Initiating buprenorphine in New Jersey emergency departments: a mixed methods study

JEM reports Pub Date : 2026-03-01 Epub Date: 2026-01-29 DOI:10.1016/j.jemrpt.2026.100210
Cadence F. Bowden , Peter Treitler , Jennifer Miles , Hannah Shepherd , Kylie Davidson , Stephen Crystal
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Abstract

Background

Emergency departments (EDs) represent a critical touchpoint in the treatment of opioid use disorder (OUD), yet evidence-based practices such as buprenorphine initiation have not been widely adopted.

Objectives

This study describes state-wide uptake of buprenorphine by Medicaid-enrolled patients with OUD who are seen in New Jersey (NJ) EDs and examines related clinical ED practices.

Methods

This sequential mixed-methods study used NJ Medicaid claims and qualitative interviews with ED leaders. Quantitative analyses included NJ Medicaid enrollees aged 18–64 treated in NJ EDs for OUD-related diagnoses. The primary quantitative outcome was ED-associated buprenorphine utilization, defined as buprenorphine that was dispensed or filled 0–4 days after ED discharge. Results of the quantitative analyses were used to classify EDs as higher and lower prescribing, from which ED leaders were then purposively sampled to participate in semi-structured interviews. Qualitative data were analyzed inductively.

Results

Overall buprenorphine initiation peaked at 14.4 % in 2022 and there was wide variation across EDs. Interviewees commonly reported that peer navigator programs, availability of community-based providers, and a positive culture toward MOUD facilitated buprenorphine initiation. Conversely, provider hesitancy, limited community resources, and regulatory factors were reported as major barriers.

Conclusions

While volumes of patients presenting to NJ EDs with OUD remain high, low rates of buprenorphine initiation and prescription persist. Providers and institutions possess great variation in their comfort with and ability to initiate buprenorphine in the ED and future work to standardize this evidence-based practice is needed.
在新泽西州急诊科启动丁丙诺啡:一项混合方法研究
背景急诊科(ed)是治疗阿片类药物使用障碍(OUD)的关键接触点,但基于证据的实践,如丁丙诺啡起始治疗尚未被广泛采用。目的:本研究描述了在新泽西州急诊科(NJ)接受医疗补助的OUD患者对丁丙诺啡的全州摄取情况,并检查了相关的临床ED实践。方法:这项连续的混合方法研究使用了新泽西州医疗补助申请和对急诊科领导的定性访谈。定量分析包括年龄在18-64岁的新泽西州医疗补助计划入选者,他们在新泽西州急诊科接受了与oud相关的诊断。主要定量指标是ED相关的丁丙诺啡利用率,定义为ED出院后0-4天配药或填充丁丙诺啡。定量分析的结果被用于将急诊科划分为高处方和低处方,然后有目的地从中抽取急诊科领导参加半结构化访谈。定性资料进行归纳分析。结果2022年丁丙诺啡起始率最高,为14.4%,各急症患者差异较大。受访者普遍报告说,同伴导航计划、社区提供者的可用性以及对mod的积极文化促进了丁丙诺啡的开始。相反,提供者的犹豫、有限的社区资源和监管因素被报道为主要障碍。结论:虽然因OUD就诊的新泽西州急诊科患者数量仍然很高,但丁丙诺啡的起始率和处方率仍然很低。提供者和机构在ED中使用丁丙诺啡的舒适度和能力方面存在很大差异,未来的工作需要将这种基于证据的实践标准化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
JEM reports
JEM reports Emergency Medicine
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