Indices Flashcards

1
Q

Hgb Male

A

14.0-18.0

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2
Q

Hgb Female

A

12.0-15.0

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3
Q

Hct Male

A

40-54

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4
Q

Hct Female

A

35-49

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5
Q

RBC Male

A

4.60-6.00

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6
Q

RBC Female

A

4.0-5.40

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7
Q

MCV Normal

A

80-100

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8
Q

MCH Normal

A

26-32

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9
Q

MCHC Normal

A

32-36

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10
Q

MCV Formula

A

MCV = Hct X 10 / RBC

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11
Q

MCH Formula

A

MCH = Hb X 10 / RBC

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12
Q

MCHC Formula

A

MCHC = Hb X 100 / Hct

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13
Q

WBC normal

A

4.5 - 11.5 x 10^9

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14
Q

RDW normal

A

11.5 - 14.5

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15
Q

RBC are decreased in

A
Iron deficiency
Vitamin B6, B12, Folic Acid
Chronic Disease
Hereditary anemia(s)
Toxic metals
Catabolic Metabolism
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16
Q

What chronic diseases can cause lower RBC

A
Liver dysfunction
Kidney dysfunction
(chemistry tests and BUN, creatinine may be abnormal)
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17
Q

Why should you asses the RBC

A

Check for anemia and evaluate normal erythropoiesis

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18
Q

What determines the number of RBCs

A
age
sex
altitude
exercise
diet
pollution
drug use
tobacco/nicotine use
kidney function
etc.
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19
Q

What does hemoglobin contribute to your blood

A

Red color

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20
Q

What does hemoglobin contain and its function

A

iron, carries oxygen to the cells

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21
Q

What ides the hemoglobin level indicate

A

amount of intracellular iron, which its value determines anemia

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22
Q

What determines anemia

A

HCT, RBC, and the indices (MCV)

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23
Q

Reasons hemoglobin is increased

A
Dehydration with prolonged or severe diarrhea
Emphysema, severe asthma, or long standing respiratory distress
Macrocytosis 
Adrenal cortex overactivity
Polycythemia vera
High altitube adaptation
Splenic hypofunction
Testosterone supplementation
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24
Q

What causes macrocytosis

A

Deficiency of B6 or B12
Folic Acid
Hypothyroid

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25
Q

Reasons hemoglobin is decreased

A
Digestive inflammation (hidden or obvious blood loss)
Free radical pathology
Adrenal cortical hypofunction
Hereditary anemia
Hemodilution (pregnancy, edema)
Blood loss
Deficiency
Chronic disease
Bone marrow insufficiency
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26
Q

Reasons MCV is increased

A
Hereditary anemia
Megaloblastic anemia
Reticulocytosis
Artifact
Liver disease
Hypothyroidism
Drugs
AIDS treatment (Zidovidune)
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27
Q

Reasons MCV is decreased

A
Copper deficiency
Low stomach acid
Vitamine C insufficiency
Vitamin B6 deficiency
Rheumatoid arthritis
Toxic effects of lead and other toxic elements
Herediatry (thalassemias, sideroblastic)
Iron deficicency (blood loss, parasites, poor intake, low stomach acid)
After a splenectomy
Hemolytic anemia
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28
Q

What is MCH

A

Variation of the MCv. Indicates amount of hemoglobin in a single RBC

29
Q

What is the RDW

A

Random Distribution of red cell Width

30
Q

What does the RDW measure

A

How consistent the size of the red blood cells are.

31
Q

Reasons the RDW is increased

A
B12 and Pernicious anemia
Folic acid anemia
IDA combined with other anemia
Hemolytic anemia
Transfusions
Sideroblastic anemia
Alcohol abuse
Various less common and hereditary anemias
32
Q

Reasons RDW is decreased

A

IDA
Vitamin B6 anemia
Rheumatoid arthritis

33
Q

What index effects hypochromasia

A

Low MCHC

34
Q

What index effects microcyte/macrocyte

A

MCV

35
Q

What does the MCV measure

A

volume in femtoliters

36
Q

What cells are seen with high/low MCV

A

Small - microcytes
Big - macrocytes
Both - anisocytosis

37
Q

What does MCH measure

A

hemoglobin by weight in picograms

38
Q

What is MCH nonspecific for

A

hypochromasia

39
Q

What does MCHC measure

A

% hgb concentration (reflects rule of 3)

40
Q

What should the MCHC be

A

approx 33%

41
Q

What does a low MCHC mean?

