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chemotherapy goals
to kill cancer cells with limited injury to normal tissues
cure, control, or palliation (relieve pain)
chemotherapy barriers
not possible to know if 100% of cells are killed
limited dosing due to toxicity and damage to normal cells
drug resistance over time
solid tumours have low growth fraction
high tumor load hard to treat
strategies to help chemotherapry
intermittent therapy
allow normal cells to grow between treatment
combination therapy
reduce resistance, inc cancer cell kill, less toxicity to normal cells
dosing schedules
regional drug delivery
localized delivery to decrease systemic effects
chemotherapy toxicities
myelosuppresion
neutropenia, thrombocytopenia, anemia
GI dysfunction
stomatitis, diarrhea, n/v
alopecia
hair loss
reproductive toxicity
etraversion
Iv therapy become interstital
carcinogensis
can inmate or promote cancer
bone marrow suppression with chemotherapy
myelosuppression - chemo toxic to bone marrow due to tissue rapidly proliferating and active
reduce neutrophil, erthtrocytes and plateletes
risk for infection (low neutrophil) bleeding (low platelet) + anemia (low erythrocyte)
use hematopoietic growth factor for medh
hematopoietic growth factors
colony stimulating factors / biologic response modifiers - stimulate hematopoietic stem cells of bone marrow
erythropoietic growth factors / erythropoietin - stem RBC production, rarely for cancer patients
leukopoteic growth factors / filgrastim - neutrophil production stimulated
thromboporietic growth factors - stimulate platelet prodcution
neutropenia
neutrophils below 500, life span 2-3 days - with cytotoxic drugs, neutropenia first happens
Nadir - lowest neutrophil count at day 10-14
at highest risk during nadir + risk from normal flora of body
neutrophils monitored carefully, hold chemotherapy until improve
signs of infection, 38 C, pus, abscesses, infiltrates
nursing considération w neutropenia
educate infection + risk + avoiding others
38 C report immediately
hygiene
reverse isolation (protect patient)
avoid food w pathogen risk - meat, veggies, fruit
cultures on patient
filgarastrim (Neupogen)
leukoporietic growth factor therapy
identical to naturally occurring granulocyte colony stimul factor
elevates neutrophil count, acto n bone marrow
dec risk of injfection
caution with cancer originating in bone marrow
IV or SC
thrombocytoponea
low circulating platelets, inc risk of bleeding
common - bleeding gum and nose
monitor hematuria, gi bleed, hemoptysis (cough blood)
avoid meds that inc bleeding, vigour tooth brush, shaving, iv insert, avoid injections, overinflated bp - bruising
oprelevekin / neumega
thromboporietic growth factor therapy - identical to cytokine prod in bone marrow
stim platelet production, proliferation of hematopoietic stem cells and inc megakaryocytic synthesis (become platelets)
not for patients with myeloid cancers (bone marrow/blood cancer)
dec thrombocyopenia and dec need for platelet transfusion
SC
anemia
dec erythrocyte
less common than neutropenia and thrombocypotneia (long life span 120 days) - full recovery happen before levels go low
monitor signs of anemia - fatigue, pallor, SOB, HGB
o2 if needed
erythropoietin/ Epoetin alpha
ertyhopoeitic growth factor therapy - hormone, stimulate RBC production in bone marrow
not for patients with myeloid malignancies + leukemias (blood/bone marrow)
admin iv or SC
increases risk of stroke, HF, blood clot, MI, death
can accelerate tumour progression + shorten life in some patients
not for patients except palliative
stomatitis
inflamed oral mucous, 2-3days after chemo - continue up to more than 2 weeks
inflammation to ulcer, lead to infection
pain when eating, speaking, swallowing - weigh patient and intake
diarrhea with chem
destruction of epithelial lining - impaired absorption of nutrient, fluid lead to diarrhea
impair nutrition, hydration, lead to infection
nausea and vomitting with chemo
with chemotherapy due to stimulation of CTZ, immeidcatley with first dose and contiue for hours to days
anticipatory emesis (prior), acute emesis (within treatment 24 Horus), delayed (1 day after to a few days
use antiemetics 30 min prior to chemo
