Sener Mesut, Yilmazer Cuneyt, Yilmaz Ismail, Bozdogan Nesrin, Ozer Cem, Donmez Asli, Arslan Gulnaz
Department of Anesthesiology and Reanimation, Baskent University Faculty of Medicine, Ankara, Turkey.
J Clin Anesth. 2008 Mar;20(2):103-8. doi: 10.1016/j.jclinane.2007.09.009.
To compare the efficacy of injectable lornoxicam with diclofenac, ketoprofen, and dipyrone for acute postoperative pain.
Prospective, randomized, placebo-controlled, double-blind study.
University hospital.
200 ASA physical status I patients who were scheduled for elective septoplasty with general anesthesia.
Patients were divided into 5 groups according to the intramuscularly administered analgesic drug: lornoxicam 8 mg (twice daily), diclofenac 75 mg (twice daily), ketoprofen 100 mg (twice daily), dipyrone 1 g (three times daily), and placebo (twice daily).
Pain intensity was evaluated with a 0 to 100 mm Visual Analog Scale (VAS) at the 2nd, 4th, 6th, 8th, 12th, 16th, 20th, and 24th hour postoperatively. Intramuscular pethidine 1 mg/kg was administered to patients requiring additional analgesia, and treatment-related adverse effects were noted.
Pethidine requirement was found to be significantly higher in the placebo group (1.8 mg/kg per 24 hours; 95% confidence interval, 1.5-2.2) than in the other groups (P = 0.001). No significant difference in opioid requirement was found among the treated groups (P > 0.05). Postoperative VAS scores were significantly lower at specific hours in the treatment groups when compared with placebo group (P < 0.05). No statistically significant difference in adverse effects was found among the groups studied (P > 0.05).
Efficacy of lornoxicam in the management of acute postoperative pain was not superior to that of other nonopioid analgesics used in this study.
比较注射用氯诺昔康与双氯芬酸、酮洛芬和安乃近治疗术后急性疼痛的疗效。
前瞻性、随机、安慰剂对照、双盲研究。
大学医院。
200例拟行择期鼻中隔成形术并接受全身麻醉的美国麻醉医师协会(ASA)身体状况I级患者。
根据肌肉注射的镇痛药物将患者分为5组:氯诺昔康8毫克(每日两次)、双氯芬酸75毫克(每日两次)、酮洛芬100毫克(每日两次)、安乃近1克(每日三次)和安慰剂(每日两次)。
术后第2、4、6、8、12、16、20和24小时,使用0至100毫米视觉模拟评分法(VAS)评估疼痛强度。对需要额外镇痛的患者给予肌肉注射哌替啶1毫克/千克,并记录与治疗相关的不良反应。
发现安慰剂组的哌替啶需求量(每24小时1.8毫克/千克;95%置信区间,1.5 - 2.2)显著高于其他组(P = 0.001)。各治疗组之间的阿片类药物需求量无显著差异(P > 0.05)。与安慰剂组相比,治疗组在特定时间的术后VAS评分显著更低(P < 0.05)。各研究组之间的不良反应无统计学显著差异(P > 0.05)。
氯诺昔康治疗术后急性疼痛的疗效并不优于本研究中使用的其他非阿片类镇痛药。