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一项随机、双盲、平行组研究,采用牙阻生疼痛模型比较依托考昔与安慰剂、萘普生钠及对乙酰氨基酚加可待因的镇痛效果。

A randomized, double-blind, parallel-group study comparing the analgesic effect of etoricoxib to placebo, naproxen sodium, and acetaminophen with codeine using the dental impaction pain model.

作者信息

Malmstrom Kerstin, Kotey Paul, Coughlin Heather, Desjardins Paul J

机构信息

Department of Clinical Immunology & Analgesia and Department of Biostatistics, Merck Research Laboratories, Rahway, NJ 07065, USA.

出版信息

Clin J Pain. 2004 May-Jun;20(3):147-55. doi: 10.1097/00002508-200405000-00004.

Abstract

OBJECTIVE

To compare the overall analgesic effect, including time to onset, peak and duration of effect for etoricoxib 120 mg, a new COX-2 selective inhibitor, in patients with acute pain to that of placebo. Naproxen sodium 550 mg and acetaminophen/codeine 600/60 mg were the active comparators.

METHODS

A total of 201 patients with moderate to severe pain following surgical extraction of > or = 2 third molars, of which at least the mandibular tooth was impacted, were randomly allocated to receive single oral doses of placebo (n = 50), etoricoxib 120 mg (n = 50), naproxen sodium 550 mg (n = 51), or acetaminophen/codeine 600/60 mg (n = 50). The endpoints included total pain relief over 8 hours (TOPAR8, primary end point), sum of pain intensity difference over 8 hours, patient's global evaluation, onset, peak, and duration of analgesia.

RESULTS

Etoricoxib 120 mg had a significantly greater least squares (LS) mean TOPAR8 score than placebo (20.9 vs 5.4; P < 0.001) and acetaminophen/codeine 600/60 mg (20.9 vs 11.5; P < 0.001), and a similar LS mean TOPAR8 score to naproxen sodium 550 mg (20.9 vs 21.3). All three active treatments had rapid onset of analgesia, median time approximately 30 minutes. The duration of analgesic effect, defined as median time to rescue medication use, was >24 hours for etoricoxib, 20.8 hours for naproxen sodium, 3.6 hours for acetaminophen/codeine, and 1.6 hours for placebo.

DISCUSSION

Etoricoxib is a new COX-2 selective inhibitor under development for treatment of osteoarthritis, rheumatoid arthritis, and acute pain. In this study, etoricoxib 120 mg provided rapid and long-lasting pain relief to patients with moderate-to-severe postdental surgery pain. Etoricoxib was generally well tolerated.

摘要

目的

比较新型环氧化酶-2(COX-2)选择性抑制剂依托考昔120毫克对急性疼痛患者的总体镇痛效果,包括起效时间、效应峰值和持续时间,与安慰剂进行对比。以550毫克萘普生钠和对乙酰氨基酚/可待因600/60毫克作为活性对照药。

方法

总共201例因拔除≥2颗第三磨牙后出现中至重度疼痛的患者,其中至少有一颗下颌牙为阻生齿,被随机分配接受单剂量口服安慰剂(n = 50)、依托考昔120毫克(n = 50)、萘普生钠550毫克(n = 51)或对乙酰氨基酚/可待因600/60毫克(n = 50)。观察终点包括8小时内的总疼痛缓解情况(TOPAR8,主要终点)、8小时内疼痛强度差值总和、患者总体评估、镇痛的起效时间、峰值和持续时间。

结果

依托考昔120毫克的最小二乘(LS)平均TOPAR8评分显著高于安慰剂(20.9对5.4;P < 0.001)和对乙酰氨基酚/可待因600/60毫克(20.9对11.5;P < 0.001),与550毫克萘普生钠的LS平均TOPAR8评分相似(20.9对21.3)。所有三种活性治疗药物的镇痛起效迅速,中位时间约为30分钟。镇痛效果持续时间定义为使用解救药物的中位时间,依托考昔>24小时,萘普生钠20.8小时,对乙酰氨基酚/可待因3.6小时,安慰剂1.6小时。

讨论

依托考昔是一种正在研发用于治疗骨关节炎、类风湿关节炎和急性疼痛的新型COX-2选择性抑制剂。在本研究中,依托考昔120毫克为中至重度牙拔除术后疼痛患者提供了快速且持久的疼痛缓解。依托考昔总体耐受性良好。

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