Oncology 4 Flashcards

1
Q
  1. Harmful properties of chemotherapeutic drugs.
  2. Where can they been excreted/secreted in patients receiving chemotherapeutic treatment?
A
  1. Mutagenic, abortifacient, teratogenic, carcinogenic, irritant, vesicant.
  2. Faeces, urine, saliva.
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2
Q

What is the individual prescribing the product responsible for?

A

Ensuring their own health and safety, as well as that of other staff, the patient, the client, other individuals in the patient’s household and the environment.

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3
Q

Examples of safe handling.

A
  • Protocols for spillages and readily prepared spill-kits.
  • Pregnant women should NEVER handle cytotoxic drugs.
  • Appropriate chemo-specific PPE.
  • All employees and owners must be informed of risks.
  • Provide owner guidance to limiting exposure w/ saliva, urine, vomit, faeces.
  • Closed systems for drawing up and administering meds.
  • Never re-cap needles (risk accidental inoculation).
  • Purple flagged containers for disposal.
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4
Q
  1. Toxicity relating to which area of the body are most common in patients receiving chemo?
  2. What other systems can be affected by chemotherapeutic drugs?
  3. What protocols help reduce the effects of chemo on body systems?
A
  1. GIT and bone marrow.
  2. Dermatological, urinary, cardiac, renal, hepatic.
  3. Recovery time gives tissues time to repair.
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5
Q
  1. GIT toxicity as a result of chemo clinical signs.
  2. How is GIT toxicity a contributing factor of sepsis risk in chemo patients?
  3. Management of clinical signs associated w/ GIT?
  4. Examples of chemo drugs that can cause GIT toxicity.
A
  1. Vomiting, diarrhoea, nausea, stomatitis.
  2. Decreased gut integrity increases risk of bacterial translocation into the blood and sepsis.
  3. Depends on side effects encountered e.g. nausea managed w/ anti-emetics.
  4. Doxorubicin, cisplatin (stimulate chemoreceptor trigger zone).
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6
Q
  1. Examples of drugs that can cause bone marrow toxicity.
  2. How do we check patients bone marrow condition before chemo?
  3. Examples of conditions caused by chemo relating to bone marrow toxicity.
A
  1. Doxorubicin, vinblastine, cyclophosphamide.
  2. Routine haematology.
  3. leukopenia, neutrophilia.
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7
Q
  1. Dermatological effects of chemo drugs.
  2. Examples of chemo drugs that can cause dermatological problems.
A
  1. Many are irritants and vesicants.
    Tissue inflammation/even necrosis if administered inappropriately e.g. if the drug extravasates during IV admin.
  2. Vincristine, cisplatin, doxorubicin.
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8
Q
  1. Clinical signs of urinary toxicity due to chemo drugs.
  2. Example of chemo drug that can cause urinary toxicity.
  3. How do we monitor patients on these drugs and ensure we cause as little damage as possible.
A
  1. Stranguria, dysuria, pollakiuria, haematuria.
  2. Cyclophosphamide.
  3. Provide dipsticks to owner to use daily to look for signs of haematuria, and at first sign of haematuria, that drug is stopped and different drug used.
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9
Q
  1. Types of cardiac toxicity that chemo drugs can cause.
  2. Give example of chemo drug and its cardiac effect. – mitigation in place to help reduce risk.
A
  1. Acute and chronic.
  2. Doxorubicin can cause tachyarrhythmias (acute) and cardiomyopathies which may lead to congestive heart failure (chronic). – Doxorubicin given slowly to avoid development of arrhythmias.
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10
Q
  1. Renal effects of chemo drugs.
  2. Examples of chemo drugs that have renal effect.
  3. Mitigations to help avoid renal effects.
A
  1. Some have potential to cause proximal tubular necrosis > irreversible loss of renal function > development of acute and/or chronic kidney disease.
  2. Cisplatin, methotrexate, doxorubicin (cats).
  3. Admin alongside IV fluids, monitoring urea and creatinine, avoid use of such drugs in patients w/ pre-existing renal disease.
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11
Q
  1. Hepatic effects of chemo drugs.
  2. Example of drug that can cause hepatotoxicity.
  3. Mitigations to help avoid hepatotoxicity.
A
  1. Transient or irreversible loss of liver function.
  2. Lomustine.
  3. Monitor hepatocellular enzymes, concurrent admin of anti-oxidant (e.g. SAMe = s-adenosyl methionine).
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