10.3 Pain Management & Opioids

Key Takeaways

  • Use a modernised WHO-style ladder: optimise non-opioid and adjuvant strategies first for most chronic non-cancer pain; match intensity and mechanism of pain to the regimen.
  • Paracetamol and NSAIDs have real risks (hepatic toxicity in overdose/misuse; GI, renal and cardiovascular harm with NSAIDs) — counsel maximum doses and comorbidities.
  • Distinguish weak and strong opioids conceptually; S8 controlled-drug supply rules apply to many strong opioids — legal compliance is non-negotiable.
  • Anticipate opioid-induced constipation and offer prophylaxis; educate on overdose risk and naloxone access where appropriate.
  • Neuropathic pain often needs different agents (e.g. amitriptyline, duloxetine, gabapentinoids) rather than escalating opioids alone.
Last updated: August 2026

10.3 Pain Management & Opioids

Quick Answer: Start with non-drug care + non-opioids (paracetamol/NSAIDs when appropriate), add adjuvants for neuropathic pain, and reserve opioids for carefully selected indications with goals, review dates, and risk mitigation. Know paracetamol ceilings, NSAID organ risks, S8 controls, constipation prophylaxis, overdose + naloxone, and that neuropathic pain often needs amitriptyline, duloxetine or gabapentinoids rather than endless opioid escalation.

Pain is one of the most frequent community presentations. Intern Written items test whether you can match medicine to pain type, minimise harm, and comply with controlled-drug law while remaining patient-centred.

Modernised WHO-style analgesic approach

The classic WHO cancer pain ladder (non-opioid → weak opioid → strong opioid) is still a useful teaching scaffold, but modern practice for chronic non-cancer pain emphasises:

  1. Assess pain type (nociceptive, neuropathic, nociplastic/mixed), severity, function, red flags, and psychosocial context.
  2. Non-pharmacological care first-line or concurrent: activity pacing, physiotherapy, heat/cold, psychological strategies, sleep, weight management where relevant.
  3. Non-opioid analgesics and disease-specific treatment of the cause.
  4. Adjuvants for neuropathic features.
  5. Opioids only when benefits are likely to outweigh harms, with defined goals (function, not only pain score), time-limited trials, and exit plans.

For acute severe pain (trauma, post-operative, cancer-related pain pathways), opioids may be appropriate earlier — the exam still expects risk counselling and legal compliance.

Paracetamol and NSAIDs — not “harmless basics”

Paracetamol

Effective for many mild–moderate pains and often preferred when NSAIDs are unsuitable. Risks centre on hepatotoxicity in overdose, in chronic supra-therapeutic dosing, and in high-risk hosts (malnutrition, chronic heavy alcohol use, interacting products with hidden paracetamol).

Counselling:

  • State the maximum daily dose clearly (product-specific; many adult OTC products use 4 g/day as a traditional ceiling — check current labelling and AMH, and lower in risk groups as advised).
  • Check combination products (cold/flu, opioid combinations) to avoid double-dosing.
  • Suspect intentional or accidental overdose → urgent emergency referral; antidote pathways are time-critical in hospital.

NSAIDs

Examples: ibuprofen, naproxen, diclofenac, meloxicam, celecoxib (COX-2 selective). Useful for inflammatory pain but carry:

Risk domainPractical points
GastrointestinalDyspepsia, ulcer, bleeding — higher with age, prior ulcer, corticosteroids, anticoagulants, SSRIs
RenalReduce glomerular filtration in volume depletion, heart failure, CKD; caution with ACEI/ARB + diuretic (“triple whammy”)
CardiovascularIncreased thrombotic risk with some NSAIDs, especially longer use / higher CV risk patients
AsthmaAspirin/NSAID-exacerbated respiratory disease in susceptible people
PregnancyAvoid especially later pregnancy unless specialist-directed

Prefer lowest effective dose and shortest duration; consider gastroprotection strategies when indicated by the prescriber.

Weak vs strong opioids — conceptual map

“Weak” opioids historically include codeine and tramadol (and related agents). They still cause sedation, constipation, dependence, and respiratory depression risk, especially with other CNS depressants. Tramadol has additional seizure and serotonergic risks.

