Relative risk between sputum strategy and clinical strategy from Cox regression models for the time to the first exacerbation and Andersen-Gill models for the multiple exacerbations during maintenance phase
Time to first exacerbation# | Multiple event analysis¶ | |||||
RR | 95% CI | p-value | RR | 95% CI | p-value | |
All exacerbations | 0.61 | (0.37–1.02) | 0.06 | 0.71 | (0.45–1.12) | 0.14 |
By type of exacerbation | ||||||
Eosinophilic | 0.19 | (0.05–0.83) | 0.03 | 0.28 | (0.10–0.74) | 0.01 |
Noneosinophilic | 0.82 | (0.44–1.53) | 0.53 | 1.07 | (0.61–1.85) | 0.82 |
By use of LABA | ||||||
Not on LABA | 0.84 | (0.44–1.63) | 0.61 | 1.05 | (0.62–1.79) | 0.85 |
On LABA | 0.40 | (0.18–0.88) | 0.02 | 0.53 | (0.24–1.14) | 0.11 |
By asthma severity | ||||||
Very mild to mild | 0.99 | (0.34–2.81) | 0.98 | 1.34 | (0.52–3.46) | 0.54 |
Moderate to severe | 0.51 | (0.29–0.90) | 0.02 | 0.63 | (0.38–1.03) | 0.07 |
RR: relative risks; 95% CI; 95% confidence intervals; LABA: long-acting β2-agonists. #: RR is relative risk from a Cox regression model. ¶: RR is relative risk from an Anderson-Gill model. Asthma severity was based on minimum daily maintenance fluticasone equivalent dose, very mild: 0; mild: <250 µg; moderate: ≥250–500 µg; severe: >500 µg.