Responses to the consensus statements
Consensus statements | Total participants (n = 26) | ||
---|---|---|---|
Disagree | Neutral | Agree | |
GINA 2022 guidelines consensus statements | |||
1. The GINA 2022 guidelines are practical in the patient population that I cover | 0 (0%) | 0 (0%) | 23 (88.5%) |
2. I am familiar with the changes in the GINA 2022 guidelines | 0 (0%) | 1 (3.8%) | 22 (84.6%) |
Confirmation of diagnosis and identifying risk factors | |||
3. At a global level, spirometry before and after bronchodilator is the most useful initial investigation (GINA 2022) | 1 (3.8%) | 1 (3.8%) | 21 (80.8%) |
4. Confirmation of asthma diagnosis with lung function testing, before commencing long-term treatment, is common practice | 4 (15.4%) | 4 (15.4%) | 15 (57.7%) |
5. Treatment of modifiable risk factors in every asthmatic patient is highly recommended and practiced | 1 (3.8%) | 0 (0%) | 22 (84.6%) |
6. Patients with apparently mild asthma are still at risk of serious adverse events [7, 8] | 0 (0%) | 3 (11.5%) | 20 (76.9%) |
Management | |||
7. The recommended first-line rescue inhaler, for the majority of patients is a short-acting β2 agonist (SABA) inhaler, e.g., Albuterol | 8 (30.8%) | 6 (23.1%) | 10 (38.5%) |
8. Low-dose inhaled corticosteroid (ICS)-formoterol as the reliever, is the preferred strategy because of the evidence that using ICS-formoterol as a reliever reduces the risk of exacerbations compared with using a SABA reliever, e.g., Albuterol | 0 (0%) | 3 (11.5%) | 20 (76.9%) |
9. Compared with as needed SABA, the use of ICS-formoterol reduced the risk of severe exacerbations by 60–64% [SYmbicort Given as needed in Mild Asthma (SYGMA) 1, novel Inhaled Steroid Treatment as Regular Therapy in Early Asthma (START)] | 2 (7.7%) | 3 (11.5%) | 18 (69.2%) |
10. SABA, e.g., Albuterol inhaler, as the reliever, is the non-preferred strategy; it is less effective than track 1 (the reliever is as needed low-dose ICS-formoterol) for reducing severe exacerbations | 2 (7.7%) | 5 (19.2%) | 16 (61.5%) |
11. Regular use of SABA, even for 1–2 weeks, is associated with increased airway hyperresponsiveness (AHR), reduced bronchodilator effect, increased allergic response, and increased eosinophils [9, 10] | 9 (34.6%) | 1 (3.8%) | 13 (50%) |
12. Track 2 (SABA is the reliever medication) involves using as needed SABA as a reliever, and taking the ICS whenever SABA is taken | 6 (23.1%) | 3 (11.5%) | 14 (53.8%) |
13. Patients with exacerbations should receive at least a medium dose of ICS-long-acting β2 agonist (LABA) before considering an add-on long-acting muscarinic antagonist (LAMA) | 1 (3.8%) | 2 (7.7%) | 20 (76.9%) |
14. LAMAs, e.g., Spiriva, should not be used as monotherapy for asthma (i.e. without ICS) because of the increased risk of severe exacerbations [11] | 2 (7.7%) | 0 (0%) | 21 (80.8%) |
Maintenance | |||
15. Checking the inhaler technique in every patient is highly recommended and practiced at every visit | 0 (0%) | 4 (15.4%) | 19 (73.1%) |
16. Every patient with suspected severe asthma should be seen within 12 weeks of referral to an appropriate specialist severe asthma service | 2 (7.7%) | 2 (7.7%) | 19 (73.1%) |