Intervention not reported
- Pulmonary artery catheters for adult patients in intensive care 2013 · Cochrane Headline outcomes onlyno estimate extracted2 studies · 191 participantsLow
The intervention leads to higher combined mortality of all studies (high certainty).
Combined inhalers probably leads to lower annual exacerbation rates compared with placebo (primary outcomes) (moderate certainty).
Budesonide/formoterol (BDF) showed no clear difference in adverse events—'serious'—320/94 Duration of 10 months3 compared with placebo (low certainty).
Budesonide/formoterol (BDF) showed no clear difference in adverse events—'serious'—160/94 Duration of nine months 3 compared with placebo (low certainty).
Combined inhalers probably leads to lower participants with at least one exacerbation Duration of six months3 compared with placebo (primary outcomes) (moderate certainty).
Combined inhalers probably leads to lower mortality Duration of 18 months3 compared with placebo (primary outcomes) (moderate certainty).
Combined inhalers probably leads to higher pneumonia Duration of 18 months3 compared with placebo (primary outcomes) (moderate certainty).
Combined inhalers showed no clear difference in hospitalisations due to COPD exacerbations Duration of 18 months3 compared with placebo (primary outcomes) (low certainty).
Fluticasone/salmeterol (FPS) showed no clear difference in adverse events—any Duration of two years1 compared with placebo (low certainty).
Fluticasone/salmeterol (FPS) showed no clear difference in adverse events—'serious' Duration of two years1 compared with placebo (low certainty).
Budesonide/formoterol (BDF) may leads to higher adverse event—any—320/94 Duration of nine months 3 compared with placebo (low certainty).
Budesonide/formoterol (BDF) may leads to higher adverse event—any—160/94 Duration of nine months 3 compared with placebo (low certainty).
The intervention probably leads to lower exacerbation rates per participant per year (moderate certainty).
The intervention leads to lower mortality (high certainty).
The intervention showed no clear difference in pneumonia (low certainty).
The intervention showed no clear difference in hospitalisations due to COPD exacerbations (low certainty).
The intervention showed no clear difference in adverse events-serious Fluticasone/salmeterol (FPS) versus… (low certainty).
It is very uncertain whether the intervention changes adverse events-serious events Budesonide/formoterol (BDF) versus… (very low certainty).
The intervention showed no clear difference in adverse events-serious Mometasone/formoterol (MF/F) versus… (low certainty).