首页> 外文期刊>The Journal of Bone and Joint Surgery. American Volume >Early postoperative analgesic effects of a single epidural injection of ropivacaine administered preoperatively in posterior lumbar interbody spinal arthrodesis: a pilot randomized controlled trial.
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Early postoperative analgesic effects of a single epidural injection of ropivacaine administered preoperatively in posterior lumbar interbody spinal arthrodesis: a pilot randomized controlled trial.

机译:术前单次硬膜外注射罗哌卡因在腰椎后椎体间椎间盘固定术中的早期术后镇痛效果:一项随机对照试验。

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Despite the suitable characteristics of ropivacaine as an epidural analgesic agent, such as better preservation of motor function and less neurotoxicity, we are aware of no data on its clinical application in pain management following lumbar spine surgery. The purpose of the present study was to evaluate the preemptive analgesic effects and safety of a single epidural injection of ropivacaine during lumbar arthrodesis.We performed a randomized, double-blinded, intention-to-treat study. Patients with planned one-level posterior lumbar interbody arthrodesis were randomly assigned to either the injection group (n = 32) or the control group (n = 34). The injection group received a 10-mL epidural injection of 0.1% ropivacaine twenty minutes before the skin incision at the planned vertebral level, and the control group received an epidural injection of 10 mL of 0.9% saline solution. A numeric rating scale (from 0 to 10) was measured at seven time points after surgery (at two, four, eight, twelve, twenty-four, and forty-eight hours and at the time of discharge), and the frequency of pushed-button patient-controlled analgesia and total fentanyl consumption were assessed at similar time points (up to two, up to four, up to eight, up to twelve, up to twenty-four, and up to forty-eight hours after surgery). Postoperative nausea and vomiting, the duration of the hospital stay, and the Likert satisfaction score at the time of discharge were evaluated.There were no significant differences between the two groups preoperatively. The numeric rating scale score was higher until twelve hours (p < 0.05) and the frequency of button pushes was higher at every time point except eight to twelve hours (p < 0.05) in the control group as compared with the injection group. Fentanyl consumption until eight to twelve hours (p < 0.05) and total consumption (p < 0.001) at discharge were higher in the control group. There were no differences between the two groups in terms of postoperative nausea and vomiting, the duration of hospital stay, or the mean satisfaction score, and no transient motor weakness was seen in relation to epidural injection of ropivacaine.A single-dose epidural injection of 0.1% ropivacaine before lumbar spine surgery is effective for reducing early postoperative pain without related complications such as transient motor weakness.
机译:尽管罗哌卡因具有作为硬膜外镇痛药的适当特性,例如更好地保留运动功能和降低神经毒性,但我们尚无关于其在腰椎手术后疼痛治疗中的临床应用的数据。本研究的目的是评估在腰椎关节置换术中单次硬膜外注射罗哌卡因的先发镇痛作用和安全性。我们进行了一项随机,双盲,意向性治疗研究。计划中的一级腰椎后椎间关节置换术患者被随机分配至注射组(n = 32)或对照组(n = 34)。注射组在计划的椎骨水平切开皮肤前20分钟接受10 mL硬膜外注射0.1%罗哌卡因,而对照组接受硬膜外注射10 mL的0.9%生理盐水。在手术后的七个时间点(在出院时的两个小时,四个小时,八个小时,十二个小时,二十四小时和四十八小时以及出院时)测量数字评分量表(从0到10),在相似的时间点评估患者自控镇痛和芬太尼的总消耗量(手术后最多2个,最多4个,最多8个,最多12个,最多24个和最多48小时)。评估术后恶心和呕吐,住院时间,出院时的李克特满意度评分。两组术前无明显差异。与注射组相比,对照组的数字评分量表评分最高,直到十二小时(p <0.05),每个时间点的按钮按下频率都更高,除了八到十二小时(p <0.05)。对照组中直到八到十二小时的芬太尼消耗量(p <0.05)和出院时的总消耗量(p <0.001)更高。两组在术后恶心和呕吐,住院时间或平均满意度评分方面无差异,并且与硬膜外注射罗哌卡因有关的患者没有观察到短暂的运动无力。腰椎手术前使用0.1%罗哌卡因可有效减轻术后早期疼痛,而无相关并发症,如短暂性运动无力。

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