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what temp counts as fever
anything =/> 38.3 (101) or =/> 38 (100.4) that remains for at least 1 hour
what is a big complication of cancer and what is it
neutropenia- a decreased number of neutrophils (less than 1000 cells/mm3) which is white blood cells. A severe neutropenia is less than 500 cells/mm3. And profound count is less than 100 cells/mm3
what are pts with neutropenia at risk for and how can we protect them
they are at high risk for infection and needs to be placed on neutropenic precautions
what is neutropenic precautions and how do we implement it
the goal is to protect the patient, so we gear up to not infect the patient
monitor pts temp because fever is an emergency
Restrict sick visitors from coming
not allow fresh plants/flowers from being in the hospital room
dedicated equipment for the patient
Neutropenia pt teaching
Take temp daily and notify provider of any temp over 100 degrees - fever with neutropenia requires hospitlization
avoid crowds and sick people
don’t consume raw foods
avoid yard work or gardening
don’t change the litter box
wash dishes using hot water or use a dishwasher
wash toothbrush in the dishwasher or use bleach solution to disinfect
what’s the standard treatment for neutropenia/fever
single broad spectrum IV antibiotic (monotherapy) until neutrophil count goes up
what is nadir
it’s the lowest point in cancer, typically referring to the lowest level of WBC count after chemotherapy. The nadir period occurs 1-2 weeks after a chemotherapy cycle. At this point, pts are at the highest risk for cancer
what is most common non-CNS cancer?
neuroblastoma - a cancer of the sympathetic nervous system that forms in neuroblasts, which are immature nerve cells most common in under kids under 5
signs and symptoms of neuroblastoma
** with this cancer, it often metastasizes (spreads) before diagnosis
fever
fatigue
decreased appetite and weight loss
limp/refusal to walk
blueberry muffin spots
hypertension
excessive sweating
orbital ecchymosis
how to diagnose neuroblastoma
imaging test - ultrasound, CT, MRI, and bone scan
biopsy to confirm diagnosis
what’s the treatment for neuroblastoma
intensive high dose chemotherapy
surgical removal tumor
radiation
stem cell transplant
antibody therapy
iodine 131 - MIGB therapy (high risk)
what’s the most common type of pediatric bone cancer
osteosarcoma that occurs at the end of a bone, typically in sites like the distal femur, proximal tibia, proximal humerus
osteosarcoma risk factors
teenagers, especially duringa growth spurt
arfican american or hispanic descent
what are the signs and symptoms of osteosarcoma
pain/tenderness at affected area
bone pain
swelling
fractures
limp when walking
decreased range of motion
how to diagnose osteosarcoma
imaging: x-ray, MRI, CT
confirmation: biopsy
how to treat osteosarcoma
initial surgery - biopsy
adjuvant combination chemo
surgery - amputation, limb salvage - (surgery removing the tumor and the limb is reconstructed via internal prosthetic device), roationplasty (surgery rotating the leg 180 degrees to create a new knee joint)
what is glioblastoma
it’s tumor in the brain - cancer that attacks the glial cells in the brain and creates tumors - its agressive
what are the signs and symptoms of glioblastoma
headaches
nasuea/vomiting
seizures
depending on where the tumor is on the brain, can affect pts neurologically
how to diagnose glioblastoma
imaging: MRI
confirmation: guided brain biopsy
treatment options for gliobastoma
surgery
radiation
chemotherapy
glucocorticoids: aid in cerebral inflammation
antiepileptic for seizure control
what is the most common type of pediatric cancer
leukemia: the overgrowth of abnormal and immature WBC in the bone marrow which prevents the growth of RBC, platelets, and WBC
leukemia signs and symptoms
fatigue
pallor
anorexia
bruising and bleeding
fever
infection
bone/joint pain
abdominal pain
headache
vomiting
visual disturbances
tachycardia
anemia
if you completed a CBC on a child with leukemia, what would the labs look like
decrease in RBC
decrease in platelets
increase in blasts (immature WBC)
nursing care for leukemia pts
neutropenic precautions
bleeding precations
how to diagnose leukemia
bone biopsy
lumbar puncture to check for spread into CNS
how to treat for leukemia
chemotherapy
ALL - lower dose for longer time (2-3 years)
AML - higher dose for shorter time (less than a year)
induction and maintence chemo
car-t cell therapy
monoclonal antibody
blincatumomab for b-cell for ALL
stem cell transplant
what is the pathophysiology of acute lymphoblastic leukemia
ALL developed from WBC (lymphocytes) or from lymphoblasts (immature lymphocytes) within the bone marrow. Then, with a genetic mutation, abnormal blood cells multiply and overcrowd
what are potential risk factors for acute lymphoblastic leukemia
down syndrome
li-fraumeni syndrome
neurofibromatosis
prolonged exposure to chemicals and radiation
family hx
male
what’s the pathophysiology of acute myeloid leukemia (AML)
in the bone marrow, there’s a WBC called myeloblast that overcrowds
after surviving, what should pts do to take care of themselves
follow up care for the rest of their life for risk of “late effects”
survivor clinics to find support for transition to independence, peer support, fertility treatments.