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NUR 211 Exam 5 with verified detailed answers

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NUR 211 Exam 5 with verified detailed answers

Institution
NUR 211
Course
NUR 211

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NUR 211 Exam 5 with verified detailed answers
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What is hematology? - ✔✔The study of the blood and the lymphatic system.
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What are the main components of blood? - ✔✔Plasma, blood cells, oxygen, nutrients,
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carbon dioxide, antibodies, and other proteins.
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What is hematopoiesis? - ✔✔The production of blood cells in the bone marrow.
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What are the three main types of blood cells? - ✔✔Red blood cells (RBCs), white blood cells
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(WBCs), and platelets.
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What is the function of red blood cells (RBCs)? - ✔✔To carry oxygen throughout the body.
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What is anemia? - ✔✔A condition characterized by a reduction in the oxygen-carrying
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capacity of the blood. || || ||




What are the five types of white blood cells (WBCs)? - ✔✔Basophils, eosinophils,
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neutrophils, monocytes, and lymphocytes. || || ||




What role do platelets play in the body? - ✔✔They are involved in hemostasis, the process
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of stopping bleeding from damaged blood vessels.
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What happens to red blood cells in sickle cell disease (SCD)? - ✔✔They become stiff, lose
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flexibility, and can clump together, leading to blockages in blood vessels.
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,2


What is the lifespan of red blood cells in individuals with sickle cell disease? -
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✔✔Approximately 20 days, compared to the normal lifespan of 120 days. || || || || || || || || || ||




What are the four types of sickle cell crises? - ✔✔1) Vasoocclusive crisis, 2) Aplastic crisis,
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3) Sequestration crisis, 4) Hemolytic crisis.
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What precipitating factors can lead to a sickle cell crisis? - ✔✔Dehydration, cold
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temperatures, infection, and low oxygen environments. || || || || ||




What percentage of sickle cell disease patients are estimated to be African American? -
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✔✔90%.



What are common clinical manifestations of sickle cell disease? - ✔✔Anemia, pain,
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swelling, fatigue, pallor, and shortness of breath.
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What complications can arise from vasoocclusion in sickle cell disease? - ✔✔Tissue
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ischemia, organ damage, and pain in joints, bones, chest, and abdomen.
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What is the primary goal of treatment for sickle cell disease? - ✔✔To prevent crises and
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manage symptoms. ||




What is hydroxyurea and its role in sickle cell disease treatment? - ✔✔A chemotherapeutic
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agent that increases fetal hemoglobin production and reduces crisis frequency.
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What is an exchange blood transfusion? - ✔✔A treatment where the entire blood volume is
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exchanged to maintain sickled hemoglobin levels below 50%.
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What are the risks associated with repeated exchange blood transfusions? - ✔✔Increased
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risk of transfusion reactions and iron overload.
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, 2




What is the significance of bilirubin in sickle cell disease? - ✔✔Its release during hemolysis
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causes an increase in serum bilirubin levels, leading to jaundice.
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What is hand-foot syndrome in sickle cell disease? - ✔✔Swelling of the dorsal surfaces of
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the hands and feet, causing pain.
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How does sickle cell disease affect growth and development in children? - ✔✔Children may
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be smaller than peers, and puberty may be delayed.
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What is the impact of sickle cell disease on infection risk? - ✔✔Patients have an increased
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risk of infections, particularly respiratory infections.
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What is the role of patient and family education in managing sickle cell disease? - ✔✔It is
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imperative for effective management of the disease and prevention of crises.
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What is the common cause of death in sickle cell disease patients? - ✔✔Long-term organ
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damage due to multiple episodes of thrombosis and infarction.
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What is a major risk associated with repeated exchange transfusions? - ✔✔Increased risk of
|| || || || || || || || || || || || || ||




blood transfusion reactions and iron overload.
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Where is excess iron primarily stored in the body? - ✔✔In the liver.
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What can high levels of iron in the liver lead to? - ✔✔Fibrosis, cirrhosis, hepatomegaly, and
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liver failure. ||

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