首页> 外文期刊>Journal of minimally invasive gynecology >Preemptive analgesic efficacy of parecoxib vs placebo in infertile women undergoing diagnostic laparoscopy: randomized controlled trial.
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Preemptive analgesic efficacy of parecoxib vs placebo in infertile women undergoing diagnostic laparoscopy: randomized controlled trial.

机译:在接受诊断性腹腔镜检查的不育妇女中,帕瑞昔布和安慰剂的先发镇痛效果:随机对照试验。

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To compare the preemptive analgesic efficacy between parecoxib and placebo in infertile women undergoing outpatient diagnostic laparoscopy.Double-blind, randomized, placebo-controlled study (Canadian Task Force classification I).Department of Obstetrics and Gynecology, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand.Sixty infertile women undergoing diagnostic laparoscopy from November 2009 to January 2011.Patients were randomized to receive either 40 mg parecoxib (treatment group) or normal saline solution as placebo (control group) intravenously at 15 minutes before surgery. Postoperative shoulder and wound pain was self-assessed using a visual analog scale at 2, 6, 12, and 24 hours after surgery. Administration of rescue analgesic agents, and adverse effects were recorded.There were 30 patients in each group. Shoulder pain scores at each time measured, as well as wound pain score, was significantly lower in the parecoxib group compared with the placebo group (p < .001). The percentage of patients who required postoperative rescue analgesic therapy was lower in the treatment group compared with the control group (26.7% and 40.0%, respectively; p = .04). The treatment group required less rescue analgesic therapy than did the control group (mean [SD], 314.8 [53.9] and 842.6 [122.7] mg acetaminophen; p = .04). There was no significant difference in adverse effects between the 2 groups.Preoperative administration of 40 mg parecoxib, compared with placebo, provided significantly superior postoperative pain relief after diagnostic laparoscopy.
机译:为了比较帕瑞昔布和安慰剂在接受门诊诊断性腹腔镜检查的不育妇女中的先发性镇痛效果,双盲,随机,安慰剂对照研究(加拿大特别工作组I级),曼谷朱拉隆功大学医学院妇产科2009年11月至2011年1月,对60例接受诊断性腹腔镜检查的不育妇女进行了随机分组,他们在手术前15分钟接受了40 mg帕瑞昔布(治疗组)或生理盐水作为安慰剂(对照组)的治疗。术后2、6、12和24小时使用视觉模拟量表对术后肩部和伤口疼痛进行自我评估。记录急救镇痛药的使用情况及不良反应。每组30例。与安慰剂组相比,帕瑞昔布组每次测量的肩部疼痛评分以及伤口疼痛评分均显着降低(p <.001)。与对照组相比,治疗组中需要术后急救镇痛治疗的患者百分比较低(分别为26.7%和40.0%; p = .04)。与对照组相比,治疗组需要更少的急救镇痛治疗(对乙酰氨基酚的平均值[SD],314.8 [53.9]和842.6 [122.7] mg; p = .04)。两组之间的不良反应没有显着差异。术前给予40 mg帕瑞昔布与安慰剂相比,诊断性腹腔镜检查后可显着改善术后疼痛。

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