Intervention not reported
Withdrawal of methylphenidate due to serious adverse events (non‐comparative cohort studies) Measured by: proportion of participants withdrawn from treatment Average study duration (range): 7.9 months (1 month to 37 months) · children and adolescents aged 18 years and under diagnosed with ADHD
1 finding from 1 review
Intervention not reported
Withdrawal of methylphenidate due to adverse events of unknown severity Measured by: proportion of participants withdrawn from treatment Average study duration (range): 4.6 months (21 days to 36 months) · children and adolescents aged 18 years and under diagnosed with ADHD
1 finding from 1 review
Intervention not reported
Non‐serious adverse events Measured by: proportion of any non‐serious adverse events Average study duration (range): 5.99 months (1 day to 41 months) · children and adolescents aged 18 years and under diagnosed with ADHD
1 finding from 1 review
Intervention not reported
Withdrawal of methylphenidate due to non‐serious adverse events Measured by: proportion of participants withdrawn from treatment Average study duration (range): 5.60 months (0.6 months to 41 months) · children and adolescents aged 18 years and under diagnosed with ADHD
1 finding from 1 review
Intervention not reported
Withdrawal of methylphenidate for unknown reasons Measure by: proportion of participants withdrawn from treatment Average study duration (range): 6.13 months (1 day to 36 months) · children and adolescents aged 18 years and under diagnosed with ADHD
1 finding from 1 review
Intervention not reported
Mortality · Improving outcomes in older adult people admitted to a surgical service.
The intervention showed no clear difference in mortality (moderate certainty).
1 finding from 1 review
RR 0.85 [0.68, 1.05]
1316 participants
Moderate
Intervention not reported
Discharge to an increased level of care · Improving outcomes in older adult people admitted to a surgical service.
The intervention leads to lower discharge to an increased level of care (high certainty).
1 finding from 1 review
RR 0.71 [0.55, 0.92]
941 participants
High
Intervention not reported
Length of stay · Improving outcomes in older adult people admitted to a surgical service.
1 finding from 1 review
no estimate extracted
841 participants
Moderate
Intervention not reported
Re‐admission · Improving outcomes in older adult people admitted to a surgical service.
The intervention showed no clear difference in re‐admission (moderate certainty).
1 finding from 1 review
RR 1 [0.76, 1.32]
741 participants
Moderate
Intervention not reported
Total cost · Improving outcomes in older adult people admitted to a surgical service.
1 finding from 1 review
no estimate extracted
397 participants
Moderate
Intervention not reported
Major complication · Improving outcomes in older adult people admitted to a surgical service.
1 finding from 1 review
no estimate extracted
579 participants
Low
Intervention not reported
Major complication ‐ delirium · Improving outcomes in older adult people admitted to a surgical service.
The intervention may leads to lower major complication ‐ delirium (low certainty).
1 finding from 1 review
RR 0.75 [0.6, 0.94]
705 participants
Low
Rate of caesarean section · Low risk pregnant women. All of the women were in labour.
Admission cardiotocography showed no clear difference in incidence of caesarean section compared with intermittent auscultation (low‐risk women) (moderate certainty).
1 finding from 1 review
Instrumental vaginal birth · Low risk pregnant women. All of the women were in labour.
Admission cardiotocography showed no clear difference in incidence of operative vaginal birth compared with intermittent auscultation (low‐risk women) (low certainty).
1 finding from 1 review
Perinatal mortality rate (fetal and neonatal deaths excluding lethal congenital anomalies) · Low risk pregnant women. All of the women were in labour.
Admission cardiotocography showed no clear difference in perinatal mortality rate (fetal and neonatal deaths excluding lethal… compared with intermittent auscultation (low‐risk women) (moderate certainty).
1 finding from 1 review
Severe neurodevelopmental disability assessed ≥ 12 months of age · Low risk pregnant women. All of the women were in labour.
1 finding from 1 review
Incidence of continuous electronic fetal monitoring during labour · Low risk pregnant women. All of the women were in labour.
Admission cardiotocography may leads to higher incidence of continuous electronic fetal monitoring during labour compared with intermittent auscultation (low‐risk women) (low certainty).
1 finding from 1 review
Incidence and severity of hypoxic ischaemic encephalopathy (incidence only reported) · Low risk pregnant women. All of the women were in labour.
It is very uncertain whether admission cardiotocography changes incidence and severity of hypoxic ischaemic encephalopathy… compared with intermittent auscultation (low‐risk women) (very low certainty).
1 finding from 1 review
Neonatal seizures · Low risk pregnant women. All of the women were in labour.
Admission cardiotocography showed no clear difference in incidence of seizures in the neonatal period compared with intermittent auscultation (low‐risk women) (low certainty).
1 finding from 1 review
Instrumental vaginal birth · healthy pregnant women
Home support showed no clear difference in rate of instrumental vaginal birth compared with telephone triage (low certainty).
1 finding from 1 review