Aesthetic condition change related to patient's opinion · Adult patients with single (localised) recession-type defects (Miller Class I/II, at least 3 mm)
The review found no eligible studies for this question.
1 finding from 1 review
Sites with complete root coverage · Adult patients with single (localised) recession-type defects (Miller Class I/II, at least 3 mm)
GTR rm + CAF showed no clear difference in sites with complete root coverage compared with SCTG + CAF (low certainty).
1 finding from 1 review
Attachment change · Adult patients with single (localised) recession-type defects (Miller Class I/II, at least 3 mm)
XCM + CAF showed no clear difference in clinical attachment level change compared with CAF (low certainty).
1 finding from 1 review
Occurrence of adverse effects or postoperative complications · Adult patients with single (localised) recession-type defects (Miller Class I/II, at least 3 mm)
1 finding from 1 review
Keratinized tissue change · Adult patients with single (localised) recession-type defects (Miller Class I/II, at least 3 mm)
It is very uncertain whether GTR rm + CAF changes keratinized tissue change compared with SCTG + CAF (very low certainty).
1 finding from 1 review
Change in gingival recession (REC) · Adult patients with single (localised) recession-type defects (Miller Class I/II, at least 3 mm)
It is very uncertain whether EMP + CAF changes gingival recession change compared with SCTG + CAF (very low certainty).
1 finding from 1 review
Intervention not reported
Disability‐worsening Proportion of participants with disability‐worsening at a maximum of five years'
It is very uncertain whether the intervention changes disability‐worsening Proportion of participants with… (very low certainty).
1 finding from 1 review
OR 0.88 [0.5, 1.57]
Studies not reported
Very low
Intervention not reported
Relapse Proportion of participants with relapse at a maximum of five years'
The intervention may leads to lower relapse Proportion of participants with relapse at a maximum of five… (low certainty).
1 finding from 1 review
OR 0.35 [0.26, 0.48]
Studies not reported
Low
Primary anaesthesia failure (incomplete sensory block) · Adult patients undergoing hand, wrist or forearm surgery
Double leads to lower primary anaesthesia failure (incomplete sensory block) compared with single‐injection technique (high certainty).
1 finding from 1 review
Secondary analgesia failure: Intraoperative sedation required · Adult patients undergoing hand, wrist or forearm surgery
Double showed no clear difference in secondary analgesia failure ‐ intraoperative sedation required compared with single‐injection technique (moderate certainty).
1 finding from 1 review
Secondary analgesia failure : Tourniquet pain · Adult patients undergoing hand, wrist or forearm surgery
Double showed no clear difference in secondary analgesia failure ‐ tourniquet pain compared with single‐injection technique (moderate certainty).
1 finding from 1 review
Complete failure of block3 · Adult patients undergoing hand, wrist or forearm surgery
Double showed no clear difference in complete failure of block3 compared with single‐injection technique (low certainty).
1 finding from 1 review
Time to readiness for surgery2 (minutes) · Adult patients undergoing hand, wrist or forearm surgery
1 finding from 1 review
Intravascular injection · Adult patients undergoing hand, wrist or forearm surgery
Double showed no clear difference in intravascular injection compared with single‐injection technique (low certainty).
1 finding from 1 review
Adverse effects lasting more than 24 hours3 · Adult patients undergoing hand, wrist or forearm surgery
1 finding from 1 review
Intervention not reported
Clearance of proven sepsis · neonates with suspected or proven sepsis
It is very uncertain whether the intervention changes clearance of proven sepsis (very low certainty).
1 finding from 1 review
Intervention not reported
Failure to achieve peak levels of at least 5 microgram/ml (measured 0.5 to one hour after administration of any dose of gentamicin) · neonates with suspected or proven sepsis
The intervention probably leads to lower failure to achieve peak levels of at least 5 microgram/ml (measured… (moderate certainty).
1 finding from 1 review
Intervention not reported
Nephrotoxicity (End of study period or before discharge) · neonates with suspected or proven sepsis
1 finding from 1 review
Intervention not reported
Ototoxicity (End of study period or before discharge) · neonates with suspected or proven sepsis
It is very uncertain whether the intervention changes ototoxicity (End of study period or before discharge) (very low certainty).
1 finding from 1 review
Intervention not reported
Failure to achieve trough levels of ≤2 microgram/ml ( · neonates with suspected or proven sepsis
The intervention probably leads to lower failure to achieve trough levels of ≤2 microgram/ml ( (moderate certainty).
1 finding from 1 review