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非致死性药物过量后阿片类药物处方与重复药物过量的关联:一项队列研究。

Opioid Prescribing After Nonfatal Overdose and Association With Repeated Overdose: A Cohort Study.

出版信息

Ann Intern Med. 2016 Jan 5;164(1):1-9. doi: 10.7326/M15-0038. Epub 2015 Dec 29.

Abstract

BACKGROUND

Nonfatal opioid overdose is an opportunity to identify and treat substance use disorders, but treatment patterns after the overdose are unknown.

OBJECTIVE

To determine prescribed opioid dosage after an opioid overdose and its association with repeated overdose.

DESIGN

Retrospective cohort study.

SETTING

A large U.S. health insurer.

PARTICIPANTS

2848 commercially insured patients aged 18 to 64 years who had a nonfatal opioid overdose during long-term opioid therapy for noncancer pain between May 2000 and December 2012.

MEASUREMENTS

Nonfatal opioid overdose was identified using International Classification of Diseases, Ninth Revision, Clinical Modification, codes from emergency department or inpatient claims. The primary outcome was daily morphine-equivalent dosage (MED) of opioids dispensed from 60 days before to up to 730 days after the index overdose. We categorized dosages as large (≥100 mg MED), moderate (50 to <100 mg MED), low (<50 mg MED), or none (0 mg MED). Secondary outcomes included time to repeated overdose stratified by daily dosage as a time-varying covariate.

RESULTS

Over a median follow-up of 299 days, opioids were dispensed to 91% of patients after an overdose. Seven percent of patients (n = 212) had a repeated opioid overdose. At 2 years, the cumulative incidence of repeated overdose was 17% (95% CI, 14% to 20%) for patients receiving high dosages of opioids after the index overdose, 15% (CI, 10% to 21%) for those receiving moderate dosages, 9% (CI, 6% to 14%) for those receiving low dosages, and 8% (CI, 6% to 11%) for those receiving no opioids.

LIMITATION

The cohort was limited to commercially insured adults.

CONCLUSION

Almost all patients continue to receive prescription opioids after an overdose. Opioid discontinuation after overdose is associated with lower risk for repeated overdose.

PRIMARY FUNDING SOURCE

Health Resources and Services Administration.

摘要

背景

非致命性阿片类药物过量是识别和治疗药物使用障碍的机会,但过量后的治疗模式尚不清楚。

目的

确定阿片类药物过量后开处的阿片类药物剂量及其与重复过量的关系。

设计

回顾性队列研究。

设置

一家大型美国健康保险公司。

参与者

2000 年 5 月至 2012 年 12 月期间,2848 名在长期阿片类药物治疗非癌症疼痛期间发生非致命性阿片类药物过量的 18 至 64 岁商业投保患者。

测量

非致命性阿片类药物过量使用急诊或住院索赔的国际疾病分类,第九修订版,临床修正版代码来识别。主要结果是从指数过量前 60 天到 730 天开出的阿片类药物的每日吗啡等效剂量(MED)。我们将剂量分为大剂量(≥100 mg MED)、中剂量(50 至 <100 mg MED)、低剂量(<50 mg MED)或无剂量(0 mg MED)。次要结果包括按每日剂量分层的重复过量时间,作为随时间变化的协变量。

结果

在中位数为 299 天的随访期间,91%的患者在过量后开处了阿片类药物。7%的患者(n=212)发生了重复阿片类药物过量。在 2 年内,接受高剂量阿片类药物治疗的患者指数过量后重复过量的累积发生率为 17%(95%CI,14%至 20%),接受中剂量阿片类药物治疗的患者为 15%(CI,10%至 21%),接受低剂量阿片类药物治疗的患者为 9%(CI,6%至 14%),接受无阿片类药物治疗的患者为 8%(CI,6%至 11%)。

局限性

队列仅限于商业投保成年人。

结论

几乎所有患者在过量后继续接受处方阿片类药物。过量后阿片类药物的停用与重复过量的风险较低相关。

主要资金来源

卫生资源和服务管理局。

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