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Microdose induction of buprenorphine-naloxone in a patient using high dose methadone: A case report
Shannon Menard1, Archana Jhawar1
1Clinical Pharmacy Specialist, Department of Pharmacy Services, Jesse Brown Veterans Affairs Medical Center, Chicago, Illinois; Clinical Pharmacy Specialist, University of Illinois at Chicago, College of Pharmacy, Chicago, Illinois.
Background:
Buprenorphine is a partial mu-opioid receptor agonist approved for the treatment of opioid dependence. The risk of withdrawal symptoms and wait time required to safely initiate buprenorphine provides challenges to both patients and providers. Microdose induction is proposed as a possible solution to ease the transition to buprenorphine; however, little data has been published to date on patients stabilized on methadone doses greater than 100 mg.
Case Report:
A 29-year-old patient stabilized on methadone 105 mg was successfully transitioned to sublingual buprenorphine-naloxone using a 7-day microdose protocol on an inpatient psychiatric service. During the transition, the patient reported only minimal symptoms.
Conclusion:
This report adds to the growing literature supporting the use of a microdose induction to initiate buprenorphine-naloxone. Additionally, this approach may be significant for patients stabilized on high doses of methadone who may not be able to tolerate a traditional buprenorphine induction.
Insights
Microdose buprenorphine induction effectively transitioned a patient from high-dose methadone with minimal withdrawal. This approach offers a promising alternative for patients on significant methadone doses.
Area of Science:
- Pharmacology
- Addiction Medicine
- Clinical Psychiatry
Background:
- Buprenorphine, a partial mu-opioid agonist, treats opioid dependence but initiation can be challenging due to withdrawal and wait times.
- High-dose methadone stabilization presents unique hurdles for transitioning patients to buprenorphine.
- Limited data exists on microdose buprenorphine induction for patients on methadone doses exceeding 100 mg.
Observation:
- A 29-year-old patient on 105 mg of methadone underwent a 7-day microdose induction protocol.
- The transition occurred within an inpatient psychiatric setting.
- The patient reported experiencing only minimal withdrawal symptoms during the buprenorphine-naloxone initiation.
Findings:
- Successful transition to sublingual buprenorphine-naloxone was achieved using the microdose protocol.
- The microdose strategy minimized adverse withdrawal effects in a patient on high-dose methadone.
- This case demonstrates the feasibility of microdose induction in this patient population.
Implications:
- Supports the growing evidence for microdose buprenorphine induction as a viable strategy.
- Offers a potential solution for patients stabilized on high methadone doses who struggle with traditional buprenorphine initiation.
- Highlights the utility of microdosing in managing opioid use disorder transitions in clinical psychiatry settings.
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