis of asthma. However, people with longstanding asthma may
develop fixed airflow limitation.
Reversibility in airflow limitation may not be detected if the person is already taking a long-acting beta2agonist or inhaled
corticosteroid.
Airflow limitation can be transient and does not necessarily mean that the person has asthma (e.g. when recorded during a severe
acuteinfection of the respiratory tract). Ideally, airflow limitation should be confirmed when the patient does not have a respiratory
tract infection. Reduction in lung function during a respiratory tract infection with improvement in lung function after its resolution,
commonly occurs in people with asthma, but can also be seen in patients with COPD or in healthy people without either asthma or
7,8
COPD.
Sit upright with legs uncrossed and feet flat on the floor and do not lean forward.
Breathe in rapidly until lungs feel absolutely full. (Coaching is essential to do this properly.)
18
Do not pause formorethan 1 second.
Place mouthpiece in mouth and close lips to form a tight seal.
Blast air out as hard and fast as possible and for as long as possible, until the lungs are completely empty or you are
unable to blow out any longer.
Remove mouthpiece.
Go to: National Asthma Council Australia'sspirometry technique video, Performing spirometry inprimary care
Repeat the test until you obtain three acceptable tests and these meet repeatability criteria.
Acceptability of test
A test is acceptable if all the following apply:
Record the highest FEV1 and FVC result from the three acceptable tests, even if they come from separate blows.10
Repeatability criteria
Repeatability criteria for a set of acceptable tests are met if both of the following apply:9
the difference between the highest and second-highest values for FEV1 is less than 150 mL
the difference between the highest and second-highest values for FVC is less than 150 mL.
For most people, it is not practical to make more than eight attempts to meet acceptability and repeatability criteria.10
Testing bronchodilator response (reversibility of airflow limitation)
Repeat spirometry 10-15 minutes after giving 4 separate puffs of salbutamol (100 mcg/actuation) via a pressurised
metered-dose inhaler and spacer.10 (For patients who have reported unacceptable side-effects with 400 mcg, 2 puffs can
be used.)
For adults and adolescents, record a clinically important bronchodilator response if FEV1 increases by 200 mL and
12%.10
For children, record a clinically important bronchodilator response if FEV1 increases by
12%.10
Asthma is more likely to explain the symptoms if Asthma is less likely to explain the symptoms if
any of these apply any of these apply
19
Asthma is more likely to explain the symptoms if Asthma is less likely to explain the symptoms if
any of these apply any of these apply
Symptoms worse at night or in the early morning Symptoms only present during upper respiratory
Adapted from:
Respiratory Expert Group, Therapeutic Guidelines Limited. Therapeutic Guidelines: Respiratory, Version 4. Therapeutic
Guidelines Limited, Melbourne,2009.
British Thoracic Society (BTS) Scottish Intercollegiate Guidelines Network (SIGN). British Guideline on the Management
of Asthma. A national clinical guideline. BTS/SIGN, Edinburgh; 2012. Available from: https://www.brit-
thoracic.org.uk/guidelines-and-quality-standards/asthma-guideline/.
Asset ID: 2
Although untreated asthma is usually characterised by airway hyperresponsiveness and airway inflammation
(eosinophilic and/or neutrophilic), these features are not essential for making the diagnosis of asthma in clinical practice.
The evidence for asthma must be documented at the time of diagnosis, because characteristic clinical, physiological and
pathological features may improve spontaneously or with treatment, and because fixed(irreversible or incompletely
reversible)airflow limitation may develop over time. It is often difficult to confirm the diagnosis of asthma after a patient
has been started on preventertreatment.
References
1. Respiratory Expert Group, Therapeutic Guidelines Limited. Therapeutic Guidelines: Respiratory, Version 4. Therapeutic
Guidelines Limited, West Melbourne, 2009.
2. British Thoracic Society (BTS), Scottish Intercollegiate Guidelines Network (SIGN). British Guideline on the
Management of Asthma. A national clinical guideline. BTS, SIGN, Edinburgh, 2012. Available from: https://www.brit-
thoracic.org.uk/guidelines-and-quality-standards/asthma-guideline/
3. Pellegrino R, Viegi G, Brusasco V, et al. Interpretative strategies for lung function tests. Eur Respir J. 2005; 26: 948-
968. Available from: http://erj.ersjournals.com/content/26/5/948
4. National Heart Lung and Blood Institute (NHLBI) National Asthma Education and Prevention Program. Expert Panel
Report 3: guidelines for the diagnosis and management of asthma. Full report 2007. US Department of Health and Human
Services National Institutes of Health, Bethesda, 2007. Available from: http://www.nhlbi.nih.gov/health-
pro/guidelines/current/asthma-guidelines/full-report
20
5. Quanjer PH, Stanojevic S, Cole TJ, et al. Multi-ethnic reference values for spirometry for the 3-95-yr age range: the
global lung function 2012 equations. Eur Respir J. 2012; 40: 1324-43. Available from:
http://www.ncbi.nlm.nih.gov/pubmed/22743675
6. Levy ML, Quanjer PH, Booker R, et al. Diagnostic Spirometry in Primary Care: Proposed standards for general
practice compliant with American Thoracic Society and European Respiratory Society recommendations. Prim Care
Respir J. 2009; 18: 130-147. Available from: http://www.ncbi.nlm.nih.gov/pubmed/19684995
