Schmidt-Hansen Mia, Bennett Michael I, Arnold Stephanie, Bromham Nathan, Hilgart Jennifer S
National Guideline Alliance, Royal College of Obstetricians and Gynaecologists, London, UK.
Leeds Institute of Health Sciences, University of Leeds, Leeds, UK.
BMJ Support Palliat Care. 2018 Jun;8(2):117-128. doi: 10.1136/bmjspcare-2017-001457. Epub 2018 Jan 13.
To assess the efficacy, tolerability and acceptability of oxycodone for cancer pain in adults METHODS: We searched CENTRAL, MEDLINE, MEDLINE In-Process, Embase, SCI, Conference Proceedings Citation Index-Science, BIOSIS, PsycINFO and four trials registries to November 2016.
We included 23 randomised controlled trials with 2144 patients analysed for efficacy and 2363 for safety. Meta-analyses showed no significant differences between controlled-release (CR) and immediate-release oxycodone in pain intensity or adverse events but did show significantly better pain relief after treatment with CR morphine compared with CR oxycodone. However, sensitivity analysis did not corroborate this result. Meta-analyses of the adverse events showed a significantly lower risk of hallucinations after treatment with CR oxycodone compared with CR morphine, but no other differences. The remaining studies either compared oxycodone in various formulations or compared oxycodone to different alternative opioids. None found any clear superiority or inferiority of oxycodone in pain relief or adverse events. The quality of this evidence base was limited by the high/unclear risk of bias of the studies and the low event rates for many outcomes.
Oxycodone offers similar levels of pain relief and adverse events to other strong opioids. However, hallucinations occurred less with CR oxycodone than with CR morphine, but the quality of this evidence was very low, so this finding should be treated with utmost caution. Our conclusions are consistent with other reviews and suggest that oxycodone can be used first line as an alternative to morphine. However, because it is cheaper, morphine generally remains the first-line opioid of choice.
评估羟考酮用于成人癌痛的疗效、耐受性及可接受性。方法:检索截至2016年11月的Cochrane系统评价数据库、医学期刊数据库、医学期刊数据库(在研)、荷兰医学文摘数据库、科学引文索引、会议论文引文索引-科学版、生物学文摘数据库、心理学文摘数据库以及四个试验注册库。
我们纳入了23项随机对照试验,其中2144例患者接受疗效分析,2363例患者接受安全性分析。荟萃分析显示,控释羟考酮与即释羟考酮在疼痛强度或不良事件方面无显著差异,但与控释吗啡相比,控释羟考酮治疗后疼痛缓解明显更佳。然而,敏感性分析并未证实这一结果。不良事件的荟萃分析显示,与控释吗啡相比,控释羟考酮治疗后幻觉风险显著更低,但无其他差异。其余研究要么比较了不同剂型的羟考酮,要么将羟考酮与不同的替代阿片类药物进行了比较。没有研究发现羟考酮在疼痛缓解或不良事件方面有任何明显的优势或劣势。这一证据基础的质量受到研究中高/不明确的偏倚风险以及许多结局的低事件发生率的限制。
羟考酮与其他强效阿片类药物在疼痛缓解和不良事件方面水平相似。然而,控释羟考酮导致的幻觉比控释吗啡少,但这一证据的质量非常低,因此这一发现应极其谨慎地对待。我们的结论与其他综述一致,表明羟考酮可作为吗啡的替代药物一线使用。然而,由于吗啡价格更低,它通常仍是首选的一线阿片类药物。