Speech and language therapy vs healthy lifestyle advice
- no estimate extracted1 study · 75 participantsLow
Single inhaler therapy showed no clear difference in fatal serious adverse events compared with fixed dose ICS (moderate certainty).
Single inhaler therapy showed no clear difference in serious adverse events (non‐fatal) compared with fixed dose ICS (moderate certainty).
It is very uncertain whether oral + inhaled dual therapy changes serious adverse events. Outcome assessed on day 42 compared with oral monotherapy (very low certainty).
160/4.5 mcg BDF single inhaler therapy showed no clear difference in fatal serious adverse events compared with current best practice (low certainty).
160/4.5 mcg BDF single inhaler therapy showed no clear difference in serious adverse events (non‐fatal) compared with current best practice (low certainty).
Sublingual immunotherapy showed no clear difference in serious adverse events Weighted mean duration of studies: 56 weeks compared with control (moderate certainty).
The review found no eligible studies for this question.
Alteplase may leads to higher serious adverse events compared with urokinase (low certainty).
Fibrinolytics showed no clear difference in serious adverse events compared with placebo (low certainty).
Streptokinase showed no clear difference in serious adverse events compared with urokinase (low certainty).
The review found no eligible studies for this question.
The review found no eligible studies for this question.
Intermittent ICS showed no clear difference in serious adverse events compared with placebo (moderate certainty).
Intermittent ICS showed no clear difference in serious adverse events compared with placebo (low certainty).
Antibiotics showed no clear difference in serious adverse events WMD of compared with placebo (moderate certainty).
SiT for maintenance/relief showed no clear difference in patients with serious adverse events compared with higher‐dose ICS/LABA + SABA (moderate certainty).
It is very uncertain whether macrolide+tetracycline changes all‐cause serious adverse events 60 weeks (end of study) compared with macrolide (very low certainty).