Desjardins Paul J, Shu Vincent S, Recker David P, Verburg Kenneth M, Woolf Clifford J
Clinical Site Administration, Analgesia Department, SCIREX Corporation, Austin, Texas, USA.
Anesthesiology. 2002 Sep;97(3):565-73. doi: 10.1097/00000542-200209000-00008.
The trend toward day-case surgery, with discharge on oral medication, has highlighted the need for effective and safe analgesics that facilitate a rapid recovery and discharge time. This study evaluated the analgesic efficacy, dose dependency, duration of action, and safety of the cyclooxygenase-2 specific inhibitor, valdecoxib, administered before oral or orthopedic surgery.
Eligible healthy adult patients were scheduled to undergo either extraction of two impacted third molar teeth (n = 284) or bunionectomy surgery (n = 223) with local anesthesia in two randomized, double-blind, placebo-controlled studies conducted at three centers in the United States. Patients received a single, preoperatively administered oral dose of placebo or 10 (oral surgery only), 20, 40, or 80 mg valdecoxib. Analgesic efficacy was assessed postoperatively, over a 24-h treatment period, or until the patient required rescue medication. Efficacy measures included time to rescue medication, proportion of patients requiring such rescue, pain intensity, and the Patient's Global Evaluation of Study Medication.
In both studies, all doses of valdecoxib produced analgesia with a duration (time to rescue analgesia) and magnitude (Pain Intensity, Patient's Global Evaluation) significantly greater than placebo. A dose-dependent effect was observed up to 40 mg valdecoxib, with an 80-mg dose providing no additional analgesic benefit. In both models, all doses of valdecoxib were well tolerated, with no clinically significant treatment-related gastrointestinal, renal, or platelet-derived adverse events, and no evidence of a dose-related increase in adverse events.
Preoperative orally administered valdecoxib provides well-tolerated and effective analgesia for mild to moderate postoperative pain.
日间手术并口服药物出院的趋势凸显了对有效且安全的镇痛药的需求,这类药物有助于快速康复和缩短出院时间。本研究评估了环氧化酶-2特异性抑制剂伐地昔布在口腔或骨科手术前给药时的镇痛效果、剂量依赖性、作用持续时间及安全性。
在美国三个中心进行的两项随机、双盲、安慰剂对照研究中,符合条件的健康成年患者计划接受局部麻醉下的两颗阻生第三磨牙拔除术(n = 284)或拇囊炎切除术(n = 223)。患者术前口服单剂量安慰剂或10 mg(仅口腔手术)、20 mg、40 mg或80 mg伐地昔布。术后在24小时治疗期内或直至患者需要急救药物时评估镇痛效果。疗效指标包括至急救药物的时间、需要此类急救的患者比例、疼痛强度以及患者对研究药物的整体评价。
在两项研究中,所有剂量的伐地昔布均产生了镇痛作用,其持续时间(至急救镇痛的时间)和强度(疼痛强度、患者整体评价)均显著优于安慰剂。观察到伐地昔布剂量达40 mg时存在剂量依赖性效应,80 mg剂量未提供额外的镇痛益处。在两种模型中,所有剂量的伐地昔布耐受性良好,未出现具有临床意义的与治疗相关的胃肠道、肾脏或血小板源性不良事件且无不良事件剂量相关增加的证据。
术前口服伐地昔布可为轻至中度术后疼痛提供耐受性良好且有效的镇痛作用。