Cochrane · systematic review · CD015087

Diclofenac for acute postoperative pain in children

Ringsten, M, Kredo, T, Ebrahim, S, et al. · Cochrane Database of Systematic Reviews · 2023 · Cochrane Library

SoF tableOnly the outcomes this review put in its Summary of Findings table are listed (the Cochrane Handbook caps them at about seven per comparison). Its other analyses are not shown here.
Questions
32
current version
GRADE rated
13
No studies
6
Included studies
NR
No studies 6 · 18.8%Ungraded 13 · 40.6%Very low 11 · 34.4%Low 0 · 0%Moderate 2 · 6.3%High 0 · 0%

Ungraded means an effect was reported without a GRADE rating; it is not a gap. No studies means the review found nothing to answer the question. The six categories are a display order, not a score.

Questions and results

Diclofenac versus placebo for treating postoperative pain in children

Population: children with acute postoperative pain
8 questions
OutcomeEffectEvidenceStatus / GRADE
Outcome№ of participants(studies)
Diclofenac vs placebo
no estimate extractedNRNo studies
Pain relief 50% ‐ as reported by child, at 0 to 2 hours (not reported)
Diclofenac vs placebo
no estimate extracted50 participantsUngraded
Pain relief 50% ‐ as reported by child, at 2 to 24 hours (not reported)
Diclofenac vs placebo
no estimate extracted50 participantsUngraded
Pain intensity ‐ as reported by child, at 0 to 2 hours (not reported)
Diclofenac vs placebo
no estimate extracted0 participantsUngraded
Pain intensity ‐ as reported by child, at 2 to 24 hours (not reported)
Diclofenac vs placebo
no estimate extracted2 participantsUngraded
Nausea, vomiting, or both during study period № of participants: 100(2 RCTs)
Diclofenac vs placebo
RR 0.83 [0.38, 1.8]2 studies · 100 participantsVery low
Downgraded: risk of bias, imprecision
Any bleeding during study period № of participants: 100(2 RCTs)d
Diclofenac vs placebo
RR 3 [0.34, 26.45]2 studies · 100 participantsVery low
Downgraded: risk of bias, imprecision
Serious adverse events during study period (not reported)
Diclofenac vs placebo
no estimate extractedNRNo studies

Diclofenac versus opioids for treating postoperative pain in children

Population: children with acute postoperative pain
8 questions
OutcomeEffectEvidenceStatus / GRADE
Outcome№ of participants(studies)
Diclofenac vs opioids
no estimate extractedNRNo studies
Pain relief 50% ‐ as reported by child, at 0 to 2 hours (not reported)
Diclofenac vs opioids
no estimate extracted50 participantsUngraded
Pain relief 50% ‐ as reported by child, at 2 to 24 hours (not reported)
Diclofenac vs opioids
no estimate extracted50 participantsUngraded
Pain intensity ‐ as reported by child, at 0 to 2 hours (not reported)
Diclofenac vs opioids
no estimate extracted0 participantsUngraded
Pain intensity ‐ as reported by child, at 2 to 24 hours № of participants: 50 (1 RCT)
Diclofenac vs opioids
no estimate extracted1 study · 2 participantsVery low
Downgraded: risk of bias, imprecision
Nausea, vomiting, or both during study period № of participants: 463 (7 RCTs)
Diclofenac vs opioids
RR 0.75 [0.58, 0.96]7 studies · 463 participantsModerate
Downgraded: risk of bias
Any bleeding during study period № of participants: 222 (2 RCTs)
Diclofenac vs opioids
RR 3.06 [1.31, 7.13]2 studies · 222 participantsModerate
Downgraded: imprecision
Serious adverse events during study period (not reported)
Diclofenac vs opioids
no estimate extractedNRNo studies

Diclofenac versus paracetamol for treating postoperative pain in children

Population: children with acute postoperative pain
8 questions
OutcomeEffectEvidenceStatus / GRADE
Outcome№ of participants(studies)
Diclofenac vs paracetamol
no estimate extractedNRNo studies
Pain relief 50% ‐ as reported by child, at 0 to 2 hours (not reported)
Diclofenac vs paracetamol
no estimate extracted50 participantsUngraded
Pain relief 50% ‐ as reported by child, at 2 to 24 hours (not reported)
Diclofenac vs paracetamol
no estimate extracted50 participantsUngraded
Pain intensity ‐ as reported by child, at 0 to 2 hours № of participants: 180 (2 RCTs)
Diclofenac vs paracetamol
no estimate extracted0 studies · 2 participantsVery low
Downgraded: risk of bias, imprecision
Pain intensity ‐ as reported by child, at 2 to 24 hours № of participants: 300 (3 RCTs)
Diclofenac vs paracetamol
no estimate extracted2 studies · 3 participantsVery low
Downgraded: risk of bias, inconsistency
Nausea, vomiting, or both during study period № of participants: 348 (5 RCTs)
Diclofenac vs paracetamol
RR 0.47 [0.25, 0.87]5 studies · 348 participantsVery low
Downgraded: risk of bias, imprecision, inconsistency
Any bleeding during study period № of participants: 332 (5 RCTs)
Diclofenac vs paracetamol
RR 0.57 [0.12, 2.62]5 studies · 332 participantsVery low
Downgraded: risk of bias, imprecision
Serious adverse events during study period № of participants: 60 (1 RCT)
Diclofenac vs paracetamol
RR 0.5 [0.05, 5.22]1 study · 60 participantsVery low
Downgraded: imprecision

Diclofenac versus bupivacaine for treating postoperative pain in children

Population: children with acute postoperative pain
8 questions
OutcomeEffectEvidenceStatus / GRADE
Outcome№ of participants(studies)
Diclofenac vs bupivacaine
no estimate extractedNRNo studies
Pain relief 50% ‐ as reported by child, at 0 to 2 hours (not reported)
Diclofenac vs bupivacaine
no estimate extracted50 participantsUngraded
Pain relief 50% ‐ as reported by child, at 2 to 24 hours (not reported)
Diclofenac vs bupivacaine
no estimate extracted50 participantsUngraded
Pain intensity ‐ as reported by child, at 0 to 2 hours (not reported)
Diclofenac vs bupivacaine
no estimate extracted0 participantsUngraded
Pain intensity ‐ as reported by child, at 2 to 24 hours (not reported)
Diclofenac vs bupivacaine
no estimate extracted2 participantsUngraded
Nausea, vomiting, or both during study period № of participants: 128 (3 RCTs)
Diclofenac vs bupivacaine
RR 1.28 [0.58, 2.78]3 studies · 128 participantsVery low
Downgraded: risk of bias, imprecision
Any bleeding during study period № of participants: 38 (1 RCTs)
Diclofenac vs bupivacaine
RR 1.8 [0.18, 18.21]1 study · 38 participantsVery low
Downgraded: risk of bias, imprecision
Serious adverse events during the study period № of participants: 38 (1 RCTs)
Diclofenac vs bupivacaine
RR 4.52 [0.23, 88.38]1 study · 38 participantsVery low
Downgraded: risk of bias, imprecision