Which percent of iron deficient children develop Iron deficiency anemia?
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Question 2 of 57
Which of the following is least likely to be associated with prolonged thrombocytopenia in children?
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Question 3 of 57
A 13-month-old girl presented with progressive pallor for the last 3 months. The mother noticed that she started to eat a non-nutritive and dirty substance. She is on breast feeding till this age. On examination, she is pale, apathetic looking, no LAP, no organomegaly, and no skin bleeds. Of the following, the MOST likely diagnosis is:
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Question 4 of 57
All of the following are true about Fanconi anemia EXCEPT
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Question 5 of 57
Anemia and reticulocytopenia that occur in the 2nd half of infancy period is LEAST likely due to
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Question 6 of 57
The urgency for packed cell transfusion in childhood anemia should be dictated by
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Question 7 of 57
Which laboratory test is ordered to determine the presence of the HIV antigen in an infant whose parent is HIV+?
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Question 8 of 57
Blood transfusion therapy in a child with sickle cell anemia is indicated in all the following conditions EXCEPT
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Question 9 of 57
One of the following features DOES NOT fit hemophilia A
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Question 10 of 57
Matching: Hemolytic anemia - Thermal sensitivity
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Question 11 of 57
A 10-month-old white male presents with a 1-day history of persistent bleeding after cutting his lip slightly. The family history is unremarkable, and the patient is receiving no medications. Laboratory data reveal a hemoglobin value of 11 g/dL, platelets of 350,000, a prothrombin time of 11.8 seconds, and a partial thromboplastin time (PTT) of 100 seconds, which is corrected by mixing of normal plasma. The most likely diagnosis is
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Question 12 of 57
Of the following, the LEAST likely feature of acute immune thrombocytopenia (ITP) is
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Question 13 of 57
A 55-year-old man presented to his primary care physician for evaluation of fatigue. He was previously healthy with the exception of chronic musculoskeletal low back pain, for which he occasionally takes nonsteroidal anti-inflammatory drugs. On examination, he is pale. Complete blood cell count results are as follows: hemoglobin 8.3 g/dL, mean corpuscular volume 73 fL, leukocyte count 6.9 × 10^9/L, and platelet count 398 × 10^9/L. Results of the fecal occult blood test are positive. During upper and lower endoscopy, a 1.2 × 2.5-cm ulcerative lesion is noted in the lesser curvature of the stomach. The lesion is biopsied and identified as a MALT lymphoma. Which of the following is characteristic of MALT lymphoma?
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Question 14 of 57
The bleeding time is a test for
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Question 15 of 57
A blood smear taken from the patient described in Question 10 shows microcytic hypochromic anemia. Iron supplementation therapy is started. When will the reticulocyte response be at maximum?
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Question 16 of 57
The BEST treatment option for factor VIII hemophiliacs with high titer inhibitor is
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Question 17 of 57
Folic acid deficiency may develop in the following children EXCEPT
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Question 18 of 57
A 15-year-old is diagnosed with non-Hodgkin lymphoma. Which of the following should the nurse include in teaching the parents about this lymphoma? (Select one that does not apply.)
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Question 19 of 57
What are the clinical manifestations of non-Hodgkin lymphoma?
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Question 20 of 57
Chronic thrombocytopenia in a male with eczema should suggest
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Question 21 of 57
A 9-month-old boy appears pale. Examination reveals a palpable liver $3 \mathrm{~cm}$ below the right costal margin and palpable spleen $4 \mathrm{~cm}$ below the left costal margin. Lab findings include: hemoglobin concentration, 6.4 g/dl; mean corpuscular volume (MCV), 67 fL; and WBC, 15,000/mm3. Of the following, The MOST valuable test to confirm the diagnosis is
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Question 22 of 57
A child with sickle cell anemia is scheduled for an exchange transfusion. What should the nurse teach the family?
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Question 23 of 57
A healthy 5-day-old male neonate develops bruising and melena. The pregnancy, and delivery course were unremarkable. The mother received heparin therapy for recurrent abortions secondary to lupus anticoagulants. The infant is vigorously breastfeeding. Examination reveals only multiple bruises. Lab tests reveals: hemoglobin, 8.4 g/dL; WBC, 8600/mm3; platelets count, 200000/mm3; PTT, 74 seconds; PT, 28 seconds; serum fibrinogen is normal. Of the following, the MOST likely cause of this bleeding is
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Question 24 of 57
In hemophilia A, factor VIII level activity should be increased to $100 \%$ in
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Question 25 of 57
Which of the following is FALSE about factor V Leiden mutation?
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Question 26 of 57
All the following are true regarding factor XIII EXCEPT
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Question 27 of 57
A child with leukemia has a white blood cell count of 5000/mm³ with 5% polys and 3% bands. Which analysis is most appropriate?