7. Collier AM, Pimmel RL, Hasselblad V, et al. Spirometric changes in normal children with upper respiratory infections.
Am Rev Respir Dis. 1978; 117: 47-53. Available from: http://www.ncbi.nlm.nih.gov/pubmed/619724
8. Melbye H, Kongerud J, Vorland L. Reversible airflow limitation in adults with respiratory infection. Eur Respir J. 1994;
7: 1239-1245. Available from: http://www.ncbi.nlm.nih.gov/pubmed/7925901
9. Miller MR, Hankinson J, Brusasco V, et al. Standardisation of spirometry. Eur Respir J. 2005; 26: 319-338. Available
from: http://erj.ersjournals.com/content/26/2/319
10. Johns DP, Pierce R. Pocket guide to spirometry. 3rd edn. McGraw Hill, North Ryde, 2011.
21
HOME > DIAGNOSIS > ADULTS > STARTING TREATMENT
After making the diagnosis of asthma, begin treatment for 46 weeks with either of the following:
Table. Initial treatment choices (adults and adolescents not already using a preventer)
Symptoms twice per month or more Regular ICS starting at a low Montelukast
dose (plus SABA as needed)
Cromones
Waking due to asthma symptoms at Regular ICS starting at a low If patient also has frequent
least once during the past month dose (plus SABA as needed) daytime symptoms consider
either of:
22
Clinical situation Suggested starting regimen Alternative options and notes
Patient not currently taking a Regular ICS (plus SABA as Consider (private prescription)
preventerwhose symptoms are needed) combination ICS/LABA#
severely uncontrolled or very
For very uncontrolled asthma at
troublesome
presentation (e.g. frequent night
waking, low lung function),
consider (either of):
When prescribing inhaled asthma medicines, take into account the persons preferences, ability to use the device,
and cost issues.
Requires multiple daily doses and daily maintenance of inhaler.
PBS status as at October 2016: Montelukast treatment is not subsidised by the PBS for people aged 15 years or over.
Special Authority is available for Department of Veterans Affairs gold card holders or white card holders with
approval for asthma treatments.
# PBS status as at October 2016: ICS/LABA combination therapy as first-line preventer treatment is not subsidised by
the PBS, except for patients with frequent symptoms while taking oral corticosteroids.
Asset ID: 32
Arrange to check response to treatment after 46 weeks. Depending on the severity of initial symptoms, consider also
monitoring progress and clinical signs during the treatment trial.
Asset ID: 36
23
Note: Although response to initial asthma treatment supports the diagnosis of asthma, respiratory symptoms and low lung function
may improve spontaneously (e.g. if they were due to a respiratory infection). Conversely, lack of response to treatment does not
necessarily rule out asthma.
Also consider a treatment trial if asthma is strongly suspected butspirometry before and after bronchodilator does not
demonstrate clinically important reversible airflow limitation (change in FEV1 of at least 200 mL and 12% from baseline)
and other investigations have not confirmed variable airflow limitation.
If there is no clear response to initial treatment, after confirming correct inhaler technique and good adherence,
consider further investigations or referral to confirm or exclude the diagnosis of asthma.
Table. Conditions that can be confused with asthma in adults and adolescents
Gastro-oesophageal reflux
Bronchiectasis
Pulmonary fibrosis
Habit-cough syndrome
Respiratory infections
COPD
Hyperventilation
24
Conditions characterised by cough
Anxiety
Pulmonary hypertension
Lung cancer
Sources
Therapeutic Guidelines Limited. Therapeutic Guidelines: respiratory. Version 4. West Melbourne: Therapeutic Guidelines
Limited; 2009.
Weinberger M, Abu-Hasan M. Pseudo-asthma: when cough, wheezing, and dyspnea are not asthma. Pediatrics 2007;
120: 855-64. Available from: http://pediatrics.aappublications.org/content/120/4/855
Asset ID: 83
More information
In children, it is less useful to define expiratory airflow limitation according to a specific cut-off for FEV1/FVC ratio,
because normal values in children change considerably with age.3
Some spirometers provide predicted normal values specific to age group. If these are available, a FEV1/FVC ratio less than
the lower limit of normal (i.e. less than the 5th percentile of normal population) indicates airflow limitation.
Variableexpiratory airflow limitation (beyond the range seen in healthy populations) can be documented if any of the
following are recorded:
a clinically important increase in FEV1 (change in FEV1 of at least 200mL and 12% from baseline for adults, or at least
12% from baseline for children) 1015 minutes after administration of bronchodilator
clinically important variation in lung function (at least 20% change in FEV1) when measured repeatedly over time (e.g.
spirometry on separate visits)
a clinically important reduction in lung function (decrease in FEV1 of at least 200mL and 12% from baseline on
spirometry, or decrease in peak expiratory flow rate by at least 20%) after exercise(formal laboratory-based exercise
challenge testing uses different criteria for exercise-induced bronchoconstriction)
a clinically important increase in lung function (at least 200mL and 12% from baseline) after a trial of 4 or moreweeks
of treatment with an inhaled corticosteroid
clinically importantvariation in peak expiratory flow (diurnal variability of more than 10%)
a clinically important reduction in lung function (1520%, depending on the test)during a test for airway
hyperresponsiveness (exercise challenge test or bronchial provocation test) measured by a respiratory function
laboratory.
Notes
25
Patients referred to a respiratory function laboratory may be asked not to take certain medicines within a few hours to days before a
spirometry visit.
A clinically important increase or decrease in lung function is defined as a change in FEV1of at least 200mL and 12% from baseline for
4,1
adults, or at least 12% from baseline for children, or a change in peak expiratory flow rate of at least 20% on the same meter. A
clinically important increase in FVC after administering bronchodilator may also indicate reversible airflow limitation, but FVC is a less
reliable measure in primary care because FVC may varydue to factors such as variation in inspiratory volume or expiratory time.
The finding of normal lung function during symptoms reduces the probability that a patient has asthma, but a clinically important
improvement in response to bronchodilator or inhaled corticosteroid can occur in patients whose baseline value is within the predicted
normal range.
The greater the variation in lung function, the more certain is the diagnosis of asthma. However, people with longstanding asthma may
develop fixed airflow limitation.
