Questão 1
Questão
All of the following would decrease WBC levels EXCEPT
Responda
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trauma
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immunosuppression
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drug toxicity
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overwhelming infection
Questão 2
Responda
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6,200-17,000
-
5,000-10,000
-
9,000-30,000
Questão 3
Questão
WBC level in >2 to adult
Responda
-
5,000-10,000
-
6,200-17,000
-
9,000-30,000
Questão 4
Responda
-
5,000-10,000
-
6,200-17,000
-
9,000-30,000
Questão 5
Questão
What are the panic values for WBC
Responda
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< 1,000
> 30,000
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< 2,000
> 30,000
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< 2,500
> 30,000
Questão 6
Questão
All of the following are granulocytes EXCEPT
Responda
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monocytes
-
neutrophils
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basophils
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eosinophils
Questão 7
Questão
T and B cells are part of what type of agranulocyte?
Responda
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lymphocyte
-
monocyte
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eosinophil
Questão 8
Questão
How many days are neutrophils in circulation?
Questão 9
Questão
Critical value of actual neutrophil count (ANC)
Questão 10
Questão
Eosinophils are what % of WBC's
Questão 11
Questão
Eosinophils and basophils respond to viral and bacterial infections.
Questão 12
Questão
Eosinophils and Basophils respond in allergic reactions and parasitic infections
Questão 13
Questão
What is responsible for hives and skin reactions due to cytoplasm containing heparin, histamine, and serotonin?
Responda
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neutrophil
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eosinophil
-
basophil
Questão 14
Questão
What type of cells provide humoral immunity?
Questão 15
Questão
What type of cell produces interferon?
Responda
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lymphocyte
-
monocyte
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neutrophil
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eosinophil
Questão 16
Questão
All of the following are true for hemoglobin EXCEPT
Questão 17
Questão
Hemoglobin panic values:
Responda
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< 10
> 30
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< 5
> 20
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< 8
> 15
Questão 18
Questão
Hematocrit critical value:
Responda
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< 20
> 60
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< 15
> 45
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< 10
> 60
Questão 19
Responda
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% of hemoglobin in a single RBC (color)
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Average weight of hemoglobin within a RBC
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Average volume/size of single RBC
Questão 20
Questão
Increased reticulocyte means all of the following EXCEPT
Questão 21
Questão
Normal or low reticulocyte count with anemia indicates all of the following EXCEPT
Questão 22
Questão
All would be included in the work-up for macrocytic anemia EXCEPT?
Responda
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B12 and folate
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iron studies
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peripheral smear
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TSH
Questão 23
Questão
All would be included in microcytic anemia work-up EXCEPT
Responda
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iron studies
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peripheral smear
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Hgb electrophoresis
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bone marrow biopsy
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B12 and folate
Questão 24
Responda
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all proteins available for binding to iron
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the major iron-storage protein
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quantity of iron bound to transferrin
Questão 25
Responda
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the major iron storage protein
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quantity of iron bound to transferrin
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all proteins available for binding to iron
Questão 26
Questão
What are the iron-binding proteins?
Questão 27
Questão
What is the major iron-storage protein?
Questão 28
Questão
What is needed for adequate functioning of the RBC's and WBC's due to synthesis of amino acids and DNA?
Responda
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ferritin
-
folic acid
-
transferrin
Questão 29
Questão
What does B12 activate?
Responda
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folate
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transferrin
-
ferritin
Questão 30
Questão
The Schilling Test is used for all of the following EXCEPT:
Questão 31
Questão
Increases LDH, increased bilirubin, and decreased haptoglobin are indicative of:
Responda
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acute blood loss
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hemolysis
Questão 32
Questão
Fetal hemoglobin contains all of the following EXCEPT:
Responda
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2 alpha chains
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2 beta chains
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2 gamma chains
Questão 33
Questão
What is the most common type of hemoglobin in adults?
Questão 34
Questão
All of the following are found in sickle cell disease except?
Questão 35
Questão
What type of hemoglobin doesn't carry oxygen well?
Questão 36
Questão
What type of hemoglobin is found in people of Southeast Asian descent?
