Department of Anesthesiology, Northwestern Memorial Hospital, Chicago, IL 60611, USA.
Anesth Analg. 2012 Feb;114(2):424-33. doi: 10.1213/ANE.0b013e3182334d68. Epub 2011 Sep 29.
Preventive analgesia using non-opioid analgesic strategies is recognized as a pathway to improve postoperative pain control while minimizing opioid-related side effects. Ketorolac is a nonsteroidal antiinflammatory drug frequently used to treat postoperative pain. However, the optimal dose and route of administration for systemic single dose ketorolac to prevent postoperative pain is not well defined. We performed a quantitative systematic review to evaluate the efficacy of a single dose of perioperative ketorolac on postoperative analgesia.
We followed the PRISMA statement guidelines. A wide search was performed to identify randomized controlled trials that evaluated the effects of a single dose of systemic ketorolac on postoperative pain and opioid consumption. Meta-analysis was performed using a random-effects model. Effects of ketorolac dose were evaluated by pooling studies into 30- and 60-mg dosage groups. Asymmetry of funnel plots was examined using Egger regression. The presence of heterogeneity was assessed by subgroup analysis according to the route of systemic administration (IV versus IM) and the time of drug administration (preincision versus postincision).
Thirteen randomized clinical trials with 782 subjects were included. The weighted mean difference (95% confidence interval [CI]) of combined effects showed a difference for ketorolac over placebo for early pain at rest of -0.64 (-1.11 to -0.18) but not at late pain at rest, -0.29 (-0.88 to 0.29) summary point (0-10 scale). Opioid consumption was decreased by the 60-mg dose, with a mean (95% CI) IV morphine equivalent consumption of -1.64 mg (-2.90 to -0.37 mg). The opioid-sparing effects of ketorolac compared with placebo were greater when the drug was administered IM compared with when the drug was administered IV, with a mean difference (95% CI) IV morphine equivalent consumption of -2.13 mg (-4.1 to -0.21 mg). Postoperative nausea and vomiting were reduced by the 60-mg dose, with an odds ratio (95% CI) of 0.49 (0.29-0.81).
Single dose systemic ketorolac is an effective adjunct in multimodal regimens to reduce postoperative pain. Improved postoperative analgesia achieved with ketorolac was also accompanied by a reduction in postoperative nausea and vomiting. The 60-mg dose offers significant benefits but there is a lack of current evidence that the 30-mg dose offers significant benefits on postoperative pain outcomes.
使用非阿片类镇痛策略进行预防性镇痛被认为是改善术后疼痛控制的途径,同时最大限度地减少阿片类药物相关的副作用。酮咯酸是一种常用于治疗术后疼痛的非甾体抗炎药。然而,全身单次剂量酮咯酸预防术后疼痛的最佳剂量和给药途径尚未明确。我们进行了一项定量系统评价,以评估围手术期单次给予酮咯酸对术后镇痛的疗效。
我们遵循 PRISMA 声明指南。进行了广泛的搜索,以确定评估全身单次剂量酮咯酸对术后疼痛和阿片类药物消耗影响的随机对照试验。使用随机效应模型进行荟萃分析。通过将研究纳入 30mg 和 60mg 剂量组来评估酮咯酸剂量的效果。使用 Egger 回归检查漏斗图的不对称性。根据全身给药途径(IV 与 IM)和药物给药时间(切口前与切口后)进行亚组分析,评估异质性的存在。
纳入了 13 项随机临床试验,共 782 名受试者。联合效应的加权均数差值(95%置信区间[CI])显示,酮咯酸与安慰剂相比,早期静息疼痛的差异为-0.64(-1.11 至-0.18),但晚期静息疼痛的差异无统计学意义,为-0.29(-0.88 至 0.29)总结点(0-10 量表)。60mg 剂量可减少阿片类药物的消耗,静脉吗啡等效消耗量平均减少 1.64mg(-2.90 至-0.37mg)。与静脉给药相比,肌内给药时酮咯酸与安慰剂相比,阿片类药物的节省作用更大,静脉吗啡等效消耗量平均差值为-2.13mg(-4.1 至-0.21mg)。60mg 剂量可减少术后恶心和呕吐,优势比(95%CI)为 0.49(0.29-0.81)。
单次全身给予酮咯酸是多模式方案中的有效辅助手段,可减轻术后疼痛。酮咯酸改善的术后镇痛效果也伴随着术后恶心和呕吐的减少。60mg 剂量可带来显著益处,但目前尚无证据表明 30mg 剂量可显著改善术后疼痛结局。