Fleckenstein J, Kohls N, Evtouchenko E, Lehmeyer L, Kramer S, Lang P M, Siebeck M, Mussack T, Hatz R, Heindl B, Conzen P, Rehm M, Czerner S, Zwißler B, Irnich D
Department of Anaesthesiology, University of Munich, Germany.
Division Integrative Health Promotion, University of Applied Sciences and Arts Coburg, Germany.
Eur J Pain. 2016 Feb;20(2):186-95. doi: 10.1002/ejp.699. Epub 2015 Mar 31.
Pre-emptive analgesia in perioperative care has potential benefits for patients. The pre-emptive and postoperative analgesic effects of the cyclooxygenase-2 inhibitor etoricoxib have been investigated using a 2 × 2 factorial trial design.
According to the 2 × 2 factorial study design, 103 patients scheduled for visceral surgery, were randomly allocated to two groups prior to surgery. Patients could receive either etoricoxib or placebo (to investigate pre-emptive analgesia). Subsequent to surgery, patients randomly received either etoricoxib or placebo, again. It follows, that four treatment modalities (continuous or replaced intervention) result, to investigate postoperative analgesia. Main Outcome Measure was the cumulative morphine use 48 h post-surgery. Other outcomes included pain intensities, pain thresholds and sensory detection.
Eighty-six patients (female n = 42; mean age 53.82 ± 13.61 years) were evaluated on the basis of an intention to treat analysis. Pre-emptive administration of 120 mg etoricoxib did not significantly reduce the cumulative morphine dose within the first 48 h after surgery, when compared to the administration of placebo. The analysis of the post-operative treatment groups showed a non-significant 8% reduction in morphine dose during the continuous administration of etoricoxib. There were no changes in sensory perception as detected with QST before and after surgery or between groups.
The effect of administering etoricoxib was not superior to placebo in reducing the morphine dose required for postoperative analgesia. The lack of changes in peripheral nociception suggests that central algetic mechanisms are of higher impact in the development of postoperative pain following abdominal or thoracic surgery.
围手术期护理中的超前镇痛对患者有潜在益处。已使用2×2析因试验设计研究了环氧化酶-2抑制剂依托考昔的超前镇痛和术后镇痛效果。
根据2×2析因研究设计,103例计划进行内脏手术的患者在手术前被随机分为两组。患者可接受依托考昔或安慰剂(以研究超前镇痛)。手术后,患者再次随机接受依托考昔或安慰剂。由此产生了四种治疗方式(持续或替代干预),以研究术后镇痛。主要观察指标是术后48小时的吗啡累积用量。其他观察指标包括疼痛强度、疼痛阈值和感觉检测。
基于意向性分析对86例患者(女性n = 42;平均年龄53.82±13.61岁)进行了评估。与给予安慰剂相比,术前给予120 mg依托考昔并未显著降低术后头48小时内的吗啡累积剂量。对术后治疗组的分析显示,持续给予依托考昔期间吗啡剂量无显著降低8%。术前和术后或组间通过定量感觉测试检测到的感觉知觉没有变化。
在减少术后镇痛所需的吗啡剂量方面,给予依托考昔的效果并不优于安慰剂。外周伤害感受无变化表明,中枢痛觉机制在腹部或胸部手术后的术后疼痛发生中影响更大。