Questão 37
Responda
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inherited 1 sickle cell gene and 1 abnormal hemoglobin gene
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inherited 2 sickle cell genes
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inherited 1 sickle cell gene and 1 normal hemoglobin gene
Questão 38
Questão 39
Questão
What test is used to differentiate hemolytic anemia into hereditary spherocytosis or thalassemia?
Questão 40
Questão
Decreased osmotic fragility test indicates:
Questão 41
Questão
What should be suspected in people with hemolysis reactions after certain medications and foods?
Responda
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G6PD deficiency
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pernicious anemia
-
hereditary spherocytosis
Questão 42
Questão 43
Questão
All of the following cause prolonged bleeding time EXCEPT
Responda
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iron deficiency
-
ASA/NSAIDs
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Von Willebrand
-
scurvy
-
renal failure
Questão 44
Questão
What is used to monitor heparin therapy
Responda
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aPTT
-
bleeding time
-
platelet count
Questão 45
Questão
aPTT/PTT evaluate what pathways?
Responda
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extrinsic and common coagulation pathways
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intrinsic and common coagulation pathways
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intrinsic and extrinsic pathways
Questão 46
Questão
Warfarin therapy and liver synthetic function is monitored using:
Questão 47
Questão
PT/INR evaluates what pathways?
Responda
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intrinsic and common
-
extrinsic and common
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intrinsic and extrinsic
Questão 48
Questão
Fibrinogen is a measure of what pathway?
Responda
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intrinsic and common
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extrinsic and common
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factor I and common
Questão 49
Questão
A decrease in antithrombin III leads to
Responda
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increased bleeding
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hypercoagulation
Questão 50
Questão
Protein C inhibits:
Responda
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Va and VIIIa
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II, X, XI, XII
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V, VI, VII
Questão 51
Questão
Antithrombin III inhibits:
Responda
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Va, VIIIa
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II, X, XI, XII
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V, VI, VII
Questão 52
Questão
What is the co-factor to Protein C
Responda
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Protein S
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antithrombin III
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factor Va
Questão 53
Questão
Proteins C and S are decreased in all of the following EXCEPT
Responda
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Coumadin
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liver disease
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renal disease
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nutritional deficiency
Questão 54
Questão
C4 binding protein from autoimmune diseases can inactivate:
Responda
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protein S
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antithrombin III
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factor Va
Questão 55
Questão
What is the most common hereditary coagulation disorder in the US?
Responda
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Factor V-Leiden
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sickle cell disease
-
hereditary spherocytosis
Questão 56
Questão
In Factor V-Leiden, protein C can't break it down which results in all of the following EXCEPT
Responda
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increased thrombin generation
-
increased antithrombin III generation
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mild hypercoaguable state
Questão 57
Questão
APC is a natural anticoagulant that inactivates
Responda
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X, XII, XI
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fVa and fVIIIa
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V, VI, VII
Questão 58
Questão
patients with factor V leiden will be resistant to WHAT when exposed to APC
Questão 59
Questão
In what disorder is the clotting mechanism inappropriately triggered producing thrombosis and hemorrhage?
Questão 60
Questão
In DIC, fibrin clots form intravascularly consuming platelets and clotting factors leading to what?
Responda
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decreased bleeding time
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increased clotting
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excessive bleeding
Questão 61
Questão
The following image shows:
Responda
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sickle cell
-
iron deficiency
-
sideroblastic
Questão 62
Questão
What is the following smear depicting?
Responda
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Heinz bodies
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nucleated RBC's
-
sideroblastic anemia
Questão 63
Questão
What acts as a carrier protein for factor VIII?
Responda
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antithrombin III
-
Von Willebrand Factor
-
Hemophilia A
Questão 64
Questão
What is the most common bleeding disorder?
Responda
-
VWD
-
hemophilia A
-
hemophilia B
Questão 65
Questão
What is a Factor VIII deficiency?
Responda
-
Hemophilia A
-
Hemophilia B
-
Hemophilia C
Questão 66
Questão
What is a Factor IX deficiency?
Responda
-
Hemophilia A
-
Hemophilia B
Questão 67
Questão
Which hemophilia disorder is common among Ashkenazi Jews?
Responda
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Hemophilia A
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Hemophilia B
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Hemophilia C
Questão 68
Questão
What would be high on your differential with mucosal and cutaneous bleeding?
Questão 69
Questão
What would be high on your differential with bleeding in joints, muscle, and GI tract?