When to Start Sublocade 100 mg for Opioid Use Disorder
Sublocade 100 mg should be initiated after patients have achieved clinical stability on a transmucosal buprenorphine-containing product, delivering at least 8-24 mg per day for a minimum of 7 days. 1
Patient Selection and Preparation
- Sublocade (buprenorphine extended-release) 100 mg is indicated for patients with opioid use disorder (OUD) who have already been stabilized on a transmucosal (sublingual or buccal) buprenorphine product 1
- The patient must demonstrate tolerance to buprenorphine before initiating Sublocade to minimize risk of precipitated withdrawal 1
- Patients should be assessed for their risk of relapse, expected level of opioid withdrawal symptoms, and comorbid conditions before determining the appropriate timing for Sublocade initiation 1
Specific Initiation Protocol
- First, stabilize the patient on 8-24 mg daily of sublingual or buccal buprenorphine for a minimum of 7 consecutive days 1
- Ensure the patient is not experiencing withdrawal symptoms and is comfortable on their oral buprenorphine dose 1
- After stabilization, transition to Sublocade 100 mg monthly subcutaneous injection 1
- The first two monthly doses should be 300 mg, followed by maintenance doses of 100 mg monthly (though this can be increased to 300 mg monthly based on patient response) 2
Clinical Considerations
- Individualize the decision to initiate Sublocade based on the patient's daily buprenorphine dose, indication for treatment (pain vs. dependency), and risk of relapse 1
- Be aware that concomitant use of buprenorphine with QT-prolonging agents is contraindicated 1
- Multiple drug-drug interactions can result in QT-interval prolongation, serotonin syndrome, paralytic ileus, reduced analgesic effect, or precipitation of withdrawal symptoms 1
Special Situations
- For patients with inadequate analgesia on buprenorphine maintenance, consider increasing the dosage in divided doses before transitioning to Sublocade 1
- For patients with chronic pain who are transitioning from full opioid agonists, ensure they are in mild withdrawal before initiating any form of buprenorphine to avoid precipitated withdrawal 1
- For patients who cannot tolerate withdrawal symptoms during traditional induction, consider low-dose initiation (microdosing) of oral buprenorphine before transitioning to Sublocade 3
Monitoring After Initiation
- Monitor patients closely after the first injection of Sublocade for signs of precipitated withdrawal, especially if the patient was recently using full opioid agonists 1
- Assess for adequate control of opioid cravings and withdrawal symptoms 4
- Higher doses of buprenorphine (up to 32 mg/day) have been associated with improved outcomes including decreased opioid use, reduced frequency of use, and better retention in treatment 4
Potential Pitfalls
- Avoid abrupt discontinuation of Sublocade as it may lead to withdrawal symptoms that can persist for weeks or months due to the long-acting nature of the formulation 5
- Be cautious with patients who may require surgery, as Sublocade's high binding affinity may interfere with perioperative pain management 1
- Do not attempt to remove Sublocade after administration, as the risks include surgical complications, infection, and damage to surrounding tissue 2