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单剂量安乃近用于术后急性疼痛。

Single dose dipyrone for acute postoperative pain.

作者信息

Edwards Jayne, Meseguer Fuensanta, Faura Clara, Moore R Andrew, McQuay Henry J, Derry Sheena

机构信息

Training Team, UK Cochrane Centre, National Institute for Health Research, Summertown Pavilion, Middle Way, Oxford, UK, OX2 7LG.

出版信息

Cochrane Database Syst Rev. 2010 Sep 8(9):CD003227. doi: 10.1002/14651858.CD003227.pub2.

DOI:10.1002/14651858.CD003227.pub2
PMID:20824835
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4160844/
Abstract

BACKGROUND

Dipyrone (metamizole) is a non-steroidal anti-inflammatory drug used in some countries to treat pain (postoperative, colic, cancer, and migraine); it is banned in others because of an association with life-threatening blood agranulocytosis. This review updates a 2001 Cochrane review, and no relevant new studies were identified, but additional outcomes were sought.

OBJECTIVES

To assess the efficacy and adverse events of single dose dipyrone in acute postoperative pain.

SEARCH STRATEGY

The earlier review searched CENTRAL, MEDLINE, EMBASE, LILACS and the Oxford Pain Relief Database to December 1999. For the update we searched CENTRAL, MEDLINE,EMBASE and LILACS to February 2010.

SELECTION CRITERIA

Single dose, randomised, double-blind, placebo or active controlled trials of dipyrone for relief of established moderate to severe postoperative pain in adults. We included oral, rectal, intramuscular or intravenous administration of study drugs.

DATA COLLECTION AND ANALYSIS

Studies were assessed for methodological quality and data extracted by two review authors independently. Summed total pain relief over six hours (TOTPAR) was used to calculate the number of participants achieving at least 50% pain relief. Derived results were used to calculate, with 95% confidence intervals, relative benefit compared to placebo, and the number needed to treat (NNT) for one participant to experience at least 50% pain relief over six hours. Use and time to use of rescue medication were additional measures of efficacy. Information on adverse events and withdrawals was collected.

MAIN RESULTS

Fifteen studies tested mainly 500 mg oral dipyrone (173 participants), 2.5 g intravenous dipyrone (101), 2.5 g intramuscular dipyrone (99); fewer than 60 participants received any other dose. All studies used active controls (ibuprofen, paracetamol, aspirin, flurbiprofen, ketoprofen, dexketoprofen, ketorolac, pethidine, tramadol, suprofen); eight used placebo controls.Over 70% of participants experienced at least 50% pain relief over 4 to 6 hours with oral dipyrone 500 mg compared to 30% with placebo in five studies (288 participants; NNT 2.4 (1.9 to 3.2)). Fewer participants needed rescue medication with dipyrone (7%) than with placebo (34%; four studies, 248 participants). There was no difference in participants experiencing at least 50% pain relief with 2.5 g intravenous dipyrone and 100 mg intravenous tramadol (70% vs 65%; two studies, 200 participants). No serious adverse events were reported.

AUTHORS' CONCLUSIONS: Based on very limited information, single dose dipyrone 500 mg provides good pain relief to 70% of patients. For every five individuals given dipyrone 500 mg, two would experience this level of pain relief who would not have done with placebo, and fewer would need rescue medication, over 4 to 6 hours.

摘要

背景

安乃近是一种非甾体类抗炎药,在一些国家用于治疗疼痛(术后疼痛、绞痛、癌症疼痛和偏头痛);但在其他一些国家,因其与危及生命的粒细胞缺乏症有关联而被禁用。本综述更新了2001年的Cochrane综述,未发现相关新研究,但寻求了更多的结局指标。

目的

评估单剂量安乃近治疗急性术后疼痛的疗效和不良事件。

检索策略

早期综述检索了截至1999年12月的Cochrane中心对照试验注册库(CENTRAL)、医学期刊数据库(MEDLINE)、荷兰医学文摘数据库(EMBASE)、拉丁美洲和加勒比地区卫生科学数据库(LILACS)以及牛津疼痛缓解数据库。本次更新检索了截至2010年2月的CENTRAL、MEDLINE、EMBASE和LILACS。

入选标准

关于单剂量安乃近用于缓解成人已确诊的中度至重度术后疼痛的随机、双盲、安慰剂对照或活性药物对照试验。研究药物的给药途径包括口服、直肠、肌肉注射或静脉注射。

数据收集与分析

由两位综述作者独立评估研究的方法学质量并提取数据。使用6小时内总的疼痛缓解量(TOTPAR)来计算至少有50%疼痛缓解的参与者数量。得出的结果用于计算与安慰剂相比的相对获益及95%置信区间,以及一名参与者在6小时内至少有50%疼痛缓解所需的治疗人数(NNT)。使用解救药物的情况及使用时间是疗效的额外衡量指标。收集了不良事件和退出研究的信息。

主要结果

15项研究主要测试了口服500mg安乃近(173名参与者)、静脉注射2.5g安乃近(101名)、肌肉注射2.5g安乃近(99名);接受其他任何剂量的参与者少于60名。所有研究均使用活性对照(布洛芬、对乙酰氨基酚、阿司匹林、氟比洛芬、酮洛芬、右酮洛芬、酮咯酸、哌替啶、曲马多、舒洛芬);8项研究使用了安慰剂对照。在5项研究(288名参与者)中,与安慰剂组30%的参与者相比,口服500mg安乃近组超过70%的参与者在4至6小时内经历了至少50%的疼痛缓解(NNT为2.4(1.9至3.2))。与安慰剂组(34%;4项研究,248名参与者)相比,使用安乃近的参与者需要解救药物的更少(7%)。静脉注射2.5g安乃近与静脉注射100mg曲马多相比,经历至少50%疼痛缓解的参与者比例无差异(70%对65%;2项研究,200名参与者)。未报告严重不良事件。

作者结论

基于非常有限的信息,单剂量500mg安乃近能使70%的患者获得良好的疼痛缓解。在4至6小时内,每给5名服用500mg安乃近的患者中,就有两名患者会获得这种程度的疼痛缓解,而服用安慰剂则不会有此效果,且需要解救药物的患者更少。

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