27 - Blood, Lymph Flashcards
During childhood, RBCs are formed in ;
the marrow of the long bones
By adolescence, hematopoiesis takes place in
the marrow of the ribs, sternum, vertebrae, pelvis, skull, clavicle, and bone marrow
An enlargement of lymph nodes
Lymphadenopathy
Largest organ of the lymphatic system
Spleen
The rate of RBC production is regulated by __
erythropoietin
Fetus: The __ produces erythropoietin
liver
At birth, the __ takes over erythropoietin production
kidneys
The spleen enlarges during (splenomegally) (3)
- infections
- congenital and acquired hemolytic anemias
- liver malfunction
An Hgb below 8 g/dL results in (2)
- increased cardiac output
2. shunting of blood from the periphery to the vital organs
Anemia can result in (5)
- pallor
- weakness
- tachypnea
- SOB
- CHF
Iron Deficiency Anemia may be caused by (4)
- severe hemorrhage
- inability to absorb iron
- excessive growth requirements
- inadequate diet
Iron Deficiency Anemia: Blood tests
RBC count Hgb and hematocrit Morphological cell changes Iron concentrations Stool may be tested for occult blood
Iron Deficiency Anemia: Treatment
Iron, usually ferrous sulfate
po, bid or tid
(Vitamin C aids in absorption)
Administering Iron to children (5)
- Vitamin C aids in absorption
- Drink through straw (stains teeth)
- Take with food
- Dark stools (increase fluids)
- No milk (interferes absorption)
Inherited defect in the formation of hemoglobin
Sickle Cell Disease
Sickle Cell Disease: Sickling (clumping) caused by decreased blood oxygen levels - May be triggered by (4)
- dehydration
- infection
- physical / emotional stress
- exposure to cold
Two Types of Sickle Cell Disease
- Sickle cell TRAIT (asymptomatic)
2. Sickle cell ANEMIA (more severe)
Sickle cell disease: Diagnosis can be detected before birth by
The sickling test, “Sickledex”
chorionic villi sampling
Sickle cell crises : Symptoms
severe abdominal pain,
muscle spasms,
leg pain, or painful swollen joints
Fever, vomiting, hematuria, convulsions, stiff neck, coma, or paralysis can result
4 Types of Sickle Cell Crises
- Vaso-occlusive
- Splenic sequestration
- Aplastic crises
- Hyperhemolytic