Intervention not reported
Changes in cognitive function testing from baseline (96 weeks trial period) · Patients with a clinical and EEG diagnosis of BECTS
1 finding from 1 review
no estimate extracted
39 participants
Very low
Intervention not reported
Proportion of patients who are seizure free at 3 months · Patients between three and 12 years old with clinical and EEG diagnosis of BECTS
It is very uncertain whether the intervention changes proportion of patients who are seizure free at 3 months (very low certainty).
1 finding from 1 review
Intervention not reported
Proportion of patients who are seizure free at 12 months · Patients between three and 12 years old with clinical and EEG diagnosis of BECTS
It is very uncertain whether the intervention changes proportion of patients who are seizure free at 12 months (very low certainty).
1 finding from 1 review
Intervention not reported
Proportion of patients who discontinued treatment due to adverse events ( · Patients between three and 12 years old with clinical and EEG diagnosis of BECTS
The intervention showed no clear difference in proportion of patients who discontinued treatment due to adverse… (low certainty).
1 finding from 1 review
Intervention not reported
Low Hb deferral ‐ at first donation visit after commencement of treatment · patients with iron deficiency and/or anaemia in blood donors
The intervention probably leads to lower low Hb deferral ‐ at first donation visit after commencement of… (moderate certainty).
1 finding from 1 review
Intervention not reported
Low Hb deferral ‐ after multiple donation visits · patients with iron deficiency and/or anaemia in blood donors
The intervention probably leads to lower low Hb deferral ‐ after multiple donation visits (moderate certainty).
1 finding from 1 review
Intervention not reported
Hb (g/L) ‐ before further donation Scale from: 123 to 152 · patients with iron deficiency and/or anaemia in blood donors
1 finding from 1 review
Intervention not reported
Hb (g/L) ‐ after subsequent donation(s) Scale from: 127.3 to 129 · patients with iron deficiency and/or anaemia in blood donors
1 finding from 1 review
Intervention not reported
Serum ferritin (ng/mL) ‐ before further donation Scale from: 12.9 to 57.8 · patients with iron deficiency and/or anaemia in blood donors
1 finding from 1 review
Intervention not reported
Serum ferritin (ng/mL) ‐ after subsequent donation(s) Scale from: 18 to 19 · patients with iron deficiency and/or anaemia in blood donors
1 finding from 1 review
Intervention not reported
Adverse effects (any) · patients with iron deficiency and/or anaemia in blood donors
The intervention probably leads to higher adverse effects (any) (moderate certainty).
1 finding from 1 review
Patient‐reported pain intensity or pain relief (VAS, NRS or categorical scale) · patients with knee replacement surgery
1 finding from 1 review
Neurological injury · patients with knee replacement surgery
1 finding from 1 review
Opioid consumption at 24 hours using morphine equivalents Scale from zero to 150 mg · patients with knee replacement surgery
1 finding from 1 review
Maternal nausea and/or vomiting · patients with knee replacement surgery
FNB (any type) probably leads to lower nausea and/or vomiting compared with epidural analgesia (moderate certainty).
1 finding from 1 review
Knee flexion range of motion (degree) · patients with knee replacement surgery
1 finding from 1 review
Participant satisfaction with analgesia (point) Scale from zero to 10 · patients with knee replacement surgery
1 finding from 1 review
Patient‐reported pain intensity or pain relief (VAS, NRS or categorical scale) · patients with knee replacement surgery
1 finding from 1 review
Pain on movement at 24 hours Visual analogue scale Scale from zero to 10 · patients with knee replacement surgery
1 finding from 1 review
Neurological injury: not reported · patients with knee replacement surgery
The review found no eligible studies for this question.
1 finding from 1 review
no estimate extracted
Studies not reported
No studies found