Opioid Conversion
Opioid conversion (rotation) involves switching between opioid formulations or agents, requiring knowledge of equianalgesic ratios and dose reduction for incomplete cross-tolerance to ensure safe and effective pain management.
Key Facts
Opioid conversion is needed when: changing route (oral → SC/IV), switching opioid (rotation for side effects), or converting between preparations Oral morphine to SC morphine: divide by 2 (e.g. 60mg oral/24h = 30mg SC/24h) Oral morphine to oral oxycodone: divide by 1.5-2 (e.g. 30mg morphine = 15-20mg oxycodone) Oral morphine to fentanyl patch: 60mg oral morphine/24h ≈ 25mcg/h fentanyl patch (72-hourly) Oral morphine to SC diamorphine: divide by 3 (e.g. 60mg oral morphine = 20mg SC diamorphine) Incomplete cross-tolerance: when switching opioids, reduce calculated equianalgesic dose by 25-50% (except fentanyl patches — manufacturer conversion used) Always calculate and document: show working; use local guidelines/conversion charts Breakthrough dose: always 1/6th of total 24-hour opioid dose in morphine equivalent, given as immediate-release preparation
Overview
Key Facts
Opioid conversion is a high-risk prescribing activity. Errors in conversion cause significant harm. Always use conversion tables, show calculations, and seek advice if unsure.
Epidemiology
- Opioid rotation is needed in approximately 20-30% of patients on long-term opioids
- Common reasons: side effects (nausea, confusion, myoclonus), renal impairment (accumulation of metabolites), route change (inability to swallow)
Aetiology
Indications for opioid conversion:
- Route change: oral to subcutaneous/transdermal (swallowing difficulty, bowel obstruction, dying patient)
- Opioid rotation: intolerable side effects despite dose titration, poor analgesia despite dose escalation, renal impairment (morphine → oxycodone or fentanyl), development of opioid-induced hyperalgesia
- Formulation change: immediate-release to modified-release
Pathophysiology
- Incomplete cross-tolerance: different opioids act on different μ-receptor subtypes and have different receptor binding profiles; tolerance to one opioid does not fully transfer to another
- This is why dose reduction (25-50%) is needed when switching opioids
- Renal impairment: morphine-6-glucuronide (active metabolite) accumulates → toxicity; switch to oxycodone, fentanyl, or buprenorphine (hepatically metabolised)
- Fentanyl: highly lipophilic; onset and offset depend on tissue distribution; requires stable pain (not for titration)
Clinical Presentation
When to Convert
- Patient unable to swallow (convert oral → SC or transdermal)
- Intolerable opioid side effects (rotate to different opioid)
- Renal impairment (switch from morphine to safer alternative)
- Starting syringe driver (convert oral to CSCI)
- Stepping up from weak to strong opioid
Assessment Before Conversion
- Current opioid, dose, route, frequency
- Total 24-hour opioid consumption (including breakthrough doses used)
- Pain control (adequate or inadequate?)
- Side effects
- Renal and hepatic function
- Reason for conversion
Red Flags
- Prescriber unsure of conversion ratios (seek specialist advice)
- Large dose conversions (high risk of error)
- Renal impairment + morphine (accumulation risk)
- Patient on mixed opioid agonists/partial agonists (buprenorphine + morphine — interactions)
Differential Diagnosis
| Scenario | Action |
|---|---|
| Pain controlled, switching route | Convert using equianalgesic table; no dose change |
| Pain controlled, switching opioid | Convert then reduce by 25-50% for cross-tolerance |
| Pain NOT controlled, switching opioid | Convert but do NOT reduce (or reduce less); titrate |
| Renal impairment on morphine | Switch to oxycodone, fentanyl, or buprenorphine |
| Starting syringe driver | Convert total 24h oral dose to SC equivalent |
Diagnosis / Investigation
Bedside
- Current pain score
- Current opioid dose (include all breakthrough doses used in last 24-48h)
- Calculate total 24-hour morphine equivalent dose
- Check renal function and hepatic function
Bloods
- U&Es (essential — renal function affects opioid choice)
- LFTs (hepatic function affects metabolism)
Imaging
- Not applicable to conversion itself
Special Tests
- Conversion calculation (show working, document clearly)
- Double-check with pharmacist or palliative care team
Management
Key Conversion Ratios
- Oral morphine → SC/IV morphine: ÷ 2 (e.g. 60mg PO = 30mg SC)
- Oral morphine → SC/IV diamorphine: ÷ 3 (e.g. 60mg PO = 20mg SC diamorphine)
- Oral morphine → oral oxycodone: ÷ 1.5-2 (e.g. 30mg morphine ≈ 15-20mg oxycodone)
- Oral oxycodone → SC oxycodone: ÷ 1.5-2 (e.g. 20mg PO = 10-13mg SC)
- Oral morphine → fentanyl patch: use conversion table (60-90mg/24h oral morphine = 25mcg/h patch)
- Oral morphine → oral hydromorphone: ÷ 5 (e.g. 50mg morphine ≈ 10mg hydromorphone)
Conversion Steps
- Calculate total 24-hour oral morphine equivalent (include MR + IR + breakthrough doses used)
- Apply conversion ratio to target opioid
- If rotating opioids: reduce by 25-50% for incomplete cross-tolerance
- Calculate new breakthrough dose (1/6th of new 24h total)
- Document calculation clearly in notes and prescription
- Monitor closely after conversion (pain, sedation, respiratory rate)
Pharmacological
- Fentanyl patch: apply when starting; takes 12-24 hours to reach therapeutic levels; continue oral opioid for first 12 hours
- Syringe driver (CSCI): convert oral dose to SC diamorphine (÷3) or SC morphine (÷2); run over 24 hours
- Renal impairment: avoid morphine; use oxycodone (÷1.5-2 from morphine), fentanyl, or alfentanil in CSCI
Surgical/Interventional
- Not applicable
Referral Criteria
- Complex conversions: palliative care pharmacist or specialist
- High-dose opioid conversions (>300mg oral morphine equivalent/day): specialist mandatory
- Methadone conversion: specialist only (complex, variable half-life)
- Mixed agonist/antagonist issues: specialist advice
Prognosis
- Safe opioid conversion maintains pain control while reducing side effects
- Errors in conversion can cause significant harm (overdose or under-dosing)
- Most conversions are straightforward with appropriate use of conversion tables
- Close monitoring in first 24-48 hours after conversion is essential
Other Relevant Information
Opioid Equianalgesic Conversion Table
| Opioid | Oral Dose | SC/IV Dose | Relative to 10mg Oral Morphine |
|---|---|---|---|
| Morphine | 10mg | 5mg | Reference |
| Oxycodone | 5-7mg | 3-5mg | 1.5-2× more potent |
| Diamorphine | N/A | 3.3mg | 3× more potent SC |
| Hydromorphone | 2mg | 1mg | 5× more potent |
| Codeine | 60-100mg | N/A | 10× less potent |
| Fentanyl patch | 12mcg/h ≈ 30-60mg/24h oral morphine |
Opioid Safety in Renal Impairment
| Opioid | Safety in CKD |
|---|---|
| Morphine | AVOID (M6G accumulates) |
| Codeine | AVOID (unpredictable metabolism) |
| Oxycodone | Use with caution (reduced dose) |
| Fentanyl | Preferred (hepatic metabolism) |
| Buprenorphine | Preferred (hepatic, no active metabolites) |
| Alfentanil | Preferred for CSCI in renal failure |