Gomes Tara, Mamdani Muhammad M, Dhalla Irfan A, Paterson J Michael, Juurlink David N
Institute for Clinical Evaluative Sciences, G Wing 106, 2075 Bayview Ave, Toronto, ON M4N 3M5, Canada.
Arch Intern Med. 2011 Apr 11;171(7):686-91. doi: 10.1001/archinternmed.2011.117.
Opioids are widely prescribed for chronic nonmalignant pain, often at doses exceeding those recommended in clinical practice guidelines. However, the risk-benefit ratio of high-dose opioid therapy is not well characterized. The objective of this study was to characterize the relationship between opioid dose and opioid-related mortality.
We conducted a population-based nested case-control study of Ontario, Canada, residents aged 15 to 64 years who were eligible for publicly funded prescription drug coverage and had received an opioid from August 1, 1997, through December 31, 2006, for nonmalignant pain. The outcome of interest was opioid-related death, as determined by the investigating coroner. The risk of opioid-related death was compared among patients treated with various daily doses of opioids.
Among 607,156 people aged 15 to 64 years prescribed an opioid over the study period, we identified 498 eligible patients whose deaths were related to opioids and 1714 matched controls. After extensive multivariable adjustment, we found that an average daily dose of 200 mg or more of morphine (or equivalent), was associated with a nearly 3-fold increase in the risk of opioid-related mortality (odds ratio [OR], 2.88; 95% confidence interval [CI], 1.79-4.63) relative to low daily doses (<20 mg of morphine, or equivalent). We found significant but attenuated increases in opioid-related mortality with intermediate doses of opioids (50-99 mg/d of morphine: OR, 1.92; 95% CI, 1.30-2.85; 100-199 mg/d of morphine: OR, 2.04; 95% CI, 1.28-3.24).
Among patients receiving opioids for nonmalignant pain, the daily dose is strongly associated with opioid-related mortality, particularly at doses exceeding thresholds recommended in recent clinical guidelines.
阿片类药物被广泛用于治疗慢性非恶性疼痛,其剂量常常超过临床实践指南中的推荐剂量。然而,高剂量阿片类药物治疗的风险效益比尚未得到充分描述。本研究的目的是描述阿片类药物剂量与阿片类药物相关死亡率之间的关系。
我们对加拿大安大略省15至64岁的居民进行了一项基于人群的巢式病例对照研究,这些居民有资格享受公共资助的处方药保险,并且在1997年8月1日至2006年12月31日期间因非恶性疼痛接受过阿片类药物治疗。感兴趣的结局是由验尸官判定的阿片类药物相关死亡。比较了接受不同日剂量阿片类药物治疗的患者中阿片类药物相关死亡的风险。
在研究期间,607156名15至64岁开具了阿片类药物处方的人中,我们确定了498名符合条件的患者,其死亡与阿片类药物有关,以及1714名匹配的对照。经过广泛的多变量调整后,我们发现,相对于低日剂量(<20毫克吗啡或等效物),平均每日剂量200毫克或更多的吗啡(或等效物)与阿片类药物相关死亡率增加近3倍相关(比值比[OR],2.88;95%置信区间[CI],1.79 - 4.63)。我们发现,中等剂量的阿片类药物会使阿片类药物相关死亡率显著增加,但增幅有所减弱(50 - 99毫克/天吗啡:OR,1.92;95% CI,1.30 - 2.85;100 - 199毫克/天吗啡:OR,2.04;95% CI,1.28 - 3.24)。
在接受阿片类药物治疗非恶性疼痛的患者中,日剂量与阿片类药物相关死亡率密切相关,尤其是在剂量超过近期临床指南推荐阈值时。