Department of Anesthesiology, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou 510060, China.
Department of Anesthesiology, State Key Laboratory of Ophthalmology, Zhongshan Ophthalmic Center, Sun Yat-sen University, Guangzhou 510060, China.
Ophthalmic Plast Reconstr Surg. 2023;39(3):260-265. doi: 10.1097/IOP.0000000000002308. Epub 2023 Jan 24.
To evaluate the effect of either flurbiprofen axetil or nalbuphine combined with retrobulbar block (RB) before surgery on postoperative pain control and enhanced recovery in day-care patients undergoing orbital implantation.
A total of 45 patients undergoing orbital implantation with general anesthesia were randomly divided into three groups: flurbiprofen axetil (1 mg/kg) combined with RB (group F), nalbuphine (0.1 mg/kg) combined with RB (group N), and placebo as normal saline with RB (group C). The primary outcome was the average pain score (numeric rating scale: 0-10) within the first 24 hours. Other outcomes including the peak pain score, paracetamol requirement, quality of recovery (QoR)-15, and adverse effects (AEs) were assessed.
The average and peak pain scores within 24 hours after surgery in group F were significantly lower than in other groups ( p < 0.0167). Compared with group C, the NRS scores were significantly decreased at 2 and 4 hours in group F, and 2 hours in group N after surgery ( p < 0.0167), but without significant differences at other measured time points. The time to first paracetamol oral intake displayed a significant difference among the three groups ( p < 0.0167).
Preemptive use of flurbiprofen axetil 1 mg/kg combined with RB is an optimal choice for multimodal analgesia for day-care patients undergoing orbital implantation in terms of efficient acute pain control, without impeding patient-enhanced recovery.
评估手术前氟比洛芬酯或纳布啡联合球后阻滞(RB)对日间手术患者眶内植入术后疼痛控制和加速康复的影响。
将 45 例行全身麻醉眶内植入术的患者随机分为三组:氟比洛芬酯(1mg/kg)联合 RB(F 组)、纳布啡(0.1mg/kg)联合 RB(N 组)和 RB 生理盐水(C 组)。主要结局是术后 24 小时内的平均疼痛评分(数字评分量表:0-10)。其他结局包括峰值疼痛评分、扑热息痛需求、恢复质量(QoR)-15 和不良反应(AE)。
F 组术后 24 小时内的平均和峰值疼痛评分明显低于其他两组(p<0.0167)。与 C 组相比,F 组在术后 2 小时和 4 小时,N 组在术后 2 小时时 NRS 评分明显降低(p<0.0167),但在其他测量时间点无显著差异。首次口服扑热息痛的时间在三组之间存在显著差异(p<0.0167)。
对于行日间手术眶内植入术的患者,氟比洛芬酯 1mg/kg 联合 RB 作为多模式镇痛的预防性应用,可有效控制急性疼痛,不影响患者的加速康复,是一种最佳选择。