Clinical Epidemiology Program, Ottawa Hospital Research Institute, University of Ottawa, Ottawa, ON, Canada; Department of Anesthesiology and Pain Medicine, University of Ottawa, The Ottawa Hospital, Ottawa, ON, Canada; Population Health and Optimal Health Practices Research Unit (Trauma - Emergency - Critical Care Medicine), CHU de Québec - Université Laval Research Center, Québec City, QC, Canada; Department of Anesthesiology and Critical Care Medicine, Faculty of Medicine, Université Laval, Québec City, QC, Canada; School of Epidemiology and Public Health, University of Ottawa, Ottawa, ON, Canada; Quebec Pain Research Network, Sherbrooke, QC, Canada.
Clinical Epidemiology Program, Ottawa Hospital Research Institute, University of Ottawa, Ottawa, ON, Canada; Faculty of Medicine, University of Ottawa, Ottawa, ON, Canada.
Br J Anaesth. 2024 Sep;133(3):615-627. doi: 10.1016/j.bja.2024.06.007. Epub 2024 Jul 16.
Dexmedetomidine is increasingly used for surgical patients requiring general anaesthesia. However, its effectiveness on patient-centred outcomes remains uncertain. Our main objective was to evaluate the patient-centred effectiveness of intraoperative dexmedetomidine for adult patients requiring surgery under general anaesthesia.
We conducted a systematic search of MEDLINE, Embase, CENTRAL, Web of Science, and CINAHL from inception to October 2023. Randomised controlled trials (RCTs) comparing intraoperative use of dexmedetomidine with placebo, opioid, or usual care in adult patients requiring surgery under general anaesthesia were included. Study selection, data extraction, and risk of bias assessment were performed by two reviewers independently. We synthesised data using a random-effects Bayesian regression framework to derive effect estimates and the probability of a clinically important effect. For continuous outcomes, we pooled instruments with similar constructs using standardised mean differences (SMDs) and converted SMDs and credible intervals (CrIs) to their original scale when appropriate. We assessed the certainty of evidence using the Grading of Recommendations Assessment, Development and Evaluation (GRADE) methodology. Our primary outcome was quality of recovery after surgery. To guide interpretation on the original scale, the Quality of Recovery-15 (QoR-15) instrument was used (range 0-150 points, minimally important difference [MID] of 6 points).
We identified 49,069 citations, from which 44 RCTs involving 5904 participants were eligible. Intraoperative dexmedetomidine administration was associated with improvement in postoperative QoR-15 (mean difference 9, 95% CrI 4-14, n=21 RCTs, moderate certainty of evidence). We found 99% probability of any benefit and 88% probability of achieving the MID. There was a reduction in chronic pain incidence (odds ratio [OR] 0.42, 95% CrI 0.19-0.79, n=7 RCTs, low certainty of evidence). There was also increased risk of clinically significant hypotension (OR 1.98, 95% CrI 0.84-3.92, posterior probability of harm 94%, n=8 RCTs) and clinically significant bradycardia (OR 1.74, 95% CrI 0.93-3.34, posterior probability of harm 95%, n=10 RCTs), with very low certainty of evidence for both. There was limited evidence to inform other secondary patient-centred outcomes.
Compared with placebo or standard of care, intraoperative dexmedetomidine likely results in meaningful improvement in the quality of recovery and chronic pain after surgery. However, it might increase clinically important bradycardia and hypotension.
PROSPERO (CRD42023439896).
右美托咪定越来越多地用于需要全身麻醉的手术患者。然而,其对以患者为中心的结果的有效性仍不确定。我们的主要目的是评估成人全身麻醉下手术患者术中使用右美托咪定的以患者为中心的效果。
我们对 MEDLINE、Embase、CENTRAL、Web of Science 和 CINAHL 进行了系统检索,检索时间从创建到 2023 年 10 月。纳入了比较成人全身麻醉下手术患者术中使用右美托咪定与安慰剂、阿片类药物或常规护理的随机对照试验(RCT)。两名评审员独立进行研究选择、数据提取和偏倚风险评估。我们使用随机效应贝叶斯回归框架综合数据,得出效应估计值和临床重要效应的概率。对于连续结局,我们使用相似结构的工具进行汇总,使用标准化均数差(SMD),并在适当情况下将 SMD 和可信区间(CrI)转换回其原始尺度。我们使用推荐评估、制定与评价(GRADE)方法学评估证据的确定性。我们的主要结局是手术后恢复质量。为了在原始尺度上进行指导解释,使用了恢复质量-15(QoR-15)工具(范围 0-150 分,最小重要差异 [MID] 为 6 分)。
我们确定了 49069 条引文,其中 44 项 RCT 涉及 5904 名参与者符合条件。术中给予右美托咪定与术后 QoR-15 改善相关(平均差异 9,95%CrI 4-14,n=21 RCT,中等确定性证据)。我们发现任何获益的概率为 99%,达到 MID 的概率为 88%。慢性疼痛发生率降低(比值比 [OR] 0.42,95%CrI 0.19-0.79,n=7 RCT,低确定性证据)。还存在临床显著低血压的风险增加(OR 1.98,95%CrI 0.84-3.92,伤害后验概率为 94%,n=8 RCT)和临床显著心动过缓的风险增加(OR 1.74,95%CrI 0.93-3.34,伤害后验概率为 95%,n=10 RCT),两者的证据确定性都非常低。有有限的证据可以说明其他以患者为中心的次要结局。
与安慰剂或标准护理相比,术中给予右美托咪定可能会显著改善术后恢复质量和慢性疼痛。然而,它可能会增加临床显著的心动过缓和低血压。
PROSPERO(CRD42023439896)。