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长期阿片类药物释放制剂处方患者的阿片类药物耐受和临床公认的阿片类药物中毒。

Opioid tolerance and clinically recognized opioid poisoning among patients prescribed extended-release long-acting opioids.

机构信息

Department of Epidemiology, Gillings School of Global Public Health, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.

Injury Prevention Research Center, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.

出版信息

Pharmacoepidemiol Drug Saf. 2019 Jan;28(1):39-47. doi: 10.1002/pds.4572. Epub 2018 Jun 11.

Abstract

BACKGROUND

In recognition of potential for increased overdose risk, drug labels for extended-release and long-acting (ER/LA) opioids emphasize the need for established opioid tolerance prior to initiating high dosages.

OBJECTIVES

Describe the proportion of patients with opioid tolerance prior to initiation of 90 morphine milligram equivalents (MME) ER/LA opioids and examine subsequent risk of opioid poisoning.

METHODS

We used Truven Health Analytics' MarketScan Databases (2006-2015) to identify patients initiating ER/LA opioids ≥90 MME. We examined prescription histories and describe the proportion of initiators with opioid tolerance (defined as ≥7 days of 60 MME in the prior 14 days). We adjusted for age, sex, year of initiation, and baseline comorbidities using inverse probability of treatment weighted Cox proportional hazards models. We estimated adjusted hazard ratios and 95% confidence intervals for the effect of opioid tolerance on the risk of clinically recognized opioid poisoning (based on diagnosis codes) in specific periods (0-7, 8-30, 31-90, and 91-365 days) following initiation.

RESULTS

Among 372 038 initiators, 38% did not meet opioid tolerance criteria. The proportion of nontolerant initiators was highest among those initiating methadone (44%) and fentanyl (42%). Nontolerant patients were 37% more likely to be diagnosed with opioid poisoning (adjusted hazard ratios = 1.37 [1.07, 1.76]) in the week following ER/LA initiation.

CONCLUSIONS

Over one-third of patients initiating ≥90 MME ER/LA opioids did not have evidence of opioid tolerance. The 7 days following high dose ER/LA initiation may represent a high-risk period for clinically diagnosed opioid poisoning in patients who do not have prior opioid tolerance.

摘要

背景

鉴于潜在的过量风险增加,延长释放和长效(ER/LA)类阿片药物的药品标签强调在开始高剂量治疗之前,需要建立阿片类药物耐受。

目的

描述开始使用 90 吗啡毫克当量(MME)ER/LA 类阿片药物之前具有阿片类药物耐受的患者比例,并检查随后发生阿片类药物中毒的风险。

方法

我们使用 Truven Health Analytics 的 MarketScan 数据库(2006-2015 年)来识别开始使用 ER/LA 类阿片药物≥90 MME 的患者。我们检查了处方记录,并描述了具有阿片类药物耐受的患者比例(定义为在过去 14 天内至少有 7 天使用 60 MME)。我们使用逆概率治疗加权 Cox 比例风险模型,根据年龄、性别、起始年份和基线合并症对数据进行了调整。我们根据诊断代码,在特定时间段(0-7、8-30、31-90 和 91-365 天)内,估计了阿片类药物耐受对临床确诊的阿片类药物中毒风险的调整后危害比和 95%置信区间。

结果

在 372038 名开始使用药物的患者中,38%的患者不符合阿片类药物耐受标准。在开始使用美沙酮(44%)和芬太尼(42%)的患者中,未耐受患者的比例最高。在 ER/LA 开始后的一周内,未耐受的患者被诊断为阿片类药物中毒的可能性增加了 37%(调整后的危害比=1.37[1.07,1.76])。

结论

开始使用≥90 MME ER/LA 类阿片药物的患者中,有三分之一以上的患者没有阿片类药物耐受的证据。在开始使用高剂量 ER/LA 后的 7 天内,对于没有先前阿片类药物耐受的患者,可能是临床诊断为阿片类药物中毒的高风险期。

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