Does literature support stopping Suboxone (buprenorphine/naloxone) after a one-time injection of Brixadi (buprenorphine) or Sublocade (buprenorphine) to wean off buprenorphine?

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Using Extended-Release Buprenorphine (Brixadi/Sublocade) for Weaning Off Suboxone

Current literature does support using a one-time injection of extended-release buprenorphine (Brixadi or Sublocade) to facilitate discontinuation of Suboxone (buprenorphine/naloxone), as this approach provides a gradual taper with minimal withdrawal symptoms.

Evidence Supporting This Approach

Extended-release buprenorphine formulations offer several advantages for discontinuing buprenorphine therapy:

  • A 2023 case series demonstrated that patients interested in voluntarily discontinuing sublingual buprenorphine were successfully transitioned to extended-release buprenorphine, allowing them to discontinue treatment with minimal withdrawal symptoms 1

  • The long terminal half-life of extended-release buprenorphine provides a natural, gradual taper effect that helps minimize withdrawal symptoms compared to abrupt discontinuation of sublingual formulations 1

  • This approach maintains therapeutic buprenorphine levels while avoiding the daily decision-making process associated with taking sublingual medications

Implementation Considerations

When implementing this approach, consider the following:

  1. Patient Selection

    • Best candidates are those who:
      • Have demonstrated stable recovery
      • Have strong psychosocial support systems
      • Are not experiencing active co-occurring mental health issues
      • Have a clear understanding of the increased risk of relapse after discontinuation
  2. Preparation

    • Ensure the patient is on a stable dose of Suboxone before transition
    • Discuss the increased risk of overdose following discontinuation due to reduced tolerance
    • Provide naloxone and overdose prevention education
  3. Transition Process

    • Administer the extended-release injection (Brixadi or Sublocade)
    • Discontinue daily Suboxone after the injection is administered
    • The extended-release formulation will provide a gradual, physiologic taper over 1-2 months

Monitoring and Follow-Up

  • Schedule regular follow-up appointments to monitor for withdrawal symptoms
  • Use the Clinical Opiate Withdrawal Scale (COWS) to objectively assess withdrawal
  • Continue counseling and support services throughout the process
  • Monitor for signs of relapse or cravings

Risks and Considerations

  • There is a risk of relapse to opioid use after discontinuation of buprenorphine therapy
  • The risk of overdose is significantly increased after discontinuation due to reduced tolerance
  • Extended-release formulations cannot be removed once administered, so patient commitment is essential
  • Limited research exists on this specific approach, though preliminary evidence is promising 1

Alternative Approaches

If the one-time injection approach is not suitable:

  • Traditional tapering of sublingual buprenorphine over several weeks/months
  • Transition to a lower dose of sublingual buprenorphine before attempting discontinuation
  • Continued maintenance therapy if risks of discontinuation outweigh benefits

Conclusion

While the literature supporting this specific approach is still emerging, the 2023 case series provides promising evidence that a one-time injection of extended-release buprenorphine can facilitate the discontinuation of Suboxone with minimal withdrawal symptoms 1. This approach leverages the pharmacokinetic properties of extended-release formulations to provide a gradual, physiologic taper that may be more comfortable and successful than traditional tapering methods.

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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