Rosenow D E, Albrechtsen M, Stolke D
Neurosurgical Department, University of Essen Medical School, Germany.
Anesth Analg. 1998 May;86(5):1045-50. doi: 10.1097/00000539-199805000-00026.
The analgesic efficacy and tolerability of lornoxicam (Xefo; Nycomed Pharma A/S, Roskilde, Denmark), a new nonsteroidal antiinflammatory drug, was compared with that of morphine in a double-blind, randomized, parallel-group study of 96 patients with at least moderate pain after lumbar microsurgical discectomy. Both drugs were administered i.v. via a patient-controlled analgesia (PCA) for up to 24 h postoperatively. Efficacy was assessed by comparing mean hourly pain intensity differences, mean hourly pain relief, and total pain relief (TOTPAR) values derived from a 5-point verbal rating scores of pain intensity and pain relief at several time points over 24 h. Of 79 patients included in a per-protocol analysis, statistically significant equivalence of lornoxicam and morphine was shown by TOTPAR values of 31.6 and 28.9, respectively (P = 0.048). Trends toward slightly faster onset of analgesia with morphine and slightly greater PCA demands with lornoxicam were observed initially, which may partly have been due to a higher baseline pain intensity in the lornoxicam group. Lornoxicam caused fewer adverse events than morphine (21.7% vs 38.0% of patients, respectively), most of which were mild or moderate in severity. These results suggest that lornoxicam is an alternative to morphine when administered by PCA for the treatment of moderate to severe postoperative pain.
After surgery for lumbar disk disease, patients obtained statistically equivalent pain relief with lornoxicam and morphine when administered by patient-controlled analgesia. However, lornoxicam was associated with a lower incidence of adverse events. This study suggests that lornoxicam provides an alternative to morphine for the treatment of postoperative pain.
在一项针对96例腰椎显微椎间盘切除术后至少有中度疼痛患者的双盲、随机、平行组研究中,将新型非甾体抗炎药氯诺昔康(Xefo;Nycomed Pharma A/S,罗斯基勒,丹麦)的镇痛效果和耐受性与吗啡进行了比较。两种药物均通过患者自控镇痛(PCA)静脉给药,术后持续24小时。通过比较24小时内多个时间点的平均每小时疼痛强度差异、平均每小时疼痛缓解程度以及根据5分语言疼痛强度和疼痛缓解评分得出的总疼痛缓解(TOTPAR)值来评估疗效。在符合方案分析纳入的79例患者中,氯诺昔康和吗啡的TOTPAR值分别为31.6和28.9,显示出统计学上的显著等效性(P = 0.048)。最初观察到吗啡的镇痛起效略快,而氯诺昔康的PCA需求略高,这可能部分归因于氯诺昔康组较高的基线疼痛强度。氯诺昔康引起的不良事件比吗啡少(分别为21.7%和38.0%的患者),大多数不良事件的严重程度为轻度或中度。这些结果表明,通过PCA给药时,氯诺昔康可作为吗啡的替代药物用于治疗中度至重度术后疼痛。
腰椎间盘疾病手术后,通过患者自控镇痛给药时,氯诺昔康和吗啡在患者获得的疼痛缓解方面具有统计学上的等效性。然而,氯诺昔康的不良事件发生率较低。这项研究表明,氯诺昔康为治疗术后疼痛提供了一种替代吗啡的药物。