McQuay Henry J, Moore R Andrew
Pain Research and Nuffield Department of Anaesthetics, (University of Oxford), Churchill Hospital, Oxford, UK.
Br J Clin Pharmacol. 2007 Mar;63(3):271-8. doi: 10.1111/j.1365-2125.2006.02723.x. Epub 2006 Jul 21.
Establishing the dose-response relationship for clinically useful doses of aspirin, ibuprofen and paracetamol has been difficult. Indirect comparison from meta-analysis is compromised by too little information at some doses.
A systematic review of randomized, double-blind trials in acute pain comparing different doses of aspirin, ibuprofen and paracetamol was therefore undertaken.
Fifty trials were found. Numerical superiority of higher over lower dose was found by the original authors in 37/50 trials (74%) and statistical superiority in 11/50 (22%). Twenty-eight trials had design, quality and data reporting characteristics to allow pooling of common doses; in 3/28 (11%) of the individual trials our calculations showed statistical superiority of higher over lower dose. Pooled comparison of 1000/1200 mg aspirin over 500/600 mg was statistically superior, with a number-needed-to-treat (NNT) for higher over lower dose of 16 (8 to > 100). Pooled comparison of 400 mg ibuprofen over 200 mg was statistically superior, with an NNT for higher over lower dose of 10 (6-23). Pooled comparison of 1000 mg paracetamol over 500 mg was statistically superior, with an NNT for higher over lower dose of 9 (6-20).
Use of trials making direct comparison of two different doses of target drugs revealed the underlying dose-response curve for clinical analgesia.
确定阿司匹林、布洛芬和对乙酰氨基酚临床有效剂量的剂量-反应关系一直很困难。荟萃分析的间接比较因某些剂量的信息过少而受到影响。
因此,对比较不同剂量阿司匹林、布洛芬和对乙酰氨基酚治疗急性疼痛的随机双盲试验进行了系统评价。
共找到50项试验。原作者在37/50项试验(74%)中发现高剂量在数值上优于低剂量,在11/50项试验(22%)中发现高剂量在统计学上优于低剂量。28项试验具有设计、质量和数据报告特征,允许汇总常用剂量;在3/28项(11%)个体试验中,我们的计算显示高剂量在统计学上优于低剂量。1000/1200mg阿司匹林与500/600mg阿司匹林的汇总比较在统计学上具有优势,高剂量优于低剂量的需治疗人数(NNT)为16(8至>100)。400mg布洛芬与200mg布洛芬的汇总比较在统计学上具有优势,高剂量优于低剂量的NNT为10(6-23)。1000mg对乙酰氨基酚与500mg对乙酰氨基酚的汇总比较在统计学上具有优势,高剂量优于低剂量的NNT为9(6-20)。
使用对两种不同剂量目标药物进行直接比较的试验揭示了临床镇痛的潜在剂量-反应曲线。