“…Data from eligible studies were extracted using standardized forms and were independently checked by the two reviewers. Outcomes analyzed were postoperative pain (swallowing or resting pain scores after leaving the operation room), 2,6,8-12 postoperative (24 hours) analgesic requirements (either doses or percentage of patient receiving postoperative opioids or nonopioids analgesics), 2,6,[8][9][10]12,13 time to first analgesic administration (opioids or nonopioids analgesics administered with a defined pain intensity target), [9][10][11] time to first oral uptake, 2,5,12,13 the occurrence of postoperative nausea and vomiting (incidence or percentage of patients), 2,6,[8][9][10][11][12][13] dizziness, 6,8,12 and headache, 6,8,12 or sedation (sedation scores). 2,11 These outcomes were compared between the preoperative gabapentinoids group, in which there was intravenous and oral administration, and the control group, in which there was no treatment or use of opioids during the 24-hour postoperative period.…”