Nüesch Eveline, Rutjes Anne Ws, Trelle Sven, Reichenbach Stephan, Jüni Peter
Division of Clinical Epidemiology and Biostatistics, Institute of Social and Preventive Medicine, University of Bern, Finkenhubelweg 11, Bern, Switzerland, 3012.
Cochrane Database Syst Rev. 2009 Oct 7(4):CD007323. doi: 10.1002/14651858.CD007323.pub2.
Osteoarthritis is a chronic joint disease that involves degeneration of articular cartilage. Pre-clinical data suggest that doxycycline might act as a disease-modifying agent for the treatment of osteoarthritis, with the potential to slow cartilage degeneration.
To examine the effects of doxycycline compared with placebo or no intervention on pain and function in patients with osteoarthritis of the hip or knee.
We searched CENTRAL ( The Cochrane Library 2008, issue 3), MEDLINE, EMBASE and CINAHL up to 28 July 2008, checked conference proceedings, reference lists, and contacted authors.
We included studies if they were randomised or quasi-randomised controlled trials that compared doxycycline at any dosage and any formulation with placebo or no intervention in patients with osteoarthritis of the knee or hip.
We extracted data in duplicate. We contacted investigators to obtain missing outcome information. We calculated differences in means at follow-up between experimental and control groups for continuous outcomes and risk ratios for binary outcomes.
We found one randomised controlled trial that compared doxycycline with placebo in 431 obese women. After 30 months of treatment, clinical outcomes were similar between the two treatment groups, with a mean difference of -0.20 cm (95% confidence interval (CI) -0.77 to 0.37 cm) on a visual analogue scale from 0 to 10 cm for pain and -1.10 units (95% CI -3.86 to 1.66) for function on the WOMAC disability subscale, which ranges from 17 to 85. These differences correspond to clinically irrelevant effect sizes of -0.08 and -0.09 standard deviation units for pain and function, respectively. The difference in changes in minimum joint space narrowing was in favour of doxycycline (-0.15 mm, 95% CI -0.28 to -0.02 mm), which corresponds to a small effect size of -0.23 standard deviation units. More patients withdrew from the doxycycline group compared with placebo due to adverse events (risk ratio 1.69, 95% CI 1.03 to 2.75).
AUTHORS' CONCLUSIONS: The symptomatic benefit of doxycycline is minimal to non-existent. The small benefit in terms of joint space narrowing is of questionable clinical relevance and outweighed by safety problems. Doxycycline should not be recommended for the treatment of osteoarthritis of the knee or hip.
骨关节炎是一种涉及关节软骨退变的慢性关节疾病。临床前数据表明,强力霉素可能作为一种改善病情的药物用于治疗骨关节炎,具有减缓软骨退变的潜力。
比较强力霉素与安慰剂或不干预措施对髋或膝骨关节炎患者疼痛和功能的影响。
我们检索了截至2008年7月28日的Cochrane系统评价数据库(CENTRAL,2008年第3期)、医学期刊数据库(MEDLINE)、荷兰医学文摘数据库(EMBASE)和护理学与健康领域数据库(CINAHL),检查了会议论文集、参考文献列表,并联系了作者。
纳入的研究需为随机或半随机对照试验,比较任何剂量和任何剂型的强力霉素与安慰剂或不干预措施对膝或髋骨关节炎患者的影响。
我们对数据进行了双人提取。我们联系了研究人员以获取缺失的结局信息。我们计算了试验组和对照组随访时连续结局的均值差异以及二分类结局的风险比。
我们发现一项随机对照试验,该试验在431名肥胖女性中比较了强力霉素与安慰剂。治疗30个月后,两个治疗组的临床结局相似,在0至10厘米的视觉模拟量表上,疼痛的平均差异为-0.20厘米(95%置信区间(CI)-0.77至0.37厘米),在WOMAC残疾分量表(范围为17至85)上,功能的平均差异为-1.10单位(95%CI -3.86至1.66)。这些差异分别对应于疼痛和功能的临床无关效应量,分别为-0.08和-0.09标准差单位。最小关节间隙狭窄变化的差异有利于强力霉素组(-0.15毫米,95%CI -0.28至-0.02毫米),这对应于一个小的效应量-0.23标准差单位。与安慰剂组相比,更多患者因不良事件退出强力霉素组(风险比1.69,95%CI 1.03至2.75)。
强力霉素的症状改善益处微乎其微或不存在。在关节间隙狭窄方面的微小益处临床相关性存疑,且被安全性问题所抵消。不建议使用强力霉素治疗膝或髋骨关节炎。