Oral Buprenorphine Equivalence to Butrans 20 mcg/hour Patch
The equivalent oral buprenorphine dose to a Butrans 20 mcg/hour transdermal patch is approximately 1.6-1.8 mg per day of oral buprenorphine.
Conversion Calculation
The conversion from transdermal buprenorphine to oral buprenorphine requires understanding several key conversion factors:
According to ESMO guidelines, the relative potency ratio of oral to transdermal buprenorphine is approximately 75:1 1.
More recent data suggests that a more accurate conversion ratio may be between 110:1 and 115:1 for transdermal buprenorphine to oral morphine equivalents 2.
Using these conversion factors:
- Butrans 20 mcg/hour = 0.48 mg/day transdermal buprenorphine
- Using the 75:1 ratio: 0.48 mg × 75 = 36 mg oral morphine equivalent
- Using the 110:1 ratio: 0.48 mg × 110 = 52.8 mg oral morphine equivalent
For conversion back to oral buprenorphine:
- Oral buprenorphine is approximately 30 times more potent than oral morphine 1
- Therefore: 36 mg oral morphine ÷ 30 = 1.2 mg oral buprenorphine
- Or using the higher ratio: 52.8 mg oral morphine ÷ 30 = 1.76 mg oral buprenorphine
Clinical Considerations
Partial Agonist Properties: Buprenorphine is a partial mu-opioid receptor agonist with a ceiling effect for respiratory depression but not necessarily for analgesia 1. This makes it potentially safer than full agonists in terms of respiratory depression risk.
Renal Function: Buprenorphine is primarily metabolized in the liver and excreted in the stool, making it one of the safest opioids for patients with renal impairment 1.
Dose Limitations: The NCCN guidelines recommend limiting transdermal buprenorphine to a maximum of 20 mcg/hour due to concerns about QT prolongation 1.
Conversion Complexity: The NCCN panel notes that dose conversion from other opioids to buprenorphine can be complex and suggests pain specialty consultation for complex cases 1.
Practical Application
When converting from Butrans 20 mcg/hour to oral buprenorphine:
- Remove the transdermal patch
- Begin oral buprenorphine at 1.6-1.8 mg daily, divided into 3-4 doses
- Monitor for:
- Adequate pain control
- Withdrawal symptoms
- Side effects such as sedation, nausea, or constipation
Potential Pitfalls
Precipitated Withdrawal: As a partial agonist, buprenorphine can displace full agonists from receptors without fully activating them, potentially causing withdrawal in opioid-dependent patients.
Ceiling Effect: Higher doses may not provide additional analgesia but could increase side effects.
Individual Variability: There is significant interpatient variability with buprenorphine 3, so close monitoring and dose adjustment may be necessary.
QT Prolongation: Monitor for QT prolongation, especially in patients with cardiac risk factors or on other medications that affect QT interval.
The conversion between transdermal and oral buprenorphine requires careful consideration of the patient's pain control, side effect profile, and individual response to ensure optimal outcomes in terms of morbidity, mortality, and quality of life.