Opioid toxicity and opioid-induced hyperalgesia in palliative care
Why opioid toxicity develops in palliative patients (renal accumulation of active metabolites, dose escalation, interactions), how to tell opioid-induced neurotoxicity and hyperalgesia from tolerance and disease progression, and the pharmacology behind dose reduction, rotation, naloxone titration and NMDA antagonists.
Tier 2Medical sciences concept
Written with AI assistance and fact-checked against the sources below. For exam study, not clinical decisions. How notes are made
At a glance
- Opioid toxicity in palliative care is usually iatrogenic and gradual: renal function falls, a dose is escalated, an interacting drug is added, or pain is relieved by radiotherapy or a nerve block so the same dose is now too much.
- Two pictures overlap. Classical mu toxicity (sedation, miosis, slow breathing) and opioid-induced neurotoxicity (OIN): myoclonus, delirium, hallucinations, allodynia and hyperalgesia.
- Opioid-induced hyperalgesia (OIH) is increased pain sensitivity caused by the opioid itself. Pain becomes diffuse and worsens as the dose goes up.
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Sources
- Therapeutic Guidelines: Palliative Care (eTG complete), version 5AU/NZTherapeutic Guidelines Limited, 2024 (version 5, December 2024)
- Faculty of Pain Medicine, ANZCA. Opioid CalculatorAU/NZFaculty of Pain Medicine, Australian and New Zealand College of Anaesthetists, accessed November 2026
- Lovell MR et al. Update of the Australian Guideline for the Management of Cancer Pain in Adults. Asia Pac J Clin Oncol 2026;22(5):705-716AU/NZWiley (Asia-Pacific Journal of Clinical Oncology), 2026 (online November 2025)
- Lee M et al. A comprehensive review of opioid-induced hyperalgesia. Pain Physician 2011;14:145-61American Society of Interventional Pain Physicians, 2011
- Australian Medicines HandbookAU/NZAustralian Medicines Handbook Pty Ltd, 2026
- Last updated
- 14 November 2026
What changed
- 14 November 2026 Personal emails, About story and Australian-style copy