Hematology Flashcards

1
Q

How much blood is in the body?

A

6 quarts (5.5 L)

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2
Q

List the functions of blood

A
  1. Delivery of substances needed for cellular metabolism
  2. Removal of wastes of cellular metabolism
  3. Defense against invading microorganisms
  4. Regulation of body temp
  5. Maintenance of acid-base balance
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3
Q

What % of whole blood is plasma?

A

55%

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4
Q

What % of whole blood is formed elements?

A

45%

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5
Q

List the 3 types of plasma proteins

A
  1. Albumin
  2. Globulins
  3. Fibrinogen
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6
Q

Albumin

A

Plays a role in vascular, transport, & metabolic processes

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7
Q

List 3 types of globulin plasma proteins

A
  1. Alpha
  2. Beta
    A &B helps transport iron, fat soluble (lipids)
  3. Gamma
    Immunoglobulins or Ab that help fight infection
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8
Q

Fibrinogen

A

Plays a role in clotting

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9
Q

All plasma proteins are manufactured by what organ?

A

liver

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10
Q

Formed elements

A

Suspended in plasma
Finite lifespan (limited)
Originate from stem cells

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11
Q

List examples of formed elements

A

Erythrocytes (RBCs)
Leukocytes (WBCs)
-Granular
-Agranular
Thrombocytes (PLTs)

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12
Q

Erythrocytes (RBCs)

A

Most abundant
Make up ~ half of the blood volume
Play a role in tissue oxygenation

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13
Q

Erythrocytes (RBCs) contains

A

Hemoglobin
-Gases → Mainly transports O2 throughout the body & minor role of carrying CO2
-Electrolyte → imbalances can effect how O2 is transported
-Regulates diffusion through the cell membrane

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14
Q

List some characteristics of erythrocytes (RBCs)

A

Biconcave disc
Has no nucleus
Flexible
Has no cytoplasmic organelles (No protein synthesis)
Life span of 120 days

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15
Q

RBCs concave structure is…

A

Ideal for gas exchange & diffusion in & out of the cell

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16
Q

RBCs have ____ ____ to move throughout the body

A

Reversible deformity

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17
Q

List the different types of Hgb

A
  1. Hb A → Adult (normal)
    -Oxygen carrying protein
  2. Hb F → fetal
  3. Hb S → sickle cell
  4. Hb A1c → Glycosylated
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18
Q

Hemoglobin molecule is composed of…

A

4 polypeptide chains
- Alpha 1, Alpha 2
- Beta 1, Beta 2

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19
Q

1 Hgb molecule carries how many oxygen atoms?

A

1 Hgb molecule carries 4 oxygen atoms

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20
Q

Iron → Hemoglobin → O2

A

Synthesis of hemoglobin (Hgb) is greatly dependent on availability of iron

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21
Q

How can we as humans get iron?

A

Iron comes from diet or is recycled

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22
Q

What happens to aged RBCs?

A

They are broken down in the spleen & iron returns to bone marrow for new RBCs

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23
Q

A lack of iron results in…

A

A lack of Hgb in each RBC which results in low O2 carriage in the blood

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24
Q

Break down of the term “hemoglobin”

A

Heme → iron
Globin → protein

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25
Q

Where are phagocytic cells located?

A

Spleen
Liver
Bone marrow
Lymph nodes

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26
Q

Where are RBCs destroyed?

A

Liver & spleen

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27
Q

Destruction of RBCs:

Recycling to form new RBCs

A

Iron from heme group is recycled & reused to create new RBCs & globulin chains break down into individual AA to be recycled & build new proteins

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28
Q

List the steps of destruction of RBCs

A

Heme broken down into → bilirubin → transported in blood bound to plasma proteins → until it reaches the liver where it’s made water soluble to be eliminated from body via bile

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29
Q

Unconjugated bilirubin

A

Yellow pigment produced when RBCs break down

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30
Q

Conjugated bilirubin

A

Water-soluble form of bilirubin that is produced by the liver & excreted in the bile

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31
Q

Abnormal RBC destruction in circulation

A

Hgb remains in plasma
Combines w/ protein in plasma (haptoglobin) & other proteins (i.e. albumin)

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32
Q

What may happen during RBC destruction in circulation associated with haptoglobin?

