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首页> 外文期刊>Rheumatology >A randomized placebo-controlled trial of arthroscopic lavage versus lavage plus intra-articular corticosteroids in the management of symptomatic osteoarthritis of the knee.
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A randomized placebo-controlled trial of arthroscopic lavage versus lavage plus intra-articular corticosteroids in the management of symptomatic osteoarthritis of the knee.

机译:关节镜下灌洗与灌洗加关节内注射皮质类固醇治疗膝关节有症状的骨关节炎的随机安慰剂对照试验。

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OBJECTIVE: To assess the efficacy of intra-articular steroid injections following arthroscopy and joint lavage in symptomatic OA of the knee. METHODS: Seventy-seven patients with OA of the knee were randomized to receive either 120 mg methylprednisolone acetate (MPA) or placebo following arthroscopy. Clinical assessments included severity of pain on movement and at rest, stiffness, the presence of joint effusions, range of movement, WOMAC (Western Ontario and McMaster Universities Osteoarthritis Index) score and Lequesne functional assessment. The outcome measures were evaluated at baseline and 2, 4, 8, 12 and 24 weeks. Further arthroscopies and synovial biopsies were performed at the time of clinical response and at relapse. RESULTS: An intention-to-treat analysis was performed on 71 patients (38 MPA, 33 placebo). Using the OARSI (Osteoarthritis Research Society International) response criteria, 58% of the steroid group vs 33% of the placebo group (adjusted relative risk = 2.38) (P = 0.004) responded at 4 weeks. At other time points, there were no significant differences between the treatment groups. There were no significant differences between the two treatment groups for pain, stiffness or WOMAC or Lequesne assessments at any time point. CONCLUSIONS: The response to intra-articular corticosteroids following joint lavage is short-lived (2-4 weeks), achievement of an OARSI response criterion being the only difference between the two groups.
机译:目的:评估关节镜检查和关节灌洗后关节内注射类固醇激素对膝部有症状OA的疗效。方法:77例膝关节炎患者被随机分配接受关节镜检查后接受120 mg醋酸甲泼尼龙(MPA)或安慰剂治疗。临床评估包括运动和休息时疼痛的严重程度,僵硬,关节积液的存在,运动范围,WOMAC(西安大略和麦克马斯特大学骨关节炎指数)评分和Lequesne功能评估。在基线,第2、4、8、12和24周评估结果指标。在临床反应时和复发时进行进一步的关节镜检查和滑膜活检。结果:对71例患者进行了意向治疗分析(38 MPA,33例安慰剂)。使用OARSI(国际骨关节炎研究协会)反应标准,在4周时,类固醇组的58%比安慰剂组的33%(调整后的相对风险= 2.38)(P = 0.004)。在其他时间点,治疗组之间没有显着差异。两组在任何时间点的疼痛,僵硬或WOMAC或Lequesne评估均无显着差异。结论:关节灌洗后对关节内糖皮质激素的反应是短暂的(2-4周),达到OARSI反应标准是两组之间的唯一区别。

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