Reversibility in airflow limitation may not be detected if the person is already taking a long-acting beta2agonist or inhaled
corticosteroid.
Airflow limitation can be transient and does not necessarily mean that the person has asthma (e.g. when recorded during a severe
acuteinfection of the respiratory tract). Ideally, airflow limitation should be confirmed when the patient does not have a respiratory
tract infection. Reduction in lung function during a respiratory tract infection with improvement in lung function after its resolution,
commonly occurs in people with asthma, but can also be seen in patients with COPD or in healthy people without either asthma or
5,6
COPD.
Sit upright with legs uncrossed and feet flat on the floor and do not lean forward.
Breathe in rapidly until lungs feel absolutely full. (Coaching is essential to do this properly.)
Do not pause formorethan 1 second.
Place mouthpiece in mouth and close lips to form a tight seal.
Blast air out as hard and fast as possible and for as long as possible, until the lungs are completely empty or you are
unable to blow out any longer.
Remove mouthpiece.
Go to: National Asthma Council Australia'sspirometry technique video, Performing spirometry inprimary care
Repeat the test until you obtain three acceptable tests and these meet repeatability criteria.
Acceptability of test
A test is acceptable if all the following apply:
Record the highest FEV1 and FVC result from the three acceptable tests, even if they come from separate blows.8
Repeatability criteria
Repeatability criteria for a set of acceptable tests are met if both of the following apply:7
26
the difference between the highest and second-highest values for FEV1 is less than 150 mL
the difference between the highest and second-highest values for FVC is less than 150 mL.
For most people, it is not practical to make more than eight attempts to meet acceptability and repeatability criteria.8
Testing bronchodilator response (reversibility of airflow limitation)
Repeat spirometry 10-15 minutes after giving 4 separate puffs of salbutamol (100 mcg/actuation) via a pressurised
metered-dose inhaler and spacer.8 (For patients who have reported unacceptable side-effects with 400 mcg, 2 puffs can
be used.)
For adults and adolescents, record a clinically important bronchodilator response if FEV1 increases by 200 mL and
12%.8
For children, record a clinically important bronchodilator response if FEV1 increases by
12%.8
Highrates of incorrect inhaler use among children with asthma and adults with asthma or COPD have been reported,15,
16, 17, 18, 19
evenamong regular users.20Regardless of the type of inhaler device prescribed, patients are unlikely to use
inhalers correctly unless they receive clear instruction, including a physical demonstration,and have their inhaler
technique checked regularly.21
Poor inhaler technique has been associated with worse outcomes in asthma and COPD. It can lead to poor asthma
symptom control and overuse of relievers and preventers.15, 22, 20, 23, 24In patients with asthma or COPD, incorrect
technique is associated with a 50% increased risk of hospitalisation, increased emergency department visits and increased
use of oral corticosteroids due to flare-ups.20
Correcting patients' inhaler technique has been shown to improve asthma control, asthma-related quality of life and lung
function.25, 26
Common errors and problems with inhaler technique
Common errors with manually actuated pressurised metered dose inhalersinclude:21
27
Common errors for dry powder inhalers include:21
not keeping the device in the correct position while loading the dose (horizontal for Accuhaler and vertical for
Turbuhaler)
failing to exhale fully before inhaling
failing to inhale completely
inhaling too slowly and weakly
exhaling into the device mouthpiece before or after inhaling
failing to close the inhaler after use
using past the expiry date or when empty.
difficulty manipulating device due to problems with dexterity (e.g. osteoarthritis, stroke, muscle weakness)
inability to seal the lips firmly around the mouthpiece of an inhaler or spacer
inability to generate adequate inspiratory flow for the inhaler type
failure to use a spacer when appropriate
use of incorrect size mask
inappropriate use of a mask with a spacer in older children.
Go to: National Asthma Council Australia'sUsing your inhalerwebpagefor information, patient resources and videos
on inhaler technique
Go to: National Asthma Council Australia's information paper for health professionals onInhaler technique for people
with asthma or COPD
Go to: NPSMedicineWise information onInhaler devices for respiratory medicines
References
1. Pellegrino R, Viegi G, Brusasco V, et al. Interpretative strategies for lung function tests. Eur Respir J. 2005; 26: 948-
968. Available from: http://erj.ersjournals.com/content/26/5/948
2. National Heart Lung and Blood Institute (NHLBI) National Asthma Education and Prevention Program. Expert Panel
Report 3: guidelines for the diagnosis and management of asthma. Full report 2007. US Department of Health and Human
Services National Institutes of Health, Bethesda, 2007. Available from: http://www.nhlbi.nih.gov/health-
pro/guidelines/current/asthma-guidelines/full-report
3. Quanjer PH, Stanojevic S, Cole TJ, et al. Multi-ethnic reference values for spirometry for the 3-95-yr age range: the
global lung function 2012 equations. Eur Respir J. 2012; 40: 1324-43. Available from:
http://www.ncbi.nlm.nih.gov/pubmed/22743675
4. Levy ML, Quanjer PH, Booker R, et al. Diagnostic Spirometry in Primary Care: Proposed standards for general
practice compliant with American Thoracic Society and European Respiratory Society recommendations. Prim Care
Respir J. 2009; 18: 130-147. Available from: http://www.ncbi.nlm.nih.gov/pubmed/19684995
5. Collier AM, Pimmel RL, Hasselblad V, et al. Spirometric changes in normal children with upper respiratory infections.
Am Rev Respir Dis. 1978; 117: 47-53. Available from: http://www.ncbi.nlm.nih.gov/pubmed/619724
6. Melbye H, Kongerud J, Vorland L. Reversible airflow limitation in adults with respiratory infection. Eur Respir J. 1994;
