Department of Anaesthesia, Guy's and St Thomas' NHS Foundation Trust, London, UK.
Department of Anaesthesia, Aretaieio Hospital, National and Kapodistrian University of Athens, Athens, Greece.
Balkan Med J. 2021 May;38(3):156-164. doi: 10.5152/balkanmedj.2021.20076.
Intravenous Regional Anesthesia (IVRA) is a reliable and cost-effective anesthetic method for minor surgical procedures to the extremities. Limitations of this block include tourniquet discomfort, short duration of anesthesia, and absence of postoperative analgesia. Dexmedetomidine has been used as an adjuvant to minimize these negative characteristics with inconclusive results.
To perform a systematic review of the existing evidence on the role of dexmedetomidine as an additive to intravenous regional anesthesia in upper limb surgery.
Systematic Review and Meta-analysis.
The databases searched were MEDLINE, Embase, PubMed, CINAHL, Cochrane Database of Systematic Reviews, Cochrane Central Register of Controlled Trials databases, and clinicaltrials. gov (1990-2019). Seven randomized controlled trials (RCTs) were included. We analyzed the duration of analgesia, onset time of sensory and motor block, intraoperative tourniquet pain scores, the incidence of tourniquet pain, need for rescue analgesia, intraoperative rescue analgesia consumption, sedation scores, postoperative pain scores, and anesthesia quality.
Intraoperative analgesia duration (MD 11.08 min; 95% CI 5.42, 16.75; P < .0001) was longer and sensory block onset time (MD -2.10 min; 95% CI -3.345, -0.86; P = .00009) was shorter in the dexmedetomidine group. Anesthesia quality scores (MD 0.58; 95% CI 0.47, 0.70; P < .00001) and postoperative sedation scores (MD 1.03; 95% CI 0.88, 1.24; P < .00001) were significantly higher. There was a significant reduction in intraoperative rescue analgesia consumption (MD -19.70 mg; 95% CI -24.15, -15.26; P < .00001) in the dexmedetomidine group. The risk of tourniquet pain as well as postoperative pain scores were lower in favor of dexmedetomidine. The addition of dexmedetomidine to IVRA slightly increased the risk of sedation. A limitation of our study is that some of the interesting outcomes derive from a small number of RCTs.
The addition of dexmedetomidine to IVRA ameliorates the block's characteristics and carries a low risk of potential side effects.
静脉局部麻醉(IVRA)是一种可靠且具有成本效益的麻醉方法,适用于四肢的小手术。该阻滞的局限性包括止血带不适、麻醉持续时间短以及缺乏术后镇痛。右美托咪定已被用作辅助药物,以最小化这些负面特征,但结果尚无定论。
对右美托咪定作为上肢手术静脉局部麻醉辅助药物的现有证据进行系统评价。
系统评价和荟萃分析。
检索数据库包括 MEDLINE、Embase、PubMed、CINAHL、Cochrane 系统评价数据库、Cochrane 对照试验中心注册数据库和 clinicaltrials.gov(1990-2019 年)。共纳入 7 项随机对照试验(RCT)。我们分析了镇痛持续时间、感觉和运动阻滞的起效时间、术中止血带疼痛评分、止血带疼痛的发生率、需要解救性镇痛、术中解救性镇痛消耗、镇静评分、术后疼痛评分和麻醉质量。
右美托咪定组的术中镇痛持续时间(MD 11.08 分钟;95%CI 5.42,16.75;P<.0001)更长,感觉阻滞起效时间(MD-2.10 分钟;95%CI-3.345,-0.86;P=0.00009)更短。麻醉质量评分(MD 0.58;95%CI 0.47,0.70;P<.00001)和术后镇静评分(MD 1.03;95%CI 0.88,1.24;P<.00001)显著升高。右美托咪定组术中解救性镇痛消耗(MD-19.70 毫克;95%CI-24.15,-15.26;P<.00001)显著降低。右美托咪定组止血带疼痛和术后疼痛评分的风险较低。右美托咪定与 IVRA 联合应用可略微增加镇静的风险。我们研究的一个局限性是,一些有趣的结果来自少数 RCT。
右美托咪定与 IVRA 联合应用可改善阻滞特性,且潜在副作用风险较低。