Intervention not reported
HRQoL ‐ CRQ subgrouped by domain (change from baseline; mixed population) ‐ dyspnoea · patients with stable chronic obstructive pulmonary disease
1 finding from 1 review
Intervention not reported
HRQoL ‐ CRQ subgrouped by domain (change from baseline; mixed population) ‐ fatigue · patients with stable chronic obstructive pulmonary disease
1 finding from 1 review
Intervention not reported
HRQoL ‐ CRQ subgrouped by domain (change from baseline; mixed population) ‐ emotion · patients with stable chronic obstructive pulmonary disease
1 finding from 1 review
Intervention not reported
HRQoL ‐ CRQ subgrouped by domain (change from baseline; mixed population) ‐ mastery · patients with stable chronic obstructive pulmonary disease
1 finding from 1 review
Intervention not reported
Fat‐free mass index (mixed population) kg/m2 · patients with stable chronic obstructive pulmonary disease
1 finding from 1 review
Intervention not reported
Fat‐free mass index (undernourished patients) kg/m2 · patients with stable chronic obstructive pulmonary disease
1 finding from 1 review
Intervention not reported
Mid‐arm muscle circumference (mixed population) cm · patients with stable chronic obstructive pulmonary disease
1 finding from 1 review
Intervention not reported
Skinfold thickness (mixed measures and mixed population) cm · stable chronic obstructive pulmonary disease
1 finding from 1 review
Intervention not reported
Functional exercise capacity ‐ 6‐minute walk test (mixed population) metres · stable chronic obstructive pulmonary disease
1 finding from 1 review
Intervention not reported
FEV1 litres and % predicted · stable chronic obstructive pulmonary disease
1 finding from 1 review
Intervention not reported
FEV1 litres · stable chronic obstructive pulmonary disease
1 finding from 1 review
Hospital admissions · patients with acute asthma
ICS may leads to lower hospital admission compared with placebo (low certainty).
1 finding from 1 review
FEV1 (L) · patients with acute asthma
ICS showed no clear difference in FEV1 at 1 hour compared with placebo (low certainty).
1 finding from 1 review
FEV1 · patients with acute asthma
ICS showed no clear difference in FEV1 at 3 to 4 hours compared with placebo (moderate certainty).
1 finding from 1 review
Nausea and vomiting · patients with acute asthma
ICS showed no clear difference in adverse effects ‐ nausea/vomiting compared with placebo (low certainty).
1 finding from 1 review
Hospital admissions · patients with acute asthma
ICS showed no clear difference in hospital admission compared with systemic corticosteroids (low certainty).
1 finding from 1 review
Asthma relapse1at 20 to 24 days · predominantly adults with acute asthma following emergency department discharge
Any ICS plus oral corticosteroid showed no clear difference in asthma relapse1at 20 to 24 days compared with oral corticosteroid (high certainty).
1 finding from 1 review
Hospital admissions · predominantly adults with acute asthma following emergency department discharge
Any ICS plus oral corticosteroid showed no clear difference in hospital admission compared with oral corticosteroid (moderate certainty).
1 finding from 1 review
Hoarseness at 20 to 24 days · predominantly adults with acute asthma following emergency department discharge
Any ICS plus oral corticosteroid showed no clear difference in hoarseness at 20 to 24 days compared with oral corticosteroid (moderate certainty).
1 finding from 1 review
Asthma relapse1at 16 to 21 days · patients with acute asthma following emergency department discharge
Any ICS showed no clear difference in asthma relapse1at 16 to 21 days compared with oral corticosteroid (moderate certainty).
1 finding from 1 review