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单剂量羟考酮及羟考酮联合对乙酰氨基酚用于术后急性疼痛

Single dose oxycodone and oxycodone plus paracetamol (acetominophen) for acute postoperative pain.

作者信息

Edwards J E, Moore R A, McQuay H J

机构信息

Pain Research Unit, Nuffield Department of Anaesthetics, Churchill Hospital, Old Road, Oxford, UK, OX3 7LJ.

出版信息

Cochrane Database Syst Rev. 2000(4):CD002763. doi: 10.1002/14651858.CD002763.

Abstract

BACKGROUND

Oxycodone is a strong opioid agonist which is useful for the management of severe pain. It is becoming increasingly important to assess the relative efficacy and harm caused by different treatments. This can be determined when an analgesic is compared with control under similar clinical circumstances.

OBJECTIVES

To quantitatively assess the analgesic efficacy and adverse effects of single-dose oxycodone and oxycodone plus paracetamol in randomised trials in acute postoperative pain.

SEARCH STRATEGY

Published reports were identified from Medline, Biological Abstracts, Embase, the Cochrane Library and the Oxford Pain Relief Database. Additional studies were identified from the reference lists of retrieved reports.

SELECTION CRITERIA

The inclusion criteria were: full journal publication, clinical trial, random allocation of adult patients to treatment groups, double blind design, moderate to severe baseline pain, postoperative administration of study drugs, treatment arms which included oxycodone or oxycodone plus paracetamol and placebo (or active control for which comparable efficacy data exist), and oral, intramuscular or intravenous administration of study drugs.

DATA COLLECTION AND ANALYSIS

Summed pain intensity and pain relief data over 4-6 hours were extracted and converted into dichotomous information yielding the number of patients obtaining at least 50% pain relief. Estimates of relative benefit and number-needed-to-treat were calculated. Single-dose adverse effect data were collected.

MAIN RESULTS

Seventy-seven reports were identified. Seven reports met the inclusion criteria; all assessed oral oxycodone. For efficacy, a significant benefit of active drug over placebo was shown for all doses of oxycodone and oxycodone plus paracetamol, except oxycodone 5 mg. For adverse effects, the number of patients reporting adverse effects was extracted for each dose of active drug versus placebo. When these data were pooled for the individual doses significantly more adverse effects with active drug than with placebo were shown for all doses, except oxycodone 5 mg and its combination with paracetamol 325 mg. This was also shown for drowsiness/somnolence. Significantly more nausea, vomiting and dizziness/lightheadedness were reported with oxycodone 10 mg plus paracetamol (650 mg and 1000 mg) than with placebo.

REVIEWER'S CONCLUSIONS: Single-dose oral oxycodone, with or without paracetamol, appears to be of comparable efficacy to intramuscular morphine and non-steroidal anti-inflammatory drugs. Central nervous system adverse effects were common.

摘要

背景

羟考酮是一种强效阿片类激动剂,对重度疼痛的治疗很有用。评估不同治疗方法的相对疗效和危害变得越来越重要。当在相似临床情况下将一种镇痛药与对照进行比较时,这一点可以确定。

目的

在急性术后疼痛的随机试验中,定量评估单剂量羟考酮以及羟考酮加对乙酰氨基酚的镇痛效果和不良反应。

检索策略

从医学文献数据库、生物学文摘数据库、荷兰医学文摘数据库、考克兰图书馆和牛津疼痛缓解数据库中识别已发表的报告。从检索到的报告的参考文献列表中识别其他研究。

选择标准

纳入标准为:完整的期刊发表、临床试验、将成年患者随机分配至治疗组、双盲设计、中度至重度基线疼痛、术后给予研究药物、治疗组包括羟考酮或羟考酮加对乙酰氨基酚以及安慰剂(或存在可比疗效数据的活性对照),以及口服、肌肉注射或静脉注射研究药物。

数据收集与分析

提取4至6小时内的疼痛强度总和及疼痛缓解数据,并转化为二分类信息,得出至少获得50%疼痛缓解的患者数量。计算相对获益估计值和需治疗人数。收集单剂量不良反应数据。

主要结果

识别出77份报告。7份报告符合纳入标准;均评估了口服羟考酮。对于疗效,除5毫克羟考酮外,所有剂量的羟考酮以及羟考酮加对乙酰氨基酚与安慰剂相比,活性药物均显示出显著获益。对于不良反应,提取了各剂量活性药物与安慰剂相比报告不良反应的患者数量。当将这些数据按个体剂量汇总时,除5毫克羟考酮及其与325毫克对乙酰氨基酚的组合外,所有剂量的活性药物与安慰剂相比均显示出更多的不良反应。嗜睡/昏睡情况也是如此。与安慰剂相比,10毫克羟考酮加对乙酰氨基酚(650毫克和1000毫克)报告的恶心、呕吐和头晕/眩晕明显更多。

综述作者结论

单剂量口服羟考酮,无论是否加用对乙酰氨基酚,其疗效似乎与肌肉注射吗啡和非甾体抗炎药相当。中枢神经系统不良反应很常见。

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