首页> 外文期刊>Scandinavian journal of rheumatology >Etoricoxib reduced pain and disability and improved quality of life in patients with chronic low back pain: a 3 month, randomized, controlled trial.
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Etoricoxib reduced pain and disability and improved quality of life in patients with chronic low back pain: a 3 month, randomized, controlled trial.

机译:依托昔布减少了慢性下腰痛患者的疼痛和残疾,并改善了生活质量:一项为期3个月的随机对照试验。

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Background: Chronic low back pain (LBP) is a growing health problem. Non-steroidal anti-inflammatory drugs (NSAIDs) are used to treat this condition, but have not demonstrated efficacy beyond 2 weeks, and no studies have shown that NSAIDs produce durable improvements in disability. Methods: To evaluate the efficacy and durability of effect of etoricoxib for chronic LBP, a randomized, double blind, placebo-controlled trial was conducted at 46 centres. Three hundred and twenty-five patients with chronic LBP requiring treatment with an NSAID or paracetamol were randomized 1:1:1 to etoricoxib 60 mg (n=109), 90 mg (n=106), or placebo (n=110), daily for 3 months. Pre-specified endpoints over 3 months included LBP intensity scale (visual analog scale 0-100 mm) time-weighted average change from baseline, the Roland-Morris Disability Questionnaire (RMDQ), the LBP bothersomeness scale, patient and investigator global assessments, and measures of quality of life. Results: Both etoricoxib groups experienced significant reductions in LBP intensity at 4 weeks versus placebo [-15.15 mm and -13.03 mm for 60 and 90 mg, respectively, probability (p)<0.001 for each], which was maintained over 3 months. Treatment resulted in significant improvement from baseline compared to placebo in RMDQ scores (etoricoxib 60 mg, -2.82 and 90 mg, -2.38, p<0.001 for each) over 12 weeks and most other efficacy endpoints. There were no significant differences between treatments in incidence of adverse events (AEs) or discontinuations due to AEs. Conclusion: Etoricoxib provided significant relief of symptoms and disability associated with chronic LBP detected at 1 week, confirmed at 4 weeks, and maintained over 3 months. Reductions in chronic LBP severity corresponded to improvements in physical functioning and quality of life. All treatments were generally well tolerated.
机译:背景:慢性下腰痛(LBP)是一个日益严重的健康问题。非甾体类抗炎药(NSAIDs)用于治疗该疾病,但超过2周未显示出疗效,也没有研究表明NSAIDs能够持久改善残疾。方法:为了评估依托昔布治疗慢性LBP的疗效和持久性,在46个中心进行了一项随机,双盲,安慰剂对照试验。将需要用NSAID或扑热息痛治疗的325名患有慢性LBP的患者按1:1的比例随机分配至60 mg(n = 109),90 mg(n = 106)或安慰剂(n = 110)的依托考昔,每天3个月。在3个月内预先指定的终点包括LBP强度量表(视觉模拟量表0-100 mm)与基线相比的时间加权平均变化,Roland-Morris残疾问卷(RMDQ),LBP烦恼量表,患者和研究者总体评估,以及生活质量的衡量标准。结果:两组依托昔布组在4周时LBP强度均显着降低,而安慰剂组分别为60 mg和90 mg [-15.15 mm和-13.03 mm,每组概率(p)<0.001),并维持3个月以上。与安慰剂相比,在12周内以及大多数其他功效终点中,与安慰剂相比,治疗的RMDQ评分(依托昔布60 mg,-2.82和90 mg,-2.38,p <0.001)显着改善。不良事件(AE)发生率或因AE停药的治疗之间无显着差异。结论:依托考昔可显着缓解与慢性LBP相关的症状和残疾,这些症状在1周时被发现,在4周时得到确认,并维持了3个月以上。慢性LBP严重程度的降低与身体机能和生活质量的提高相对应。所有治疗通常耐受良好。

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