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布洛芬-可待因组合用于治疗下颌第三磨牙拔除术后疼痛患者的效果。

The effect of an ibuprofen-codeine combination for the treatment of patients with pain after removal of lower third molars.

作者信息

Petersen J K, Hansson F, Strid S

机构信息

Department of Oral and Maxillofacial Surgery, Royal Dental College, Faculty of Health Sciences, University of Aarhus, Denmark.

出版信息

J Oral Maxillofac Surg. 1993 Jun;51(6):637-40. doi: 10.1016/s0278-2391(10)80262-9.

Abstract

A double-blind randomized crossover analgesic trial was carried out on 70 patients undergoing surgical removal of one lower third molar at each visit. The analgesic efficacy of a two-dose regimen of the combination ibuprofen-codeine, 400 to 60 mg, was compared with ibuprofen, 400 mg. Each of the two doses was taken when the patient needed pain relief and the pain intensity was measured on a visual analog scale during the 10-hour period after the first medication. Because of carryover effects between periods 1 and 2, the analysis was carried out only for period 1 according to a parallel group design. Of the 60 patients who were evaluated for analgesic effect, the mean pain reduction of dose 1 was 63% for the 29 patients given ibuprofen-codeine and 50% for the 31 patients given ibuprofen; the mean duration of effect was 7.5 and 6.3 hours, respectively. The difference in pain reduction index (pain reduction X duration of effect) between the two treatments was significant in favor of the combination, whereas the separate variables of pain reduction and duration of effect were not significantly different. The mean pain reduction was 67% after doses 1 and 2 for patients on ibuprofen-codeine and 52% for those on ibuprofen; the mean duration of effect was 9.4 and 9.2 hours, respectively. For doses 1 and 2, the difference in pain reduction index per dose between the two treatments was significant but not the difference for the separate variables, pain reduction, and duration of effect.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

对70例每次就诊时接受下颌第三磨牙拔除术的患者进行了一项双盲随机交叉镇痛试验。将布洛芬 - 可待因两剂量方案(400至60毫克)的镇痛效果与400毫克布洛芬进行了比较。当患者需要缓解疼痛时服用两种剂量中的每一种,并在首次用药后的10小时内通过视觉模拟量表测量疼痛强度。由于第1阶段和第2阶段之间存在残留效应,因此仅根据平行组设计对第1阶段进行分析。在60例接受镇痛效果评估的患者中,给予布洛芬 - 可待因的29例患者第1剂的平均疼痛减轻为63%,给予布洛芬的31例患者为50%;平均起效持续时间分别为7.5小时和6.3小时。两种治疗之间的疼痛减轻指数(疼痛减轻×起效持续时间)差异显著,有利于联合用药,而疼痛减轻和起效持续时间的单独变量没有显著差异。服用布洛芬 - 可待因的患者在第1剂和第2剂后的平均疼痛减轻为67%,服用布洛芬的患者为52%;平均起效持续时间分别为9.4小时和9.2小时。对于第1剂和第2剂,两种治疗之间每剂的疼痛减轻指数差异显著,但疼痛减轻和起效持续时间的单独变量差异不显著。(摘要截断于250字)

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