Foster Jeffrey A, Kavolus Matthew W, Landy David C, Pectol Richard W, Sneed Chandler R, Kinchelow Daria L, Griffin Jarod T, Hawk Gregory S, Bernard Andrew C, Oyler Douglas R, Aneja Arun
Department of Orthopaedic Surgery & Sports Medicine, University of Kentucky, Lexington, KY; and.
Dr. Bing Zhang Department of Statistics, University of Kentucky, Lexington, KY.
J Orthop Trauma. 2023 Dec 1;37(12):633-639. doi: 10.1097/BOT.0000000000002703.
To determine whether scheduled low-dose, short-term ketorolac is associated with reduced length of stay, opioid use, and pain in orthopaedic polytrauma patients.
Double-blinded, randomized controlled trial.
One Level 1 trauma center.
From August 2018 to October 2022, 70 orthopaedic polytrauma patients between 18 and 75 years of age with a New Injury Severity Score > 9 were randomized. Seventy participants were enrolled, with 35 randomized to the ketorolac group and 35 to the placebo group.
The intervention used was 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.
Length of stay (LOS), morphine milligram equivalents, visual analog scale, and complications.
Study groups were not significantly different regarding age, body mass index, and New Injury Severity Score ( P > 0.05). The median LOS was 8 days (interquartile range, 4.5-11.5) in the ketorolac group compared with 7 days (interquartile range, 3-10) in the placebo group ( P = 0.275). Over the 5-day treatment period, the ketorolac group experienced a 32% reduction in average morphine milligram equivalents ( P = 0.013) and a 12-point reduction in baseline-adjusted mean visual analog scale ( P = 0.037) compared with the placebo group. There were no apparent short-term adverse effects in either group.
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.
Therapeutic Level I. See Instructions for Authors for a complete description of levels of evidence.
确定定期给予低剂量、短期酮咯酸是否与骨科多发伤患者住院时间缩短、阿片类药物使用减少及疼痛减轻相关。
双盲、随机对照试验。
一家一级创伤中心。
2018年8月至2022年10月,70例年龄在18至75岁之间、新损伤严重程度评分>9的骨科多发伤患者被随机分组。招募了70名参与者,35名被随机分配到酮咯酸组,35名被随机分配到安慰剂组。
采用的干预措施是每6小时静脉注射(IV)15毫克酮咯酸,最多持续5个住院日,或以类似方式注射2毫升静脉生理盐水。
住院时间(LOS)、吗啡毫克当量、视觉模拟评分及并发症。
研究组在年龄、体重指数和新损伤严重程度评分方面无显著差异(P>0.05)。酮咯酸组的中位住院时间为8天(四分位间距,4.5 - 11.5),而安慰剂组为7天(四分位间距,3 - 10)(P = 0.275)。在5天的治疗期内,与安慰剂组相比,酮咯酸组的平均吗啡毫克当量降低了32%(P = 0.013),基线调整后的平均视觉模拟评分降低了12分(P = 0.037)。两组均未出现明显的短期不良反应。
定期给予低剂量、短期静脉注射酮咯酸与骨科多发伤患者住院期间阿片类药物使用显著减少及疼痛减轻相关,住院时间无显著差异,且无明显短期不良反应。结果支持在骨科多发伤患者中使用定期给予低剂量、短期静脉注射酮咯酸来控制急性疼痛。需要进一步研究以明确其持久的临床效果和潜在的长期影响,如骨折愈合。
治疗性I级。有关证据水平的完整描述,请参阅作者指南。