Your browser doesn't support javascript.
loading
Low-Dose Short-Term Scheduled Ketorolac Reduces Opioid Use and Pain in Orthopaedic Polytrauma Patients: A Randomized Clinical Trial.
Foster, Jeffrey A; Kavolus, Matthew W; Landy, David C; Pectol, Richard W; Sneed, Chandler R; Kinchelow, Daria L; Griffin, Jarod T; Hawk, Gregory S; Aneja, Arun.
Affiliation
  • Foster JA; Department of Orthopaedic Surgery & Sports Medicine, University of Kentucky.
  • Kavolus MW; Department of Orthopaedic Surgery & Sports Medicine, University of Kentucky.
  • Landy DC; Department of Orthopaedic Surgery & Sports Medicine, University of Kentucky.
  • Pectol RW; Department of Orthopaedic Surgery & Sports Medicine, University of Kentucky.
  • Sneed CR; Department of Orthopaedic Surgery & Sports Medicine, University of Kentucky.
  • Kinchelow DL; Department of Orthopaedic Surgery & Sports Medicine, University of Kentucky.
  • Griffin JT; Department of Orthopaedic Surgery & Sports Medicine, University of Kentucky.
  • Hawk GS; Department of Statistics, University of Kentucky.
  • Aneja A; Department of Orthopaedic Surgery & Sports Medicine, University of Kentucky.
J Orthop Trauma ; 2023 Sep 25.
Article in En | MEDLINE | ID: mdl-37752630
OBJECTIVE: To determine whether scheduled low-dose, short-term ketorolac is associated with reduced length of stay, opioid use, and pain in orthopaedic polytrauma patients. DESIGN: Double-blinded, randomized controlled trial. SETTING: One Level 1 trauma center. PATIENTS: From August 2018 to October 2022, 70 orthopaedic polytrauma patients between 18-75 years-old with a New Injury Severity Score (NISS) > 9 were randomized. 70 participants were enrolled, with 35 randomized to the ketorolac group and 35 to the placebo group. INTERVENTION: 15 mg of intravenous (IV) ketorolac every 6 hours for up to 5 inpatient days or 2 mL of IV saline in a similar fashion. MAIN OUTCOME MEASUREMENTS: Length of Stay (LOS), Morphine Milligram Equivalents (MME), Visual Analogue Scale (VAS), and Complications. RESULTS: Study groups were not significantly different with respect to age, BMI, and NISS (p>0.05). Median LOS was 8 days (interquartile range [IQR], 4.5 to 11.5) in the ketorolac group compared to 7 days (IQR, 3 to 10) in the placebo group (p = 0.275). Over the 5-day treatment period, the ketorolac group experienced a 32% reduction in average MME (p = 0.013) and a 12-point reduction in baseline-adjusted mean VAS (p = 0.037) compared to the placebo group. There were no apparent short-term adverse effects in either group. CONCLUSION: Scheduled low-dose, short-term IV ketorolac was associated with significantly reduced inpatient opioid use and pain in orthopaedic polytrauma patients with no significant difference in LOS and no apparent short-term adverse effects. The results support the use of scheduled low-dose, short-term IV ketorolac for acute pain control among orthopaedic polytrauma patients. Further studies are needed to delineate lasting clinical effects and potential long-term effects, such as fracture healing. LEVEL OF EVIDENCE: Therapeutic Level I. See Instructions for Authors for a complete description of levels of evidence.

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Clinical_trials Language: En Journal: J Orthop Trauma Journal subject: ORTOPEDIA / TRAUMATOLOGIA Year: 2023 Document type: Article Country of publication: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Clinical_trials Language: En Journal: J Orthop Trauma Journal subject: ORTOPEDIA / TRAUMATOLOGIA Year: 2023 Document type: Article Country of publication: United States