Hematology, Immunology, and Oncology Flashcards
Hematological Disorders
- Hemophilia A
- Sickle Cell Disease
- Iron Deficiency Anemia
Common Medical Treatments for Hematological Disorders
- Blood Product Transfusion
- IV PRBCs, platelets, or plasma
- Requires 2 RN signatures
- Monitor VS frequently
- Supplemental O2
Iron Deficiency Anemia
The body does not have enough iron to produce hemoglobin
** Common in 6-20 month year olds, and in adolescents
S/Sx of Iron Deficiency Anemia
- Irritability
- Pica
- Spoon-shaped nails
- Headache
- Weakness
- Dizziness
- SOB
- Pallor
What is a major contributing factor of iron deficiency anemia in young children?
Cow’s milk consumption contributes to iron-deficiency anemia in older infants and young children due to its poor iron availability
Iron Deficiency Anemia Treatment
Iron Supplements
- Vitamin C can increase absorption
- Do not administer with cow’s milk
- May color stools/urine black
- May stain teeth, provide straw
- Increase fiber intake
Iron Deficiency Anemia Nursing Management
- Protect child from injury
- Dietary Education
- Iron fortified infant cereal
- Avoid fast foods
- Increase amount of iron rich foods
Sickle Cell Disease
- Severe chronic blood disorder
- Affects 1 in 400 African Americans
- Recessive pattern of inheritance
- Elongated RBCs with a shorter life span
- Sickling triggered by any stress or traumatic event
- Sickled cells clump together and prevent normal blood flow to tissues
Sickle Cell Disease Nursing Management
- First = pulse ox
- Prevent infection
- Scheduled pain medication
- Supplemental oxygen during sickle cell crisis (during a pain crisis these patients are shallow breathers)
- IVF
- Closely monitor Hgb, Hct, and electrolytes (potassium)
- Educate family on early recognition of vaso-occlusive events
Prevention or Early Recognition of Vaso-Occlusive Events
- Seek immediate attention for ANY febrile illness
- Obtain vaccinations and penicillin prophylaxis
- Encourage adequate fluid intake daily
- Avoid temperatures that are too hot or too cold
- Avoid overexertion or stress
- Have 24-hour access to physician, nurse practitioner, or facility familiar with sickle cell care
- Contact MCP if you suspect pain crisis
For a child with sickle cell disease, seek medical attention immediately if…
- Child is pale and listless
- Abdominal pain
- Limp or swollen joints
- Cough, shortness of breath, chest pain
- Increasing fatigue
- Unusual headache, loss of feeling, or sudden weakness
- Sudden vision change
- Painful erection that won’t go down (priapism)
Hemophilia A
- X-linked disorder (passed from mother to sons; daughters are carriers)
- Factor 8 deficiency leads to inability to activate Factor 10 which means they can’t convert prothrombin to thrombin which leads to the inability of platelets to be used in clot formation
- Ranges from mild to severe
Hemophilia Nursing Management
- Preventing bleeding
- Managing a bleeding episode
- Factor 8 replacement IVP
- Cold compress - Education
- Risk for vitamin D deficiency (because they stay inside so much)
Preventing Bleeding in the Child with Hemophilia
- Protect toddlers with soft helmets, padding on the knees, carpets in the home, and softened or covered corners
- Children should stay active: swimming, baseball, basketball, and bicycling (wearing a helmet) are good physical activities
- Avoid intense contact sports
- Avoid trampoline use and ATVs
- Arrange premedication with Amicar is oral surgery is indicated
Immunological Disorders
- HIV
- Juvenile Idiopathic Arthritis
- Allergies/Anaphylaxis
Causes of Infant HIV
- Perinatal transmission
2. Breastmilk
Causes of Adolescent HIV
Nonsterile needles or sexual contact
Infant HIV Diagnostics
Polymerase chain reaction (PCR) test to diagnose
Adolescent HIV Diagnostics
Platelets and CD4 to diagnose
Is there a cure for HIV
No, but survival rates improved with highly active antiretroviral therapy (HAART)
** COMPLIANCE very important
S/Sx of Infant HIV
- Failure to thrive
- Recurrent bacterial infections
- Chronic or recurrent diarrhea
- Fever
- Developmental delay
- Prolonged candidiasis
HIV Nursing Management
- Early recognition and prevention
- Promote HAART compliance
- Promote nutrition
- Provide family education and support
Juvenile Idiopathic Arthritis
- Autoimmune disorder mainly affecting the joints (pain, redness, warmth, stiffness, and swelling)
- Chronic disease (healthy periods with flare ups)
- Three types
Three Types of Juvenile Idiopathic Arthritis
- Pauciarticular (least severe)
- Polyarticular
- Systemic (severe)
S/Sx of Juvenile Idiopathic Arthritis
- Fussiness
- Withdrawal from play
- Limping or guarding
- Joint swelling
Juvenile Idiopathic Arthritis Pharmacological Treatment
- NSAIDs
- Corticosteroids
- DMARDs
NSAIDs for Juvenile Idiopathic Arthritis
- With food to decrease GI upset
- Monitor liver enzymes and renal function
- GI bleeding risk
- Do not crush or chew extended release
* * NSAIDs are helpful with pain relief, but antirheumatic drugs are necessary to prevent disease progression
Corticosteroids for Juvenile Idiopathic Arthritis
- With food to decrease GI upset
- May mask s/sx of infection
- Do not stop abruptly, taper over time
- Monitor BP