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奈福泮用于腹腔镜妇科手术后患者自控镇痛的疗效:一项随机、双盲、非劣效性研究。

The Analgesic Efficacy of Nefopam in Patient-Controlled Analgesia after Laparoscopic Gynecologic Surgery: A Randomized, Double-Blind, Non-Inferiority Study.

作者信息

Lee Soomin, Lee Seounghun, Kim Hoseop, Oh Chahyun, Park Sooyong, Kim Yeojung, Hong Boohwi, Yoon Seokhwa, Noh Chan, Ko Youngkwon

机构信息

Department of Anesthesiology and Pain Medicine, Chungnam National University Hospital, Daejeon 35015, Korea.

Department of Anesthesiology and Pain Medicine, Chungnam National University Sejong Hospital, Sejong 30099, Korea.

出版信息

J Clin Med. 2021 Mar 3;10(5):1043. doi: 10.3390/jcm10051043.

Abstract

Opioid-sparing effects of nefopam during patient-controlled analgesia (PCA) are well demonstrated. We hypothesized that postoperative pain control with an opioid-equivalent dose of nefopam as a single analgesic agent for PCA would not be inferior to fentanyl in laparoscopic gynecologic surgery. In total, 135 patients were randomly assigned to the N (nefopam 200 mg), NF (fentanyl 500 mcg + nefopam 100 mg), and F (fentanyl 1000 mcg) groups ( = 45 patients per group). The primary outcome was the numerical rating scale (NRS) score at rest at 6 h postoperatively, and the non-inferiority limit was set to 1. Secondary outcomes were pain severity and incidence of nausea and vomiting for 48 h postoperatively. Mean differences (MD) in primary outcome between the N and F groups were 0.4 (95% confidence interval (CI) -0.5 to 1.3). The upper limit of 95% CI exceeded the non-inferiority limit. The N group showed higher pain scores than the NF group (MD, 1.1; 95% CI, 0.3-1.9) in pairwise comparisons. No significant intergroup differences were observed in the cumulative dose of PCA usage and incidence of postoperative nausea and vomiting (PONV). In laparoscopic gynecological surgery, nefopam alone showed limited efficacy for postoperative pain control.

摘要

奈福泮在患者自控镇痛(PCA)中的阿片类药物节省效应已得到充分证实。我们假设,在腹腔镜妇科手术中,使用等效阿片类剂量的奈福泮作为PCA单一镇痛剂的术后疼痛控制效果不会逊于芬太尼。总共135例患者被随机分为N组(奈福泮200 mg)、NF组(芬太尼500 mcg + 奈福泮100 mg)和F组(芬太尼1000 mcg)(每组 = 45例患者)。主要结局是术后6小时静息时的数字评分量表(NRS)评分,非劣效性界限设定为1。次要结局是术后48小时的疼痛严重程度以及恶心和呕吐的发生率。N组和F组之间主要结局的平均差异(MD)为0.4(95%置信区间(CI)-0.5至1.3)。95%CI的上限超过了非劣效性界限。在两两比较中,N组的疼痛评分高于NF组(MD,1.1;95%CI,0.3 - 1.9)。在PCA使用的累积剂量和术后恶心呕吐(PONV)的发生率方面,未观察到显著的组间差异。在腹腔镜妇科手术中,单独使用奈福泮对术后疼痛控制的疗效有限。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/92ba/7959469/d854691e97cf/jcm-10-01043-g001.jpg

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