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Microdosing and standard-dosing take-home buprenorphine from the emergency department: A feasibility study
Jessica Moe1,2, Katherin Badke3, Megan Pratt4
1Department of Emergency Medicine University of British Columbia Vancouver British Columbia Canada.
Objective:
Emergency department (ED)-initiated buprenorphine may prevent overdose. Microdosing is a novel approach that does not require withdrawal, which can be a barrier to standard inductions. We aimed to evaluate the feasibility of an ED-initiated buprenorphine/naloxone program providing standard-dosing and microdosing take-home packages and of randomizing patients to either intervention.
Methods:
We broadly screened patients ≥18 years old for opioid use disorder at a large, urban ED. In a first phase, we provided consecutive patients with 3-day standard-dosing packages, and then we provided a subsequent group with 6-day microdosing packages. In a second phase, we randomized patients to standard dosing or microdosing. We attempted 7-day telephone follow-ups and 30-day in-person community follow-ups. The primary feasibility outcome was number of patients enrolled and accepting randomization. Secondary outcomes were numbers screened, follow-up rates, and 30-day opioid agonist therapy retention.
Results:
We screened 3954 ED patients and identified 94 with opioid use disorders. Of the patients, 26 (27.7%) declined participation: 10 identified a negative prior experience with buprenorphine/naloxone as the reason, 5 specifically cited precipitated withdrawal, and none cited randomization. We enrolled 68 patients. A total of 14 left the ED against medical advice, 8 were excluded post-enrollment, 21 received standard dosing, and 25 received microdosing. The 7-day and 30-day follow-up rates were 9/46 (19.6%) and 15/46 (32.6%), respectively. At least 5/21 (23.8%) provided standard dosing and 8/25 (32.0%) provided microdosing remained on opioid agonist therapy at 30 days.
Conclusions:
ED-initiated take-home standard-dosing and microdosing buprenorphine/naloxone programs are feasible, and a randomized controlled trial would be acceptable to our target population.
Insights
Emergency department buprenorphine/naloxone initiation is feasible using standard or microdosing take-home packages. A randomized controlled trial is acceptable to patients with opioid use disorder, suggesting potential for wider implementation.
Area of Science:
- Emergency Medicine
- Addiction Medicine
- Pharmacology
Background:
- Emergency department (ED) initiation of buprenorphine/naloxone can prevent opioid overdose.
- Microdosing is a novel buprenorphine induction method that may overcome barriers associated with precipitated withdrawal.
- Standard induction requires patients to be in withdrawal, which can deter treatment initiation.
Purpose of the Study:
- To evaluate the feasibility of an ED-initiated buprenorphine/naloxone program.
- To assess the acceptability of providing take-home standard-dosing and microdosing packages.
- To determine the feasibility of randomizing patients to either standard or microdosing interventions.
Main Methods:
- Broad screening of adult patients in a large, urban ED for opioid use disorder.
- Phase 1: Consecutive patients received 3-day standard-dosing or 6-day microdosing packages.
- Phase 2: Patients were randomized to standard or microdosing, with attempted 7-day telephone and 30-day in-person follow-ups.
Main Results:
- 94 patients with opioid use disorder were identified out of 3954 screened ED patients.
- 68 patients were enrolled, with 21 receiving standard dosing and 25 receiving microdosing.
- 30-day follow-up rates were 32.6%, with 23.8% on standard dosing and 32.0% on microdosing remaining on opioid agonist therapy.
Conclusions:
- ED-initiated buprenorphine/naloxone programs using take-home standard and microdosing packages are feasible.
- The study population found randomization to be acceptable, supporting future randomized controlled trials.
- These findings suggest a viable strategy for increasing access to medication for opioid use disorder in the ED setting.
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