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Question 28 of 57
Transfusion of fresh frozen plasma (FFP) is efficacious for the treatment of deficiency of all the following coagulation factors EXCEPT
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Question 29 of 57
A previously normal 10-year-old male experiences pallor, fatigue, and a fall in hemoglobin level from 13 to 8 g/dL without evidence of bleeding. His spleen is slightly enlarged. The reticulocyte count is 10%, and his WBC and platelet counts are normal. Many spherocytes are observed on the blood film. The most likely diagnosis is
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Question 30 of 57
A 6-year- old boy presented three hours after receiving blood transfusion with urticaria, pruritus, maculopapular rash, progressively developed facial edema, and respiratory distress. Of the following, the MOST likely diagnosis is
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Question 31 of 57
Mentzer index of less than 12.5 suggests thalassemia trait, it represents
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Question 32 of 57
An 18-month-old male is brought in by his mother. He is pale, and his hematocrit is 20%. Which questions should help the nurse make a diagnosis?.)
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Question 33 of 57
A 72-year-old man with chronic atrial fibrillation has been receiving dabigatran 75 mg twice daily for the past 6 months. He has not had any thrombotic or hemorrhagic complications. He has a history of colon polyps, for which he needs to undergo a colonoscopy with possible polypectomy. Apart from an irregular pulse, his physical examination findings are normal. Results were normal for a complete blood cell count and tests of renal and liver function. The calculated creatinine clearance is 28 mL/min. For how long should dabigatran use be discontinued before the colonoscopy?
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Question 34 of 57
Which analgesic is most effective for a child with sickle cell pain crisis?
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Question 35 of 57
Which of the following conditions causes profound thrombocytopenia?
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Question 36 of 57
A healthy 5-mo-old boy appears pale. Examination is unremarkable. Lab findings include: Hb 8.1 g/dl; WBC 4,800/mm3; platelets 144,000/mm3; MCV, 111 fl; blood film showed hypersegmented neutrophils; serum B12, 65 pg/mL (low). The infant is vigorously breast fed. Of the following, the NEXT step of the management is
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Question 37 of 57
Inherited thrombocytopenias include all the following EXCEPT
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Question 38 of 57
Which of the following tests measures the step from fibrinogen to fibrin conversion?
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Question 39 of 57
Which factors should be included in a teaching plan for a child with sickle cell anemia? (Select one that does not apply..)
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Question 40 of 57
Deficiency of which of the following factors is asymptomatic?
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Question 41 of 57
Which of the following symptoms/sings is a manifestation of anemia?
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Question 42 of 57
Constrictive pericarditis secondary to radiation exposure with sings of increase in pulmonary pressure. The child received a course of irradiation which leads to
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Question 43 of 57
Matching: Red blood cell aplasia - X-linked recessive
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Question 44 of 57
The best treatment option for hereditary spherocytosis is
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Question 45 of 57
A 22-year-old man is admitted to the hospital for an elective cholecystectomy. You are asked to see him because he had anemia on preoperative testing. He tells you that he has always been told by his physicians that he has mild anemia; his medical history is otherwise unremarkable. His vital signs are normal. His conjunctivae are mildly icteric, and the spleen is palpable in the left upper quadrant. Findings on the remainder of the physical examination are normal. Diagnostic testing results are shown in Table 9.Q3. Which of the following tests would most likely help confirm the diagnosis?
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Question 46 of 57
In hereditary spherocytosis, all the following will resolve postsplenectomy EXCEPT
All the following are correct regarding treatment of cold agglutinin disease EXCEPT
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Question 49 of 57
The nurse is taking care of a child with sickle cell disease. The nurse is aware that which of the following problems is (are) associated with sickle cell disease? (Select all that apply.)
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Question 50 of 57
The parent of a 2-year-old HIV-positive child questions whether the child can attend day care. Which is the best response?
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Question 51 of 57
Which of the following is not a feature of Wiskott-Aldrich Syndrome (WAS)
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Question 52 of 57
Which liver protein plays a key role in iron homeostasis?
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Question 53 of 57
A child who has completed treatment for leukemia comes to the clinic with the parents. The parents express that they are glad their child has been cured and is safe from getting cancer later in life. Which of the following should the nurse consider in responding?
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Question 54 of 57
Which of the following agents helps in decreasing the frequency of vasoocclusive crises in children with sickle cell disease?
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Question 55 of 57
Which would you expect to administer to a child with ITP and a platelet count of 5000/mm³?
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Question 56 of 57
The increment in hemoglobin after instituting oral iron therapy for iron deficiency anemia is about
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Question 57 of 57
A 62-year-old man underwent right total knee replacement 8 days ago. Swelling has developed in his right lower extremity, and Doppler ultrasonography confirms the presence of a right superficial femoral vein thrombosis. His current medications include oxycodone and subcutaneous unfractionated heparin. Results of preoperative tests, including a complete blood cell count and liver and kidney function, were normal. Other laboratory data include the following: hemoglobin 12.2 g/dL, leukocyte count 8.5 × 10^9/L, and platelet count 60 × 10^9/L. In addition to stopping the use of subcutaneous heparin, what is the next most appropriate step in management of this patient?
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