Adults: higher dose/longer course vs lower dose/shorter course
- no estimate extracted2 studies · 41 participantsVery low
It is very uncertain whether adults: higher dose/longer course changes all adverse events compared with lower dose/shorter course (very low certainty).
Comparison 12.8: Long‐term therapy showed no clear difference in repetition of SH at post‐intervention compared with TAU or another comparator (low certainty).
Children: higher dose/longer course showed no clear difference in asthma symptoms Symptom free by 7 days compared with lower dose/shorter course (moderate certainty).
Children: higher dose/longer course showed no clear difference in new exacerbation during compared with lower dose/shorter course (low certainty).
Children: higher dose/longer course showed no clear difference in all adverse events compared with lower dose/shorter course (moderate certainty).
It is very uncertain whether prolonged feeding: hydrolysed formula changes all allergic disease ‐ Infancy (incidence) compared with cow's milk formula (very low certainty).
It is very uncertain whether prolonged feeding: hydrolysed formula changes all allergic disease ‐ Childhood (incidence) compared with cow's milk formula (very low certainty).
It is very uncertain whether prolonged feeding: hydrolysed formula changes asthma ‐ Infancy (incidence) compared with cow's milk formula (very low certainty).
It is very uncertain whether prolonged feeding: hydrolysed formula changes eczema ‐ Infancy (incidence) compared with cow's milk formula (very low certainty).
It is very uncertain whether prolonged feeding: hydrolysed formula changes rhinitis ‐ Infancy (incidence) compared with cow's milk formula (very low certainty).
It is very uncertain whether prolonged feeding: hydrolysed formula changes food allergy ‐ Infancy (incidence) compared with cow's milk formula (very low certainty).
It is very uncertain whether prolonged feeding: hydrolysed formula changes cow's milk allergy ‐ Infancy (incidence) compared with cow's milk formula (very low certainty).
Longer intervals (5‐15 days) (intervention) showed no clear difference in catheter‐related blood stream infection (CRBSI) compared with shorter intervals (2‐5 days) (control) between dressing changes (low certainty).
Longer intervals (5‐15 days) (intervention) showed no clear difference in all‐cause mortality compared with shorter intervals (2‐5 days) (control) between dressing changes (low certainty).
Longer intervals (5‐15 days) (intervention) showed no clear difference in pain № of participants: 193 (2 RCTs) compared with shorter intervals (2‐5 days) (control) between dressing changes (low certainty).