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首页> 外文期刊>Journal of Clinical Pharmacy and Therapeutics >No need for rescue medication (NNR) as an easily interpretable efficacy outcome measure in analgesic trials: Validation in an individual-patient meta-analysis of dental pain placebo-controlled trials of naproxen
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No need for rescue medication (NNR) as an easily interpretable efficacy outcome measure in analgesic trials: Validation in an individual-patient meta-analysis of dental pain placebo-controlled trials of naproxen

机译:在镇痛试验中无需使用急救药物(NNR)作为易于解释的疗效指标:在对萘普生进行的牙科疼痛安慰剂对照试验的逐项患者荟萃分析中进行验证

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What is known and Objective: In analgesic trials, pain relief is often assessed using a pain-relief score. We aimed to assess, through a meta-analysis, whether absence of need for rescue medication (NNR) is a reliable outcome measure in the evaluation of acute pain relief. Methods: Individual-patient meta-analysis of placebo-controlled trials of single-dose naproxen sodium 220 or 440 mg in dental pain. Efficacy estimates were based on NNR and compared with the more commonly used 50% maximum total pain relief score (50% TOTPAR). The trials included were the full set of trials sponsored by one manufacturer. Results and Discussion: Need for rescue medication and 50% TOTPAR gave comparable estimates of efficacy of naproxen sodium (220 and 440 mg) relative to placebo in dental pain at both 8 and 12 h after dosing. What is new and Conclusion: No need for rescue medication is a reliable outcome measure for use in acute pain trials. As it is more readily understandable than 50% TOTPAR, it should be the preferred primary outcome measure in acute pain trials.
机译:已知和目的:在止痛试验中,通常使用缓解评分来评估缓解疼痛。我们旨在通过荟萃分析评估是否需要急救药物(NNR)是评估急性疼痛缓解的可靠结果。方法:对单剂萘普生钠220或440 mg的牙科疼痛进行安慰剂对照试验的逐项患者荟萃分析。疗效评估基于NNR,并与更常用的50%最大总疼痛缓解评分(50%TOTPAR)进行比较。其中包括由一家制造商赞助的全套试验。结果与讨论:给药后8小时和12小时,对急救药物和50%TOTPAR的需要,萘普生钠(220和440 mg)相对于安慰剂在牙痛中的疗效具有可比的估计。新功能和结论:不需要急救药物是用于急性疼痛试验的可靠结果指标。因为它比50%TOTPAR更容易理解,所以它应该是急性疼痛试验中首选的主要结局指标。

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