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首页> 外文期刊>BMC Anesthesiology >Effect of local anesthetic concentration, dose and volume on the duration of single-injection ultrasound-guided axillary brachial plexus block with mepivacaine: a randomized controlled trial
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Effect of local anesthetic concentration, dose and volume on the duration of single-injection ultrasound-guided axillary brachial plexus block with mepivacaine: a randomized controlled trial

机译:局麻药浓度,剂量和体积对单注射超声引导的甲吡卡因腋下臂丛神经阻滞持续时间的影响:一项随机对照试验

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Background In what way volume, concentration and dose affect block duration is controversial. The purpose of the present study is to investigate the effect of dose, volume and concentration of mepivacaine on the duration of sensory and motor blockade in ultrasound-guided single shot axillary brachial plexus blockade. Methods In this parallel group randomized trial conducted in the Sint Maartenskliniek Nijmegen, 45 adult patients undergoing minor orthopaedic forearm, wrist or hand surgery were randomized to 3 groups. Group A: 20?mL mepivacaine 1.5?%, Group B: 30?mL mepivacaine 1?% and Group C: 30?mL mepivacaine 1.5?%. Randomization was computer-generated, with allocation concealment by opaque sequentially numbered sealed envelopes. Patients and observers were blinded to group allocation. Primary outcome measure: duration of sensory block. Results Forty-five patients were randomized, four patients were excluded and replaced, and 15 patients in each group were included in the analysis. Mean (95?% CI) sensory and motor block duration was 256 (230–282) and 254 (226–282) minutes in Group A, 226 (209–243) and 220 (200–240) minutes in Group B and 270 (249–291) and 264 (244–284) minutes in Group C. Duration of sensory and motor block duration differed significantly between groups (p?=?0.012 and p?=?0.016 respectively). Post-hoc analysis showed a significantly reduced sensory and motor block duration in Group B when compared to Group C of 44?min. No local anesthetic systemic toxicity was reported. Conclusions When using mepivacaine for axillary brachial plexus block, a higher dose and concentration was associated with a longer duration of sensory and motor blockade, but not a higher volume. Trial Registration The Netherlands National Trial Register NTR3648 . Registered October 3, 2012.
机译:背景技术体积,浓度和剂量以何种方式影响阻滞持续时间是有争议的。本研究的目的是研究在超声引导的单发腋下臂丛神经阻滞中,甲哌卡因的剂量,体积和浓度对感觉和运动阻滞持续时间的影响。方法在Sint Maartenskliniek Nijmegen进行的平行组随机试验中,将45例行小骨科前臂,手腕或手部手术的成年患者随机分为3组。 A组:20?mL甲哌卡因1.5?%,B组:30?mL甲哌卡因1?%,C组:30?mL甲哌卡因1.5?%。随机化是由计算机生成的,通过不透明的顺序编号的密封信封隐藏分配。患者和观察者对组分配不知情。主要结局指标:感觉障碍的持续时间。结果对45例患者进行了随机分组,排除并替换了4例患者,每组中有15例患者被纳入分析。 A组的平均(95%CI)感觉和运动阻滞持续时间分别为256(230-282)和254(226-282)分钟,A组为226(209-243)和220(200-240)分钟C组分别为(249–291)分钟和264(244–284)分钟。两组之间的感觉和运动阻滞持续时间显着不同(分别为p?=?0.012和p?=?0.016)。事后分析显示,与C组相比,B组的感觉和运动阻滞持续时间显着减少了44分钟。尚无局部麻醉药全身毒性的报道。结论当使用甲哌卡因治疗腋下臂丛神经阻滞时,较高的剂量和浓度与较长的感觉和运动阻滞持续时间有关,但与容积无关。试用登记荷兰国家试验登记册NTR3648。 2012年10月3日注册。

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