Sun Mingyang, Liao Qin, Wen Lingling, Yan Xuebin, Zhang Fan, Ouyang Wen
Department of Anesthesiology, Third Xiangya Hospital, Central South University, Changsha 410013; Department of Anesthesiology, Henan Provincial People Hospital, Zhengzhou 450000, China.
Zhong Nan Da Xue Xue Bao Yi Xue Ban. 2013 Jul;38(7):653-60. doi: 10.3969/j.issn.1672-7347.2013.07.001.
To explore whether perioperative intravenous flurbiprofen axetil can reduce the incidence and intensity of chronic pain for breast cancer after surgical treatment.
This randomized, double-blind, controlled trial enrolled 60 patients undergoing mastectomy and axillary lymph node dissection under general anesthesia. All patients accepted Hospital Anxiety and Depression Scale (HAD) tests the day before the surgery to evaluate depression and anxiety. The patients were randomly assigned to receive either 50 mg flurbiprofen axetil intravenously 15 minutes before the surgical incision and 6 hours later (group F) or intravenous 5 mL intralipid as a control (group C). All patients received patient-controlled intravenous analgesia (PCIA) with fentanyl postoperatively. Peripheral venous blood samples were drawn before the surgery, at 4 and 24 h after the surgery to detect the plasma level of PGE2 and tumor necrosis factor-α (TNF-α). Postoperative fentanyl consumption, Numerical Rating Scale (NRS) scores and adverse effects were recorded at 2, 6, 12, 24 and 48 h after the surgery. The duration and intensity of pain were followed up by telephone at the 2nd-12th month after the surgery.
The incidence of pain at 2, 4, 6, and 12 months after the breast surgery was 33%, 20%, 15%, and 10%, respectively, and the average pain score was 0.77, 0.57, 0.28, and 0.18, respectively. Compared with group C, the scores of pain in group F were significantly lower at 2, 4, 6 and 12 months postoperatively (F=7.758, P=0.007). The incidence of pain in group F was significantly lower at 2, 4 and 6 months postoperatively (P<0.05). There was no significant difference in the incidence of pain between the groups at 12 months postoperatively (P>0.05). Preoperatively and at 4 and 24 h after the surgery, there was no significant difference in the level of TNF-α between the two groups (F=0.530, P=0.470); but plasma concentration of PGE2 in group F was significantly lower than that in group C (F=5.646, P=0.021). No patients developed abnormal bleeding, peptic ulcer, impaired liver or renal function and respiratory depression.
Perioperative intravenous infusion of 100 mg flurbiprofen axetil can decrease the intensity and incidence of chronic pain for breast cancer after surgical treatment.
探讨围手术期静脉注射氟比洛芬酯能否降低乳腺癌手术治疗后慢性疼痛的发生率及疼痛强度。
本随机、双盲、对照试验纳入了60例在全身麻醉下行乳房切除术和腋窝淋巴结清扫术的患者。所有患者在手术前一天接受医院焦虑抑郁量表(HAD)测试,以评估抑郁和焦虑情况。患者被随机分为两组,一组在手术切口前15分钟静脉注射50mg氟比洛芬酯,6小时后再注射一次(F组);另一组静脉注射5mL脂肪乳作为对照(C组)。所有患者术后均接受芬太尼患者自控静脉镇痛(PCIA)。在手术前、术后4小时和24小时采集外周静脉血样本,检测血浆中前列腺素E2(PGE2)和肿瘤坏死因子-α(TNF-α)的水平。记录术后2、6、12、24和48小时的芬太尼用量、数字评分量表(NRS)评分及不良反应。在术后第2至12个月通过电话随访疼痛的持续时间和强度。
乳腺癌手术后2、4、6和12个月的疼痛发生率分别为33%、20%、15%和10%,平均疼痛评分分别为0.77、0.57、0.28和0.18。与C组相比,F组术后2、4、6和12个月的疼痛评分显著更低(F=7.758,P=0.007)。F组术后2、4和6个月的疼痛发生率显著更低(P<0.05)。术后12个月时,两组间疼痛发生率无显著差异(P>0.05)。术前及术后4小时和24小时,两组间TNF-α水平无显著差异(F=0.530,P=0.470);但F组血浆PGE2浓度显著低于C组(F=5.646,P=0.021)。无一例患者出现异常出血、消化性溃疡、肝肾功能损害及呼吸抑制。
围手术期静脉输注100mg氟比洛芬酯可降低乳腺癌手术治疗后慢性疼痛的强度和发生率。