Adverse events mild adverse events · adolescent and adult male circumcisions
It is very uncertain whether circumcision devices changes mild adverse events compared with standard surgical techniques (very low certainty).
1 finding from 1 review
Operating time · adolescent and adult male circumcisions
1 finding from 1 review
Pain during the first 24 hours (VAS means) · adolescent and adult male circumcisions
1 finding from 1 review
Pain during the first 7 days (VAS means) · adolescent and adult male circumcisions
1 finding from 1 review
Participant satisfaction · adolescent and adult male circumcisions
Circumcision devices may leads to higher participant satisfaction compared with standard surgical techniques (low certainty).
1 finding from 1 review
Death (any case) Time frame: 2 to 4 weeks · solid organ transplant recipients
It is very uncertain whether extended changes death (any cause) Time frame: 30 days compared with short duration antibiotics (very low certainty).
1 finding from 1 review
Graft loss including death · solid organ transplant recipients
It is very uncertain whether extended changes graft loss (including death with functioning graft) Time frame: 30… compared with short duration antibiotics (very low certainty).
1 finding from 1 review
UTI · solid organ transplant recipients
It is very uncertain whether extended changes other infection: UTI Time frame: 30 days compared with short duration antibiotics (very low certainty).
1 finding from 1 review
Other infection: septicaemia Time frame: 2 to 6 weeks · solid organ transplant recipients
It is very uncertain whether extended changes other infection: septicaemia Time frame: 30 days compared with short duration antibiotics (very low certainty).
1 finding from 1 review
Other infection: pneumonia Time frame: 30 days · solid organ transplant recipients
It is very uncertain whether extended changes other infection: pneumonia Time frame: 30 days compared with short duration antibiotics (very low certainty).
1 finding from 1 review
Adverse drug reactions · solid organ transplant recipients
The review found no eligible studies for this question.
1 finding from 1 review
no estimate extracted
Studies not reported
No studies found
Serious maternal morbidity (renal or respiratory failure, cardiac arrest or multiple organ failure) · treating primary postpartum haemorrhage
The review found no eligible studies for this question.
1 finding from 1 review
no estimate extracted
Studies not reported
No studies found
Number of women with total blood loss 1000 mL or more after randomisation · treating primary postpartum haemorrhage
The review found no eligible studies for this question.
1 finding from 1 review
no estimate extracted
Studies not reported
No studies found
Mean blood loss (mL) (trialist defined) · treating primary postpartum haemorrhage
The review found no eligible studies for this question.
1 finding from 1 review
no estimate extracted
Studies not reported
No studies found
Blood transfusion (red cell or whole blood) · treating primary postpartum haemorrhage
The review found no eligible studies for this question.
1 finding from 1 review
no estimate extracted
Studies not reported
No studies found
Side effects of the intervention (e.g. trauma, necrosis) · treating primary postpartum haemorrhage
It is very uncertain whether one uterine devascularisation technique (uterine arterial… changes side effects of the intervention (e.g. trauma, necrosis) compared with another uterine devascularisation technique (surgical… (very low certainty).
1 finding from 1 review
Mortality due to bleeding · women with complete placenta praevia and intractable bleeding following caesarean section
1 finding from 1 review
Hysterectomy to control bleeding · women with complete placenta praevia and intractable bleeding following caesarean section
1 finding from 1 review
Serious maternal morbidity (renal or respiratory failure, cardiac arrest or multiple organ failure) · women with complete placenta praevia and intractable bleeding following caesarean section
1 finding from 1 review
Number of women with total blood loss 1000 mL or more after randomisation · women with complete placenta praevia and intractable bleeding following caesarean section
The review found no eligible studies for this question.
1 finding from 1 review
no estimate extracted
Studies not reported
No studies found