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首页> 外文期刊>Pain. >Pain therapy with high risk: One-sided presentation of the results from the latest phase III study on tanezumab in osteoarthritis pain.
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Pain therapy with high risk: One-sided presentation of the results from the latest phase III study on tanezumab in osteoarthritis pain.

机译:疼痛治疗风险高:坦尼斯单抗治疗骨关节炎疼痛的最新III期研究结果的单方面介绍。

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The International Headache Society (IHS) provides guidance on the conduct of trials for acute treatment of episodic tension-type headache (TTH), a common disorder with considerable disability. Electronic and other searches identified randomised, double-blind trials of oral drugs treating episodic TTH with moderate or severe pain at baseline, or that tested drugs at first pain onset. The aims were to review methods, quality, and outcomes reported (in particular the IHS-recommended primary efficacy parameter pain-free after 2hours), and to assess efficacy by meta-analysis. We identified 58 reports: 55 from previous reviews and searches, 2 unpublished reports, and 1 clinical trial report with results. We included 40 reports of 55 randomised trials involving 12,143 patients. Reporting quality was generally good, with potential risk of bias from incomplete outcome reporting and small size; the 23 largest trials involved 82% of patients. Few trials reported IHS outcomes. The number needed to treat values for being pain-free at 2hours compared with placebo were 8.7 (95% confidence interval [CI] 6.2 to 15) for paracetamol 1000mg, 8.9 (95% CI 5.9 to 18) for ibuprofen 400mg, and 9.8 (95% CI 5.1 to 146) for ketoprofen 25mg. Lower (better) number needed to treat values were calculated for outcomes of mild or no pain at 2hours, and patient global assessment. These were similar to values for these drugs in migraine. No other drugs had evaluable results for these patient-centred outcomes. There was no evidence that any one outcome was better than others. The evidence available for treatment efficacy is small in comparison to the size of the clinical problem.
机译:国际头痛协会(IHS)为急性发作性紧张型头痛(TTH)的急性治疗试验提供指导。电子搜索和其他搜索确定了治疗基线时中度或重度疼痛或发作初期就测试药物的发作性TTH口服药物的随机,双盲试验。目的是审查报告的方法,质量和结果(特别是IHS推荐的2小时后无痛的主要疗效参数),并通过荟萃分析评估疗效。我们确定了58份报告:其中55份来自以前的评论和搜索,2份未发表的报告以及1份具有结果的临床试验报告。我们纳入了55项随机试验的40份报告,涉及12,143例患者。报告质量总体良好,由于结果报告不完整和规模小,存在潜在的偏差风险; 23个最大的试验涉及82%的患者。很少有试验报告IHS结果。与安慰剂相比,在2小时内无痛治疗所需的数值为:对乙酰氨基酚1000mg为8.7(95%置信区间[CI] 6.2至15),布洛芬400mg为8.9(95%CI 5.9至18)和9.8(酮洛芬25mg的95%CI 5.1至146)。计算2小时轻度疼痛或无疼痛的结局所需的较低(更好)数值,并进行患者总体评估。这些与偏头痛中这些药物的值相似。对于以患者为中心的结果,没有其他药物具有可评估的结果。没有证据表明任何一项结果都优于其他结果。与临床问题的规模相比,可用于治疗功效的证据很小。

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