1/4
Looks like no tags are added yet.
Name | Mastery | Learn | Test | Matching | Spaced |
---|
No study sessions yet.
manifestations of infection
neuro
temp
oral mucosa
skin
resp.
GI
GU
neutropenia
abnormally low absolute neutrophil count (ANC) less than 2,000/mm3. result of decreased prod. of neutrophils or increased destruction of cells. associated with RISK OF INFECTION
below 1500 cells, risk of infection rises
less than 500 cells: high risk
less than 100 cells: greatest risk of infection
(increased duration of neutropenia, increases risk of infection)
assessment & diagnostic findings:
no definitive symptoms until patient develops an infection
CBC with ‘diff’
medical management:
discontinue med
corticosteroids
growth factor (GCS-F: Filgrastim)
witholding/reducing chemo
febrile neutropenia
-cultures (blood, sputum, urine), CXR
-antibiotics
nursing management:
neutropenic precautions: initiated when ANC is less than 1,000 cells
-private room, precautions sign on door
-mask when leaving room
-proper hand hygiene/standard precautions
-staff/visitors with a contagious illness restricted
-follow institution policy
check VS and temp q4h
monitor WBC with diff daily
administer filgrastim as prescribed
avoid rectal/vaginal procedures
use oral stool softeners
assist pt with personal hygiene
instruct pt to use electric razor
encourage ambulation is room
change water pitcher, denture cleaning fluids, and respiratory equipment daily
assess IV sites daily
encourage IS
fluid intake
no IM injections nor CATH
no plants, fresh fruit
-patient education/discharge planning
maintain good hand hygiene, personal hygiene, oral hygiene, skin integrity
avoid cleaning birdcages & pet litter boxes
avoid garden work
high cal, high protein diet
fluid intake @ least 3L a day
no large crowds
deep breathing & IS
no vaginal or rectal manipulation during sex
discuss dental procedures with providers
provide fam & patient ed on food hygiene & safe food handling
REPORT S/S of infection ASAP to provider
leukemia
unregulated proliferation of leukocytes in bone marrow, leads to overcrowding, leaving little room of normal cell production. can affect other organs in body such as liver, spleen, lymph nodes, and skin
occurs in all age groups: acute myeloid leukemia (AML), chronic myeloid leukemia (CML), acute lymphocytic leukemia (ALL), chronic lymphocytic leukemia (CLL)
no single causative agent
-risk factors include prior radiation and chemotherapy, smoking, occupation and chemical exposure, increasing age, family hx, and certain genetic disorders
clinical manifestations
L: lymph node swelling
E: enlargement of spleen and liver
U: unexplained weight loss, fever
K: K as in WeaKness
E: easily bleeding & bruising
M: midnight sweats
I: infections
A: anemia s/s, appetite loss
diagnostic procedures
CBC w/ diff, coagulation studies, cytogenic studies, creatinine, electrolytes, LFTs, and C&S
bone marrow biopsy or aspiration will confirm diagnosis
patient problems
risk for infection and/or bleeding
impaired nutritional status
acute pain
fatigue and activity intolerance
fluid imbalance
impaired ability to perform hygiene, dress, self-toileting
anxiety and grief
risk for spiritual distress
lack of knowledge
planning/goals
absence of complications and pain
maintenance of adequate nutrition and activity tolerance
ability to provide self care and cops with diagnosis and prognosis
positive body image
understanding of disease process and tx
medical management
combination chemotherapy
immunotherapy
targeted cell therapy
radiation therapy
hematopoietic stem cell transplant
nursing interventions/care
diminish risk of infection & bleeding
-neutropenic precautions
-bleeding precautions
managing mucositis
improving nutritional intake
easing pain & discomfort
decreasing fatigue & activity intolerance
maintaining fluid & electrolyte imbalance
improving self care
managing anxiety and grief
encourage spiritual well-being
lymphoma
a neoplasm of lymphocyte cells. cells overgrow & multiply causes tumors within lymph nodes, lymphomas can metastasize to almost any organ
hodgkin lymphoma
arises in single location, spreads along adjacent lymphatics
15-35 years of age, more than 50
2x in males
weight loss, fatigue, weakness, fever, chills, tachycardia, night sweats, alcohol induced pain, generalized pruritus w/out lesions
reed-sternberg cells
chemo & radiation
monoclonal aB
high dose chemo & stem cell transplant
non-hodgkin lymphoma
older than 60
exposed to certain chemicals, radiation exposure
immune system deficiency and HIV infection
enlarged lymph nodes, swollen abdomen, feeling full after only a small amount of food. chest pain or pressure. SOB or cough
more than 3 types of NHL
chemo, radiation, immunotherapy, targeted therapy, stem cell transplant
multiple myeloma
malignant disease of the most mature form of B lymphocyte- the plasma cell. the malignant plasma cells produce a specific immunoglobin that is nonfunctional, referred to as the monoclonal protein or M protein
-these malignant plasma cells build up in the bone marrow and form tumors in many bones in the body
-multiple myeloma may evolve from a precursor condition known as monoclonal gammopathy of undetermined significance (MGUS) and the next stage, smoldering (or asymptomatic) multiple myeloma SMM
risk factors
increasing age
fam hx
male gender
african americans
exposure to radiation, chemicals
obesity
plasma cell disease hx
clinical manifestations/assessment
C: as in hyperCalcemia
R: renal dysfunction
A: anemia
B: bone destruction
diagnostic findings
CBC with diff, BUN, creatinine, creatinine clearance, electrolytes, LDH
total protein level, electrophoresis, urine protein level
cytogenic studies
CT scan, MRI, PET scan
BMA or biopsy
medical management
NO CURE
hematopoietic stem cell transplant (bone marrow)
chemo, steroids, monoclonal aB, immunomodulary drugs
nursing management
pain management
-opioids or NSAIDs as prescribed
preventing infection
activity/mobility assistance to prevent pathologic fractures (braces, 10 lb. lifting restriction, gentle repositioning)
oral hygiene
monitoring renal function, fluid & electrolytes
VTE prevention
monitoring sensory motor function
patient education on preventing infection, blood clots, sensory motor impairment, pain management, as well as s/s
HYPERCALCEMIA INTERVENTIONS
maintain pt safety & ease comfort
ECG monitoring
3-4L daily fluid intake
biphosphate therapy
encourage mobilization & weight bearing activities as tolerated
high fiber diet/stool softeners/laxatives for constipations
antiemetics for n/v
avoid dietary supplements and meds that increase serum Ca lvls