7: 1239-1245. Available from: http://www.ncbi.nlm.nih.gov/pubmed/7925901
7. Miller MR, Hankinson J, Brusasco V, et al. Standardisation of spirometry. Eur Respir J. 2005; 26: 319-338. Available
from: http://erj.ersjournals.com/content/26/2/319
8. Johns DP, Pierce R. Pocket guide to spirometry. 3rd edn. McGraw Hill, North Ryde, 2011.
28
9. Lucas AE, Smeenk FW, Smeele IJ, van Schayck CP. Overtreatment with inhaled corticosteroids and diagnostic
problems in primary care patients, an exploratory study. Fam Pract. 2008; 25: 86-91. Available from:
http://fampra.oxfordjournals.org/content/25/2/86.full
10. Luks VP, Vandemheen KL, Aaron SD. Confirmation of asthma in an era of overdiagnosis. Eur Respir J. 2010; 36: 255-
260. Available from: http://erj.ersjournals.com/content/36/2/255.full
11. Marklund B, Tunster A, Bengtsson C. How often is the diagnosis bronchial asthma correct?. Fam Pract. 1999; 16:
112-116. Available from: http://fampra.oxfordjournals.org/content/16/2/112.full
12. Aaron SD, Fergusson D, Dent R, et al. Effect of weight reduction on respiratory function and airway reactivity in
obese women. Chest. 2004; 125: 2046-52. Available from: http://www.ncbi.nlm.nih.gov/pubmed/15189920
13. Basheti IA, Armour CL, Bosnic-Anticevich SZ, Reddel HK. Evaluation of a novel educational strategy, including
inhaler-based reminder labels, to improve asthma inhaler technique. Patient Educ Couns. 2008; 72: 26-33. Available
from: http://www.ncbi.nlm.nih.gov/pubmed/18314294
14. Bosnic-Anticevich, S. Z., Sinha, H., So, S., Reddel, H. K.. Metered-dose inhaler technique: the effect of two educational
interventions delivered in community pharmacy over time. The Journal of asthma : official journal of the Association for
the Care of Asthma. 2010; 47: 251-6. Available from: https://www.ncbi.nlm.nih.gov/pubmed/20394511
15. Price, D., Bosnic-Anticevich, S., Briggs, A., et al. Inhaler competence in asthma: common errors, barriers to use and
recommended solutions. Respiratory medicine. 2013; 107: 37-46. Available from:
https://www.ncbi.nlm.nih.gov/pubmed/23098685
16. Capanoglu, M., Dibek Misirlioglu, E., Toyran, M., et al. Evaluation of inhaler technique, adherence to therapy and their
effect on disease control among children with asthma using metered dose or dry powder inhalers. The Journal of
asthma : official journal of the Association for the Care of Asthma. 2015; 52: 838-45. Available from:
https://www.ncbi.nlm.nih.gov/pubmed/20394511
17. Lavorini, F., Magnan, A., Dubus, J. C., et al. Effect of incorrect use of dry powder inhalers on management of patients
with asthma and COPD. Respiratory medicine. 2008; 102: 593-604. Available from:
https://www.ncbi.nlm.nih.gov/pubmed/18083019
18. Federman, A. D., Wolf, M. S., Sofianou, A., et al. Self-management behaviors in older adults with asthma: associations
with health literacy. Journal of the American Geriatrics Society. 2014; 62: 872-9. Available from:
https://www.ncbi.nlm.nih.gov/pubmed/24779482
19. Crane, M. A., Jenkins, C. R., Goeman, D. P., Douglass, J. A.. Inhaler device technique can be improved in older adults
through tailored education: findings from a randomised controlled trial. NPJ primary care respiratory medicine. 2014;
24: 14034. Available from: https://www.ncbi.nlm.nih.gov/pubmed/25188403
20. Melani AS, Bonavia M, Cilenti V, et al. Inhaler mishandling remains common in real life and is associated with reduced
disease control. Respir Med. 2011; 105: 930-8. Available from: http://www.ncbi.nlm.nih.gov/pubmed/21367593
21. National Asthma Council Australia. Inhaler technique for people with asthma or COPD. National Asthma Council
Australia, Melbourne, 2016. Available from: https://www.nationalasthma.org.au/living-with-
asthma/resources/health-professionals/information-paper/hp-inhaler-technique-for-people-with-asthma-or-copd
22. Bjermer, L.. The importance of continuity in inhaler device choice for asthma and chronic obstructive pulmonary
disease. Respiration; international review of thoracic diseases. 2014; 88: 346-52. Available from:
https://www.ncbi.nlm.nih.gov/pubmed/25195762
23. Haughney, J., Price, D., Barnes, N. C., et al. Choosing inhaler devices for people with asthma: current knowledge and
outstanding research needs. Respiratory medicine. 2010; 104: 1237-45. Available from:
https://www.ncbi.nlm.nih.gov/pubmed/20472415
24. Giraud, V., Roche, N.. Misuse of corticosteroid metered-dose inhaler is associated with decreased asthma stability.
The European respiratory journal. 2002; 19: 246-51. Available from: https://www.ncbi.nlm.nih.gov/pubmed/11866004
25. Basheti IA, Reddel HK, Armour CL, Bosnic-Anticevich SZ. Improved asthma outcomes with a simple inhaler technique
intervention by community pharmacists. J Allergy Clin Immunol. 2007; 119: 1537-8. Available from:
http://www.jacionline.org/article/S0091-6749(07)00439-3/fulltext
26. Giraud, V., Allaert, F. A., Roche, N.. Inhaler technique and asthma: feasability and acceptability of training by
pharmacists. Respiratory medicine. 2011; 105: 1815-22. Available from:
https://www.ncbi.nlm.nih.gov/pubmed/21802271
27. Basheti, I. A., Reddel, H. K., Armour, C. L., Bosnic-Anticevich, S. Z.. Counseling about turbuhaler technique: needs
assessment and effective strategies for community pharmacists. Respiratory care. 2005; 50: 617-23. Available from:
https://www.ncbi.nlm.nih.gov/pubmed/15871755
28. Lavorini, F.. Inhaled drug delivery in the hands of the patient. Journal of aerosol medicine and pulmonary drug delivery.
