for the main comparison.
Ibuprofen plus codeine compared with placebo for acute postoperative pain | ||||||
Population: adults with moderate or severe acute postoperative pain Settings: community or hospital Intervention: ibuprofen 400 mg + codeine 25.6 mg to 60 mg Comparison: placebo | ||||||
Outcomes | Probable outcome with |
Relative effect and NNT or NNH (95% CI) |
Number of studies, events | Quality of the evidence (GRADE) | Comments | |
Comparator | Intervention | |||||
At least 50% of maximum pain relief over 4 to 6 h | 180 in 1000 | 640 in 1000 | RR 4.1 (2.8 to 5.9) NNT 2.2 (1.8 to 2.6) |
4 studies 443 participants 208 events |
High | Adequate numbers of studies, participants and events. Consistency across studies |
Participants with at least 1 adverse event | 180 in 1000 | 280 in 1000 | RR 1.2 (0.84 to 1.7) NNH not calculated |
4 studies 443 participants 109 events |
Moderate | Adequate numbers of studies, participants, but moderate number of events. Consistency across studies. Single dose studies may not reflect clinical practice |
Participants with a serious adverse event | No serious adverse events | Low | Studies underpowered to detect rare events | |||
Deaths | No deaths | Low | Studies underpowered to detect rare events | |||
CI: confidence interval; NNH: number needed to treat to harm; NNT: number needed to treat for benefit; RR: Risk Ratio | ||||||
GRADE Working Group grades of evidence High quality: Further research is very unlikely to change our confidence in the estimate of effect. Moderate quality: Further research is likely to have an important impact on our confidence in the estimate of effect and may change the estimate. Low quality: Further research is very likely to have an important impact on our confidence in the estimate of effect and is likely to change the estimate. Very low quality: We are very uncertain about the estimate. |