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The comparing of ultrasound-guided techniques:sciatic block with continous lumbar plexus block or continous femoral nerve block for aneshtesia and analgesia of total knee replacement

机译:超声引导技术的比较:坐骨神经阻滞与连续腰丛神经阻滞或连续股神经阻滞对全膝关节置换的麻醉和镇痛作用

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摘要

Abstract: Background and Aims: This double blind prospective randomized clinical trial evaluated the efficacy and safety of continuous ultrasound-guided lumbar plexus block compared to continuous ultrasound-guided femoral nerve block, in the intra-operative and postoperative periods after total knee replacement.udMethods: Forty ASA I-III patients were randomized to receive: continuous femoral block (n= 20, 30 ml of ropivacaine 5 mg/ml) or continuous lumbar plexus block (n= 20, 30 ml of ropivacaine 5 mg/ml) both in association with single injection sciatic nerve block. All patients received continuous infusion of 2 mg/ml of ropivacaine at 8 ml/h for 48 hours and intra- venous morphine for patient-controlled analgesia. Primary outcomes were intra-operative sufentanil consumption and verbal analogue scale (VAS) score at rest at 24h follow up.udResults: Intra-operative sufentanil consumption was higher in the femoral block (FEM) group compared to the lumbar plexus block (PSOAS) group (FEM: 10.00 (10.00, 17.50) μg; PSOAS: 2.50 (0.00, 10.00) μg. p= 0.002).udObturator motor blockade occurred more frequently in the PSOAS group (70%) than in the FEM group (40%) (p=0.1); however, we found no differences in sensory blockade (p=0.6).udVAS at rest was similar in the two groups at 24h postoperatively (FEM: 29.50 ± 14.74 mm; PSOAS: 25.60 ±17.42 mm. p=0.4), and throughout the follow-up period. No differences were detected in pain scores during physiotherapy.udConclusion: Continuous femoral and lumbar plexus blocks, both in association with sciatic nerve block, provided similar VAS scores at 24h, and throughout the follow-up period; intra-operative sufentanil consumption was, however, lower in the lumbar plexus block group.
机译:摘要:背景与目的:这项双盲前瞻性随机临床试验评估了在全膝关节置换术后的术中和术后,连续超声引导的腰丛神经阻滞与连续超声引导的股神经阻滞的疗效和安全性。 udMethods:40例ASA I-III患者随机接受:连续股骨阻滞(n = 20、30 ml罗哌卡因5 mg / ml)或连续腰丛神经阻滞(n = 20、30 ml罗哌卡因5 mg / ml)与单次注射坐骨神经阻滞有关。所有患者均以48 ml / h的速度连续注入2 mg / ml罗哌卡因,持续48小时,并静脉注射吗啡以进行患者自控镇痛。主要结局为术中摄入舒芬太尼和24h时静息状态的口头类似量表(VAS)评分。 ud结果:股骨阻滞(FEM)组的术中舒芬太尼的摄入量高于腰丛神经阻滞(PSOAS) (FEM:10.00(10.00,17.50)μg; PSOAS:2.50(0.00,10.00)μg。p = 0.002)。 udPSOAS组(70%)的闭塞性运动阻滞发生率高于FEM组(40% )(p = 0.1);然而,我们发现在感觉阻滞方面没有差异(p = 0.6)。 udVAS两组在术后24h静止时相似(FEM:29.50±14.74 mm; PSOAS:25.60±17.42mm。p= 0.4),并且贯穿整个过程随访期。结论:连续性股骨和腰丛神经阻滞与坐骨神经阻滞有关,在24h及整个随访期间,VAS评分相似。然而,腰丛神经阻滞组的术中舒芬太尼消耗量较低。

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