FINAL REVIEW
(40:39 on BB Collab)
1. Treatment for Pulmonary Atresia
Prostagladin E to keep PDA
Treat symptoms of CHF
Surgery
2. Where to give intramuscular injection
Infants = vastus lateralis
Peds = d
...
FINAL REVIEW
(40:39 on BB Collab)
1. Treatment for Pulmonary Atresia
Prostagladin E to keep PDA
Treat symptoms of CHF
Surgery
2. Where to give intramuscular injection
Infants = vastus lateralis
Peds = deltoid
3. Anatomy and physiology of infant’s heart
4. Childhood patent ductus arteriosus... What to find on
assessment?
dyspnea , tachycardia
Full, bounding pulses
Hypotension
“Machine” murmur
5. Know what pertussis (Whooping Cough) is
Patho:
Pertussis is primarily a toxin-mediated disease. The bacteria
attach to the cilia of the respiratory epithelial cells, produce
toxins that paralyze the cilia, and cause inflammation of the
respiratory tract, which interferes with the clearing of
pulmonary secretions.
s/s:
Runny nose
Low-grade fever (generally minimal throughout the course of the
disease)
Mild, occasional cough
Apnea – a pause in breathing (in babies)
Vaccine for it is → DTap
6. Kawasaki disease.... Know what they are likely to develop
While the majority of heart disease in children is congenital (present at
birth), it is possible for kids to develop heart disease later in childhood.
Kawasaki disease is the leading cause of acquired heart disease
in kids.
Acute:
Irritability
high fever lasting 5 or more days
red throat
Subacute:
afebrile,
cracking lips and fissures,
desquamation of skin on tips of toes and fingers,
7. Know how to treat Rheumatic fever
Antibiotics
Aspirin
Prophylactic antibiotics for invasive procedure and dental
work
8. Know what successive vaccinations are releasing antibody
antigen response ??
9. Know the evaluation of the infants that are septic
Infants under 2 months → Any fever in an infant under 1-2 months
needs to be evaluated for neonatal sepsis
At risk for neonatal sepsis
Workup → LP , Blood & urine cultures, IV antibiotics ASAP &
monitoring
10. Atrial septic defect.. what kind of shunt is it?
LEFT to RIGHT shunting of blood
11. know different disorders that fall under the umbrella of cyanotic
disease
Pulmonary Atresia
Tricuspid Atresia
Tetralogy of Fallot
12. therapeutic regimen for patient with heart failure will be
Maintain fluid and electrolyte balance
Decrease workload of the heart
Provide adequate nutrition
Increase tissue oxygenation
-- not sure? maybe?
Meds: diuretics, ACE inhibitors
13. client education for sickle cell disease
Often at an early age this child becomes opioid tolerant
Seizure precaution
14. parenteral education for patient with hemophilia (Things they
need to avoid)
AVOID BLEEDING EPISODES
15. Foods they need to take for iron deficiency anemia
Foods high in iron such as
Shellfish
Spinach
Live and other organ meats
Legumes (beans, lentils, chickpeas, peas, soybeans)
Red meat
Pumpkin seeds
16. Long term complications of thalassemia major
Severe anemia?
17. If child has ITP and given steroids what do you need to monitor
for?
PLATELETS
Monitor for Infection and hyperglycemia
18. Aplastic Anemia know pathophysiology
Patho: Failure of bone marrow to produce blood cells resulting in
pancytopenia
Develops after treatment with radiation, medications, infections or
congenital in nature.
19. Know what STAGE 2 WILMS TUMOR MEANS
Patho: Intrarenal tumor that grows rapidly (doubling in size approx
11-13 days
Manifestations:
Firm, lobated mass on one side or midline of abdomen
If symptomatic: HTN, abdominal pain and or hematuria
Management:
Nephrectomy of affected tumor
Chemo and/or radiation
Don’t palpate mass aggressively
Stage II: (graph in textbook)
-tumor extends beyond the kidney and is completely excised
-regional extension of the tumor is presented
-vessels outside the kidney are infiltrated or contain tumor thrombus
20. Lymphatic Leukemia
Patho: Stem cells in the bone marrow produce immature WBCs that do
not function normally and are produced at a rapid rate that replaces the
normal functioning cells leaving the body at an increased risk for infection.