2014; 27: 414-8. Available from: https://www.ncbi.nlm.nih.gov/pubmed/25238005
29. Newman, S.. Improving inhaler technique, adherence to therapy and the precision of dosing: major challenges for
pulmonary drug delivery. Expert opinion on drug delivery. 2014; 11: 365-78. Available from:
https://www.ncbi.nlm.nih.gov/pubmed/24386924
29
Table. Confirming the diagnosis of asthma in a person using
preventer treatment
Few respiratory Variable airflow limitation not Obtain historical documentation of variable airflow
symptoms demonstrated limitation if possible.
30
Clinical profile Lung function Interpretation or action
Table applies to patients taking maintenance inhaled corticosteroid or combination inhaled corticosteroid/long-acting beta2
agonist
When spirometry is performed as a diagnostic test, inhaled bronchodilators should be withheld before the test.
Withholding times vary between medicines:
at least 4 hours for short-acting beta2 agonists (e.g. salbutamol, terbutaline) and short-acting muscarinic antagonists
(e.g. ipratropium)
at least 12 hours for preventers containing long-acting beta2 agonists for which twice-daily dosing is recommended
(e.g. formoterol, salmeterol)
at least 24 hours for long-acting muscarinic antagonists (e.g. aclidinium, glycopyrronium, tiotropium) and preventers
containing long-acting beta2 agonists with once-daily dosing (e.g. fluticasone furoate plus vilanterol).
Note: Requested withholding times may vary between centres that conduct formal lung function testing.
For patients using inhaled corticosteroid/long-acting beta2 agonist combinations, reduce the dose of inhaled corticosteroid
component by 50%. For those already using the lowest possible dose of inhaled corticosteroid/long-acting beta2 agonist
combination, consider switching to low-dose inhaled corticosteroid or stopping preventer.
Beforestepping down, document the patient's currentasthma status and risk factors, andensure that the person has a
written asthma action plan and an appointment for asthma review.
Back to top
Asset ID: 9
31
HOME > DIAGNOSIS > ADULTS > FURTHER INVESTIGATIONS
General considerations
Allergy tests
Imaging
32
HOME > DIAGNOSIS > ADULTS > FURTHER INVESTIGATIONS > GENERAL CONSIDERATIONS
Consider arranging further investigations and referral to appropriate specialists if the diagnosis cannot be made with
confidence from clinical features, spirometry and response to treatment.
Consider investigation for conditions that may affect or mimic asthma symptoms (e.g. coronary heart disease,
obstructive sleep apnoea, gastro-oesophageal reflux disease or aspirin-exacerbated respiratory disease).
the timing of asthma symptoms is associated with work activities (especially if symptoms improve when the person is
away from the workplace)
the person is exposed to substances known to cause occupational asthma
co-workers have respiratory symptoms.
Note: Do not rule out the possibility of work-related asthma if the persons occupation is not among those commonly associated with
asthma triggers (e.g. bakers, vehicle spray painters, electronics manufacturing workers who perform soldering, woodworkers,
healthcare workers, laboratory animal workers, agriculture workers), because many substances and occupations have been
associated with asthma and more are being identified continually.
Dykewics, 20091
Henneberger et al.2011 2
Hoy et al.20103
Tarloet al.20084
if the diagnosis is uncertain (consider referral for diagnostic assessment and further investigation by a respiratory
physician or general physician)
if signs and symptoms do not respond to a treatment trial (consider further investigations or referral to an
appropriate specialist)
if work-related asthma is suspected (consider referral to a respiratory physician, occupational physician and/or
allergist, or allergist with experience in work-related asthma, if possible. Investigation is complex and involves a very
detailed history,detailed lung function testing,site visits and sometimeschallenge testing).
33
s How this recommendation was developed
Consensus
Based on clinical experience and expert opinion (informed by evidence, where available).
More information
Sit upright with legs uncrossed and feet flat on the floor and do not lean forward.
Breathe in rapidly until lungs feel absolutely full. (Coaching is essential to do this properly.)
Do not pause formorethan 1 second.
Place mouthpiece in mouth and close lips to form a tight seal.
Blast air out as hard and fast as possible and for as long as possible, until the lungs are completely empty or you are
unable to blow out any longer.
Remove mouthpiece.
Go to: National Asthma Council Australia'sspirometry technique video, Performing spirometry inprimary care
Repeat the test until you obtain three acceptable tests and these meet repeatability criteria.
Acceptability of test
A test is acceptable if all the following apply:
Record the highest FEV1 and FVC result from the three acceptable tests, even if they come from separate blows.7
Repeatability criteria
Repeatability criteria for a set of acceptable tests are met if both of the following apply:5
the difference between the highest and second-highest values for FEV1 is less than 150 mL
the difference between the highest and second-highest values for FVC is less than 150 mL.
For most people, it is not practical to make more than eight attempts to meet acceptability and repeatability criteria.7
Testing bronchodilator response (reversibility of airflow limitation)
Repeat spirometry 10-15 minutes after giving 4 separate puffs of salbutamol (100 mcg/actuation) via a pressurised
metered-dose inhaler and spacer.7 (For patients who have reported unacceptable side-effects with 400 mcg, 2 puffs can
be used.)
For adults and adolescents, record a clinically important bronchodilator response if FEV1 increases by 200 mL and
12%.7
34
For children, record a clinically important bronchodilator response if FEV1 increases by
12%.7
cough is episodic
cough with exercise is associated with other symptoms that suggest airflow limitation(expiratory wheeze or
breathlessness)
spirometry confirms reversible airflow limitation.