aprepitatnt and dexamethasone and ondastron - high risk emesis comb
alopecia
hair loss, from injury to follicles because rapid proliferation
with many cytotoxic meds
7-10 days start of treatment, peak at 1-2 months
1-2 month after, reverse alopecia (grow back)
reproductive toxicity
cytoxitoc med interfere w early embryo development
fetal malformation, death (first trim common)
low risk after 18 weeks
irreversible sterility in men
affects ovaries - amenorrhea (no period) + menopausal symptom
extravasation
vesicants, highly reactive
admin via central line to lower risk of direct contact to tissues
extroversion - leakage / infliltration of drug (vesicant) from blood vessel to surrounding area, major tissue damage
pain, infection, loss of mobility, necrosis, sloughing
carcinogenesis
cytotoxic drugs damage DNA, promote cancer to develop, years after treatment
with alkylating agents comonly
type of anticancer cytotoxic drug / chemotherapry
cell cycle phase specific - toxic to cells passing through phases of cell cycle
bc its cell phase specific, cannot target inactive cells in g0 phase
cell cycle phase nonspecific - act at any part of phase including g0
given in combination
doxorubicin
treats leukaemia, lymphoma and solid breast and ovarian tumours in adult and paediatric patients
cardiotoxicity - acute (arythmias last 2 weeks) or delayed and lead to HF
assess egg changes, chest pain, irregular HR, signs of HF, VS
paclitaxel
used in advanced ovarian cane,r breast cancer, non smalll cell lung cancer
cardiotoxitcity - acute (arthymias, Brady) or delayed HF
ekg changes, chest pain, HR, vs, HF signs
neuropathy - autonomic nerve dysfunction, in 30-50% of people - contipaiton, urinary hesitancy
risk of severe hypersensitive reactions - hypotension, dynspea, hives, angioedema (rapid swelling skin, mucous, airways)
consider glucocorticoid or histamine receptor antagonist
monitor signs of hypersensitivity
vincristine
chemo for hematologic cancers (Hodgkin and non-hodghkin) - little effect on bone marrow
toxic to peripheral nerves, neuropathy - autonomic nerve dysfunction, in 30-50%. of people, constipation and urianry hesitancy
almost all patients experiences sensory or motor dyfynciton
minimal brain injury bc rarely enter CNS
assess reflex, sensory and motor nerve injruy
cisplatin
chemo - treat bladder, ovarian, testicular cancer
toxic to peripheral nerves
assess reflex, sensory and motor nerve injury
major nephrotoxic properties - Renal damage and renal failure
assess I and o, serum cr, fluid overload, uremias,
minimize renal damage with pre infusion iv hydration (also help with fluid loss due to vomitting)
highly emetic properties
ocular toxic and otoxic - vision and hearing loss
risk of severe hypersensitive reactions - hypotension, dynspea, hives, angioedema (rapid swelling skin, mucous, airways)
consider glucocorticoid or histamine receptor antagonist
monitor signs of hypersensitivity
cyclophosphamide
commonly used with combination to treat variety of ccancer
hard on bladder, lead to bladder injury - hemorrhagic cystitis - inflammation and bleeding of bladder lining
assess urine output, hematuria, increase fluids
bleomycin
treats testicular cancer and Hodgkin lymphoma
canc cause severe injury to lungs in 10% patients
starts as pneuomintis (inflammation) progress to fibrosis or scarring, respiratory failure/death
assess pulmonary function, CXR (chest X-ray), vital signs
tamoxifen
breast cancer hormonal therapy - anti estrogen
used for premenopausal women mainly
block estrogen receptor on breast cancer
risk of endometrial cancer and thrombosis
hot flash, fluid retention, menstrual irregularities, vaginal discharge, n/v
not safe with pregnancy
oral, adjuvant therapy to suppress growth of cancer cells after surgery for years
longer treatment decrease reuccurance
not same toxicity as other chemotherapy agents
anastrozole
aromatase inhibitor
ONLY for post menopausal women - block production of estrogen from adrgenic precursors
does not block estrogen production from ovaries - why they dont benefit premenopausal women (they produce estrogen from ovaries)
less hot flashes, weight gain, N/V
no estrogen at all = no endometrial cancer or thromboembolic events
musk pain, osteoperiois, fracture risk