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术后疼痛单剂量口服对乙酰氨基酚(扑热息痛)。

Single dose oral paracetamol (acetaminophen) for postoperative pain.

作者信息

Barden J, Edwards J, Moore A, McQuay H

机构信息

Pain Research Unit, University of Oxford, Churchill Hospital, Old Road, Oxford, UK, OX3 7LJ.

出版信息

Cochrane Database Syst Rev. 2004(1):CD004602. doi: 10.1002/14651858.CD004602.

Abstract

BACKGROUND

Paracetamol (acetaminophen) and non-steroidal anti-inflammatory drugs (NSAIDs) are widely used for the relief of mild and moderate pain arising from headache, musculoskeletal conditions and dysmenorrhoea. A prior Cochrane systematic review concluded that paracetamol is also effective for postoperative pain, but additional trials have since been published. This review sought to evaluate the efficacy and safety of paracetamol using current data, and to compare the findings with other analgesics evaluated in the same way.

OBJECTIVES

To assess the efficacy of single dose oral paracetamol for the treatment of acute postoperative pain.

SEARCH STRATEGY

We searched the Cochrane Library (Issue 3, 2002), the trials register of the Cochrane Pain, Palliative and Supportive Care group (November 2002); MEDLINE (1966 to May 1996); PubMed (1996 to August 2001); EMBASE (1980 to 1996); the Oxford Pain Relief Database (1950 to 1994); and reference lists of articles in order to update an existing version of the review.

SELECTION CRITERIA

Randomised, double-blind, placebo-controlled clinical trials of paracetamol for acute postoperative pain in adults.

DATA COLLECTION AND ANALYSIS

Two reviewers independently assessed trial quality and extracted data. The area under the 'pain relief versus time' curve was used to derive the proportion of patients with paracetamol or placebo experiencing least 50% pain relief over four to six hours using validated equations. The number-needed-to-treat (NNT) was calculated using 95% confidence intervals. Information on adverse effects was also collected.

MAIN RESULTS

Forty-seven reports that enrolled 4186 patients (2561 patients were treated with a single oral dose of paracetamol and 1625 with placebo) met the inclusion criteria and were included in the analyses. The NNTs for at least 50% pain relief over four to six hours following a single dose of paracetamol were as follows: 325 mg NNT 3.8 (2.2 to 13.3); 500 mg NNT 3.5 (2.7 to 4.8); 600/650 mg NNT 4.6 (3.9 to 5.5); 975/1000 mg NNT 3.8 (3.4 to 4.4); and 1500 mg NNT 3.7 (2.3 to 9.5). Sub-group analysis showed no significant differences between smaller and larger trials, or lower and higher quality trials. Drug-related study withdrawals were rarely reported. Studies reported a variable incidence of adverse effects that were generally mild and transient. There were no statistically significant differences in the frequency of reported adverse effects between paracetamol 975/1000 mg and placebo.

REVIEWER'S CONCLUSIONS: Single doses of paracetamol are effective analgesics for acute postoperative pain and give rise to few adverse effects.

摘要

背景

对乙酰氨基酚(扑热息痛)和非甾体抗炎药(NSAIDs)被广泛用于缓解由头痛、肌肉骨骼疾病和痛经引起的轻中度疼痛。先前一项Cochrane系统评价得出结论,对乙酰氨基酚对术后疼痛也有效,但此后又发表了其他试验。本评价旨在使用当前数据评估对乙酰氨基酚的疗效和安全性,并将结果与以同样方式评估的其他镇痛药进行比较。

目的

评估单剂量口服对乙酰氨基酚治疗急性术后疼痛的疗效。

检索策略

我们检索了Cochrane图书馆(2002年第3期)、Cochrane疼痛、姑息和支持治疗组的试验注册库(2002年11月);MEDLINE(1966年至1996年5月);PubMed(1996年至2001年8月);EMBASE(1980年至1996年);牛津疼痛缓解数据库(1950年至1994年);以及文章的参考文献列表,以便更新该评价的现有版本。

选择标准

对乙酰氨基酚用于成人急性术后疼痛的随机、双盲、安慰剂对照临床试验。

数据收集与分析

两名评价员独立评估试验质量并提取数据。使用经过验证的公式,通过“疼痛缓解与时间”曲线下的面积来计算服用对乙酰氨基酚或安慰剂的患者在4至6小时内疼痛缓解至少50%的比例。使用95%置信区间计算需治疗人数(NNT)。还收集了不良反应的信息。

主要结果

47篇报告纳入了4186例患者(2561例患者接受单剂量口服对乙酰氨基酚治疗,1625例接受安慰剂治疗),符合纳入标准并纳入分析。单剂量对乙酰氨基酚后4至6小时内疼痛缓解至少50%的NNT如下:325mg,NNT为3.8(2.2至13.3);500mg,NNT为3.5(2.7至4.8);600/650mg,NNT为4.6(3.9至5.5);975/1000mg,NNT为3.8(3.4至4.4);1500mg,NNT为3.7(2.3至9.5)。亚组分析显示,大小试验之间或低质量与高质量试验之间无显著差异。很少有与药物相关的研究撤稿报告。研究报告的不良反应发生率各不相同,一般为轻度且短暂。975/1000mg对乙酰氨基酚组和安慰剂组报告的不良反应频率无统计学显著差异。

评价员结论

单剂量对乙酰氨基酚是治疗急性术后疼痛的有效镇痛药,且不良反应较少。

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