Duloxetine for post-operative analgesia after modified radical mastectomy: A prospective randomized study

Dina Abdel Monem Elfeky, Ashraf Elsayed Alzeftawy, Mohamed Samir Abdel Ghafar, Motaz Amr Abdel Moez
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Abstract

Background: Insufficient management of postoperative pain has been shown to be correlated with prolonged hospitalization, escalated healthcare expenses, disrupted sleep patterns, heightened risk of depression, compromised functional abilities, and a worse quality of life. The objective of this research is to assess the efficacy of duloxetine in managing postoperative pain following radical mastectomy.Methods: This prospective randomised controlled work was performed on (40) individuals scheduled for modified radical mastectomy in Tanta University Hospital. The criteria for inclusion for this study consisted of adult female patients between the ages of 18 and 60 who were scheduled to have a modified radical mastectomy (MRM), ASA I, II and III. A total of 20 participants were recruited for this research, with an equal number of participants being randomly assigned to each of the two groups. The process of randomization was conducted using a computer-generated method. The patients were allocated by closed envelop into 2 groups: Group (1) (control group): Participants received 500 mg of IV acetaminophen (every 6 hours post operatively). Group (2): Participants received duloxetine 30 mg every 12 h for 3 days prior to operation, 30 mg 2 h prior to surgery and 30 mg 12 h following surgery and 500 mg of IV acetaminophen (every 6 hours following surgery).Results: There was significant decrease at 2,4,6,18,30,36 and 48 h in group 2 contrasted to group 1 (P value <0.001) and statistically insignificant difference in postoperative HR at baseline, PACU, 12, 24 and 42 h among both groups. A substantial decrease in postoperative MAP was existed at 2,4,6,18,30,36 and 48 h in group 2 contrasted to group 1 and statistically insignificant difference at baseline, PACU, 12, 24 and 42 h among both groups (P value <0.001). A statistically substantial decrease in intraoperative fentanyl consumption was existed in group 2 compared to groups 1 (P value <0.001). There was substantial decrease in VAS at 2,4,6,18,30,36 and 48 hours in group 2 contrasted to group 1 (P value<0.05). The satisfied patients in group 2 were significantly higher in group 2 compared to group 1.Conclusions: The current work showed that the use of perioperative duloxetine was safe and effective in controlling pain after modified radical mastectomy.
度洛西汀用于改良乳房根治术后的术后镇痛:一项前瞻性随机研究
背景:术后疼痛管理不足与住院时间延长、医疗费用增加、睡眠模式紊乱、抑郁风险增加、功能能力受损和生活质量下降有关。本研究的目的是评估度洛西汀治疗根治性乳房切除术后疼痛的疗效。方法:这项前瞻性随机对照研究在坦塔大学医院进行了40例计划进行改良乳房根治术的患者。纳入本研究的标准包括年龄在18至60岁之间的成年女性患者,她们计划接受改良乳房根治术(MRM), ASA I, II和III。这项研究共招募了20名参与者,两组中随机分配了相同数量的参与者。随机化过程采用计算机生成方法进行。采用密闭包膜法将患者分为两组:1组(对照组):术后每6小时静脉滴注对乙酰氨基酚500 mg。组(2):术前3天每12小时给予度洛西汀30 mg,术前2小时30 mg,术后12小时30 mg,术后每6小时静脉给予对乙酰氨基酚500 mg。结果:2组术后2、4、6、18、30、36、48 h与1组比较,差异均有统计学意义(P值<0.001),两组术后基线、PACU、12、24、42 h HR差异均无统计学意义。2组术后2、4、6、18、30、36、48 h MAP较1组明显降低,两组基线、PACU、12、24、42 h差异无统计学意义(P值<0.001)。2组术中芬太尼用量明显低于1组(P值<0.001)。2组VAS评分在2、4、6、18、30、36、48 h较1组明显降低(P值<0.05)。2组患者满意度明显高于1组。结论:改良乳房根治术后围手术期应用度洛西汀控制疼痛安全有效。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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