Time to first exacerbation for participants where treatment was guided by FENO compared to standard care | Interaction p-value | ||
HR (95% CI) | p-value | ||
LTRA treatment | |||
Yes | 0.76 (0.57–0.99) | 0.048 | 0.049 |
No | 1.26 (0.82–1.90) | 0.292 | |
ICS dose | |||
≤400 μg BUD | 0.76 (0.52–1.12) | 0.166 | 0.393 |
>400 μg BUD | 0.94 (0.71–1.25) | 0.667 | |
Obese | |||
Yes | 0.96 (0.74–1.25) | 0.787 | 0.456 |
No | 0.78 (0.48–1.27) | 0.321 | |
Atopic | |||
Yes | 0.61 (0.29–1.31) | 0.207 | 0.347 |
No | 0.90 (0.70–1.16) | 0.412 | |
Ethnic group | |||
White | 1.24 (0.76–2.02) | 0.391 | 0.268 |
Non-white | 0.90 (0.67–1.20) | 0.469 |
FENO: exhaled nitric oxide fraction; HR: hazard ratio; LTRA: leukotriene receptor antagonist; ICS: inhaled corticosteroids; BUD: budesonide equivalent. #: these models are fitted as time = subgroup + treatment group + subgroup * treatment + age + study ID + baseline ICS. Baseline ICS was not included in the model where outcomes between ICS subgroups were analysed.