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Cancer pain & opioids flashcards

28 high-yield MRCP Part 1 cards from the Intellect Medicos Geriatrics & Palliative Care course. Try to answer each question before you open it — then study them properly with spaced repetition, which brings each card back just before you would forget it.

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  1. ______ pain is sudden, transient pain that occurs despite adequate baseline analgesia.

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    Breakthrough

    Why? It needs an immediate-release PRN dose on top of the regular modified-release opioid.

  2. Name three psychosocial factors that increase cancer pain perception.

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    Any three of: anger, anxiety, grief, depression, fatigue/insomnia, boredom, social isolation, lack of understanding.

    Why? Total pain has physical, psychological, social and spiritual parts; sleep, company, relaxation and clear information reduce it.

  3. What is the NICE starting regimen for strong opioids in a palliative patient with no comorbidities (normal renal and hepatic function)?

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    Oral modified-release morphine 20–30 mg/day plus immediate-release oral morphine 5 mg PRN for breakthrough pain.

    Why? NICE CG140: e.g. MR morphine 10–15 mg twice daily, with 5 mg IR morphine for rescue doses while titrating. Oral MR morphine is the first-line maintenance treatment.

  4. How is the breakthrough (PRN) opioid dose calculated?

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    One-tenth to one-sixth of the total 24-hour regular opioid dose (the course notes use one-sixth).

    Why? Give it as immediate-release of the same opioid when breakthrough pain occurs, every 2–4 hours as needed.

  5. A woman with metastatic breast cancer takes MR morphine 60 mg twice daily. Using the one-sixth rule, what is her immediate-release morphine breakthrough dose?

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    20 mg PRN.

    Why? 60 mg BD = 120 mg/24 h; one-sixth of 120 mg = 20 mg.

  6. Which drug must be prescribed for everyone started on a regular strong opioid?

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    A laxative (e.g. senna, or macrogol).

    Why? Opioid constipation is almost universal and tolerance to it does not develop.

  7. By how much should a strong opioid dose be increased when pain is not controlled?

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    By 30–50%.

    Why? Smaller steps under-treat pain; larger steps risk toxicity.

  8. A man takes MR morphine 20 mg twice daily and has needed two 5 mg doses of IR morphine in each of the last few days. What should his new regular MR morphine dose be?

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    MR morphine 25 mg twice daily (with a new PRN of about 8 mg, one-sixth of 50 mg, rounded to a practical dose).

    Why? Add regular (40 mg) and PRN (10 mg) use = 50 mg/24 h, then give half as each 12-hourly MR dose. This is a 25% rise, within the 50% limit.

  9. When re-titrating opioids, if the new total daily dose would be more than ______ above the previous dose, increase by only that amount.

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    50%

    Why? This caps each step and avoids opioid toxicity from a large jump.

  10. How do you convert an oral codeine or tramadol dose to the equivalent oral morphine dose?

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    Divide by 10.

    Why? Both are about 10 times weaker than oral morphine, e.g. codeine 240 mg/24 h ≈ oral morphine 24 mg/24 h.

  11. To convert oral morphine to subcutaneous morphine, divide by ______; to subcutaneous diamorphine, divide by 3.

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    2

    Why? SC morphine is twice and SC diamorphine three times as potent as oral morphine, e.g. oral morphine 15 mg ≈ SC diamorphine 5 mg.

  12. To convert oral morphine to subcutaneous morphine, divide by 2; to subcutaneous diamorphine, divide by ______.

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    3

    Why? SC morphine is twice and SC diamorphine three times as potent as oral morphine, e.g. oral morphine 15 mg ≈ SC diamorphine 5 mg.

  13. According to the course conversion chart, how do you convert oral morphine to oral oxycodone?

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    Divide by 1.5 (oral oxycodone is about 1.5 times as potent as oral morphine).

    Why? e.g. oral morphine 7.5 mg ≈ oral oxycodone 5 mg. SC oxycodone is twice as potent as oral oxycodone.

  14. A fentanyl 25 microgram/hour patch is roughly equal to ______ oral morphine per 24 h; a 12 microgram/hour patch to 30 mg.

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    60 mg

    Why? Transdermal fentanyl is about 100 times as potent as oral morphine.

  15. A fentanyl 25 microgram/hour patch is roughly equal to 60 mg oral morphine per 24 h; a 12 microgram/hour patch to ______.

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    30 mg

    Why? Transdermal fentanyl is about 100 times as potent as oral morphine.

  16. A buprenorphine 10 microgram/hour patch is roughly equivalent to how much oral morphine per 24 hours?

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    24 mg oral morphine per 24 h.

    Why? A 5 microgram/hour patch ≈ 12 mg/24 h; the conversion scales linearly.

  17. How potent is SC alfentanil compared with SC diamorphine?

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    About 10 times more potent (SC alfentanil 1 mg ≈ SC diamorphine 10 mg).

    Why? Alfentanil is used in syringe drivers in severe renal impairment, so the conversion matters.

  18. Which opioid side effect does NOT usually improve with continued use?

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    Constipation.

    Why? Tolerance develops to nausea and drowsiness over days, but not to the gut effect, so laxatives are continued.

  19. Name four signs of opioid toxicity.

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    Any four of: drowsiness/sedation, confusion or hallucinations, pinpoint pupils (miosis), respiratory depression, myoclonus, hypotension, bradycardia, urinary retention.

    Why? In palliative care, new drowsiness, confusion or myoclonus are the early clues, often after a dose rise or worsening renal function.

  20. What is the antidote for opioid toxicity?

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    IV naloxone.

    Why? Naloxone is a competitive opioid receptor antagonist. Its half-life is shorter than most opioids, so repeat doses or an infusion may be needed.

  21. Why is morphine risky in renal impairment?

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    Its active metabolites (morphine-3- and -6-glucuronide) are renally excreted and accumulate.

    Why? Accumulation causes sedation, respiratory depression and neurotoxicity (myoclonus, confusion, hallucinations).

  22. Which opioids are preferred in severe renal impairment (eGFR below 30)?

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    Alfentanil, fentanyl or buprenorphine.

    Why? They are mainly metabolised by the liver and have little renally cleared active metabolite, so they accumulate far less than morphine in renal failure.

  23. According to the notes, which strong opioid can be used in mild to moderate renal impairment (eGFR 30–60)?

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    Oxycodone (at a reduced dose).

    Why? Oxycodone has fewer active renally cleared metabolites than morphine. The notes also list meptazinol, a partial agonist rarely used in UK palliative care.

  24. Which adjuvant analgesics are used for neuropathic cancer pain?

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    Amitriptyline, duloxetine, gabapentin or pregabalin (the course notes name a tricyclic or gabapentin).

    Why? They act on nerve-pain pathways that respond poorly to opioids alone. NICE CG173 offers a choice of these four as initial treatment.

  25. Which drug is used for intestinal colic in palliative care?

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    Hyoscine butylbromide.

    Why? It is an antimuscarinic antispasmodic that relaxes gut smooth muscle and does not cross the blood–brain barrier.

  26. Which adjuvant is used for pain from liver capsule stretch (hepatic metastases) or raised intracranial pressure?

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    Dexamethasone.

    Why? It reduces tumour-related oedema and swelling.

  27. Which drugs are used for painful muscle spasm in palliative care?

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    Diazepam or baclofen.

    Why? Both reduce skeletal muscle tone (GABA-mediated).

  28. Name the three main treatment options for metastatic bone pain.

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    Strong opioids, bisphosphonates and radiotherapy.

    Why? Single-fraction palliative radiotherapy gives good relief for localised bone pain; bisphosphonates help widespread bone metastases.

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