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首页> 外文期刊>Canadian journal of anesthesia: Journal canadien d'anesthesie >Intrathecal bupivacaine with morphine or neostigmine for postoperative analgesia after total knee replacement surgery.
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Intrathecal bupivacaine with morphine or neostigmine for postoperative analgesia after total knee replacement surgery.

机译:鞘内注射布比卡因与吗啡或新斯的明用于全膝关节置换术后的镇痛。

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PURPOSE: To compare the postoperative analgesic efficacy and safety of intrathecal (IT) neostigmine and IT morphine in patients undergoing total knee replacement under spinal anesthesia. METHODS: Sixty patients scheduled for elective total knee replacement under spinal anesthesia were randomly divided into three equal groups which received IT 0.5% hyperbaric bupivacaine 15 mg with either normal saline 0.5 mL, neostigmine 50 microg, or morphine 300 microg. The maximal level of sensory block, duration of analgesia, time to use of rescue analgesics, the overall 24-hr and four-hour interval visual analogue scale (VAS) pain score, and the incidence of adverse effects were recorded for 24 hr after administration. RESULTS: There was no significant difference in maximal level of sensory block among the three groups. The morphine group had a later onset of postsurgical pain and longer time to first rescue analgesics than the neostigmine group (P <0.05). Overall 24-hr VAS pain scores were significantly higher in the saline group vs the morphine and neostigmine groups (P <0.05). Motor block lasted significantly longer in the neostigmine group than in the morphine and saline groups (P <0.05). The incidence of adverse effects was similar in the neostigmine and morphine groups except for pruritus (70%) occurring more frequently in the morphine group than in the neostigmine and saline groups (0%; P ]0.05). Overall satisfaction rates were better in the neostigmine group than in the morphine and saline groups (P <0.05). CONCLUSIONS: IT neostigmine 50 microg produced postoperative analgesia lasting about seven hours with fewer side effects and better satisfaction ratings than IT morphine 300 microg.
机译:目的:比较椎管内麻醉下全膝关节置换患者鞘内(IT)新斯的明和IT吗啡的镇痛效果和安全性。方法:将60名计划在脊柱麻醉下进行选择性全膝关节置换的患者随机分为三组,分别接受IT 0.5%高压布比卡因15 mg,生理盐水0.5 mL,新斯的明50μg或吗啡300μg。给药后24小时记录最大感觉阻滞水平,镇痛持续时间,使用救援镇痛剂的时间,24小时和4小时间隔的视觉模拟量表(VAS)总体疼痛评分以及不良反应的发生率。结果:三组之间最大的感觉障碍水平无显着差异。与新斯的明组相比,吗啡组术后疼痛发作较晚,首次抢救镇痛的时间更长(P <0.05)。盐水组的总24小时VAS疼痛评分明显高于吗啡和新斯的明组(P <0.05)。新斯的明组的运动阻滞持续时间明显长于吗啡和生理盐水组(P <0.05)。在新斯的明和吗啡组中,不良反应的发生率相似,除了在吗啡组中比在新的斯的明和生理盐水组中,瘙痒的发生率更高(70%)(0%; P = 0.05)。新斯的明组的总满意度高于吗啡和生理盐水组(P <0.05)。结论:与IT吗啡300微克相比,IT新斯的明50微克可使术后镇痛持续约7小时,且副作用更少,满意度更高。

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