If cough is due to asthma, it should respond to treatment with an inhaled corticosteroid preventer taken regularly and
reliever as needed).8
Findings that suggest a serious alternative or comorbid diagnosis that requires further investigationinclude:8
haemoptysis
smoker with > 20 packyear smoking history
smoker aged over 45 years with a new cough, altered cough, or cough with voice disturbance
prominent dyspnoea, especially at rest or at night
substantial sputum production
hoarseness
fever
weight loss
complicated gastro-oesophageal reflux disease
swallowing disorders with choking or vomiting
recurrent pneumonia
abnormal clinical respiratory examination.
For information on diagnosis and management of COPD, refer to the COPD-X Concise Guide for Primary Care.11
The Global Initiative for Asthma (GINA) and Global Initiative Obstructive Lung Disease (GOLD) recommend the following
stepwise approach for adults presenting with respiratory symptoms:12
1. Identify whether the patient has clinical features of, or is at risk of, chronic airway disease. This may be suggested
by the clinical history and physical examination.
2. Identify features that favour a diagnosis of typical asthma or typical COPD. If several features of both are present,
asthma-COPD overlap is likely.
3. Perform spirometry to confirm airflow limitation.
4. Start treatment, selected according to whether the assessment favoured the single diagnosis of asthma, the single
diagnosis of COPD, or asthma-COPD overlap.
5. Refer for specialist assessment and other investigations, if necessary.
35
Other diagnostic tests in adults
For patients with incompletely reversible airflow limitation, a careful history will often clarify which investigation is most
appropriate. Lung volume tests and diffusing capacity tests may be helpful to identify emphysema or pulmonary fibrosis.
High-resolution computed tomography is useful if bronchiectasis is suspected.
References
1. Dykewics MS. Occupational asthma: Current concepts in pathogenesis, diagnosis, and management. J Allergy Clin
Immunol. 2009; 123: 519-528. Available from: http://www.jacionline.org/article/S0091-6749(09)00214-0/fulltext
2. Henneberger PK, Redlich CA, Callahan DB, et al. An official american thoracic society statement: work-exacerbated
asthma. Am J Respir Crit Care Med. 2011; 184: 368-78. Available from:
http://ajrccm.atsjournals.org/content/184/3/368.long
3. Hoy RF, Abramson MJ, Sim MR. Work related asthma - diagnosis and management. Aust Fam Physician. 2010; 39: 39-
42. Available from: http://www.racgp.org.au/afp/201001/35841
4. Tarlo SM, Balmes J, Balkissoon R, et al. Diagnosis and management of work-related asthma: American College Of
Chest Physicians Consensus Statement. Chest. 2008; 134(3 Suppl): 1S-41S. Available from:
http://journal.publications.chestnet.org/article.aspx?articleid=1044851
5. Miller MR, Hankinson J, Brusasco V, et al. Standardisation of spirometry. Eur Respir J. 2005; 26: 319-338. Available
from: http://erj.ersjournals.com/content/26/2/319
6. Levy ML, Quanjer PH, Booker R, et al. Diagnostic Spirometry in Primary Care: Proposed standards for general
practice compliant with American Thoracic Society and European Respiratory Society recommendations. Prim Care
Respir J. 2009; 18: 130-147. Available from: http://www.ncbi.nlm.nih.gov/pubmed/19684995
7. Johns DP, Pierce R. Pocket guide to spirometry. 3rd edn. McGraw Hill, North Ryde, 2011.
8. Gibson PG, Chang AB, Glasgow NJ, et al. CICADA: cough in children and adults: diagnosis and assessment. Australian
cough guidelines summary statement. Med J Aust. 2010; 192: 265-271. Available from:
http://www.lungfoundation.com.au/professional-resources/guidelines/cough-guidelines
9. Abramson MJ, Crockett AJ, Dabscheck E, et al. The COPD-X Plan: Australian and New Zealand guidelines for the
management of chronic obstructive pulmonary disease. Version 2.34. The Australian Lung Foundation and The Thoracic
Society of Australia and New Zealand, 2012. Available from: http://www.copdx.org.au/
10. Gibson PG, McDonald VM, Marks GB. Asthma in older adults. Lancet. 2010; 376: 803-813. Available from:
http://www.ncbi.nlm.nih.gov/pubmed/20816547
11. Abramson M, Frith P, Yang I, et al. COPD-X Concise Guide for Primary Care. Lung Foundation Australia, Brisbane, 2016.
Available from: http://lungfoundation.com.au/health-professionals/guidelines/copd/copd-x-concise-guide-for-
primary-care/
12. Global Initiative for Asthma (GINA). Global strategy for asthma management and prevention. GINA, 2016. Available
from: http://ginasthma.org/
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HOME > DIAGNOSIS > ADULTS > FURTHER INVESTIGATIONS > AIRWAY HYPERRESPONSIVENESS TESTS
Consider arranging bronchial provocation (challenge) tests for airway hyperresponsiveness if asthma is suspected but
initial spirometry does not demonstrate reversible airflow limitation.
Notes:
If challenge testing is needed, consider referring to a respiratory physician for investigation, or discussing with a respiratory physician
before selecting which test to order.
Dont test during a respiratory infection, or initiate inhaled corticosteroid treatment in the few weeks before challenge testing,
because these could invalidate the result.
Bronchial provocation (challenge) tests should be performed only in accredited respiratory function laboratories.
Note: A list of accredited laboratories is available from the Australian and New Zealand Society of Respiratory Science
Do not routinely order tests for airway hyperresponsiveness (challenge tests) for all patients with suspected asthma. It
is not necessary to demonstrate airway hyperresponsiveness if the patient shows clinical features of asthma and there is
a high probability that these are not due to another cause.
