Reuben S S, Connelly N R
Department of Anesthesiology, Baystate Medical Center, Springfield, Massachusetts 01199, USA.
Anesth Analg. 2000 Nov;91(5):1221-5. doi: 10.1097/00000539-200011000-00032.
Nonsteroidal antiinflammatory drugs are recommended for the multimodal management of postoperative pain and may have a significant opioid-sparing effect after major surgery. The analgesic efficacy of the cyclooxygenase-2 nonsteroidal antiinflammatory drugs, celecoxib and rofecoxib, have not been evaluated after major orthopedic surgery. This study was designed to determine whether the administration of a preoperative dose of celecoxib or rofecoxib to patients who have undergone spinal stabilization would decrease patient-controlled analgesia (PCA) morphine use and/or enhance analgesia. We evaluated 60 inpatients undergoing spine stabilization by one surgeon. All patients received PCA morphine. The patients were divided into three groups. Preoperatively, they were given oral celecoxib 200 mg, rofecoxib 50 mg, or placebo. The outcome measures included pain scores and 24-h morphine use at six times during the first 24 postoperative h. The total dose of morphine and the cumulative doses for each of the six time periods were significantly more in the placebo group than in the other two groups. The morphine dose was significantly less in five of the six time intervals in the rofecoxib group compared with the celecoxib group. The pain scores were significantly less in the rofecoxib group than in the other two groups at two of the six intervals, and less than the placebo group in an additional interval. Although both rofecoxib and celecoxib produce similar analgesic effects in the first 4 h after surgery, rofecoxib demonstrated an extended analgesic effect that lasted throughout the 24-h study. We thus recommend that rofecoxib be used as a preoperative component of pain management that includes PCA morphine in patients undergoing spine stabilization surgery.
The cyclooxygenase-2-specific nonsteroidal antiinflammatory drugs, celecoxib and rofecoxib, both demonstrate an opioid-sparing effect after spinal fusion surgery. Celecoxib resulted in decreased morphine use for the first 8 h after surgery, whereas rofecoxib demonstrated less morphine use throughout the 24-h study period.
非甾体类抗炎药被推荐用于术后疼痛的多模式管理,并且在大手术后可能具有显著的阿片类药物节省效应。环氧化酶-2非甾体类抗炎药塞来昔布和罗非昔布在大骨科手术后的镇痛效果尚未得到评估。本研究旨在确定对接受脊柱固定手术的患者术前给予一剂塞来昔布或罗非昔布是否会减少患者自控镇痛(PCA)吗啡的使用和/或增强镇痛效果。我们评估了由一位外科医生进行脊柱固定手术的60例住院患者。所有患者均接受PCA吗啡治疗。患者被分为三组。术前,他们分别口服200毫克塞来昔布、50毫克罗非昔布或安慰剂。观察指标包括术后24小时内六个时间点的疼痛评分和24小时吗啡使用量。安慰剂组的吗啡总剂量以及六个时间段中每个时间段的累积剂量均显著高于其他两组。与塞来昔布组相比,罗非昔布组在六个时间间隔中的五个间隔内吗啡剂量显著更低。在六个间隔中的两个间隔,罗非昔布组的疼痛评分显著低于其他两组,在另一个间隔中低于安慰剂组。尽管罗非昔布和塞来昔布在术后最初4小时产生相似的镇痛效果,但罗非昔布在整个24小时研究期间都表现出持续的镇痛效果。因此,我们建议将罗非昔布用作脊柱固定手术患者疼痛管理的术前组成部分,该疼痛管理包括PCA吗啡。
环氧化酶-2特异性非甾体类抗炎药塞来昔布和罗非昔布在脊柱融合手术后均显示出阿片类药物节省效应。塞来昔布导致术后最初8小时吗啡使用量减少,而罗非昔布在整个24小时研究期间吗啡使用量更少。