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Implementation of low-dose buprenorphine induction at a syringe services program.
Maia H Hauschild1, Peyton V Warp2, William H Eger3,4
1Division of Infectious Diseases, Department of Medicine, University of Miami Miller School of Medicine, Miami, USA. maiahaus@gmail.com.
Low-dose induction (LDI) shows promise for treating opioid use disorder (OUD) by mitigating withdrawal symptoms, but high follow-up loss in real-world settings requires further study.
Area of Science:
- Addiction Medicine
- Pharmacology
- Public Health
Background:
- Fentanyl complicates opioid use disorder (OUD) treatment, increasing risks like buprenorphine-precipitated opioid withdrawal (BPOW).
- Traditional buprenorphine induction can be difficult for fentanyl users.
- Low-dose induction (LDI) offers a gradual titration method to reduce BPOW risk.
Purpose of the Study:
- To assess the feasibility and acceptability of LDI in a low-barrier syringe services program (SSP).
- To evaluate LDI as an alternative induction method for OUD patients using fentanyl.
Main Methods:
- A mixed-methods prospective cohort study was conducted at an SSP in Miami, Florida.
- A 4-day LDI protocol was offered to 30 OUD patients interested in buprenorphine.
- Outcomes included urine drug screens, symptom surveys, and qualitative interviews within four weeks.
Main Results:
- 53% of participants returned for follow-up.
- 56% of those followed up tested positive for buprenorphine.
- Most participants reported LDI success and acceptability, citing reduced withdrawal and increased autonomy.
Conclusions:
- LDI is perceived as acceptable and empowering, despite low objective induction rates.
- High participant attrition and environmental instability limit conclusions.
- Further research is needed to optimize LDI protocols and address barriers to treatment success.
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