More information
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Challenge tests for exercise-induced bronchoconstriction
Role of challenge tests
Self-reported symptoms are not sensitive enough to detect exercise-induced bronchoconstriction reliably or specific
enough to rule out other conditions, particularly in elite athletes.5,6,7Single office FEV1 readings or peak expiratory flow
measurement are not adequate to demonstrate exercise-induced bronchoconstriction.8
Standardised, objective bronchial provocation (challenge) tests using spirometry are necessary for the investigation of
suspected exercise-induced bronchoconstriction in elite athletes. These tests involve serial spirometry measurements
after challenge with exercise (or exercise surrogates e.g. dry powder mannitol, eucapnic voluntary hyperpnoea or
hyperventilation, or hyperosmolar aerosols such as 4.5% saline).5,8, 9,10Severity of exercise-induced bronchoconstriction
is assessed by percentage fall in FEV1 after challenge.8
Challenge testing is mandated by sports governing bodies before the athlete is given permission to use some asthma
medicines, and the required testing protocol varies between specific sports. The latest information is available from the
Australian Sports Anti-Doping Authority (ASADA) and the World Anti-Doping Agency(WADA).
Challenge tests are also used in the investigation of exercise-related symptoms in recreational and non-athletes, when
objective demonstration of exercise-induced bronchoconstriction is needed to guide management decisions.
The eucapnic voluntary hyperpnoea test can provoke a severe response.5For safety reasons, the eucapnic voluntary
hyperpnoea test should only be used in adultswho regularly exercise at high intensity (e.g. elite athletes).5 It should
not be used in children.
When an exercise challenge test is used, inhalation of dry air is recommended to diagnose or exclude exercise-induced
bronchoconstriction because it increases the sensitivity of the test.5
Mannitol challenge can be used as an alternative to exercise provocation testing to investigate suspected exercise-
induced bronchoconstriction, 5, 11, 12including in children.13, 14
For safety reasons, exercise challenge in dry air should be avoided in patients with FEV1<70% predicted5
Referral
If challenge testing is needed, consider referring to a respiratory physician for investigation, or discussing with a
respiratory physician before selecting which test to order. Do not test during a respiratory infection, or initiate inhaled
corticosteroid treatment in the few weeks before challenge testing, because these could invalidate the result.
A list of accredited respiratory function laboratories is available from the Australian and New Zealand Society of
Respiratory Science.
References
1. Anderson SD. Indirect challenge tests: Airway hyperresponsiveness in asthma: its measurement and clinical
significance. Chest. 2010; 138(2 Suppl): 25S-30S. Available from:
http://journal.publications.chestnet.org/article.aspx?articleid=1086636
2. Anderson SD. Bronchial challenge tests: usefulness, availability and challenges. Breathe. 2011; 8: 53-60. Available
from: http://www.ers-education.org
3. Cockcroft DW. Direct challenge tests: airway hyperresponsiveness in asthma: its measurement and clinical
significance. Chest. 2010; 138(2 Suppl): 18S-24S. Available from:
http://journal.publications.chestnet.org/article.aspx?articleid=1086632
4. Anderson SD, Pearlman DS, Rundell KW, et al. Reproducibility of the airway response to an exercise protocol
standardized for intensity, duration, and inspired air conditions, in subjects with symptoms suggestive of asthma.
Respir Res. 2010; Sept 1: 120. Available from: http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2939602/
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5. Weiler JM, Anderson SD, Randolph C, et al. Pathogenesis, prevalence, diagnosis, and management of exercise-
induced bronchoconstriction: a practice parameter. Ann Allergy Asthma Immunol. 2010; 105: S1-47. Available from:
http://www.ncbi.nlm.nih.gov/pubmed/21167465
6. Rundell KW, Im J, Mayers LB, et al. Self-reported symptoms and exercise-induced asthma in the elite athlete. Med Sci
Sports Exerc. 2001; 33: 208-13. Available from: http://www.ncbi.nlm.nih.gov/pubmed/11224807
7. Holzer K, Anderson SD, Douglass J. Exercise in elite summer athletes: Challenges for diagnosis. J Allergy Clin Immunol.
2002; 110: 374-80. Available from: http://www.ncbi.nlm.nih.gov/pubmed/12209082
8. Parsons JP, Hallstrand TS, Mastronarde JG, et al. An official American Thoracic Society clinical practice guideline:
exercise-induced bronchoconstriction. Am J Respir Crit Care Med. 2013; 187: 1016-27. Available from:
http://www.ncbi.nlm.nih.gov/pubmed/23634861
9. Fitch KD, Sue-Chu M, Anderson SD, et al. Asthma and the elite athlete: Summary of the International Olympic
Committee's Consensus Conference, Lausanne, Switzerland, January 22-24, 2008. J Allergy Clin Immunol. 2008; 122:
254-260. Available from: http://www.ncbi.nlm.nih.gov/pubmed/18678340
10. Anderson SD, Kippelen P. Assessment and prevention of exercise-induced bronchoconstriction. Br J Sports Med.
2012; 46: 391-6. Available from: http://www.ncbi.nlm.nih.gov/pubmed/22247297
11. Brannan JD, Koskela H, Anderson SD, Chew N. Responsiveness to mannitol in asthmatic subjects with exercise- and
hyperventilation-induced asthma. Am J Respir Crit Care Med. 1998; 158: 1120-6. Available from:
http://www.atsjournals.org/doi/full/10.1164/ajrccm.158.4.9802087
12. Holzer K, Anderson SD, Chan HK, Douglass J. Mannitol as a challenge test to identify exercise-induced
bronchoconstriction in elite athletes. Am J Respir Crit Care Med. 2003; 167: 534-7. Available from:
