Department of Anesthesiology, Northwestern University, Feinberg School of Medicine, Chicago, Illinois 60611, USA.
Anesthesiology. 2011 Sep;115(3):575-88. doi: 10.1097/ALN.0b013e31822a24c2.
Dexamethasone is frequently administered in the perioperative period to reduce postoperative nausea and vomiting. In contrast, the analgesic effects of dexamethasone are not well defined. The authors performed a meta-analysis to evaluate the dose-dependent analgesic effects of perioperative dexamethasone.
We followed the PRISMA statement guidelines. A wide search was performed to identify randomized controlled trials that evaluated the effects of a single dose systemic dexamethasone on postoperative pain and opioid consumption. Meta-analysis was performed using a random-effect model. Effects of dexamethasone dose were evaluated by pooling studies into three dosage groups: low (less than 0.1 mg/kg), intermediate (0.11-0.2 mg/kg) and high (≥ 0.21 mg/kg).
Twenty-four randomized clinical trials with 2,751 subjects were included. The mean (95% CI) combined effects favored dexamethasone over placebo for pain at rest (≤ 4 h, -0.32 [0.47 to -0.18], 24 h, -0.49 [-0.67 to -0.31]) and with movement (≤ 4 h, -0.64 [-0.86 to -0.41], 24 h, -0.47 [-0.71 to -0.24]). Opioid consumption was decreased to a similar extent with moderate -0.82 (-1.30 to -0.42) and high -0.85 (-1.24 to -0.46) dexamethasone, but not decreased with low-dose dexamethasone -0.18 (-0.39-0.03). No increase in analgesic effectiveness or reduction in opioid use could be demonstrated between the high- and intermediate-dose dexamethasone. Preoperative administration of dexamethasone appears to produce a more consistent analgesic effect compared with intraoperative administration.
Dexamethasone at doses more than 0.1 mg/kg is an effective adjunct in multimodal strategies to reduce postoperative pain and opioid consumption after surgery. The preoperative administration of the drug produces less variation of effects on pain outcomes.
地塞米松在围手术期经常被用于减少术后恶心和呕吐。相比之下,地塞米松的镇痛效果尚未明确。作者进行了一项荟萃分析,以评估围手术期地塞米松的剂量依赖性镇痛作用。
我们遵循 PRISMA 声明指南。进行了广泛的搜索,以确定评估单次全身给予地塞米松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。通过将研究纳入三个剂量组(低剂量组(<0.1mg/kg)、中剂量组(0.11-0.2mg/kg)和高剂量组(≥0.21mg/kg))来评估地塞米松剂量的影响。
纳入了 24 项随机临床试验,共 2751 例受试者。与安慰剂相比,地塞米松的综合效果在静息时(≤4 小时,-0.32[0.47 至-0.18];24 小时,-0.49[-0.67 至-0.31])和运动时(≤4 小时,-0.64[-0.86 至-0.41];24 小时,-0.47[-0.71 至-0.24])均有利于地塞米松。中剂量-0.82(-1.30 至-0.42)和高剂量-0.85(-1.24 至-0.46)的地塞米松可使阿片类药物消耗减少到相似程度,但低剂量地塞米松(-0.18[-0.39 至 0.03])则不然。高剂量和中剂量地塞米松之间未能证明镇痛效果增加或阿片类药物使用减少。与术中给药相比,术前给予地塞米松似乎能更一致地产生镇痛效果。
剂量超过 0.1mg/kg 的地塞米松是减少手术后疼痛和阿片类药物消耗的多模式策略中的有效辅助药物。药物的术前给药对疼痛结局的影响变化较小。