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iron deficiency anemia
Inadequate iron in the diet
At birth, infant has iron stores from mom
Lasts 5-6 months in full term infant
Lasts 2-3 months in preterm infant
After birth, 0.8 mg must be absorbed until age 15
Inappropriate vegetarian diet
iron deficiency anemia symptoms
Underweight infant OR overweight infant due to excuse milk ingestion
Pale
Poor muscle development
Prone to infection
Edema
Retarded growth
Irritability
Tachycardia
Fatigue
Glossitis
Angular stomatitis
Koilonychia
Impaired neurocognitive function
iron deficiency anemia prevention
Breastmilk or iron fortified formula x 6 months (12 for premature)
Iron supplementation of 1 mg/kg/day by 4-6 months
Administer iron drops to breastfeed preterm infants after 2 months of age
Limit formula to no more than 1 L/day to encourage intake of iron-rich solid foods
Screen for anemia at 12 months of age
Infants less than 12 months should not be given cow’s milk
sickle cell train
35-45% of total hemoglobin is HgS
Typically asymptomatic but carriers of condition
sickle cell disease
60-80% of Hgb is HgS
Symptomatic, prone to sickle cell crisis
sickle cell anemia general symptoms
Possible growth retardation
Chronic anemia (Hgb 6-9)
Possible delayed sexual maturation
Marked susceptibility to sepsis
sickle cell anemia vascular occlusive crisis symptoms
Extremities - painful swelling of hands and feet, painful joints
Abdomen - severe pain
Cerebrum - stroke, visual disturbances
Chest - resembling pneumonia
Liver - obstructive jaundice, hepatic coma
Kidney - hematuria
Genitals - priapism
sickle cell anemia sequestration crisis
Pooling of large amounts of blood (hepatomegaly, splenomegaly, circulatory collapse
vaso-occlusive crisis
sickle cell anemia complication
painful episode or event
Most common types of non-life-threatening crisis
Ischemia
sequestration crisis
sickle cell anemia complication
pooling of large quantities of blood
Spleen or liver
Decreased blood volume - shock
cerebrovascular accident (CVA)
Sudden and severe complication of sickle cell anemia
acute chest syndrome
sickle cell anemia complication
Clinically appears like pneumonia (infiltrate on chest xray)
Chest pain, fever, cough, tachypnea, hypoxia
sickling triggers
Trauma
Fever
Infection
Dehydration
Stress
Hypoxia
Vasoconstriction
sickle cell anemia treatment
Bed rest
Hydration
Electrolyte replacement
Analgesia
Blood transfusion
Exchange transfusion
Antibiotics
Prevention infection
Vaccine
PVK
hemophilia types
Factor VII deficiency (hemophilia A or classic hemophilia)
Factor IX deficiency (hemophilia B or christmas disease)
hemophilia symptoms
Prolonged bleeding
Bleeding into tissue and joint cavities
hemophilia treatment
Replace missing clotting factors
DDAVP
NSAIDS only used with caution
Avoid ASA
Recognize bleeding episodes early
Avoid contact sports
immune thrombocytopenia
idiopathic thrombocytopenic purpura ITP
acquired hemorrhagic disorder
immune thrombocytopenia symptoms
Petechiae, bruising, bleeding from mucous membranes, prolonged bleeding from abrasions
immune thrombocytopenia acute treatment
Prednisone
IVIG (IV immune globulin)
anti-D antibody
immune thrombocytopenia chronic treatment
Splenectomy (if no response to meds)
henoch-schonlein purpura (HSP)
Allergic vasculitis/allergic purpura/anaphylactoid purpura
what characterizes henoch-schonlein purpura (HSP)
Nonthrombocytopenic purpura
Arthritis
Nephritis
abdominal pain
henoch-schonlein purpura (HSP) symptoms
Primary feature
Symmetric purpura (buttocks and lower extremities)
Other symptoms
Rash - maculopapular lesions, erticaria, erythema
Edema
Arthritis
GI involvement
Renal involvement
henoch-schonlein purpura (HSP) treatment
supportive
child cancer acronym
Continued, unexplained weight loss
Headaches, often with early morning vomiting
Increased swelling or persistent pain in bones, joints, back, or legs
Lump or mass especially in the abdomen, neck, chest, pelvis, or arm
Development of excessive bruising, bleeding, or rash
Constant infections
A whitish color behind the pupils
Nausea which persists or vomiting without nausea
Constant tiredness or noticeable paleness
Eye or vision changes which occur suddenly or persist
