Tirunagari Shravan Kumar, Derry Sheena, Moore R Andrew, McQuay Henry J
Anaesthesia and Critical Care, Oxford Deanery, 10, Norhaw Close, Hemel Hempstead, UK, HP2 7NH.
Cochrane Database Syst Rev. 2009 Jul 8;2009(3):CD007357. doi: 10.1002/14651858.CD007357.pub2.
Etodolac is a selective cyclo-oxygenase-2 (COX-2) inhibitor, with evidence of efficacy in osteoarthritis and rheumatoid arthritis. Its analgesic efficacy in postoperative pain has not been clearly established. There are no systematic reviews on Etodolac's use in this condition.
To assess the analgesic efficacy of etodolac in single oral doses for moderate and severe postoperative pain.
We searched Cochrane CENTRAL, MEDLINE, EMBASE and the Oxford Pain Relief Database for studies to May 2009.
Randomised, double blind, placebo-controlled trials of single dose orally administered etodolac (any formulation) in adults with moderate to severe acute postoperative pain.
Two review authors independently assessed trial quality and extracted data. Pain relief or pain intensity data were extracted and converted into the dichotomous outcome of number of participants with at least 50% pain relief over 4 to 6 hours, from which relative risk (RR) and number needed to treat to benefit (NNT) were calculated. Numbers of participants using rescue medication over specified time periods, and time to use of rescue medication, were sought as additional measures of efficacy. Information on adverse events and withdrawals were collected.
Nine studies (1459 participants) compared etodolac and placebo. Studies were of adequate reporting quality, and the majority of participants had pain following dental extractions. The dose of etodolac used was 25 mg to 1200 mg, with most of the information for 100 mg and 200 mg. For at least 50% pain relief over 4 to 6 hours compared with placebo the NNT for etodolac 100 mg (498 participants) was 4.8 (3.5 to 7.8) and for etodolac 200 mg (670 participants) it was 3.3 (2.7 to 4.2). Very limited information with the extended release formulation did not suggest improved benefit for this outcome.The proportion of participants with at least 50% pain relief was 41% with 100 mg and 44% with 200 mg. Remedication was needed by about 60% with etodolac 200 mg or 400 mg over 6 to 8 hours, compared with almost 80% with placebo.Adverse events were uncommon, and not significantly different form placebo.
AUTHORS' CONCLUSIONS: Etodolac 200 mg may be a useful analgesic in postoperative pain, with efficacy similar to paracetamol 1000 mg and celecoxib 200 mg. Higher doses may provide analgesia equivalent to more commonly used drugs, such as ibuprofen 400 mg, naproxen 500 mg and diclofenac 50 mg.
依托度酸是一种选择性环氧化酶-2(COX-2)抑制剂,在骨关节炎和类风湿关节炎中具有疗效证据。其在术后疼痛中的镇痛效果尚未明确确立。目前尚无关于依托度酸在这种情况下使用的系统评价。
评估单次口服依托度酸对中度和重度术后疼痛的镇痛效果。
我们检索了Cochrane中心对照试验注册库、医学期刊数据库、荷兰医学文摘数据库以及牛津疼痛缓解数据库,检索截至2009年5月的研究。
针对患有中度至重度急性术后疼痛的成年人,进行单次口服依托度酸(任何剂型)的随机、双盲、安慰剂对照试验。
两位综述作者独立评估试验质量并提取数据。提取疼痛缓解或疼痛强度数据,并将其转换为在4至6小时内疼痛缓解至少50%的参与者数量这一二分结果,据此计算相对危险度(RR)和需治疗获益人数(NNT)。收集在特定时间段内使用解救药物的参与者数量以及使用解救药物的时间,作为疗效的额外衡量指标。收集不良事件和退出试验的信息。
九项研究(1459名参与者)比较了依托度酸和安慰剂。研究报告质量良好,大多数参与者为拔牙后疼痛。依托度酸的使用剂量为25毫克至1200毫克,其中大部分信息涉及100毫克和200毫克。与安慰剂相比,依托度酸100毫克(498名参与者)在4至6小时内实现至少50%疼痛缓解的NNT为4.8(3.5至7.8),依托度酸200毫克(670名参与者)的NNT为3.3(2.7至4.2)。关于缓释制剂的信息非常有限,并未表明该剂型在此结果上有更好的获益。100毫克依托度酸组和200毫克依托度酸组中疼痛缓解至少50%的参与者比例分别为41%和44%。在6至8小时内,依托度酸200毫克或400毫克组约60%的参与者需要再次用药,而安慰剂组这一比例近80%。不良事件不常见,与安慰剂组无显著差异。
依托度酸200毫克可能是一种有效的术后镇痛药,疗效与对乙酰氨基酚1000毫克和塞来昔布200毫克相似。更高剂量可能提供与更常用药物(如布洛芬400毫克、萘普生500毫克和双氯芬酸50毫克)相当的镇痛效果。