What is the recommended dosing for rotating a patient from MS‑Contin (morphine sulfate controlled‑release) 30 mg twice daily to OxyContin (oxycodone controlled‑release)?

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Opioid Rotation from MS Contin 30mg BID to OxyContin

For a patient on MS Contin 30mg twice daily (total 60mg/day oral morphine), rotate to OxyContin 30mg daily given as 15mg twice daily, which represents a 25% dose reduction from the calculated equianalgesic dose to account for incomplete cross-tolerance. 1

Step-by-Step Conversion Protocol

Calculate Total Daily Morphine Dose

  • Current regimen: MS Contin 30mg BID = 60mg oral morphine per day 1

Apply Equianalgesic Conversion Ratio

  • Oral morphine to oral oxycodone ratio is 2:1 (morphine is half as potent as oxycodone) 2, 3
  • Calculated equianalgesic dose: 60mg morphine ÷ 2 = 30mg oxycodone per day 2

Reduce for Incomplete Cross-Tolerance

  • Reduce the calculated equianalgesic dose by 25-50% when rotating between opioids 1, 2
  • For well-controlled pain with minimal side effects, use a 25% reduction 1
  • For poorly controlled pain or significant side effects, use a 50% reduction 1
  • Recommended starting dose: 30mg oxycodone × 0.75 (25% reduction) = 22.5mg daily, rounded to 20-30mg daily 1

Prescribe OxyContin Regimen

  • OxyContin 10mg twice daily (20mg total) to 15mg twice daily (30mg total) is the appropriate starting range 1, 4
  • The 25% reduction (30mg daily) is preferred if pain is currently well-controlled 1
  • The 50% reduction (15mg daily as 10mg BID) is preferred if there are significant opioid side effects or concerns about tolerance 1

Breakthrough Medication Requirements

Prescribe immediate-release oxycodone at 10-20% of the total 24-hour dose for breakthrough pain, available every 4 hours as needed. 1, 5

  • For OxyContin 15mg BID (30mg total daily): breakthrough dose = 3-6mg immediate-release oxycodone every 4 hours PRN 1
  • For OxyContin 10mg BID (20mg total daily): breakthrough dose = 2-4mg immediate-release oxycodone every 4 hours PRN 1
  • If more than 3-4 breakthrough doses are required per day, increase the scheduled OxyContin dose by 25-50% 1, 2

Titration and Monitoring Protocol

Initial 24-48 Hour Period

  • Monitor closely for inadequate pain control and opioid-related adverse effects during the first 24-48 hours 1
  • Titrate liberally and rapidly to analgesic effect if pain remains severe or inadequately controlled 1
  • Review total daily opioid consumption (scheduled plus breakthrough doses) every 24 hours 5

Dose Adjustments

  • Increase the baseline OxyContin dose based on total breakthrough medication usage 1, 5
  • Add the total daily breakthrough oxycodone to the scheduled dose, then redistribute as twice-daily dosing 5
  • Example: If patient uses 30mg OxyContin daily plus 12mg breakthrough oxycodone, increase to OxyContin 21mg BID (42mg total daily) 5

Steady State Considerations

  • Steady state is achieved in approximately 24 hours for OxyContin (5 half-lives of oxycodone's 3-5 hour half-life) 1, 3
  • Reassess pain control and side effects at 24 hours, 48 hours, and 5-7 days 1

Critical Safety Considerations

Prophylactic Bowel Regimen

  • Institute stimulant laxative (senna) plus stool softener (docusate) prophylactically at initiation 2, 1
  • Start with senna/docusate 2 tablets every morning, maximum 8-12 tablets per day 2
  • Constipation does NOT improve over time with opioids and requires ongoing management 2

Monitoring for Adverse Effects

  • Common side effects include nausea, constipation, drowsiness, vomiting, pruritus, and dizziness 3
  • Oxycodone causes somewhat less nausea, hallucinations, and pruritus than morphine 3
  • Most side effects (except constipation) improve within days to weeks 2, 1

Special Population Considerations

  • No dose reduction needed in elderly patients or those with moderate hepatic or renal failure 3
  • However, avoid morphine (not oxycodone) in patients with renal disease due to accumulation of morphine-6-glucuronide 2, 1

Common Pitfalls to Avoid

Do Not Skip the Dose Reduction

  • Never use a 1:1 conversion without dose reduction – this ignores incomplete cross-tolerance and risks opioid toxicity 1
  • The 25-50% reduction is mandatory, not optional 1, 2

Do Not Use Extended-Release for Titration Alone

  • While controlled-release oxycodone CAN be used for titration (unlike transdermal fentanyl), always provide immediate-release breakthrough medication during the conversion period 2, 1, 6
  • Dose adjustments should occur no more frequently than every 24 hours 5

Do Not Forget Tablet Administration Instructions

  • OxyContin tablets must be swallowed whole and must not be broken, chewed, or crushed 4, 3
  • Breaking or crushing destroys the controlled-release mechanism and can cause rapid release of a potentially fatal dose 4

Do Not Underprescribe Breakthrough Medication

  • The breakthrough dose should equal the full 4-hourly equivalent (10-20% of daily dose), not a smaller amount 1, 5
  • Underdosing breakthrough medication leads to inadequate pain control and patient suffering 5

When to Consider Alternative Strategies

If Conversion Fails

  • If pain remains inadequately controlled after 2-3 dose adjustments, consider rotation to a different opioid (hydromorphone, methadone) or refer to pain specialist 1
  • If significant side effects persist despite dose adjustment, consider opioid rotation rather than continuing to escalate 2, 1

Adjuvant Analgesics

  • Consider adding gabapentin (300-1200mg TID) or pregabalin (75-300mg BID) for neuropathic pain components 1
  • Consider adding duloxetine (30-60mg daily) or nortriptyline (25-100mg nightly) for neuropathic pain 1

References

Guideline

Opioid Rotation Guidelines

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Research

Oxycodone: a pharmacological and clinical review.

Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico, 2007

Guideline

Opioid Dosing Regimens for Pain Management

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

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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