Sun Yiyuan, Lin Yipeng, Li Qi, Li Bohua, Wang Duan, Huang Xihao
Day Service Center, West China Hospital, Sichuan University, Chengdu Sichuan, 610041, P. R. China.
Department of Orthopaedics, Orthopedic Research Institute, West China Hospital, Sichuan University, Chengdu Sichuan, 610041, P. R. China.
Zhongguo Xiu Fu Chong Jian Wai Ke Za Zhi. 2023 Aug 15;37(8):982-988. doi: 10.7507/1002-1892.202304068.
To investigate the effectiveness of preemptive analgesia with imrecoxib on analgesia after anterior cruciate ligament (ACL) reconstruction.
A total of 160 patients with ACL injuries who met the selection criteria and were admitted between November 2020 and August 2021 were selected and divided into 4 groups according to the random number table method (=40). Group A began to take imrecoxib 3 days before operation (100 mg/time, 2 times/day); group B began to take imrecoxib 1 day before operation (100 mg/time, 2 times/day); group C took 200 mg of imrecoxib 2 hours before operation (5 mL of water); and group D did not take any analgesic drugs before operation. There was no significant difference in gender, age, body mass index, constituent ratio of meniscal injuries with preoperative MRI grade 3, constituent ratio of cartilage injury Outerbridge grade 3, and visual analogue scale (VAS) score at the time of injury and at rest among 4 groups (>0.05). The operation time, hospitalization stay, constituent ratio of perioperative American Society of Anesthesiologists (ASA) grade 1, postoperative opioid dosage, and complications were recorded. The VAS scores were used to evaluate the degree of knee joint pain, including resting VAS scores before operation and at 6, 24, 48 hours, and 1, 3, 6, and 12 months after operation, and walking, knee flexion, and night VAS scores at 1, 3, 6, and 12 months after operation. The knee injury and osteoarthritis score (KOOS) was used to evaluate postoperative quality of life and knee-related symptoms of patients, mainly including pain, symptoms, daily activities, sports and entertainment functions, knee-related quality of life (QOL); and the Lysholm score was used to evaluate knee joint function.
All patients were followed up 1 year. There was no significant difference in operation time, hospitalization time, or constituent ratio of perioperative ASA grade 1 among 4 groups (>0.05); the dosage of opioids in groups A-C was significantly less than that in group D (<0.05). Except for 1 case of postoperative fever in group B, no complications such as joint infection, deep vein thrombosis of the lower extremities, or knee joint instability occurred in each group. The resting VAS scores of groups A-C at 6 and 24 hours after operation were lower than those of group D, and the score of group A at 6 hours after operation was lower than those of group C, and the differences were significant (<0.05). At 1 month after operation, the knee flexion VAS scores of groups A-C were lower than those of group D, the walking VAS scores of groups A and B were lower than those of groups C and D, the differences were significant (<0.05). At 1 month after operation, the KOOS pain scores in groups A-C were higher than those in group D, there was significant difference between groups A, B and group D (<0.05); the KOOS QOL scores in groups A-C were higher than that in group D, all showing significant differences (<0.05), but there was no significant difference between groups A-C (>0.05). There was no significant difference in VAS scores and KOOS scores between the groups at other time points (>0.05). And there was no significant difference in Lysholm scores between the groups at 1, 3, 6, and 12 months after operation (>0.05).
Compared with the traditional analgesic scheme, applying the concept of preemptive analgesia with imrecoxib to manage the perioperative pain of ACL reconstruction can effectively reduce the early postoperative pain, reduce the dosage of opioids, and promote the early recovery of limb function.
探讨艾瑞昔布超前镇痛对前交叉韧带(ACL)重建术后镇痛的效果。
选取2020年11月至2021年8月收治的160例符合入选标准的ACL损伤患者,按随机数字表法分为4组(每组40例)。A组于术前3天开始服用艾瑞昔布(100mg/次,2次/天);B组于术前1天开始服用艾瑞昔布(100mg/次,2次/天);C组于术前2小时服用艾瑞昔布200mg(加水5mL);D组术前未服用任何镇痛药。4组患者在性别、年龄、体重指数、术前MRI 3级半月板损伤构成比、Outerbridge 3级软骨损伤构成比以及损伤时和静息时视觉模拟评分(VAS)等方面比较,差异均无统计学意义(P>0.05)。记录手术时间、住院时间、围手术期美国麻醉医师协会(ASA)1级构成比、术后阿片类药物用量及并发症情况。采用VAS评分评估膝关节疼痛程度,包括术前及术后6、24小时、48小时,1、3、6、12个月静息时VAS评分,以及术后1、3、6、12个月行走、屈膝及夜间VAS评分。采用膝关节损伤与骨关节炎评分(KOOS)评估患者术后生活质量及膝关节相关症状,主要包括疼痛、症状、日常活动、运动与娱乐功能、膝关节相关生活质量(QOL);采用Lysholm评分评估膝关节功能。
所有患者均随访1年。4组患者手术时间、住院时间及围手术期ASA 1级构成比比较,差异均无统计学意义(P>0.05);AC组阿片类药物用量均显著少于D组(P<0.05)。除B组术后有1例发热外,各组均未发生关节感染、下肢深静脉血栓形成或膝关节不稳等并发症。术后6、24小时,AC组静息VAS评分均低于D组,且A组术后6小时评分低于C组,差异均有统计学意义(P<0.05)。术后1个月,AC组屈膝VAS评分低于D组,A、B组行走VAS评分低于C、D组,差异均有统计学意义(P<0.05)。术后1个月,AC组KOOS疼痛评分高于D组,A、B组与D组比较差异有统计学意义(P<0.05);AC组KOOS QOL评分高于D组,差异均有统计学意义(P<0.05),但AC组间比较差异无统计学意义(P>0.05)。其他时间点各组VAS评分及KOOS评分比较,差异均无统计学意义(P>0.05)。术后1、3、6、12个月各组Lysholm评分比较,差异均无统计学意义(P>0.05)。
与传统镇痛方案相比,将艾瑞昔布超前镇痛理念应用于ACL重建围手术期疼痛管理,可有效减轻术后早期疼痛,减少阿片类药物用量,促进肢体功能早期恢复。