ATI LPN
Wong's Essentials of Pediatric Nursing 11th Edition Test Bank
Chapter 24 : The Child with Hematologic or Immunologic Dysfunction Questions
Question 1 of 5
What statement best describes iron deficiency anemia in infants?
Correct Answer: D
Rationale: Iron deficiency anemia reduces oxygen availability to tissues, causing symptoms like pallor and fatigue. The hematopoietic system produces smaller, less hemoglobin-rich RBCs, infants are often overweight from milk, and diagnosis requires lab confirmation, not appearance.
Question 2 of 5
What information should the nurse include when teaching the mother of a 9-month-old infant about administering liquid iron preparations?
Correct Answer: C
Rationale: Adequate iron dosage turns stools tarry green, indicating sufficient absorption. Iron is best given between meals for acidic absorption, nausea may require dose adjustment, not cessation, and liquid iron should be given through a straw to avoid tooth staining.
Question 3 of 5
Therapeutic management of a 6-year-old child with hereditary spherocytosis (HS) should include which therapeutic intervention?
Correct Answer: A
Rationale: Splenectomy corrects hemolysis in hereditary spherocytosis, typically for children over 5 with symptomatic anemia. Calcium doesn?t affect HS, transfusions suppress RBC production and carry risks, and iron supplementation is ineffective for this condition.
Question 4 of 5
What condition occurs when the normal adult hemoglobin is partly or completely replaced by abnormal hemoglobin?
Correct Answer: B
Rationale: Sickle cell anemia involves replacement of normal hemoglobin with abnormal sickled hemoglobin, a hemoglobinopathy. Aplastic anemia is bone marrow failure, thalassemia major involves reduced hemoglobin chain production, and iron deficiency affects RBC size, not hemoglobin type.
Question 5 of 5
The parents of a child with sickle cell anemia (SCA) are concerned about subsequent children having the disease. What statement most accurately reflects inheritance of SCA?
Correct Answer: C
Rationale: SCA is an autosomal recessive disorder, so each sibling has a 25% chance of inheriting SCA, 25% chance of being unaffected, and 50% chance of having the trait. SCA is inherited, not all siblings will have it, and 50% applies to the trait, not the disease.