Derry Sheena, Wiffen Philip J, Moore R Andrew
Pain Research and Nuffield Department of Clinical Neurosciences (Nuffield Division of Anaesthetics), University of Oxford, Pain Research Unit, Churchill Hospital, Oxford, Oxfordshire, UK, OX3 7LE.
Cochrane Database Syst Rev. 2015 Jul 14;2015(7):CD011509. doi: 10.1002/14651858.CD011509.pub2.
There is good evidence that combining two different analgesics in fixed doses in a single tablet can provide better pain relief in acute pain and headache than either drug alone, and that the drug-specific benefits are essentially additive. This appears to be broadly true in postoperative pain and migraine headache across a range of different drug combinations, and when tested in the same and different trials. Adding caffeine to analgesics also increases the number of people obtaining good pain relief. Combinations of ibuprofen and caffeine are available without prescription in some parts of the world.
To assess the analgesic efficacy and adverse effects of a single oral dose of ibuprofen plus caffeine for moderate to severe postoperative pain, using methods that permit comparison with other analgesics evaluated in standardised trials using almost identical methods and outcomes.
We searched the Cochrane Central Register of Controlled Trials (CENTRAL), MEDLINE, EMBASE, the Oxford Pain Relief Database, two clinical trial registries, and the reference lists of articles. The date of the most recent search was 1 February 2015.
Randomised, double-blind, placebo- or active-controlled clinical trials of single dose oral ibuprofen plus caffeine for acute postoperative pain in adults.
Two review authors independently considered trials for inclusion in the review, assessed risk of bias, and extracted data. We used the area under the pain relief versus time curve to derive the proportion of participants with at least 50% pain relief over six hours prescribed either ibuprofen plus caffeine or placebo. We calculated the risk ratio (RR) and number needed to treat to benefit (NNT). We used information on the use of rescue medication to calculate the proportion of participants requiring rescue medication and the weighted mean of the median time to use. We also collected information on adverse effects.
We identified five randomised, double-blind studies with 1501 participants, but only four had been published and had relevant outcome data. These four studies were of high quality, although two of the studies were small.Both ibuprofen 200 mg + caffeine 100 mg and ibuprofen 100 mg + caffeine 100 mg produced significantly more participants than placebo who achieved at least 50% of maximum pain relief over six hours, and both doses significantly reduced remedication rates (moderate quality evidence). For at least 50% of maximum pain relief, the NNT was 2.1 (95% confidence interval 1.8 to 2.5) for ibuprofen 200 mg + caffeine 100 mg (four studies, 334 participants) and 2.4 (1.9 to 3.1) for ibuprofen 100 mg + caffeine 100 mg (two studies, 200 participants) (moderate quality evidence). These values were close to those predicted by published models for combination analgesics in acute pain, and were supported by low (good) NNT values for prevention of remedication.Adverse event rates were low, and no sensible analysis was possible.
AUTHORS' CONCLUSIONS: For ibuprofen 200 mg + caffeine 100 mg particularly, the low NNT value is among the lowest (best) values for analgesics in this pain model. The combination is not commonly available, but can be probably be achieved by taking a single 200 mg ibuprofen tablet with a cup of modestly strong coffee or caffeine tablets. In principle, this can deliver good analgesia at lower doses of ibuprofen.
有充分证据表明,在一片药中固定剂量联合两种不同的镇痛药,相较于单独使用任何一种药物,能在急性疼痛和头痛中提供更好的疼痛缓解效果,且药物的特定益处基本是相加的。在术后疼痛和偏头痛中,在一系列不同的药物组合中,以及在相同和不同试验中进行测试时,情况似乎大致如此。在镇痛药中添加咖啡因也会增加获得良好疼痛缓解的人数。在世界某些地区,布洛芬和咖啡因的组合无需处方即可获得。
采用允许与使用几乎相同方法和结果的标准化试验中评估的其他镇痛药进行比较的方法,评估单剂量口服布洛芬加咖啡因对中度至重度术后疼痛的镇痛效果和不良反应。
我们检索了Cochrane对照试验中央注册库(CENTRAL)、MEDLINE、EMBASE、牛津疼痛缓解数据库、两个临床试验注册库以及文章的参考文献列表。最近一次检索日期为2015年2月1日。
关于单剂量口服布洛芬加咖啡因用于成人急性术后疼痛的随机、双盲、安慰剂对照或活性对照临床试验。
两位综述作者独立考虑纳入综述的试验,评估偏倚风险,并提取数据。我们使用疼痛缓解与时间曲线下的面积来得出在服用布洛芬加咖啡因或安慰剂的六个小时内至少有50%疼痛缓解的参与者比例。我们计算了风险比(RR)和治疗获益所需人数(NNT)。我们利用急救药物使用信息来计算需要急救药物的参与者比例以及使用时间中位数的加权平均值。我们还收集了不良反应信息。
我们确定了五项有1501名参与者的随机、双盲研究,但只有四项已发表且有相关结局数据。这四项研究质量较高,尽管其中两项研究规模较小。布洛芬200毫克+咖啡因100毫克和布洛芬100毫克+咖啡因100毫克在六个小时内实现至少50%最大疼痛缓解的参与者均显著多于安慰剂,且两种剂量均显著降低了补救用药率(中等质量证据)。对于至少50%的最大疼痛缓解,布洛芬200毫克+咖啡因100毫克(四项研究,334名参与者)的NNT为2.1(95%置信区间1.8至2.5),布洛芬100毫克+咖啡因100毫克(两项研究,200名参与者)的NNT为2.4(1.9至3.1)(中等质量证据)。这些数值接近已发表的急性疼痛联合镇痛药模型所预测的值,并得到预防补救用药的低(良好)NNT值的支持。不良事件发生率较低,无法进行合理分析。
特别是对于布洛芬200毫克+咖啡因100毫克,低NNT值是该疼痛模型中镇痛药的最低(最佳)值之一。这种组合并不常见,但可能通过服用一片200毫克布洛芬片加一杯浓度适中的咖啡或咖啡因片来实现。原则上,这可以在较低剂量的布洛芬下提供良好的镇痛效果。