Recurrent or persistent fevers of unknown origin
cancer diagnosis labs
CBC, CMP, LFTs, coagulation studies, UA, ANC
cancer diagnostics
LP (leukemia, brain tumors, mets)
Bone marrow aspiration, tumor biopsy
CT, MRI, PET
cancer treatments
Surgery
Chemo
Steroids
Radiation
Biologic therapy
Stem cell transplant
Immunotherapy
stem cell transplant
Kill original bone marrow
Transplant with donor marrow
risks of stem cell transplant
At risk for GVHD
At risk for infection
May cause change of blood type
chemotherapy
Primary form of treatment
Interferes with cells ability to grow and reproduce
Chemo kills rapidly growing cells
Used alone or in combo with other treatments
myelosuppression
a condition where the bone marrow's activity is reduced, leading to fewer red blood cells, white blood cells, and platelets
can be a side effect of chemo
what is golden hour associated it
Neutropenic fever in a cancer patient
acute tumor lysis syndrome
a serious, potentially life-threatening condition caused by the rapid breakdown of cancer cells, leading to a release of their contents into the bloodstream
acute tumor lysis syndrome symptoms
Anorexia
Vomiting
Weakness
Lethargy
Edema
4 metabolic abnormalities in acute tumor lysis syndrome
Hyperphosphatemia
Hypocalcemia
Hyperuricemia
Hyperkalemia
acute tumor lysis syndrome treatment
allopurinol to help with prevention
supportive care
chemotherapy side effects
Extravasation
Alopecia
GI problems
nausea/vomiting
Nutrition
Offer small meals
Give child choices
constipation/diarrhea
Mucosal ulcers
GU problems
Hemorrhagic cystitis
Neuropathy
ALL vs AML
Group of malignant diseases of the bone marrow, blood, and lymphatic system
ALL: most common form of childhood cancer
Boys more than girls
Whites more than african americans
Peak age 2-3 years
90% survival rate
AML
20% of leukemia
Boys = girls
Higher rates during first year of life
65% survival rate
are AML and ALL tumors?
no
AML and ALL treatment induction therapy
4-5 weeks
Corticosteroids to maintain high levels
Chemo
Family support
Achieves a complete remission
AML and ALL treatment consolidation therapy
Several months
Eradicates residual leukemia cells and prevents further cloning
AML and ALL treatment maintenance therapy
Chemo
Maintains the remission phase
osteogenic sarcoma
Most common bone cancer
Peak - 10-25 years
Tumors in long bones especially lower extremities
osteogenic sarcoma treatment
Surgery
May amputate
Limb salvage procedures
Chemo
Given preoperatively
Postoperatively
ewing sarcoma
Arises in the marrow spaces of bone
ewing sarcoma treatment
Limb salvage procedures are recommended for better outcomes
Chemo and radiation
hodgkin’s lymphoma
Disorder of lymphoid system
hodgkin’s lymphoma symptoms
Firm, non tender lymphadenopathy
Enlarged, moveable nodes
Supraclavicular or cervical area
Fever of unknown origin
Night sweats
Anorexia
Weight loss
Other symptoms related to locations of involvement
hodgkins lymphoma treatment
Radiation
Chemo
non-hodgkins lymphoma
More common than hodgkins
Predominantly in 15-19 year olds
Large group of cancers of lymphocytes
Lymphoblastic
Burkitt
Non-burkitt
Large cell
Aggressive or slow growing
B or T cell
non-hodgkins lymphoma symptoms
Painless swollen LN
Fever
Fatigue
Weight loss
non-hodgkins lymphoma treatment
Chemo and radiation tailored to stage of disease
Removal of tissue mass if necessary/possible
what virus does Burkitt’s lymphoma often preceed
epstein-barr virus
CNS tumor symptoms
Infants hard to detect
Symptoms increased ICP
Increased head circumference
Headache when waking and vomiting unrelated to feeding
CNS tumors treatment
Surgery
Radiation
Chemo
Maintain low ICP
neuroblastoma
Most common extracranial solid tumor
Most common cancer in infancy
Silent tumor
Arise from adrenal gland or in the neck, chest, or spinal cord
neuroblastoma treatment
Surgery to remove affected kidney
Chemo
Radiation
wilm’s tumor
Malignant tumor that arises from the kidney
Swelling or mass in abdomen
DO NOT palpate abdomen - encapsulated tumor
Rapid growing - can double size in 11-13 days
retinoblastoma
Sporadic or genetic intraocular tumor
Congenital malignant tumor
Unilateral or bilateral
Leukocoria
Strabismus - second most common sign
retinoblastoma treatment
Enucleation
Radiation
Cryotherapy
Chemo