Strong opioids include morphine, oxycodone, hydromorphone, fentanyl, methadone, buprenorphine (context-dependent), and others. High-yield counselling:

  • Start low, go slow in opioid-naïve patients; beware cumulative sedation with benzodiazepines and alcohol.
  • Tolerance and physical dependence are expected with continuous use; addiction/opioid-use disorder is a related but distinct risk requiring screening and careful supply.
  • Modified-release products must not be crushed or chewed (dose dumping).
  • Transdermal fentanyl is for opioid-tolerant patients in appropriate indications — dangerous if misused in naïve patients.
  • Breakthrough vs background dosing concepts matter in palliative and acute settings.

S8 controls reminder

Many strong opioids are Schedule 8 (controlled drugs) in Australia. Interns must know the legal supply framework at high level (valid prescription requirements, quantity/interval scrutiny, jurisdiction-specific real-time monitoring, secure storage, recording, and forgery vigilance). If legal elements are incomplete, do not supply — clarify with the prescriber. Legal detail is reinforced in the schedules chapter; here the clinical exam point is that therapeutic intent never overrides S8 compliance.

Constipation prophylaxis

Opioid-induced constipation is common and persistent (tolerance to constipation is limited). Best practice anticipates it:

  • Counsel on fluids, fibre, and mobility where suitable.
  • Recommend or ensure a plan for stimulant ± softener laxatives as appropriate (e.g. senna with docusate patterns — check AMH).
  • Do not wait until severe faecal loading develops.
  • Red flags (absolute constipation with vomiting, severe abdominal pain) need medical assessment.

Overdose risk and naloxone

Opioid overdose: reduced consciousness, slow/shallow breathing, miosis, snoring/gurgling, blue lips. Immediate actions: call emergency services, support airway/breathing per first-aid training, and administer naloxone if available and indicated.

Pharmacy role in harm reduction:

  • Educate patients and carers on not mixing opioids with alcohol/benzodiazepines.
  • Discuss safe storage away from children and others.
  • Support access to take-home naloxone programs where available and indicated (including people on high-dose opioids, history of overdose, or using opioids with other sedatives).
  • Counsel that naloxone is temporary — emergency care is still required after response because opioids may outlast naloxone.

Multimodal and neuropathic approaches

Multimodal analgesia combines complementary mechanisms (e.g. paracetamol + NSAID ± regional techniques ± low-dose opioid ± adjuvant) to improve control and reduce opioid load.

Neuropathic pain agents (high-level)

Neuropathic pain (burning, shooting, allodynia) often responds poorly to opioids alone.

Agent classExamplesCounselling / monitoring concepts
TCAsamitriptyline (often low dose for pain)Sedation, anticholinergic effects, falls, cardiac caution, suicide risk in overdose
SNRIsduloxetineNausea, blood pressure, serotonergic interactions, withdrawal if stopped abruptly
Gabapentinoidsgabapentin, pregabalinDizziness, sedation, misuse potential, renal dosing, respiratory depression risk with opioids

Titrate slowly; set expectations that benefit may be partial; review efficacy and adverse effects; avoid automatic long-term continuation without benefit.

Putting scenarios together

High-yield stems: chronic back pain escalated on oxycodone without functional goals; NSAID triple whammy in an older person; paracetamol combination product overdose risk; missing S8 prescription elements; constipation ignored for weeks; gabapentinoid + opioid + benzodiazepine sedation stack; tramadol + SSRI serotonin risk. Correct answers prioritise mechanism-matched therapy, harm reduction, and legal safety over reflexive opioid escalation.

Test Your Knowledge

Which approach best reflects a modernised analgesic strategy for many people with chronic non-cancer musculoskeletal pain?

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D
Test Your Knowledge

A patient taking an ACE inhibitor and a thiazide diuretic wants continuous high-dose ibuprofen for knee pain. What is the main concern?

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B
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D
Test Your Knowledge

When initiating a regular strong opioid for severe pain, which supportive care point is most characteristic?

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D
Test Your Knowledge

A patient describes burning, shooting leg pain with allodynia after shingles. Which statement is most accurate?

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B
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D