Transitioning from Hydromorphone (Dilaudid) to Butrans (Buprenorphine) Patch
When transitioning a patient from hydromorphone (Dilaudid) to Butrans (buprenorphine) patch, first calculate the 24-hour hydromorphone requirement, convert to morphine equivalents, then select the appropriate Butrans patch strength using established conversion tables, and reduce the calculated dose by 25-50% to account for incomplete cross-tolerance. 1, 2
Step-by-Step Conversion Process
Step 1: Calculate Total Daily Hydromorphone Dose
- Determine the total amount of hydromorphone the patient is taking in a 24-hour period
- Include all scheduled and as-needed doses
Step 2: Convert to Morphine Equivalents
- Use standard conversion ratios:
Step 3: Select Appropriate Butrans Patch Strength
- Based on the NCCN conversion table for transdermal buprenorphine 1:
- 25 mcg/h patch ≈ 60mg oral morphine or 7.5mg oral hydromorphone daily
- 50 mcg/h patch ≈ 120mg oral morphine or 15mg oral hydromorphone daily
- 75 mcg/h patch ≈ 180mg oral morphine or 22.5mg oral hydromorphone daily
- 100 mcg/h patch ≈ 240mg oral morphine or 30mg oral hydromorphone daily
Step 4: Reduce Dose for Cross-Tolerance
- Reduce the calculated dose by 25-50% to account for incomplete cross-tolerance 1, 2
- Example: If calculations indicate a 50 mcg/h patch, consider starting with a 25 mcg/h patch
Important Clinical Considerations
Timing of Transition
- Due to buprenorphine's high binding affinity for μ-opioid receptors, traditional approaches recommend waiting until the patient is in mild withdrawal before initiating buprenorphine 1
- However, newer approaches suggest using transdermal buprenorphine as a bridge to avoid the painful abstinence period 3
- For patients on lower doses of hydromorphone, apply the Butrans patch 12-24 hours after the last hydromorphone dose
- For patients on higher doses, consider a more gradual transition with overlapping therapy
Breakthrough Pain Management
- Provide short-acting non-opioid analgesics for breakthrough pain during the first 24-72 hours 1
- Options include NSAIDs, acetaminophen, or adjuvant medications appropriate to the pain syndrome
- Avoid using full opioid agonists for breakthrough pain if possible, as buprenorphine's high receptor affinity may block their effects 1
Monitoring and Dose Adjustments
- Assess pain control after 72 hours (when buprenorphine reaches steady state)
- Butrans patches are typically changed every 7 days 4
- If pain control is inadequate:
- Increase to the next patch strength
- Consider dividing buprenorphine doses if using sublingual formulations 1
Special Considerations
- Patients previously on very high doses of hydromorphone (>30mg oral daily) may have more difficulty transitioning and may require more careful monitoring 5
- Patients with renal or hepatic impairment may require lower starting doses
- Elderly patients may be more sensitive to both medications and may require dose reductions
Potential Challenges and Solutions
Inadequate Pain Control
- If maximum Butrans dose is reached with inadequate analgesia, consider adding a full opioid agonist under close monitoring 1
- Higher doses of full agonists may be needed due to buprenorphine's high receptor affinity 1
Withdrawal Symptoms
- If withdrawal symptoms occur, consider using the transdermal buprenorphine as a bridge method 3
- For severe cases, consider a microdosing approach with gradually increasing buprenorphine while tapering hydromorphone 6
Adverse Effects
- Monitor for common side effects: nausea, constipation, headache, dizziness
- Transdermal buprenorphine typically has fewer gastrointestinal side effects than sublingual formulations 7
- Assess for local skin reactions at patch application sites 4
By following this structured approach, you can safely transition patients from hydromorphone to Butrans patches while minimizing withdrawal symptoms and maintaining adequate pain control.