首页> 外文期刊>Acute pain: international journal of acute pain management >Postoperative analgesic and adverse effects of two low doses of intrathecal neostigmine and its influence on spinal bupivacaine anaesthesia after knee arthroscopy
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Postoperative analgesic and adverse effects of two low doses of intrathecal neostigmine and its influence on spinal bupivacaine anaesthesia after knee arthroscopy

机译:两种低剂量鞘内新斯的明的术后镇痛及不良反应及其对膝关节镜检查后布比卡因麻醉的影响

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Background: Neostigmine is a spinal analgesic that could be a useful adjunct. This study was conducted to evaluate the postoperative analgesic efficacy and the safety of two low doses of intrathecal (IT) neostigmine in patients undergoing knee arthroscopy under spinal bupivacaine anaesthesia. Methods: By using a double-blinded study design, 80 patients undergoing knee arthroscopy during spinal anaesthesia were divided into four groups: bupivacaine group (Group B) received 15mg hyperbaric bupivacaine; bupivacaine+fentanyl group (Group BF) received 15mg hyperbaric bupivacaine mixed with 25|xg fentanyl; bupivacaine + neostigmine group 1 (Group BN1) received 15mg hyperbaric bupivacaine mixed with 25 mug neostigmine; bupivacaine + neostigmine group 2 (Group BN2) received 15mg hyperbaric bupivacaine mixed with 35mug neostigmine. The postoperative visual analog scale (VAS) and the incidence of adverse effects were recorded for 24 h after administration of study drugs. Results: VAS scores were significantly lower in group BN2 compared with group B, group BF and group BN1 at 2, 4, 6, 12, and 24 h after operation (P<0.05). The time to the first patients' demand for morphine administration after surgery was significantly prolonged in group BN2 compared with group B or group BN1 (P< 0.05). There was no significant difference between four groups in incidence of nausea and vomiting. Conclusion: Our study showed that IT neostigmine (35 mug) enhanced bupivacaine spinal anaesthesia (15 mg) and produced prolonged postoperative analgesia for about 24 h without producing significant more adverse effects such as nausea and vomiting. Crown Copyright
机译:背景:新斯的明是一种脊髓镇痛药,可能是有用的辅助药物。这项研究的目的是评估在布比卡因麻醉下进行膝关节镜检查的患者中,两种低剂量鞘内(IT)新斯的明的镇痛效果和安全性。方法:采用双盲研究设计,将80例在脊柱麻醉期间接受膝关节镜检查的患者分为四组:布比卡因组(B组)接受15mg高压布比卡因治疗。布比卡因+芬太尼基(BF组)接受15mg高压布比卡因与25 | xg芬太​​尼混合;布比卡因+新斯的明1组(BN1组)接受15mg高压布比卡因与25杯新斯的明混合。布比卡因+新斯的明2组(BN2组)接受15mg高压布比卡因与35杯新斯的明混合。记录研究药物后24小时的术后视觉模拟量表(VAS)和不良反应的发生率。结果:术后2、4、6、12和24 h,BN2组的VAS评分明显低于B组,BF组和BN1组(P <0.05)。与B组或BN1组相比,BN2组对首例患者术后接受吗啡给药的时间显着延长(P <0.05)。四组的恶心和呕吐发生率无显着差异。结论:我们的研究表明,新斯的明(35杯)可增强布比卡因脊柱麻醉(15毫克)并在术后约24小时内产生延长的镇痛效果,而不会产生明显的更多不良反应,例如恶心和呕吐。皇冠版权

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