Group Health Research Institute, Seattle, Washington 98101, USA.
Ann Intern Med. 2010 Jan 19;152(2):85-92. doi: 10.7326/0003-4819-152-2-201001190-00006.
Long-term opioid therapy for chronic noncancer pain is becoming increasingly common in community practice. Concomitant with this change in practice, rates of fatal opioid overdose have increased. The extent to which overdose risks are elevated among patients receiving medically prescribed long-term opioid therapy is unknown.
To estimate rates of opioid overdose and their association with an average prescribed daily opioid dose among patients receiving medically prescribed, long-term opioid therapy.
Cox proportional hazards models were used to estimate overdose risk as a function of average daily opioid dose (morphine equivalents) received at the time of overdose.
HMO.
9940 persons who received 3 or more opioid prescriptions within 90 days for chronic noncancer pain between 1997 and 2005.
Average daily opioid dose over the previous 90 days from automated pharmacy data. Primary outcomes--nonfatal and fatal overdoses--were identified through diagnostic codes from inpatient and outpatient care and death certificates and were confirmed by medical record review.
51 opioid-related overdoses were identified, including 6 deaths. Compared with patients receiving 1 to 20 mg/d of opioids (0.2% annual overdose rate), patients receiving 50 to 99 mg/d had a 3.7-fold increase in overdose risk (95% CI, 1.5 to 9.5) and a 0.7% annual overdose rate. Patients receiving 100 mg/d or more had an 8.9-fold increase in overdose risk (CI, 4.0 to 19.7) and a 1.8% annual overdose rate.
Increased overdose risk among patients receiving higher dose regimens may be due to confounding by patient differences and by use of opioids in ways not intended by prescribing physicians. The small number of overdoses in the study cohort is also a limitation.
Patients receiving higher doses of prescribed opioids are at increased risk for overdose, which underscores the need for close supervision of these patients.
National Institute of Drug Abuse.
在社区实践中,长期使用阿片类药物治疗慢性非癌痛的情况越来越普遍。伴随着这种治疗实践的改变,阿片类药物过量致死的比率也在增加。目前尚不清楚在接受医学处方长期阿片类药物治疗的患者中,药物过量的风险增加到何种程度。
评估接受医学处方长期阿片类药物治疗的患者中,药物过量的发生率及其与平均处方日阿片类药物剂量(吗啡等效剂量)的关系。
Cox 比例风险模型用于根据药物过量时所接受的平均每日阿片类药物剂量(吗啡等效剂量)来评估药物过量的风险。
健康维护组织。
1997 年至 2005 年间,9940 名患有慢性非癌痛且在 90 天内接受 3 次或 3 次以上阿片类药物处方的患者。
90 天内从自动药房数据获得的平均每日阿片类药物剂量。主要结局指标——非致命性和致命性药物过量——通过住院和门诊治疗以及死亡证明的诊断代码确定,并通过病历审查进行确认。
共发现 51 例阿片类药物相关的药物过量,其中 6 例死亡。与接受 1 至 20 mg/d 阿片类药物(0.2%的年药物过量率)的患者相比,接受 50 至 99 mg/d 阿片类药物的患者药物过量风险增加 3.7 倍(95%CI,1.5 至 9.5),年药物过量率为 0.7%。接受 100 mg/d 或更高剂量阿片类药物的患者药物过量风险增加 8.9 倍(CI,4.0 至 19.7),年药物过量率为 1.8%。
接受高剂量阿片类药物治疗的患者药物过量风险增加可能是由于患者差异和处方医生意图之外的阿片类药物使用导致的混杂因素所致。研究队列中药物过量的数量较少也是一个限制。
接受较高剂量处方阿片类药物的患者发生药物过量的风险增加,这突出表明需要对这些患者进行密切监测。
国家药物滥用研究所。