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Hematologic Problems Questions with Solutions
Typology: Exams
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anemia? "Decreased erythropoietin production causes blood loss." "Iron deficiency accelerates RBC destruction." "Chronic colorectal cancer leads to decreased RBC production." "Decreased iron availability decreases RBC production.": "Decreased iron availability de- creases RBC production."
Anemia is normal in older adults due to normal aging physiology. Anemia may be overlooked because of other health problems. Older adults become anemic because of expected large changes in RBC mass. Increased production of estrogen in older females accelerates hemoglobin decline.: Anemia may be overlooked because of other health problems.
blood cell (RBC) production? Select all that apply. Pantothenic acid Ascorbic acid Amino acid Folic acid Niacinamide acid
2 / 28 Ferric acid: Pantothenic acid Ascorbic acid Amino acid Folic acid
Blurred vision Intermittent claudication Anorexia Glossitis: Glossitis
supplementation? "Avoid drinking orange juice with your iron supplements." "Take stool softeners as prescribed by the doctor." "It could take up to a week of taking iron supplements to see improvement in your hemoglobin levels." "Call the doctor immediately to report any black stools.": "Take stool softeners as pre- scribed by the doctor."
supplement? Iron can be administered intravenously (IV), intramuscularly (IM), or subcuta- neously (SQ). Z-track injection should be avoided when administering iron. The preferred method of administration of iron is parenterally. Staining of the skin may occur with IM solutions.: Staining of the skin may occur with IM solutions.
4 / 28 Nausea and vomiting Weakness
"Nearly all cases of aplastic anemia are fatal over time." "It causes a decrease in only the red blood cells." "A majority of cases are due to autoreactive T lymphocytes." "Aplastic anemia is the most common type of anemia.": "A majority of cases are due to autoreactive T lymphocytes."
Infection Nosebleed Glossitis Pruritus
5 / 28 Petechiae Ecchymosis: Infection Nosebleed Petechiae Ecchymosis
all that apply. High-dose cyclophosphamide Intravenous (IV) or subcutaneous (SQ) deferoxamine Antithimocyte globulin and cyclosporine Luspatercept-aamt (Reblozyl) Iron-binding agent: High-dose cyclophosphamide Antithimocyte globulin and cyclosporine Iron- binding agent
during normal daily activities may be at risk for anemia due to which physiologic effect of cancer treatment? Excessive blood loss Destruction of red blood cells Decreased synthesis of hemoglobin Decreased number of red blood cell precursors: Decreased number of red blood cell precur- sors
7 / 28 therapy Intrinsic factor exchange therapy High-dose cyclophosphamide: Hematopoietic stem cell transplantation (HSCT)
with thalassemia when he- moglobin (Hgb) drops to less than g/dL based on the patient's symptoms.: 7
anemia? Select all that apply. Iron deficiency anemia Pernicious anemia Megaloblastic anemia Sickle cell anemia Thalassemia Aplastic anemia: Pernicious anemia Megaloblastic anemia
Crohn's disease Celiac disease Esophageal stricture Ileitis Small-intestine diverticula: Crohn's disease Celiac disease Ileitis Small-intestine diverticula
8 / 28 with folic acid deficiency anemia? Select all that apply. Green, leafy vegetables Orange juice Lean beef and chicken Peanut butter Potatoes Strawberries: Green, leafy vegetables Orange juice Peanut butter
Thalassemia major Megaloblastic anemia Sickle cell anemia Aplastic anemia: Aplastic anemia
that apply. One, some, or all responses may be correct. Neutropenia Hypochromia Normochromia Macrocytosis Thrombocytopenia Normocytosis: Neutropenia Normochromia Thrombocytopenia Normocytosis
acute blood loss? Select all that apply.
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disease? Causes RBCs to stiffen and elongate Responds to a low hemoglobin level Decreases production of erythrocytes Causes RBCs to be phagocytized: Causes RBCs to stitten and elongate
A person inherits hemoglobin (Hgb) S from both parents. Inherits Hgb S from 1 parent and another type of abnormal Hgb from the other parent. Inheritance of Hgb S from 1 parent and normal Hgb from the other parent: A person inherits hemoglobin (Hgb) S from both parents. Sickle cell anemia Inherits Hgb S from 1 parent and another type of abnormal Hgb from the other parent. Sickle cell- thalassemia Inheritance of Hgb S from 1 parent and normal Hgb from the other parent Sickle cell trait
disease? Select all that apply. Cyclophosphamide (Cytoxan) Crizanlizumab (Adakveo) Bavencio avelumab Oral glutamine Hydroxyurea
11 / 28 (Hydrea) Voxelotor (Oxbryta): Crizanlizumab (Adakveo) Oral glutamine Hydroxyurea (Hydrea) Voxelotor (Oxbryta
Red blood cell (RBC) overproduction Hemoglobin deficiency Chromatin deficiency Iron overload: Iron overload
patient with hemochromatosis? Hydroxyurea Deferasirox Ruxolitinib ( Jakafi) Voxelotor (Oxbryta): Deferasirox
problem? Sickle cell disease Hemophilia Polycythemia vera Hemochromatosis: Polycythemia vera
Select all that apply.
