Cancer and Palliative Drugs Flashcards

1
Q

Paracetamol indications

A

Pain

Fever (anti-pyrexial)

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2
Q

Consequences/mechanism of paracetamol overdose

A

Liver failure:

  • Metabolised by cP45, forming a toxic metabolite which is eliminated
  • Overdose saturates elimination pathway
  • Toxic metabolite (NAPQI) causes liver necrosis
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3
Q

Paracetamol dose

A

0.5-1g ever 4-6 hours

MAX: 4g per day

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4
Q

Codeine indications

A

Mild-moderate pain (e.g. post-op)

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5
Q

Codeine MOA

A

Metabolised by liver to produce small amounts of morphine.

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6
Q

IV Codeine effects

A

Anaphylaxis-like reaction

DO NOT GIVE IV

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7
Q

Doses of codeine

A

Regular or PRN

30mg 4 hourly

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8
Q

Co-codamol doses

A

Combination of paracetamol and codeine

E.g. 15/500 = 15mg codeine, 500mg paracetamol

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9
Q

MST indications

A

Modified release morphine. Lasts 12 hours.

Chronic pain relief

Reduce breathlessness/anxiety in EOL and pulmonary oedema

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10
Q

Morphine MOA

A

Activates opioid μ receptors in CNS, reducing neuronal excitability and pain transmission.

Blunts response to hypoxia, reducing respiratory drive and breathlessness

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11
Q

Side effects of opioids

A

Nausea/vomiting (transient)

Constipation

Drowsiness

Itchy skin/sweating

Euphoria/hallucinations

Tolerance/dependence

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12
Q

MST contra-indications

A

Renal impairment (eGFR <50)

It is renally eliminated

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13
Q

MST doses

A

Determined by 24 hour use of immediate release morphine (e.g. oramorph).

Orally = dose is BD

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14
Q

Morphine doses at EOL

A

Opioid naive: 20-30mg SC over 24 hours

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15
Q

Oramorph indications

A

Immediate release morphine.

Acute, severe pain relief.
Lasts 20-30 mins.

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16
Q

Oramorph dose and administration

A

IV, IM, SC or oral

2-10mg depending on age, weight + background dose of morphine

17
Q

Metoclopramide drug type and MOA

A

Dopamine antagonist (prokinetic)

Prevents stimulation of d2 receptors in CTZ.

Prevents stimulation of d2 receptors in the gut, increasing gastric emptying.

18
Q

Metoclopramide indications

A

Chemotherapy induced n+v

n+v due to delayed gastric emptying (e.g. opioids, gastroparesis)

AVOID IN PARKINSON’s (crosses blood-brain barrier)

19
Q

Cyclizine drug type and MOA

A

Anti-histamine.

Blocks h1 receptors in VC

Some anti-muscarinic properties

20
Q

Cyclizine indications and dose

A

N+V due to vertigo, motion sickness and high ICP

Mechanical bowel obstruction (anti-muscarinic)

50mg 8 hourly

21
Q

Haloperidol drug type and indications

A

Dopamine antagonist (anti-psychotic)

N+V due to toxins, radiotherapy and metabolic causes (e.g. renal failure)

AVOID IN PARKINSON’s (crosses blood-brain barrier)

22
Q

Levomepromazine

A

Anti-emetic (anti-psychotic dopamine antagonist)

Wide spectrum, give when others have not worked

23
Q

Domperidone

A

Dopamine antagonist (prokinetic)

Chemotherapy induced n+v

n+v due to delayed gastric emptying (e.g. opioids, gastroparesis)

24
Q

Dexamethasone

A

Useful synergist

Chemotherapy induced n+v

n+v due to raised ICP (e.g. brain tumour)

25
Q

Drugs for EOL care (4)

A

Analgesia = diamorphine

Anti-emetic = levomeprozamine

Anti-secretory = hyoscine butylbromide

Anti-agitation = miadazolam