http://www.atsjournals.org/doi/full/10.1164/rccm.200208-916OC
13. Kersten ET, Driessen JM, van der Berg JD, Thio BJ. Mannitol and exercise challenge tests in asthmatic children.
Pediatr Pulmonol. 2009; 44: 655-661. Available from: http://www.ncbi.nlm.nih.gov/pubmed/19499571
14. Barben J, Kuehni CE, Strippoli MP, et al. Mannitol dry powder challenge in comparison with exercise testing in
children. Pediatr Pulmonol. 2011; 46: 842-8. Available from: http://www.ncbi.nlm.nih.gov/pubmed/21465681
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HOME > DIAGNOSIS > ADULTS > FURTHER INVESTIGATIONS > AIRWAY INFLAMMATION TESTS
Do not routinely orderinduced sputum eosinophilcount for all patients with suspected asthma. It is not necessary to
demonstrate airway inflammation if the patient shows clinical features of asthma and there is a low probability that
these are due to another cause.
Measurement of exhaled nitric oxide is not recommended as a diagnostic test for asthma in routine clinical practice.
Dweik et al.20111
More information
some types of asthma (i.e. asthma without eosinophilic airway inflammation) are not associated with increased
exhaled nitric oxide
patients treated with inhaled corticosteroids may show a false negative test result.
In people with a clinical diagnosis of asthma, the exhaled nitric oxide test is useful for identifying those with asthma that is
likely to respond well to inhaled corticosteroids. The exhaled nitric oxide test is easy for patients to do.
The predictive value of exhaled nitric oxide as a diagnostic test for asthma is higher than for peak expiratory flow and
spirometry, and similar to that of bronchial challenge tests.1
There are several inflammatory phenotypes in asthma: eosinophilic, neutrophilic, mixed, and asthma with sputum cell
counts within normal range (paucigranulocytic). The exhaled nitric oxide fraction is associated with eosinophilic airway
inflammation, but not with neutrophilic or paucigranulocytic asthma.1
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Impulse oscillometry in adults and adolescents
Impulse oscillometry is a noninvasive and rapid technique for measuring pulmonary function. Unlike spirometry, the test
is easy to do and requires only passive cooperation by the patient, so it is suitable for small children. It is not used
routinely in clinical practice, butis currently available insome tertiary referral centres.
Low-frequency impulse oscillometry (resistance at 5 Hz) measurements taken before and after administration of a
bronchodilator correlate with spirometry (FEV1) in people with asthma and without asthma.2Impulse oscillometrymay be
useful in identifying patients with asthma,and might possibly identify obstruction in the peripheral airways.3
This test is not used routinely in clinical practice because diagnostic cut-points are not well established yet.3 Australian
4
normal values for adults without asthma have been developed.
References
1. Dweik RA, Boggs PB, Erzurum SC, et al. An Official ATS Clinical Practice Guideline: Interpretation of Exhaled Nitric
Oxide Levels (FeNO) for Clinical Applications. Am J Respir Crit Care Med. 2011; 184: 602-615. Available from:
http://ajrccm.atsjournals.org/content/184/5/602.long
2. Nair A, Ward J, Lipworth BJ. Comparison of bronchodilator response in patients with asthma and healthy subjects
using spirometry and oscillometry. Ann Allergy Asthma Immunol. 2011; 107: 317-322. Available from:
http://www.ncbi.nlm.nih.gov/pubmed/21962091
3. Galant SP, Nickerson B. Lung function measurement in the assessment of childhood asthma: recent important
developments. Curr Opin Allergy Clin Immunol. 2010; 10: 149-154. Available from:
http://www.ncbi.nlm.nih.gov/pubmed/20035221
4. Newbury W, Crockett A, Newbury J. A pilot study to evaluate Australian predictive equations for the impulse
oscillometry system. Respirology. 2008; 13: 1070-1075. Available from:
http://www.ncbi.nlm.nih.gov/pubmed/18699802
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HOME > DIAGNOSIS > ADULTS > FURTHER INVESTIGATIONS > ALLERGY TESTS
Consider allergy testing as part of diagnostic investigations if you suspect allergic triggers, or to guide management.
To investigate allergies in a person with severe or unstable asthma, or a history of anaphylaxis, refer to a specialist
allergist for investigationto minimise risk.
If allergy testing is needed, refer to an appropriate provider for skin prick testing for common aeroallergens.
Notes
Ifstaff are trained in the skin prick test procedure and its interpretation, skin prick testing can be performed in primary care. If not,
refer to an appropriate provider.
When performing skin prick testing, follow Australasian Society of Clinical Immunology and Allergy (ASCIA)guidance:Skin prick
testing for the diagnosis of allergic disease. A manual for practitioners
Blood test (immunoassay for allergen-specific immunoglobulin E) can be used if skin prick testing is (any of):
unavailable
impractical (e.g. a patient who is unable to cooperate with test procedure, a patient taking antihistamines when
these cannot be withdrawn, or a patient taking tricyclic antidepressants or pizotifen)
contraindicated (e.g. patients with severe dermatographism, extensive skin rash, or those at risk of anaphylaxis
including patients with occupational asthma due to latex sensitivity).
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More information
References
1. Australasian Society of Clinical Immunology and Allergy (ASCIA), Skin Prick Testing Working Party. Skin prick testing
for the diagnosis of allergic disease: A manual for practitioners. ASCIA, Sydney, 2013. Available from:
http://www.allergy.org.au/health-professionals/papers/skin-prick-testing
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HOME > DIAGNOSIS > ADULTS > FURTHER INVESTIGATIONS > IMAGING
Consider arranging chest X-ray if there are respiratory symptoms that are not explained by asthma or as otherwise
indicated to investigate the possibility ofother conditions (e.g. pneumonia, cancer).
Do not routinely order chest X-ray in all patients with suspected asthma, because it is not a diagnostic test for ruling
asthma in or out.
More information
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