Yang Timin, Si Haibo, Wu Yuangang, Zeng Yi, Pei Fuxing, Weng Xisheng, Shen Bin
Department of Orthopaedics, West China Hospital, Sichuan University, Chengdu Sichuan, 610041, P. R. China.
Department of Orthopaedics, Peking Union Medical College Hospital.
Zhongguo Xiu Fu Chong Jian Wai Ke Za Zhi. 2016 Sep 8;30(9):1065-1071. doi: 10.7507/1002-1892.20160217.
To investigate the efficacy of sequential treatment with adductor canal nerve block (ACNB) and cyclooxygenase 2 (COX-2) selective inhibitor (parecoxib and celecoxib) after primary total knee arthroplasty (TKA).
Between January 2015 and December 2015, 90 osteoarthritis patients who met the inclusion criteria were treated, and randomly divided into 3 groups:ACNB+COX-2 group (group A, =30), COX-2 group (group B, =30), and control group (group C, =30). There was no significant difference in gender, age, body mass index, side, and osteoarthritis duration between groups (>0.05), and the data were comparable. ACNB was used in group A at the end of TKA. Intravenous injection of parecoxib (40 mg per 12 hours) was administrated at the first three postoperative days, and followed by oral celecoxib (200 mg per 12 hours) until 6 weeks after operation in groups A and B; while placebo was given at the same time point in group C. Oral tramadol or intravenous morphine, as remedial measures, were introduced when patients had a visual analogue scale (VAS) score more than 4. The following indicators were compared between groups:the operative time, drainage volume at 24 hours after operation, length of hospital stay, and incidence of side effect; VAS pain scores, morphine consumption, range of motion (ROM) of the knee joint, and inflammatory cytokines levels at pre-operation and at 1 day, 2 days, 3 days, 1 week, 2 weeks, 4 weeks, and 6 weeks after operation; morphine consumption within first 24 hours and at 24 hours to 6 weeks after operation; the American Hospital for Special Surgery (HSS) score at 1, 2, 4, and 6 weeks after operation; and the serum coagulation parameters at pre-operation, and at 1, 3, and 14 days after operation.
The length of hospital stay was significantly shorter and the incidence of postoperative nausea and vomiting was significantly lower in groups A and B than group C (<0.05). The VAS scores at rest (VASR) of groups A and B were significantly lower than that of group C at 1, 2, and 3 days after operation (<0.05); difference in the VAS scores at walking (VASW) was significant between groups at 1 day after operation (<0.05), and group A had the lowest VASW; and the VASW of groups A and B were significantly lower than that of group C at 2 and 3 days and at 1, 2, 4, and 6 weeks after operation (<0.05). The difference in morphine consumption was significant between groups within the first 24 hours after operation (<0.05), and group A exhibited the lowest consumption; and the morphine consumption in groups A and B was significantly lower than that in group C at 24 hours to 6 weeks after operation (<0.05). Significant difference was found in HSS scores between groups at 1, 2, 4, and 6 weeks after operation, and group A showed the highest score (<0.05). At 1 and 2 days after operation, group A showed the highest ROM (<0.05), and ROM of groups A and B was significantly higher that of group C at 3 days, 1 week, 2 weeks, 4 weeks, and 6 weeks after operation (<0.05). Groups A and B were significantly lower than group C in the serum erythrocyte sedimentation rate at 2 days, 3 days, 1 week, 2 weeks, 4 weeks, and 6 weeks, in C-reactive protein levels at 1, 2, and 3 days, in interleukin 6 (IL-6) and TNF-α levels at 1 day to 6 weeks, and in IL-8 level at 2 and 3 days (<0.05). The drainage volume within the first 24 hours and the serum coagulation parameters within the 2 weeks after operation showed no significant difference between groups (>0.05).
Sequential treatment with ACNB and COX-2 selective inhibitor is a safe and effective approach for postoperative pain management after primary TKA, and it can alleviate postoperative pain, promote the joint function recovery, and reduce the risk of adverse reactions.
探讨收肌管神经阻滞(ACNB)联合环氧化酶2(COX - 2)选择性抑制剂(帕瑞昔布和塞来昔布)序贯治疗初次全膝关节置换术(TKA)后疼痛的疗效。
选取2015年1月至2015年12月符合纳入标准的90例骨关节炎患者,随机分为3组:ACNB + COX - 2组(A组,n = 30)、COX - 2组(B组,n = 30)和对照组(C组,n = 30)。各组患者在性别、年龄、体重指数、手术侧别及骨关节炎病程方面比较,差异均无统计学意义(P > 0.05),具有可比性。A组在TKA结束时行ACNB。A组和B组术后前3天静脉注射帕瑞昔布(40 mg/12小时),之后口服塞来昔布(200 mg/12小时)至术后6周;C组在相同时间点给予安慰剂。当患者视觉模拟评分(VAS)>4分时,采用口服曲马多或静脉注射吗啡作为补救措施。比较各组手术时间、术后24小时引流量、住院时间、不良反应发生率;术前及术后1天、2天、3天、1周、2周、4周和6周的VAS疼痛评分、吗啡用量、膝关节活动度(ROM)及炎症因子水平;术后24小时内及术后24小时至6周的吗啡用量;术后1、2、4和6周的美国特种外科医院(HSS)评分;术前及术后1、3和14天的血清凝血参数。
A组和B组住院时间明显短于C组,术后恶心呕吐发生率明显低于C组(P < 0.05)。术后1、2和3天,A组和B组静息时VAS评分(VASR)明显低于C组(P < 0.05);术后1天,各组行走时VAS评分(VASW)差异有统计学意义(P < 0.05),A组VASW最低;术后2、3天及术后1、2、4和6周,A组和B组VASW明显低于C组(P < 0.05)。术后24小时内各组吗啡用量差异有统计学意义(P < 0.05),A组用量最低;术后24小时至6周,A组和B组吗啡用量明显低于C组(P < 0.05)。术后1、2、4和6周各组HSS评分差异有统计学意义,A组评分最高(P < 0.05)。术后1和2天,A组ROM最大(P < 0.05),术后3天、1周、2周、4周和6周,A组和B组ROM明显高于C组(P < 0.05)。术后2天、3天、1周、2周、4周和6周,A组和B组血清红细胞沉降率明显低于C组;术后1、2和3天,C反应蛋白水平明显低于C组;术后1天至6周,白细胞介素6(IL - 6)和肿瘤坏死因子 - α水平明显低于C组;术后2和3天,IL - 8水平明显低于C组(P < 0.05)。术后24小时内引流量及术后2周内血清凝血参数各组间比较,差异均无统计学意义(P > 0.05)。
ACNB联合COX - 2选择性抑制剂序贯治疗是初次TKA术后疼痛管理的一种安全有效的方法,可减轻术后疼痛,促进关节功能恢复,降低不良反应发生风险。