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Europeans African Americans Pacific Islanders Latinos: Europeans
that apply. Oranges Dark green leafy vegetables Uncooked seafood Lean beef Beans: Oranges Dark green leafy vegetables Uncooked seafood Lean beef Beans
High iron Low total iron-binding capacity (TIBC) Low ferritin High platelets: High iron
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newly diagnosed with polycythemia vera? Blood transfusion Phlebotomy Chelation Diuretics: Phlebotomy
Select all that apply. Petechiae Vomiting Numbness Tachycardia Hypotension Abdominal pain: Petechiae Tachycardia Hypotension Abdominal pain
thrombocytopenic purpura (TTP)? Normal red blood cell morphology Increased lactate dehydrogenase Abnormal coagulation Increased platelets: Increased lactate dehydrogenase
16 / 28 Female hemophilia occurs often. All daughters of males with hemophilia are carriers. Female carriers transmit the genetic defect to all of their sons.: All daughters of males with hemophilia are carriers.
Willebrand disease? Factor assays Thrombin time Platelet count Prothrombin time: Factor assays
factor VIII? Antifibrinolytic therapy Emicizumab Factor VIII inhibitor bypassing activity (FEIBA) Desmopressin acetate: Desmopressin acetate
disseminated intravascular coagulation (DIC)? Administer heparin. Administer whole blood. Treat the causative
17 / 28 problem. Administer fresh frozen plasma.: Treat the causative problem.
intravascular coagulation (DIC) who is hemorrhaging? Delirium Petechiae Gangrene Oliguria: Petechiae
acute disseminated intravascular coagulation (DIC) and is bleeding? Elevated D dimers Elevated fibrinogen Reduced prothrombin time (PT) Reduced fibrin degradation products (FDPs): Elevated D dimers
Hemodialysis Antiinflammatory drugs Diuretics Chemotherapy: Chemotherapy
neutropenia? "A total white blood cell count is needed." "Please assess
19 / 28 Daily nasal swabs for culture Monitoring temperature every hour Daily skin care and oral hygiene Private room with a high-efficiency particulate air (HEPA) filter: Strict hand washing Daily skin care and oral hygiene Private room with a high-efficiency particulate air (HEPA) filter
thrombocytopenia (HIT) for a patient receiving heparin subcutaneously twice a day? Prothrombin time Erythrocyte count Hemoglobin level Platelet count: Platelet count
admitted for severe hypovolemia after prolonged diarrhea and a platelet count of 43,000/μL? Insert two 18-gauge intravenous (IV) catheters. Check stools for presence of frank or occult blood. Administer prescribed enoxaparin. Monitor the patient's temperature every 2 hours.: Check stools for presence of frank or occult blood.
diagnosis of hemophilia who had a fall down an escalator earlier in the day and now has bleeding in the left knee joint? Immediate transfusion of platelets Resting the patient's knee to prevent hemarthroses Assistance with
20 / 28 intracapsular injection of corticosteroids Range-of-motion exercises to prevent thrombus formation: Resting the patient's knee to prevent hemarthroses
department with a fever, blood clots, and history of an abnormal enzyme deficiency, who has not taken any medications in the past month, is also likely to experience pain with the condition? Heparin-induced thrombocytopenia (HIT) Disseminated intravascular coagulation (DIC) Thrombotic thrombocytopenic purpura (TTP) Immune thrombocytopenic purpura (ITP): Thrombotic thrombocytopenic purpura (TTP)
thrombocytopenia? Heparin-induced therapy (HIT) and platelet count <10,000/μL Thrombocytopenic purpura (ITP), painful splenomegaly, and platelet count <60,000/μL HIT and a platelet count <30,000/μL Immune thrombocytopenic purpura (ITP) with a platelet count <10,000/μL: Im- mune thrombocytopenic purpura (ITP) with a platelet count <10,000/μL
stage cancer who has been diagnosed with chronic disseminated intravascular coagulation (DIC) but does not have hemorrhagic symptoms? Administration of fresh frozen plasma (FFP) Platelet administration