Specific Inspiratory Muscle Training in Patients With Mild Asthma With High Consumption of Inhaled β2-Agonists


      It has been known for many years that there are variations between asthmatic patients in terms of their perception of breathlessness during airway obstruction.

      Study objective

      To investigate the relationship betweenβ 2-agonist consumption and the score of perception of dyspnea, in mild asthmatics, and the relationship between the effect of specific inspiratory muscle training (SIMT) on the score of perception of dyspnea and β2-agonist consumption in “high perceivers.”


      Daily β2-agonist consumption was assessed during a 4-week run-in period in 82 patients with mild asthma. Patients with a mean β2-agonist consumption of > 1 puff/d (“high consumers”) then were randomized into two groups: one group of patients received SIMT for 3 months; the other group of patients was assigned as a control group and received sham training. Inspiratory muscle strength and perception of dyspnea were assessed before patients entered the study, following the 4-week run-in period, and after completing the training period.


      Following the 4-week run-in period, 23 high-consumer patients (mean [± SEM]β 2-agonist consumption, 2.7 ± 0.4 puffs/d) were detected. The mean Borg score during breathing against resistance was significantly higher (p < 0.05) in the patients with highβ 2-agonist consumption than in the subjects with low meanβ 2-agonist consumption. Following SIMT, the mean maximal inspiratory pressure increased significantly from 94.1 ± 5.1 to 109.7 ± 5.2 cm H2O (p < 0.005) in the training group. The increase in inspiratory muscle strength was associated with a statistically significant decrease in the mean Borg score during breathing against resistance (p < 0.05) as well as in the mean dailyβ 2-agonist consumption.


      We have shown that patients with mild asthma, who have a highβ 2-agonist consumption, have a higher perception of dyspnea than those with normal consumption. In addition, SIMT was associated with a decrease in perception of dyspnea and a decrease inβ 2-agonist consumption.

      Key words


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