Assess for, and correct, common causes of poor control (poor adherence, incorrect inhaler technique, exposure to avoidable triggers (e.g. cigarette smoke, allergens, irritants, infections, moulds/dampness, indoor/outdoor air pollution), psychosocial factors affecting the family’s or child’s ability to manage asthma (e.g. life events, financial problems, or mental health conditions).
Assess salbutamol use. Refer patients with marked overuse to a severe asthma clinic (if available) or respiratory physician for supervised reduction.
Confirm the diagnosis.
Assess comorbid conditions that could be contributing to asthma symptoms (e.g. rhinosinusitis, obesity, gastroesophageal reflux disease, obstructive sleep apnoea, inducible laryngeal obstruction) and whether respiratory symptoms may be caused by an alternative diagnosis.
Recommendation type: Adapted from GINA
Among patients with asthma that is uncontrolled despite having been prescribed medium-dose maintenance ICS-LABA or higher-intensity treatment, many can achieve good control after correcting common causes. A minority have severe asthma, which is non-responsive to high doses of ICS and requires specialist treatment with monoclonal antibody therapy.[GINA 2025]
Global Initiative for Asthma (GINA). Global Strategy for Asthma Management and Prevention, 2025. Available from: www.ginasthma.org
This recommendation applies after confirming good adherence to ICS and correct inhaler technique, and after assessing and managing other risk factors.
Refer to a specialist, regardless of spirometry findings and blood eosinophil count.
Recommendation type: Consensus recommendation
Thoracic Society of Australia and New Zealand’s list of accredited respiratory laboratories.
Suitable specialists for referral include paediatric respiratory physicians, general paediatricians with a special interest in asthma, or allergists.
Options include:
Continue ICS-LABA while trialling add-on treatment for 8–12 weeks. Stop the treatment if ineffective after 12 weeks or adverse effects occur.
Recommendation type: Consensus recommendation
Tiotropium added to ICS-LABA reduces the risk of exacerbations and achieves a small improvement in lung function in children aged 6–11 years.[Rodrigo 2017] Benefits of tiotropium in children do not appear to depend on asthma phenotype identified by IgE or eosinophil count.[Szefler 2019]
Australian product information – Spiriva Respimat tiotropium solution for inhalation (with dose counter). [Revised 17 May 2024] Therapeutic Goods Administration (www.ebs.tga.gov.au)
Rodrigo GJ, Neffen H. Efficacy and safety of tiotropium in school-age children with moderate-to-severe symptomatic asthma: A systematic review. Pediatr Allergy Immunol 2017; 28: 573-578.
Szefler SJ, Vogelberg C, Bernstein JA, et al. Tiotropium Is efficacious in 6- to 17-year-olds with asthma, independent of T2 phenotype. J Allergy Clin Immunol Pract 2019; 7: 2286-2295 e2284.
Tiotropium delivered by mist inhaler is approved by TGA as add-on maintenance bronchodilator treatment in patients aged 6 years and older with moderate-to-severe asthma.[Australian PI: tiotropium] Other tiotropium devices are not approved for asthma.