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鞘内注射布比卡因联合吗啡或新斯的明用于全膝关节置换术后镇痛

Intrathecal bupivacaine with morphine or neostigmine for postoperative analgesia after total knee replacement surgery.

作者信息

Tan P H, Chia Y Y, Lo Y, Liu K, Yang L C, Lee T H

机构信息

Department of Anesthesia, Chang-Gung Memorial Hospital, Kaohsiung, Taiwan, Republic of China.

出版信息

Can J Anaesth. 2001 Jun;48(6):551-6. doi: 10.1007/BF03016831.

Abstract

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.

摘要

目的

比较鞘内注射新斯的明和鞘内注射吗啡对脊髓麻醉下全膝关节置换患者术后的镇痛效果及安全性。

方法

60例计划在脊髓麻醉下择期行全膝关节置换术的患者被随机分为三组,每组20例,分别接受含0.5%重比重布比卡因15mg加0.5mL生理盐水、50μg新斯的明或300μg吗啡的鞘内注射。记录给药后24小时的感觉阻滞最高平面、镇痛持续时间、使用补救镇痛药的时间、24小时及每4小时间隔的视觉模拟评分(VAS)疼痛评分以及不良反应的发生率。

结果

三组间感觉阻滞最高平面无显著差异。吗啡组术后疼痛开始时间较新斯的明组晚,首次使用补救镇痛药的时间更长(P<0.05)。生理盐水组24小时总体VAS疼痛评分显著高于吗啡组和新斯的明组(P<0.05)。新斯的明组运动阻滞持续时间显著长于吗啡组和生理盐水组(P<0.05)。新斯的明组和吗啡组不良反应发生率相似,但吗啡组瘙痒发生率(70%)高于新斯的明组和生理盐水组(0%;P<0.05)。新斯的明组总体满意度高于吗啡组和生理盐水组(P<0.05)。

结论

鞘内注射50μg新斯的明产生的术后镇痛持续约7小时,与鞘内注射300μg吗啡相比,副作用更少,满意度更高。

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