Acute lymphatic leukemia- affects lymphocytes predominantly
Manifestation:
Petechiae
Ecchymosis
Abnormal bleeding
Fever
Splenomegaly
Diagnosis:
initially made by abnormal CBC (anemia, thrombocytopenia
and/or neutropenia
Confirmed by bone marrow aspiration
21. Comfort Care
22. know what to do diagnosis with terminal illness... what type of
treatments are available for that scenario
23. know what to do for immunodeficiency syndrome for HIV
Patho: HIV destroys the T cells in the body leaving the immune
system weakened and allows for opportunistics infections
Management:
Preventions of transmission
Prevent opportunistic infections
24. Child with AIDS.. as a nurse you would use to ENCOURAGE
EFFECTIVE LUNG EXPANSION. (PROF WILL CHANGE
QUESTION)
25. know the activities that children with juvenile rheumatoid
arthritis can do.. and most appropriate thing for them to do
They need extra time completing ADLs
26. Know what is caused by histamine release. KNOW
(ALLERGIC REACTION)
Patho: Antigen-antibody reaction to an allergen
Can manigest as anaphylaxis, atopic dermatitis, contact
dermatitis, serum sickness
Allergen binds to antibodies on mast cells → Histamine is released
from the mast cell → an allergic reaction ensues
27. FIRST priority for anaphylatic shock
AIRWAAAAAY! ABC’S
ALSO, Avoidance of allergen
28. Know what to do for anaphylactic shock
Avoidance of allergen
ABC’s
Epinephrine, IV, or IM
29. Pathophysiology for anaphylactic reactions
Patho: Anaphylaxis is a severe, systemic hypersensitivity reaction that is
rapid in onset and characterized by life-threatening airway, breathing, and/or
circulatory problems, and that is usually associated with skin and mucosal
changes.
30. Know histamine response (STUDY PICTURE ON SLIDE)
Sensitization: Initial exposure to allergen
Allergen (ie: pollen, grain) enters into the bloodstream → B cells
differentiate into plasma cells and make antibodies → antibodies
attach to mast cells
Allergic Reaction: Secondary exposure to same allergen
Allergen binds to antibodies on mast cells → Histamine is released
from the mast cell → an allergic reaction ensues
31. Brain Tumor (SELECT ALL THAT APPLY) 4 things on brain
tumor (4 SYMPTOMS)
Manifestations:
Behavioral and nervous system changes
Increased ICP (rapid or slowly)
o Headache
o Nausea
o Vomiting
o Abnormal gait
o Dizziness
o Vision changes
o Fatigue
+mental status changes or educational problems
Treatment:
Surgery
Chemotherapy and/or radiation
32. Non-Hodgkins lymphoma that nurse is at high risk for kidney
or renal disorders
tenks 8===D~~ SMH
*He said to focus on the difference between these two.
Hodgkin NON-Hodgkin
Patho: starts in a single lymph
node or chain
Large cell with multiple
nuclei
Patho: T-cell abnormalities that
cause immature, malignant and
diffuse T-cells
Often occurs in children with
congenital or acquired
immunodeficiency,
autoimmune diseases.
s/s
Nontender, firm
lymphadenopathy
May cause resp.
Symptoms if pressure is
placed on trachea or
bronchi
If progressed → fever,
night sweats, and weight
loss
s/s
Fever
Weight loss
Enlarged or nodular lymph
nodes may or may not be
present
o May cause resp.
Compromise if
trachea/bronchi has
pressure
Pain and swelling in
lymph nodes
Swelling of face
Enlargement of lymph
nodes:
o Neck
o Armpits
o Groin
RESP:
o SOB
o Chest pain
o Difficulty breathing
o Coughs
Abdominal pain,
distention, bloating and
constipation
Loss of appetite,
diarrhea, weight loss
Management
Chemotherapy and/or
radiation
High survival rate
Managementdisease
Chemotherapy and/or radiation
Hematopoietic stem cell
transplant for recurrent disease
33. Diagnosis of acute lymphatic leukemia know diagnosis for
this one (PATHO)
PATHO:
Stem cells in the bone marrow produce immature
WBCs that do not function normally and are
produced at a rapid rate that replaces the normal
functioning cells leaving the body at an increased
risk for infection
***ALL (acute lymphocytic leukemia) – affects
lymphocytes predominantly***
DX:
Initially made by abnormal CBC (anemia,
thrombocytopenia and/or neutropenia)
Confirmed by bone marrow aspiration
34. Hodgkins disease patient with hodgkins.. know expected
findings
Nontender, firm lymphadenopathy
Respiratory difficulty
Fever
Night sweats, weight loss
35. neuroblastoma study manifestations.. they will have an
ELEVATION IN WHAT??????
Tumor markers:
Homovanillic acid (HVA) and vanillylmandelic acid (VMA) are by-
products of adrenal hormones are usually elevated in the urine
and blood
-Elevation in dopamine, ferritin, NSE, LDH, and GD2
Manifestations:
Dependent on the location of the mass, but problems
are caused by pressure onto organs
Weight loss
Abdominal distension
Irritability, fatigue, fever
Elevation in whaaaaat???
36. Sickle Cell Disease know what it does to the tissue how it
causes pain
Obstruct capillary blood flow → tissue ischemia/hypoxia →
organ tissues become damaged and impaired function
pain results from avascular necrosis of the bone marrow
37. Lupas.. Know the highest priority nursing diagnosis
PAIN? Body Image?
Patho: Autoantibodies are produced and immune complexed form
and are deporisted into connective tissue, triggering and inflammatory
response which overtime damages the connective tissue.
Can affect all organs, but small blood vessels, glomeruli, joings,
spleen and heart valves most common
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