Butrans (Buprenorphine Transdermal) Usage Guidelines
Overview and Formulations
Butrans is the transdermal patch formulation of buprenorphine specifically FDA-approved for chronic pain management, not for opioid use disorder treatment. 1 This distinction is critical—the transdermal patch cannot be prescribed off-label for addiction treatment, while sublingual formulations (tablets, films) are approved for opioid use disorder and can be used off-label for pain in divided doses every 6-8 hours. 1
Pain Management Applications
Chronic Pain Treatment
For chronic pain management, transdermal buprenorphine (Butrans) provides effective analgesia with a superior safety profile compared to full opioid agonists. 1
- Transdermal buprenorphine bypasses the 90% first-pass hepatic metabolism of sublingual formulations, potentially providing better analgesia. 1
- In systematic reviews, transdermal buprenorphine provided comparable pain relief to transdermal fentanyl and morphine but with fewer adverse events. 1
- The respiratory depression ceiling effect makes buprenorphine safer than full mu-opioid agonists in overdose situations. 1
Dosing for Chronic Pain
- Sublingual buprenorphine for chronic pain typically ranges from 4-16 mg daily (mean 8 mg) in divided doses, with 86% of patients achieving moderate to substantial pain relief. 1
- When maximum transdermal buprenorphine doses are insufficient, add or replace with high-potency full agonists (fentanyl, hydromorphone, or morphine) rather than discontinuing buprenorphine. 1
- Buprenorphine does not occupy all opioid receptors, allowing other opioids to provide additional analgesia when needed. 1
Perioperative Management
Current Consensus (2019)
The most recent expert consensus strongly recommends continuing buprenorphine therapy throughout the perioperative period regardless of formulation or indication. 1 This represents a major shift from older guidelines that recommended discontinuation.
Preoperative Management
- Continue buprenorphine at the current dose; it is rarely appropriate to reduce the dose preoperatively. 1
- Verify the maintenance dose with the patient's prescribing physician or addiction treatment program. 1
- Distinguish whether buprenorphine is prescribed for chronic pain versus opioid use disorder, as this affects discharge planning. 1
- Notify the addiction treatment program about admission, discharge timing, and any medications given that may appear on urine drug screening. 1
Intraoperative and Postoperative Analgesia
If analgesia is inadequate after optimizing multimodal adjunct therapies, initiate a full mu-agonist opioid while continuing buprenorphine at some dose. 1
- Use scheduled continuous dosing rather than as-needed orders. 1
- Expect higher opioid requirements and shorter dosing intervals due to opioid cross-tolerance and increased pain sensitivity. 1
- High-potency opioids (fentanyl, hydromorphone) are preferred when additional analgesia is needed. 1
- Avoid mixed agonist-antagonist opioids (butorphanol, nalbuphine) as they may precipitate acute withdrawal. 1
Four Management Options for Acute Pain
For patients on buprenorphine maintenance requiring opioid analgesia, choose based on anticipated pain duration and treatment setting: 1
- Continue buprenorphine and titrate short-acting full agonists (for short-duration pain only)
- Divide buprenorphine dose to every 6-8 hours to enhance analgesic properties
- Discontinue buprenorphine temporarily, use full agonist opioids, then convert back when acute pain resolves
- For inpatients: discontinue buprenorphine, initiate methadone 20-40 mg for opioid dependence, use short-acting opioids for pain, keep naloxone at bedside, convert back to buprenorphine before discharge
Discharge Planning
- Patients should ideally be discharged on buprenorphine, though not necessarily at their preoperative dose. 1
- Depending on analgesic requirements, discharge on a full mu-agonist may be necessary temporarily. 1
- For opioid use disorder patients, long-term buprenorphine treatment retention and harm reduction must be prioritized to prevent relapse. 1
Critical Drug Interactions and Precautions
Contraindications
Concomitant use of buprenorphine with QT-prolonging agents is contraindicated. 1
Significant Interactions
- Multiple drug-drug interactions can result in QT-interval prolongation, serotonin syndrome, paralytic ileus, reduced analgesic effect, or precipitation of withdrawal. 1
- Avoid strong CYP3A4 inducers and inhibitors as they significantly alter buprenorphine metabolism. 1
- Combining with serotonergic agents increases risk of serotonin syndrome. 1
Opioid Antagonist Considerations
- Concomitant use with opioid antagonists (naloxone, naltrexone) should be avoided except for clinically significant respiratory depression, as it precipitates withdrawal and reduces efficacy. 1
- Oral naltrexone should be held 3-4 days before surgery; intramuscular naltrexone requires 24-30 days. 1
Opioid Use Disorder Treatment
Switching Formulations for Pain Management
For patients on buprenorphine/naloxone for opioid use disorder who develop chronic pain, consider switching to transdermal buprenorphine alone for better analgesia. 1
When Buprenorphine is Inadequate
If patients on buprenorphine maintenance have inadequate analgesia despite optimized strategies, transition from buprenorphine to methadone maintenance. 1
Common Pitfalls to Avoid
- Never abruptly discontinue buprenorphine perioperatively in patients with opioid use disorder—this significantly increases relapse risk. 1
- Do not assume buprenorphine will block all analgesic effects of full agonists; it does not occupy all opioid receptors. 1
- Avoid underestimating opioid requirements in buprenorphine patients; they require higher doses at shorter intervals. 1
- Do not use mixed agonist-antagonist opioids in patients on buprenorphine maintenance. 1
- Reassure patients that their addiction history will not prevent adequate pain management—this reduces anxiety and improves cooperation. 1