Intervention not reported
TDI Total scores range from ‐ 9 to +9. The lower the score, the greater the deterioration in severity of dyspnoea, MCID ≥ 1 · 18 to 80 years of age with bronchiectasis
The intervention may leads to higher TDI Total scores range from ‐ 9 to +9. The lower the score, the… (low certainty).
1 finding from 1 review
Intervention not reported
Cough‐free days Percentage of days free of cough · 18 to 80 years of age with bronchiectasis
The intervention may leads to higher cough‐free days Percentage of days free of cough (low certainty).
1 finding from 1 review
Intervention not reported
Hospitalisations, number of participants with 1 or more exacerbations · 18 to 80 years of age with bronchiectasis
The intervention showed no clear difference in hospitalisations, number of participants with 1 or more exacerbations (low certainty).
1 finding from 1 review
Intervention not reported
Exacerbation rates per participant per year · patients with COPD
The intervention probably leads to lower exacerbation rates per participant per year (moderate certainty).
1 finding from 1 review
Intervention not reported
Mortality · patients with COPD
The intervention leads to lower mortality (high certainty).
1 finding from 1 review
Intervention not reported
Pneumonia · patients with COPD
The intervention showed no clear difference in pneumonia (low certainty).
1 finding from 1 review
Intervention not reported
Hospitalisations due to COPD exacerbations · patients with COPD
The intervention showed no clear difference in hospitalisations due to COPD exacerbations (low certainty).
1 finding from 1 review
Intervention not reported
Adverse events-serious Fluticasone/salmeterol (FPS) versus fluticasone (FP) · patients with COPD
The intervention showed no clear difference in adverse events-serious Fluticasone/salmeterol (FPS) versus… (low certainty).
1 finding from 1 review
Intervention not reported
Adverse events-serious events Budesonide/formoterol (BDF) versus budesonide (BD) · patients with COPD
It is very uncertain whether the intervention changes adverse events-serious events Budesonide/formoterol (BDF) versus… (very low certainty).
1 finding from 1 review
Intervention not reported
Adverse events-serious Mometasone/formoterol (MF/F) versus Mometasone (MF) · patients with COPD
The intervention showed no clear difference in adverse events-serious Mometasone/formoterol (MF/F) versus… (low certainty).
1 finding from 1 review
PEF (L/min) · patients with adults with acute asthma
Aminophylline showed no clear difference in PEF (L/min) ‐ at 60 min compared with placebo (low certainty).
1 finding from 1 review
Hospital admissions · patients with adults with acute asthma
Aminophylline showed no clear difference in hospital admissions compared with placebo (moderate certainty).
1 finding from 1 review
Tremor · patients with adults with acute asthma
Aminophylline showed no clear difference in tremor compared with placebo (low certainty).
1 finding from 1 review
Vomiting · patients with adults with acute asthma
Aminophylline probably leads to higher vomiting compared with placebo (moderate certainty).
1 finding from 1 review
Arrhythmia/palpitations · patients with adults with acute asthma
Aminophylline probably leads to higher arrhythmia/palpitations compared with placebo (moderate certainty).
1 finding from 1 review
Convulsions · patients with adults with acute asthma
1 finding from 1 review