All‐cause mortality · people with COPD who have smoked for ≥ 10 pack‐years
Tiotropium showed no clear difference in mortality compared with placebo (moderate certainty).
1 finding from 1 review
Survival to hospital discharge · patients with out‐of‐hospital cardiac arrest
CPR plus delayed defibrillation showed no clear difference in survival to hospital discharge rate compared with immediate defibrillation: overall analysis (low certainty).
1 finding from 1 review
Neurological outcome at hospital discharge rate of good recovery · patients with out‐of‐hospital cardiac arrest
CPR plus delayed defibrillation showed no clear difference in neurological outcome at hospital discharge rate of good recovery compared with immediate defibrillation: overall analysis (low certainty).
1 finding from 1 review
ROSC rate · patients with out‐of‐hospital cardiac arrest
CPR plus delayed defibrillation showed no clear difference in ROSC rate compared with immediate defibrillation: overall analysis (low certainty).
1 finding from 1 review
Survival at 1 year rate · patients with out‐of‐hospital cardiac arrest
CPR plus delayed defibrillation showed no clear difference in survival at 1 year rate compared with immediate defibrillation: overall analysis (low certainty).
1 finding from 1 review
Intervention not reported
ICU length of stay (general intensive care patients) · Adult patients in intensive care
1 finding from 1 review
Intervention not reported
Hospital length of stay (general intensive care patients) · Adult patients in intensive care
1 finding from 1 review
Intervention not reported
Hospital length of stay (high‐risk surgical patients) · Adult patients in intensive care
1 finding from 1 review
Intervention not reported
Cost of care (hospital charges, 1000s of US dollars) · Adult patients in intensive care
1 finding from 1 review
Intervention not reported
Combined mortality of all studies · Adult patients in intensive care
The intervention leads to higher combined mortality of all studies (high certainty).
1 finding from 1 review
Annual Exacerbation Rates · COPD
Combined inhalers probably leads to lower annual exacerbation rates compared with placebo (primary outcomes) (moderate certainty).
1 finding from 1 review
Adverse events—'serious'—320/94 Duration of 10 months3 · COPD
Budesonide/formoterol (BDF) showed no clear difference in adverse events—'serious'—320/94 Duration of 10 months3 compared with placebo (low certainty).
1 finding from 1 review
OR 1.17 [0.95, 1.45]
2476 participants
Low
Adverse events—'serious'—160/94 Duration of nine months 3 · COPD
Budesonide/formoterol (BDF) showed no clear difference in adverse events—'serious'—160/94 Duration of nine months 3 compared with placebo (low certainty).
1 finding from 1 review
OR 1.2 [0.89, 1.63]
1556 participants
Low
Exacerbations (number of people experiencing ≥ 1 exacerbations) · COPD
Combined inhalers probably leads to lower participants with at least one exacerbation Duration of six months3 compared with placebo (primary outcomes) (moderate certainty).
1 finding from 1 review
OR 0.78 [0.66, 0.93]
3141 participants
Moderate
Mortality Duration of 18 months3 · COPD
Combined inhalers probably leads to lower mortality Duration of 18 months3 compared with placebo (primary outcomes) (moderate certainty).
1 finding from 1 review
Pneumonia · COPD
Combined inhalers probably leads to higher pneumonia Duration of 18 months3 compared with placebo (primary outcomes) (moderate certainty).
1 finding from 1 review
Hospitalisations due to COPD exacerbations · COPD
Combined inhalers showed no clear difference in hospitalisations due to COPD exacerbations Duration of 18 months3 compared with placebo (primary outcomes) (low certainty).
1 finding from 1 review
Adverse events—any Duration of two years1 · COPD
Fluticasone/salmeterol (FPS) showed no clear difference in adverse events—any Duration of two years1 compared with placebo (low certainty).
1 finding from 1 review
OR 1.09 [0.95, 1.25]
5574 participants
Low
Adverse events—'serious' Duration of two years1 · COPD
Fluticasone/salmeterol (FPS) showed no clear difference in adverse events—'serious' Duration of two years1 compared with placebo (low certainty).
1 finding from 1 review
OR 1.08 [0.95, 1.23]
5531 participants
Low
Adverse event—any—320/94 Duration of nine months 3 · COPD
Budesonide/formoterol (BDF) may leads to higher adverse event—any—320/94 Duration of nine months 3 compared with placebo (low certainty).
1 finding from 1 review
OR 1.42 [1.16, 1.74]
1552 participants
Low