chemotherapy Flashcards

1
Q

allopurinol indications

A
  • prevent recurrent attacks of gout
  • prevent uric acid and calcium oxalate renal stones
  • prevent hyperuricaemia and Tumour lysis syndrome pre chemo
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2
Q

MOA allopurinol

A
  • xanthine oxidase inhibitor. metabolises xanthine to uric acid. inhibiting = lower plasma uric acid and reduces precipitation of uric acid in the joints or kidneys
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3
Q

SE allopurinol

A
  • can trigger or worsen an acute attack of gout when starting . can be reduced by co prescribing NSAID or colchicine in initiation phase.
  • skin rash or SJS or TENS
  • allopurinol hypersensitivity syndrome = lofe threeatening - fever, eosinophilia, LNA, liver and skin issues
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4
Q

When should allopurinol not be started

A

acute attacks of gout

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5
Q

CI to allopurinol

A
  • recurrent skin rash or signs of more severe hypersesntiivvity
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6
Q

where is allopurinol metabolised and excreted

A
  1. liver

2. kidneys

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7
Q

reduced dose of allopurinol to which patients

A

renal impairment

hepatic impairment

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8
Q

interactions of allopurinol

A
  • azathioprines active metabolite mercaptopurinne is metabolised by xanthine oxidase therefore = increased risk of toxicity
  • co prescribe with ace-i and thiazides increase risk of hypersensitivity reaction and with amoxicillin increases risk of skin rash
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9
Q

what dose should you start allopurinol at

A

100mg daily

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10
Q

when should you give allopurinol as part of cancer therapy

A

pre chemo

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11
Q

when should allopurinol be taken

A

after meals

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12
Q

what drugs can cause acute attacks of gout

A
  • thiazodes, loops, low dose aspirin
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13
Q

methotrexate indications

A
  • DMRD for RA
  • Chemo for ca - leukaemia, lymphoma and some solid tumours
  • psoriasis that is resistant to other therapies
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14
Q

MOA methotrexate

A
  • inhibitis dihydrofolate reductase - prevents cellular replication
    also immunosupresses. and inhibits inflammatory mediators
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15
Q

SE methotrexate

A
  • mucosal damage, sore mouth, GI upset
  • BM supression

hyepersenitivity reactions - hepatitis, pneumonitis

ltm use - hepatic cirrhosis, pulmonary fibrosis

OD - as once weekly dose normally

neuro effects 0 headache,s eizure, coma

  • dose related effects with renal imapirment and hepatotoxicity

treat toxicity with folinic acid - and with hydration and urinary alkalinisation to enhance excretion

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16
Q

CI methotrexate

A
  • pregnancy
  • need contraception men and women
  • severe renal impairment

relative CI - abnormal liver function

17
Q

Interactions methotrexate

A
  • NSAis, penicillins - inhibits renal excretion - leads to toxicity
  • other folate antagonists
  • risk of neutropenia is increased if given with clozapine
18
Q

what seretonin 5HT3 receptor antagonists are used as antiemetics

A

ondansetron

granisetron

19
Q

Indications 5HT3RAN , antiemetics

A
  • N and v esp in general anesthesia and chemo
20
Q

MOA 5HT3RAN, antiemetics

A

blocks 5ht3r in chemoreceptor trigger zone. blocks 5ht release from gut which often stimulates the vagus nerve - activates vomiting by soleus nucleus

21
Q

why do Ondansetron and gansetron not work for motion sickness

A
  • 5ht is not involved in comms between vestibular system and vomiting centre. - this is where motion sickness originates from
22
Q

SE ondansetron etc

A
  • rare; constipation, diarrhoea and headaches
23
Q

what can 5h3ran do to the heart

A
  • prolong QT interval - so do not give wiht other drugs that do this
24
Q

typical starting dose of ondansetron

A

4-8mg 12hrly oral or IV. 1hr if possible before anticipated settings e.g. general anesthesia