So, you’ve read the title of the quiz and you’re still here? That must mean you’re an intellectual, but you’re going to need to prove it in this tough quiz on blood. What do you know about the fluid that keeps our bodies ticking? Take the quiz and we’ll find out together!
7.00 to 7.45
7.35 to 7.45
6.92 to 7.25
7.45 to 7.80
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Is removed from the circulation and broken down
Becomes known as a "poly"
Becomes known as a reticulocyte
Is converted ro fibrin
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Albumin
Plasma
Iron
Erythropoietin
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Causes jaundice
Prevents blood coagulation
Fights infection
Stimulates the synthesis of hemoglobin
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Leukopenia
Anemia
Jaundice
Kernicterus
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Phagocytic activity
Blood-clotting activity
Percentage of red blood cells in the blood
The amount of blirubin in the blood
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Granulocyte
Platelet
Red blood cell
Lymphocyte
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Flushed
Yellow
Blue
Ecchymotic
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A type
B type
AB type
O type
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Phagocytosis
Oxygen transport
Hemoglobin
Bilirubin
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O
AB
A
B
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The baby is Rh (-) and the mother is Rh (-)
The baby is Rh (+) and the mother is Rh (+)
The baby is Rh (+) and the mother is Rh (-)
The baby is Rh (+) and the mother is type A (+)
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Contain hemoglobin
Are thrombocytes
Are nongranular leukocytes
Are hemostatic
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Is secreted by the kidneys
Stimulates th bone marrow to produce RBCs
Is released in response to hypoxemia
All of the above
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Granulocyte
Thrombocyte
"poly"
Red blood cell
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Thrombocyte
Granulocyte
Platelet
Immature erythrocyte
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Leukocytes
Neutrophils
Red blood cells
Platelets
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Platelet
Phagocyte
Plasma protein
Oxygen carrier
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Erythrocyte
Leukocyte
Stem cell
Megakaryocyte
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Thrombolytic agents
Anticoagulants
Clotting factors
Plasminogen activators
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Granulocyte
Bilirubin
O2 transport
Stickiness
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Granulocytopenia
Thrombocytopenia
Polycythemia
Anemia
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Venous thrombosis
Hemophilia
Anemia
Myelosuppression
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Thrombocytopenia
Anemia
Jaundice
Leukocytosis
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High fever
Infection
Jaundice
Bleeding
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Thrombin
Plasmin
Bilirubin
Albumin
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Bleeding
Infection
Jaundice
Thrombosis
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Thrombocyte
Eosinophil
Neutrophil
Lymphocyte
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Are classified as either granulocytes or agranulocytes
Contain iron that acts as a binding site for oxygen
Contain hemoglobin
Are produced in the bone marrow
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Hypoxemia
Low blood volume
Low plasma pH (acidosis)
Infection
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Is necessary for the synthesis of prothrombin
Is a clotting factor
Is necessary for the absorption of vitamin B12
Stimulates the bone marrow to produce red blood cells
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The lack of gastric hydrochloric acid causes myelosuppression
Iron absorption is impaired
A major source of erythropoietin has been removed
Vitamin B12 absorption is impaired because of the lack of intrinsic factor
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Anticoagulant
Antiplatelet
"clot buster" (thrombolytic)
Antihistamine
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The average adult male has 4 to 6 L of blood
The normal pH of blood is 7.35 to 7.45
Oxygenated blood is redder than unoxygenated blood
Water is 3 to 5 times more viscous than blood
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Refers to deficiency of platelets
Is caused by myelopression
May be accompanied by aplastic anemia and granulocytopenia
All of the above
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Prevents blood coagulation
Causes thrombocytopenia
Dissolves blood clots
Prevents the formation of a platelet plug
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Vitamin B12
Iron
Heme
Prothrombin
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Lymphocytes
Granulocytes
Phagocytic
Heparin-secreting
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Results of myelosuppression: granulocytopenia, aplastic anemia, hemophilia
Antigens: A, B, Rh factor
White blood cells: granulocytes, agranulocytes
Plasma proteins: albumin, fibrinogen, globulins
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Increased numbers of white blood cells
Decreased number of white blood cells
Abnormal numbers of white blood cells
The result of myelosuppression
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Infection
Myelosuppression
Agglutination
Petechiae formation
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Form the platelet plug
Activate facot VIII (antihemophilic factor)
Are involved in coagulation
Are responsible for agglutination
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Heparin
Calcium
Hemophilic factor
Vitamin k
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Is characteristic of sickle cell anemia
Is most often prevented by a diet that is high in vitamin k
Refers to pinpoint hemorrhages under the skin
Is due to a deficiency of reticulocytes
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Prothrombin
Albumin
White blood cells
Myelin sheath
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Blood coagulation
Platelet aggregation
Fibrinolysis
Blood cell production
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Agglutination
Hemophilia
Fibrin strands
Rh factor
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Folic acid deficiency
Hemplytic
Aplastic
Sickle cell
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