A

hypocchromasia

42
Q

What does a MCHC above 36% mean

A

probable error

43
Q

What does RDW measure

A

coefficient of variation of the RBC population = anisocytosis

44
Q

Symptoms of IDA

A

Hypochromic, microcytic (not enough building materials to construct the cells)
Low hgb/hct - no symptoms/morphology until iron stores are depleted
Most common anemia
Mimicked by other conditions

45
Q

How is IDA treated

A

Nutrition or iron supplements

46
Q

What tests are done for IDA

A

Serum iron
Transferrin (elevated to carry any available iron)
Marrow stain: Perle’s Prussian Blue (marrow will show absence of iron)
Others

47
Q

Symptoms of Megaloblastic Anemia

A

Nuclear maturation issue resulting in large blasts
Oval macrocytes (MCV > 120)
hypersegemented neutrophils
HJ bodies, stippling, cabbot rings
Asynchrony in blasts (nucleus and cytoplasm mature at different rates, not in sync)

48
Q

Causes of Megaloblastic Anemia

A

Folate/B12 deficiency (only made in the gut of animals)

Nutritional

49
Q

Anemias with decreased hgb synthesis

A

IDA

Refactory anemia with ringed sideroblasts (RARS)

50
Q

IDA treatment

A

Dietary, decrease in body stores of iron

51
Q

How is RARS contracted

A

Hereditary - sex linked an autosomal recessive
Acquired: Primary Myelodysplasia
Secondary: toxins (lead, alcohol, drugs)

52
Q

Types of cells seen in IDA

A
Hypochromic
Microcytic
Aniso
Poik
Elliptocytes
53
Q

Types of cells seen in RARS

A

Ringed sideroblasts

Lead - basophilic stippling

54
Q

What does megloblastic anemia cause

A

decreased DNA synthesis

55
Q

Causes of

megaloblastic anemia - B12 deficiency

A
dietary
Malabsorption (pernicious anemia)
Racial - Scandinavia
Gastrectomy
Hemodyalisism HIV - AIDS
Drugs/alcohol
56
Q

Causes of megaloblastic anemia - folic acid deficiency

A

Dietary - critical in pregnancy
Malabsorption - tropical sprue
Gluten-sensitive enteropathy
drug induced

57
Q

Cell types in megloblastic anemia

A

Oval macrocytes
Hypersegmented neutrophils
Pancytopenia
Asynchrony Elliptocytes

58
Q

Pancytopenia

A

deficiency in all 3 components of blood (red, white, platelets)

59
Q

Treatment for megaloblastic anemia

A
Near immediate response to IM B12 (12-24 hrs)
Elevated retics (new methylene blue stain)
60
Q

Untreated megaloblastic anemia

A

Neurological issues and death

61
Q

Megaloblastic anemia test

A
Elevated LDH, Indirect bilirubin, Iron Serum and ferritin, erythropoietin
Gastric achlorhydria
Serum B12
Red cell folate
Schiling test
Methylmalonic acid
62
Q

What anemia is cause by stem cell failure

A

Aplastic anemia

63
Q

What is aplastic anemia

A

failure of blood cell production by the bone marrow

64
Q

Types of aplastic anemia

A

Acquired and congenital

65
Q

What is acquired aplastic anemia

A

Idiopathic (primary 40-70%)

secondary to marrow damage from toxins, including radiation and immune responses

66
Q

What is congenital aplastic anemia

A

Fanconi’s anemia
dyskeratosis congenital
Dyserythropoetic CDA Type 1 and 2

67
Q

Acquired aplastic anemia test results

A

pancytopenia that progresses with age
low retic count
morphology typically normal
may do bone marrow tap (replacement of tissue with fatty deposits)

68
Q

Congenital aplastic anemia test results

A

untreated - patients usually die from infections or hemorrhage
Skeletal defects may be present