Path - Cells And Tests Flashcards

1
Q

red test tube cap

A

Glass=nothing
Plastic=clot activator

Serology
Blood bank
Chemistry tests

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2
Q

Red/gray test tube cap

A

No anticoagulant but does have clot activator gel for separating cells from serum

Serology
Chemistry tests

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3
Q

Light blue test tube cap

A

Citrate anticoagulant

Coagulation tests

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4
Q

Purple test tube cap

A

EDTA anticoagulant

CBC
Ammonia

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5
Q

Green test tube cap

A

Heparin anticoagulant

Blood gases
Chemistry tests

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6
Q

Gray test tube cap

A

Fluoride with oxalate anticoagulant

Glucose
Lactate

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7
Q

Yellow test tube cap

A

Acid citrate dextrose (ACD)
Blood bank studies

or
Sodium polyanethol sulfate (SPS)
Blood cultures

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8
Q

Dark blue test tube cap

A

Nothing
Stopper is usually specially treated

Trace elements
Nutritional studies
Toxicology

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9
Q

Sensitivity equation

A

100 X (TP/(TP+FN))

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10
Q

Specificity equation

A

100 X (TN/(TN+FP))

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11
Q

PPV equation

A

100 X (TP/(TP+FP))

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12
Q

NPV equation

A

100 X (TN/(TN+FN))

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13
Q

Number of existing cases of a disease in a population

A

Prevalence

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14
Q

Number of new cases of a disease in a population per unit time

A

Incidence

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15
Q

As prevalence increases, PPV ___

A

Increases

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16
Q

Screening tests require high ___

Confirmatory tests require high ___

A

Sensitivity

Specificity

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17
Q

More sensitive = more chance of ___

More specific = more chance of ___

18
Q

True anemia is marked by what characteristic of RBCs?

A

Decreased RBC mass

19
Q

Relative anemia is due to __

Causes?

A

Increased plasma volume

Pregnancy
Excessive hydration
Macroglobulinemia

20
Q

Severe symptoms of anemia

A

Chest pain
Angina
Heart attack
Fainting

21
Q

Trauma causes what kind of anemia?

22
Q

What is the most common cause of anemia of insufficient production? Others?

A

Iron deficiency

B12 or Folate deficiency
bone marrow suppression or replacement
-parvovirus B19
-cancer

23
Q

Hereditary membrane abnormality:

A

Elliptocytosis

24
Q

Hereditary hemoglobin abnormality:

A

Thalassemia

25
Extravascular vs intravascular causes of RBC destruction
Extra-warm autoimmune hemolytic anemia | Intra-RBC fragmentation disorders
26
Large number of blue cells, which are immature RBCS, due to an increase in demand
Hyperproliferative
27
Definitions: Variation in size of RBCs? Shape?
Anisocytosis | Poikilocytosis
28
Anemia of chronic disease: | Morphologic characteristics
None
29
Thalassemia
quantitative defects of hemoglobin Reduced globin chain synthesis Alpha and beta
30
Beta thalassemia major | Characteristics
``` Severe microcytic hypochromic anemia Anisocytosis Poikilocytosis Many uncleared RBCs Polychromasia ```
31
Cytoskeletal abnormalities cause
Hereditary spherocytosis
32
Small nuclear remnants Typically single Normal in neonates
Howell Jolly bodies
33
Iron-containing mitochondrial remnants | Small clusters near cell periphery
Pappenheimer granules
34
MCV below normal Above normal Normal
Microcytic Macrocytic Normocytic Mean cell volume
35
Most common cause of microcytic hypochromic cells
Iron deficiency
36
Cells in hemoglobin C disease
Target cells Hemoglobin C crystals Irregularly contracted cells Spherocytes
37
Degmacyte vs schistocyte
Bite cell Fragmented cell
38
Aggregates of denatured hemoglobin
Heinz bodies
39
Dacrocytes
Tear drop cells
40
Blue gray color of immature RBCs due to residual ribosomal material
Polychromasia
41
Aggregates of ribosomes RNA All over the cell
Basophilic stippling