Sivrikoz Nükhet, Koltka Kemalettin, Güresti Ece, Büget Mehmet, Sentürk Mert, Özyalçın Süleyman
Department of Anesthesiology, İstanbul University İstanbul Faculty of Medicine, İstanbul, Turkey.
Agri. 2014;26(1):23-8. doi: 10.5505/agri.2014.09821.
Non-steroidal anti-inflammatory drugs (NSAIDs) are recommended for multimodal postoperative pain management. The purpose of this study was to evaluate the postoperative pain relief and opioid-sparing effects of dexketoprofen and lornoxicam after major orthopedic surgery.
After obtaining ethical committee approval and informed consent, 120 patients undergoing elective hip or knee replacement under general anesthesia were randomized to receive two intravenous injections of 50 mg dexketoprofen (GD), 8 mg lornoxicam (GL) or saline as placebo (GP) intravenously. Postoperatively, patient-controlled analgesia (PCA) morphine was started as a 0.01 mg.kg-1 bolus dose, with lockout time of 10 minutes without continuous infusion. Pain assessment was made using the Visual Analogue Scale (VAS) at rest or during movement at postoperative 1, 2, 4, 6, 8, 12, and 24 hours.
The three groups were similar in terms of age, gender, American Society of Anesthesiologists (ASA) class, number of patients who underwent hip or knee surgery, weight, height, and operation duration. Patients in GD and GL demonstrated significantly reduced pain scores at rest and active motion compared to GP, with lower scores in the dexketoprofen group. Patients in GD and GL used significantly less morphine in the postoperative period compared to GP. The total morphine consumption of patients in GD was lower than in GL.
Intravenous application of 50 mg dexketoprofen twice a day and 8 mg lornoxicam twice a day improved analgesia and decreased morphine consumption following major orthopedic surgery. When the two active drugs were compared, it was found that dexketoprofen was superior to lornoxicam in terms of analgesic efficacy and opioid consumption.
非甾体抗炎药(NSAIDs)被推荐用于多模式术后疼痛管理。本研究的目的是评估右酮洛芬和氯诺昔康在骨科大手术后的术后疼痛缓解及阿片类药物节省效应。
获得伦理委员会批准并取得知情同意后,120例在全身麻醉下接受择期髋关节或膝关节置换术的患者被随机分为三组,分别静脉注射两次50mg右酮洛芬(GD组)、8mg氯诺昔康(GL组)或生理盐水作为安慰剂(GP组)。术后,患者自控镇痛(PCA)吗啡以0.01mg·kg-1的推注剂量开始,锁定时间为10分钟且无持续输注。在术后1、2、4、6、8、12和24小时,使用视觉模拟评分法(VAS)在静息或活动时进行疼痛评估。
三组在年龄、性别、美国麻醉医师协会(ASA)分级、接受髋关节或膝关节手术的患者数量、体重、身高和手术持续时间方面相似。与GP组相比,GD组和GL组患者在静息和主动活动时的疼痛评分显著降低,右酮洛芬组的评分更低。与GP组相比,GD组和GL组患者在术后使用的吗啡显著减少。GD组患者的吗啡总消耗量低于GL组。
每天两次静脉注射50mg右酮洛芬和每天两次静脉注射8mg氯诺昔康可改善骨科大手术后的镇痛效果并减少吗啡消耗量。当比较这两种活性药物时,发现右酮洛芬在镇痛效果和阿片类药物消耗量方面优于氯诺昔康。