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鞘内注射吗啡联合低剂量布比卡因对肝切除术后镇痛的效果:一项随机对照研究

Analgesic Effect of Intrathecal Morphine Combined with Low-Dose Bupivacaine on Postoperative Analgesia after Liver Resection: A Randomized Controlled Study.

作者信息

Ban MinGi, Choi Yong Seon, Koo Bon-Nyeo

机构信息

Department of Anesthesiology and Pain Medicine, Anesthesia and Pain Research Institute, Yonsei University College of Medicine, Seoul 03722, Korea.

出版信息

J Pers Med. 2022 Feb 3;12(2):211. doi: 10.3390/jpm12020211.

Abstract

Although intrathecal morphine and bupivacaine are increasingly implemented in effective postoperative pain control, there is a lack of consensus on the dosage as high doses of bupivacaine may inadvertently cause unwanted side effects. The purpose of this study was to compare the effects of intrathecal morphine injection and low-dose bupivacaine with morphine injection. In total, 90 patients were divided into 3 groups: (1) sham injection for the control group; (2) morphine 400 mcg for the morphine group (M); and (3) morphine 400 mcg and bupivacaine 5 mg for the morphine and bupivacaine group (M + B). Our primary outcome was time to first rescue analgesic. The VAS (visual analogue scale) pain score was compared until POD (postoperative day)1. Total fentanyl dose was compared until POD2. Side effects were monitored until POD3. Although time to first rescue was significantly shorter in the control group compared to group M and group M + B ( < 0.001), both groups (M and M + B) were comparable to each other. There was a significant decrease in the VAS score and total fentanyl administration in group M and group M + B compared to the control group. Pruritus and tingling were more prevalent in the M + B group ( = 0.023; = 0.010). The addition of 5 mg bupivacaine may be insufficient in providing further analgesic benefits; however, higher doses may aggravate side effects.

摘要

尽管鞘内注射吗啡和布比卡因在有效的术后疼痛控制中应用越来越广泛,但对于剂量仍缺乏共识,因为高剂量的布比卡因可能会意外导致不良副作用。本研究的目的是比较鞘内注射吗啡与低剂量布比卡因联合吗啡注射的效果。总共90例患者被分为3组:(1)对照组进行假注射;(2)吗啡组(M)注射400微克吗啡;(3)吗啡和布比卡因组(M + B)注射400微克吗啡和5毫克布比卡因。我们的主要结局是首次使用解救镇痛药的时间。比较视觉模拟量表(VAS)疼痛评分直至术后第1天(POD1)。比较总芬太尼剂量直至术后第2天(POD2)。监测副作用直至术后第3天(POD3)。尽管与M组和M + B组相比,对照组首次使用解救镇痛药的时间明显更短(<0.001),但两组(M组和M + B组)之间具有可比性。与对照组相比,M组和M + B组的VAS评分和芬太尼总用量均显著降低。瘙痒和刺痛在M + B组中更为常见(P = 0.023;P = 0.010)。添加5毫克布比卡因可能不足以提供进一步的镇痛益处;然而,更高的剂量可能会加重副作用。

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