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. 2016 May 23;2016(5):CD007126. doi: 10.1002/14651858.CD007126.pub3

Summary of findings 6. Opioid consumption (IV morphine equivalents) over 6 hours.

IV paracetamol/propacetamol compared to placebo or other analgesics for postoperative pain
Patient or population: patients with postoperative pain
 Settings: hospital
 Intervention: IV paracetamol/propacetamol
 Comparison: placebo or other analgesics
Outcomes Illustrative comparative risks* (95% CI) No of participants
 (studies) Quality of the evidence
 (GRADE)
Para/propacetamol vs placebo
 see footnote1 The mean opioid consumption (IV morphine equivalents) over 6 hours was:
 1.92 lower (2.41 to 1.42 lower) 777
 (13 studies) ⊕⊕⊕⊝
 moderate2,3
Paracetamol vs placebo
 see footnote1 The mean opioid consumption (IV morphine equivalents) over 6 hours was:
 1.83 lower (2.35 to 1.31 lower) 404
 (8 studies) ⊕⊕⊝⊝
 low2,3,4
Propacetamol vs placebo
 see footnote1 The mean opioid consumption (IV morphine equivalents) over 6 hours was:
 2.67 lower (4.21 to 1.13 lower) 373
 (6 studies) ⊕⊕⊝⊝
 low2,4,5
Para/propacetamol vs NSAIDs
 see footnote1 The mean opioid consumption (IV morphine equivalents) over 6 hours was:
 0.12 lower (0.37 lower to 0.12 higher) 540
 (8 studies) ⊕⊝⊝⊝
 very low2,3,6
Paracetamol vs NSAIDs
 see footnote1 The mean opioid consumption (IV morphine equivalents) over 6 hours was:
 0.81 higher (0.87 lower to 2.49 higher) 160
 (3 studies) ⊕⊝⊝⊝
 very low3,5,6,7
Propacetamol vs NSAIDs
 see footnote1 The mean opioid consumption (IV morphine equivalents) over 6 hours was:
 0.14 lower (0.39 lower to 0.11 higher) 380
 (5 studies) ⊕⊝⊝⊝
 very low5,6,7
*The basis for the assumed risk (e.g. the median control group risk across studies) is provided in footnotes. The corresponding risk (and its 95% confidence interval) is based on the assumed risk in the comparison group and the relative effect of the intervention (and its 95% CI).
 CI: confidence interval; NSAIDs: nonsteroidal anti‐inflammatory drugs
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.

1Mean opioid consumption (in mg) over 6 hours in each treatment arm converted into IV morphine‐equivalents, using commonly used and widely accepted opioid conversion tables.
 2See 'Risk of bias' tables: several unclear assessments related to randomization, unclear risk for selective reporting.
 3Majority of all individual studies had < 100 participants.
 4Considerable unexplained heterogeneity exists between studies.
 5Total population size < 400.
 6Different NSAIDs studied.
 7Wide confidence interval that includes no effect and appreciable benefit and/or harm.