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A Multicentre, Randomised, Double-Blind Study Comparing the Efficacy and Tolerability of Intramuscular Dexketoprofen versus Diclofenac in the Symptomatic Treatment of Acute Low Back Pain

机译:一项多中心,随机,双盲研究比较了肌内右旋酮洛芬和双氯芬酸对症治疗急性下腰痛的疗效和耐受性

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Background: Low back pain is an important medical problem in Western industrialised countries. NSAIDs are one of the main options for symptomatic pain relief in the early management of this painful condition. Dexketoprofen is an NSAID belonging to the arylpropionic acid group that has demonstrated good analgesic efficacy and a good safety profile in different acute and chronic painful conditions. Methods: A randomised, double-blind, parallel, active controlled, multicentre study that included 370 outpatients with acute low back pain was conducted to compare the analgesic efficacy of dexketoprofen 50mg twice daily versus diclofenac 75mg twice daily administered intramuscularly for 2 days. Efficacy outcomes were assessment of pain intensity (PI) measured on a visual analogue scale, total PI scores from baseline to 6 hours after the first-dose administration (primary efficacy endpoint; SAPID_(0-6)), score on a physical disability scale using the Roland Disability Questionnaire (RDQ), and use of rescue medication. Tolerability and safety were also assessed as secondary variables. Results: The adjusted mean (SAPID_(0-6)) scores were very similar, 117.3 mm/h with dexketoprofen and 114.7 mm/h with diclofenac. The adjusted ratio of means was 1.023 and the lower 95% confidence limit was 0.81, demonstrating non-inferiority of dexketoprofen (defined by a lower limit of the 95% CI >0.80) in comparison with diclofenac (per-protocol analysis). The median change in the RDQ was -6 points for both groups (p = 0.69), showing an overall improvement on the disability scale. No significant differences between groups were observed regarding the percentage of patients needing rescue medication or in the mean values of pain after repeated doses (SAPID_(0-last)). Dexketoprofen was well tolerated, with a reported incidence of adverse events similar to that of diclofenac. No serious adverse events were reported in either treatment group. Conclusion: From the results of this study it can be concluded that dexketoprofen 50mg administered twice daily intramuscularly provides a clinically relevant analgesic effect with good tolerability after single and repeated doses in patients with acute severe low back pain.
机译:背景:腰痛是西方工业化国家的重要医学问题。非甾体抗炎药是缓解这种疼痛症状的主要方法之一。右酮洛芬是属于芳基丙酸基团的NSAID,在不同的急性和慢性疼痛情况下均显示出良好的镇痛效果和安全性。方法:一项随机,双盲,平行,主动控制,多中心研究,包括370名急性下腰痛门诊患者,比较了每天2次肌肉注射地克洛芬50mg与每日两次两次双氯芬酸75mg的镇痛效果。疗效结果是通过视觉模拟量表评估疼痛强度(PI),首次给药后从基线到6小时的总PI评分(主要功效终点; SAPID_(0-6)),身体残疾评分使用罗兰残疾问卷(RDQ)并使用急救药物。耐受性和安全性也被评估为次要变量。结果:调整后的平均值(SAPID_(0-6))评分非常相似,右酮洛芬为117.3 mm / h,双氯芬酸为114.7 mm / h。调整后的均值比为1.023,较低的95%置信限为0.81,表明右酮洛芬与双氯芬酸相比(按方案分析)的非劣效性(由95%CI> 0.80的下限定义)。两组的RDQ中位数变化为-6点(p = 0.69),显示了残疾量表的总体改善。两组之间在需要急救药物的患者百分比或重复剂量后的疼痛平均值(SAPID_(0-last))方面没有观察到显着差异。右酮洛芬的耐受性良好,据报道与双氯芬酸相似的不良事件发生率。两个治疗组均未报告严重不良事件。结论:根据这项研究的结果,可以得出结论,每天两次肌注右旋布洛芬50mg在急性重度下腰痛患者中,单次和重复给药后,具有临床相关的镇痛作用,且耐受性良好。

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