What is the recommended protocol for treating opioid use disorder with Suboxone (buprenorphine/naloxone)?

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Suboxone Protocol for Opioid Use Disorder

For standard buprenorphine/naloxone induction, patients must abstain from short-acting opioids for 12-24 hours and long-acting opioids for 36-48 hours, then demonstrate at least mild withdrawal symptoms on a validated scale before receiving the first dose to avoid precipitated withdrawal. 1

Standard Induction Protocol

Pre-Induction Requirements

  • Verify withdrawal symptoms using a validated opioid withdrawal scale (e.g., COWS score ≥8-12) before administering any buprenorphine 1
  • Abstinence periods are mandatory: 12-24 hours for short-acting opioids (heroin, oxycodone), 36-48 hours for long-acting opioids (methadone, extended-release formulations) 1
  • Failure to wait for adequate withdrawal will precipitate severe withdrawal symptoms due to buprenorphine's partial agonist properties displacing full agonists from opioid receptors 1

Day 1 Dosing

  • Administer initial dose of 2-4 mg buprenorphine/naloxone sublingually once mild withdrawal is confirmed 1
  • Reassess withdrawal symptoms 30 minutes after first dose using the same validated scale 1
  • If tolerated and withdrawal persists, give another 2-4 mg dose 1
  • Target Day 1 total: 8 mg (range 4-8 mg depending on tolerance) 1

Dose Titration

  • Target maintenance dose is 16 mg daily, which suppresses illicit opioid use in most patients 1
  • Dosing range: 4-24 mg daily, adjusted based on withdrawal symptoms and cravings 1
  • Higher doses may be needed during pregnancy (2-4 times daily dosing) with increasing gestational age 1

Alternative Induction: Microdosing Protocol

For patients unable to tolerate the abstinence period (especially those using fentanyl), microdosing allows buprenorphine initiation while continuing other opioids, avoiding precipitated withdrawal entirely. 2, 3

7-Day Microdosing Schedule

  • Day 1: 0.5 mg once daily 2
  • Day 2: 0.5 mg twice daily 2
  • Day 3: 1 mg twice daily 2
  • Day 4: 2 mg twice daily 2
  • Day 5: 3 mg twice daily 2
  • Day 6: 4 mg twice daily 2
  • Day 7: 12 mg once daily, discontinue all other opioids 2
  • Subsequently titrate to 12-32 mg daily as needed 2

This approach has shown success in patients using illicit fentanyl, prescribed methadone, or slow-release morphine without precipitated withdrawal 2, 3

Transition to Long-Acting Injectable Formulations

Patients must be stabilized on 8-24 mg daily sublingual/buccal buprenorphine for minimum 7 consecutive days before transitioning to monthly injectable buprenorphine (Sublocade). 4

Injectable Protocol

  • First two monthly doses: 300 mg subcutaneous injection 4
  • Maintenance doses: 100 mg monthly thereafter 4
  • Combine with behavioral therapies for optimal outcomes 4
  • Do not attempt removal of depot injection due to risks of surgical complications, infection, and tissue damage 4

Critical Drug Interactions and Contraindications

  • Concomitant use with QT-prolonging agents is contraindicated 1, 4
  • Risk of serotonin syndrome when combined with serotonergic agents 1
  • Risk of paralytic ileus with anticholinergic medications 1, 4
  • Benzodiazepine co-use: While methadone may be preferred with concurrent benzodiazepine use, buprenorphine should not be withheld if it's the only accessible option—use careful medication management 1

Special Populations

Pregnancy

  • Continue buprenorphine/naloxone combination if already prescribed—theoretical concerns about naloxone precipitating fetal withdrawal are not supported by evidence 1
  • Buprenorphine monotherapy (Subutex) is no longer preferentially recommended over combination therapy (Suboxone) in pregnancy 1
  • Buprenorphine results in less severe neonatal opioid withdrawal syndrome, shorter treatment duration, and shorter hospital stays compared to methadone 1
  • May require higher and more frequent dosing (2-4 times daily) as pregnancy progresses 1

Perioperative Management

  • Decision to continue or hold should reflect: prescribed daily dose, indication (pain vs dependency), relapse risk, and expected postoperative pain level 1
  • Multiple drug interactions possible during anesthesia 1
  • Coordinate closely with anesthesiology regarding timing and dosing 1

Common Pitfalls to Avoid

  • Never initiate standard buprenorphine without confirmed withdrawal symptoms—this is the most common cause of precipitated withdrawal 1
  • Do not use oral naloxone for overdose reversal (it's inactivated); use intranasal, subcutaneous, intramuscular, or intravenous routes 1
  • Switching from methadone to buprenorphine is challenging and requires close monitoring due to withdrawal risk; switching from buprenorphine to methadone can be done immediately if no sedation present 1
  • For patients on naltrexone: hold intramuscular formulation 24-30 days, oral formulation 3-4 days before buprenorphine initiation 1

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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