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Published on: June 23, 2023
Intravenous acetaminophen for postoperative pain control after open abdominal and thoracic surgery in pediatric
Victoria Archer1, Zacharie Cloutier2, Lily Park2
1Division of General Surgery, Department of Surgery, McMaster University, Hamilton, ON, Canada. vicki.archer@medportal.ca.
Insights
Intravenous acetaminophen (IVA) may reduce opioid use and minor adverse events (AEs) in children after major surgery. Evidence suggests IVA does not increase postoperative pain, but further research is needed.
Area of Science:
- Pediatric Anesthesiology
- Pharmacology
- Evidence-Based Medicine
Background:
- Pediatric opioid exposure is linked to adverse events (AEs).
- Intravenous acetaminophen (IVA) may offer an alternative or adjunct to opioids for pediatric pain management.
- Limited data exist on IVA's postoperative impact in pediatric surgical patients.
Conclusions:
- Addition of IVA to opioid-based pain management may decrease opioid use and minor AEs in pediatric surgical patients.
- IVA appears safe regarding postoperative pain levels in this population.
- Further high-quality research with long-term follow-up is warranted to confirm these findings.
Abstract:
Pediatric opioid exposure increases short- and long-term adverse events (AE). The addition of intravenous acetaminophen (IVA) to pediatric pain regimes to may reduce opioids but is not well studied postoperatively. Our objective was to quantify the impact of IVA on postoperative pain, opioid use, and AEs in pediatric patients after major abdominal and thoracic surgery. Medline, Embase, CINAHL, Web of Science, and Cochrane Library were searched systematically for randomized controlled trials (RCTs) comparing IVA to other modalities. Five RCTs enrolling 443 patients with an average age of 2.12 years (± 2.81) were included. Trials comparing IVA with opioids to opioids alone were meta-analyzed. Low to very low-quality evidence demonstrated equivalent pain scores between the groups (-0.23, 95% CI -0.88 to 0.40, p 0.47) and a reduction in opioid consumption (-1.95 morphine equivalents/kg/48 h, 95% CI -3.95 to 0.05, p 0.06) and minor AEs (relative risk 0.39, 95% CI 0.11 to 1.43, p 0.15). We conclude that the addition of IVA to opioid-based regimes in pediatric patients may reduce opioid use and minor AEs without increasing postoperative pain. Given the certainty of evidence, further research featuring patient-important outcomes and prolonged follow-up is necessary to confirm these findings.
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