• Srdjan Jelacic, Laurent Bollag, Andrew Bowdle, Cyril Rivat, Kevin C Cain, and Philippe Richebe.
• Department of Anesthesiology and Pain Medicine. Electronic address: sjelacic@uw.edu.
• J. Cardiothorac. Vasc. Anesth. 2016 Aug 1; 30 (4): 997-1004.

ObjectivesThe authors hypothesized that intravenous acetaminophen as an adjunct analgesic would significantly decrease 24-hour postoperative opioid consumption.DesignDouble-blind, randomized, placebo-controlled trial.SettingA single academic medical center.ParticipantsThe study was comprised of 68 adult patients undergoing cardiac surgery.InterventionsPatients were assigned randomly to receive either 1,000 mg of intravenous acetaminophen or placebo immediately after anesthesia induction, at the end of surgery, and then every 6 hours for the first 24 hours in the intensive care unit, for a total of 6-1,000 mg doses.Measurements And Main ResultsThe primary outcome was 24-hour postoperative opioid consumption. The secondary outcomes included 48-hour postoperative opioid consumption, incisional pain scores, opioid-related adverse effects, length of mechanical ventilation, length of intensive care unit stay, and the extent of wound hyperalgesia assessed at 24 and 48 hours postoperatively. The mean±standard deviation postoperative 24-hour opioid consumption expressed in morphine equivalents was significantly less in the acetaminophen group (45.6±29.5 mg) than in the placebo group (62.3±29.5 mg), representing a 27% reduction in opioid consumption (95% CI, 2.3-31.1 mg; p = 0.024). There were no differences in pain scores and opioid-related adverse effects between the 2 groups. A significantly greater number of patients in the acetaminophen group responded "very much" and "extremely well" when asked how their overall pain experience met their expectation (p = 0.038).ConclusionsThe administration of intravenous acetaminophen during cardiac surgery and for the first 24 hours postoperatively reduced opioid consumption and improved patient satisfaction with their overall pain experience but did not reduce opioid side effects.Copyright © 2016 Elsevier Inc. All rights reserved.

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