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首页> 外文期刊>Canadian journal of anesthesia: Journal canadien d'anesthesie >A randomized comparison between interscalene and combined infraclavicular-suprascapular blocks for arthroscopic shoulder surgery
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A randomized comparison between interscalene and combined infraclavicular-suprascapular blocks for arthroscopic shoulder surgery

机译:三甲醛与血管基颌骨组合梗死梗手术的随机比较

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Abstract Background This randomized trial aimed to evaluate combined infraclavicular-suprascapular blocks (ICB-SSBs) as a diaphragm-sparing alternative to interscalene blocks (ISBs) for arthroscopic shoulder surgery. We hypothesized that ICB-SSB would provide equivalent postoperative analgesia to ISB 30 min after surgery without the risk of hemidiaphragmatic paralysis. Methods Following research ethics board approval and written informed consent, participants in the ISB group received an ultrasound-guided ISB with 20?mL of levobupivacaine 0.25% and epinephrine 5?μg·mL ?1 . In the ICB-SSB group, ultrasound-guided ICB (20?mL) and SSB (10?mL) were carried out using the same local anesthetic. Thirty minutes after the block was performed, a blinded investigator assessed the presence of hemidiaphragmatic paralysis. Subsequently, all patients underwent general anesthesia. Postoperatively, a blinded investigator?recorded?pain scores at rest at 0.5, 1, 2, 3, 6, 12 and 24?hr.?Consumption of intra- and postoperative narcotics was?also tabulated. Results Compared to its ICB-SSB counterpart, the ISB group displayed non-equivalent (i.e., lower) postoperative pain scores at 30 min (difference of the medians, ?4; 99% confidence interval [CI], ?6 to ?3), required less cumulative morphine iv at 24 hr (difference of the means, ?6.1 mg; 95% CI, ?10.5 to ?1.6), and resulted in a higher incidence of hemidiaphragmatic paralysis (18/20 vs 0/20 patients, respectively; P ? Conclusion Compared with ICB-SSB, ISB provided non-equivalent (i.e., lower) postoperative pain scores 30 min after arthroscopic shoulder surgery. Thereafter, postoperative analgesia was comparable between the two groups. Further trials are required to compare ISB with ICB-SSB using a proximal (i.e., costoclavicular) technique for ICB. Trial registration www.clinicaltrials.gov , NCT02993939. Registered 12 December 2016.
机译:摘要背景本随机试验旨在评估基础射刺 - 初步块(ICB-SSBS)作为膈肌块(ISBS)的晶体障碍替代品,用于关节镜肩部手术。我们假设ICB-SSB在手术后30分钟提供相同的术后镇痛,而没有血糖瘫痪的风险。方法遵循研究伦理委员会批准和书面知情同意,参与者在ISB组中接收超声引导的ISB,其中20?Ml左旋蛋白0.25%和肾上腺素5?μg·mlα1。在ICB-SSB组中,使用相同的局部麻醉剂进行超声引导的ICB(20?mL)和SSB(10?ML)。在嵌段进行三十分钟后,盲盲的调查员评估了血糖瘫痪的存在。随后,所有患者都经过全身麻醉。术后,盲盲的调查员?记录?静止的疼痛评分在0.5,1,2,3,6,12和24?HR。?患有和术后麻醉剂的消耗量是?结果与其ICB-SSB对应相比,ISB组在30分钟内显示不等效(即,下部)术后疼痛分数(中位数的差异,?4; 99%置信区间[CI],?6到?3) ,在24小时时需要较少的累积吗啡IV(手段的差异,α.6.1mg; 95%CI,?10.5至?1.6),并导致30/20患者的血液瘫痪发病率较高; p?结论与ICB-SSB相比,ISB提供了在关节镜肩部手术后30分钟的不等效(即,下部)术后疼痛。此后,两组之间的术后镇痛是可比的。需要进一步的试验来与ICB比较ISB -SSB使用用于ICB的近端(即Costoclavicular)技术。试验登记www.clinicaltrials.gov,NCT02993939。2016年12月12日注册。

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