TextbookPalliative CareOpioid Conversion

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

ScenarioAction
Pain controlled, switching routeConvert using equianalgesic table; no dose change
Pain controlled, switching opioidConvert then reduce by 25-50% for cross-tolerance
Pain NOT controlled, switching opioidConvert but do NOT reduce (or reduce less); titrate
Renal impairment on morphineSwitch to oxycodone, fentanyl, or buprenorphine
Starting syringe driverConvert 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

  1. Calculate total 24-hour oral morphine equivalent (include MR + IR + breakthrough doses used)
  2. Apply conversion ratio to target opioid
  3. If rotating opioids: reduce by 25-50% for incomplete cross-tolerance
  4. Calculate new breakthrough dose (1/6th of new 24h total)
  5. Document calculation clearly in notes and prescription
  6. 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

OpioidOral DoseSC/IV DoseRelative to 10mg Oral Morphine
Morphine10mg5mgReference
Oxycodone5-7mg3-5mg1.5-2× more potent
DiamorphineN/A3.3mg3× more potent SC
Hydromorphone2mg1mg5× more potent
Codeine60-100mgN/A10× less potent
Fentanyl patch12mcg/h ≈ 30-60mg/24h oral morphine

Opioid Safety in Renal Impairment

OpioidSafety in CKD
MorphineAVOID (M6G accumulates)
CodeineAVOID (unpredictable metabolism)
OxycodoneUse with caution (reduced dose)
FentanylPreferred (hepatic metabolism)
BuprenorphinePreferred (hepatic, no active metabolites)
AlfentanilPreferred for CSCI in renal failure