# Drug Use After Emergency Department‐Initiated Injectable Buprenorphine: A Secondary Analysis of the ED‐INNOVATION Ancillary Safety and Feasibility Trial

**Authors:** Ethan Cowan, Gail D'Onofrio, Jeanmarie Perrone, Erik Anderson, James Dziura, Kathryn Hawk, Andrew Herring, Ryan McCormack, Manali Phadke, Elizabeth A. Samuels, David A. Fiellin

PMC · DOI: 10.1111/acem.70191 · Academic Emergency Medicine · 2025-11-24

## TL;DR

This study shows that starting buprenorphine treatment in emergency departments significantly reduces opioid and other drug use in the first week after discharge.

## Contribution

The study demonstrates the effectiveness of emergency department-initiated buprenorphine in reducing drug use shortly after treatment.

## Key findings

- 98% of participants reported at least one opioid-free day in the week after treatment.
- 63% of participants reported no opioid use across all 7 days.
- Urine drug screens showed reduced detection of opioids, stimulants, and benzodiazepines.

## Abstract

To characterize opioid and nonopioid drug use in the week following emergency department (ED)‐initiated extended‐release buprenorphine (XR‐BUP) treatment using both self‐reported data and urine drug screens (UDS).

This study uses data collected during a nonrandomized clinical trial of patients with untreated opioid use disorder (OUD), testing the safety and feasibility of initiating XR‐BUP in patients presenting with minimal to mild withdrawal. The study was conducted from July 2020 to May 2023 across four urban academic EDs in the Northeast, Mid‐Atlantic, and Pacific regions of the United States. A total of 100 participants, 18 years or older with OUD defined by DSM‐5 criteria, a clinical opiate withdrawal scale (COWS < 8), and a positive opioid urine screen were included. Individuals with recent MOUD treatment, presentation for overdose, or concurrent methadone use were excluded. All participants received a single subcutaneous injection of 24 mg XR‐BUP (CAM2038) during their ED visit. The primary outcomes were self‐reported daily opioid and nonopioid drug use over 7 days postinjection using daily Qualtrics surveys and UDS results on day 7.

Among participants who received XR‐BUP and completed daily surveys, 98% reported at least one opioid‐free day, and 63% reported no opioid use across all 7 days. Day 7 UDS results showed decreased detection of opioids, stimulants, and benzodiazepines. Reported polysubstance use also declined over the observation period.

ED‐initiated XR‐BUP was associated with substantial reductions in opioid and polysubstance use during the first week post‐discharge, supporting its role in early overdose risk mitigation and highlighting its value as an ED‐based intervention for opioid use disorder.

ClinicalTrials.gov Identifier: NCT03658642

## Linked entities

- **Chemicals:** buprenorphine (PubChem CID 644073), opioids (PubChem CID 126961754)

## Full-text entities

- **Diseases:** OUD (MESH:D009293), overdose (MESH:D062787)
- **Chemicals:** Buprenorphine (MESH:D002047), CAM2038 (-), benzodiazepines (MESH:D001569), methadone (MESH:D008691)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

37 references — full list in the complete paper: https://tomesphere.com/paper/PMC12937049/full.md

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Source: https://tomesphere.com/paper/PMC12937049