A

Haptoglobin may exceed ability of plasma proteins to bind → free haptoglobin in blood → excreted via urine

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33
Q

Free haptoglobin in the blood is known as _____

A

Hemoglobinemia

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34
Q

List example conditions that occur from abnormal destruction of RBCs

A

Hemolytic anemia
Hemolytic transfusion reaction

35
Q

What is erythropoiesis

A

A specific series of steps in the BM that leads to the synthesis of mature RBCs

36
Q

What do all RBCs start out as?

A

Pluripotent stem cells in the bone marrow → stimulated to become an erythroid precursor cell

37
Q

Explain what happens in the series that erythroid precursor cells go through

A

goes through series of changes until it becomes a mature RBC released by the BM

38
Q

What is an immature RBC called?

A

Reticulocyte

39
Q

What form of RBCs have NO genetic material?

A

Mature RBCs

40
Q

What are the nutritional requirements for adequate synthesis of healthy RBCs?

A

Protein
Iron
Vitamin B12
Folic acid

41
Q

Iron as a nutritional element

A

Main nutritional elements for Hgb synthesis

42
Q

What types of pts might you see high RBC levels?

A

Patients with chronic hypoxia → i.e. COPD

43
Q

Reticulocyte count

A

good indicator of BM activity, because it represents recent production of RBCs

44
Q

What does a high reticulocyte count indicate?

A

Indicates that BM is working hard to keep up with RBC loss
-I.e. of causes: Anemia & cancer

45
Q

Spleen

A

Highly vascular organ, considered “graveyard of RBCs”
Also an organ of immunity

46
Q

Role of the spleen

A

Removes aged, lysed, & dead RBCs from circulation

47
Q

What happens to RBCs in the spleen?

A

Broken down into their component parts, which are recycled to make new RBCs

48
Q

The spleen sequesters…

A

Abnormally shaped & hemolyzed RBCs & destroys them

49
Q

How does splenomegaly occur?

A

Occurs when there is a large amount of RBC breakdown occurring in the body

50
Q

Leukocytes (WBCs) Normal range & function

A

NR: 5,000 to 10,000/ μL
Function → to combat inflammation & infection

51
Q

Two types of leukocytes & their subsections

A

Granulocytes:
- neutrophils
- eosinophils
- basophils
Agranulocytes:
- lymphocytes
- monocytes

52
Q

Immature WBCs (timeline)

A

Start as myeloblast → promyelocyte → myelocyte → loss of capacity for mitosis → metamyelocytes → band cell → segmented neutrophil → that eneters blood → enters tissues (1-2 days)

53
Q

Immature WBCs → left shift

A

Increased #s of immature neutrophils
most common cause is inflammation
can also be seen in some marrow disorders (leukemia) or severe BM injury

54
Q

How are cells classified?

A

Based on their stage of maturation

55
Q

Thrombocytes (platelets)

A

Large megakaryocytes → come from myeloid stem cells

56
Q

Thrombocytes form the ____ _____

A

platelet plug

57
Q

What do thrombocytes look like?

A

Disc shaped without a nucleus

58
Q

Thrombopoietin

A

Hormone that is chief regulator of PLT production & are synthesized by liver
Stimulated by ↓ # PLTs in BM

59
Q

How much of PLTs are squestered in the spleen?

60
Q

Senescent platelets

A

Aged PLTs that have lost function & less able to respond to clotting factors
Cleared by splenic macrophages after average lifespan of 7-10 days

61
Q

When assessing for bleeding what changes to the skin should you look for?

A

Petechiae
Purpura
Ecchymosis
Spontaneous bleeding

62
Q

Petechiae

A

Pinpoint red-purple areas of bleeding that resemble a rash

63
Q

Purpura

A

Larger purple areas of bleeding

64
Q

Ecchymosis

65
Q

Spontaneous bleeding

A

I.e. Nosebleed (epistaxis)

66
Q

What do CBCs look at?

A

WBCs
Hemoglobin
Hematocrit
Platelets

67
Q

What is included in WBC part of CBC?

A

Neutrophils
Lymphocytes
Monocytes
Eosinophils
Basophils
Immature granulocytes, absolute
Neutrophils, absolute

68
Q

What is included in hematocrit on CBC?

A

Mean corpuscular volume (MCV)
Red cell distribution width (RDW)
Mean corpuscular Hgb concentration (MCHC)
Mean cell Hgb (MCH)

69
Q

Mean corpuscular volume (MCV)

A

size of RBC

70
Q

Red cell distribution width (RDW)

A

range in size & shape of RBC

71
Q

Mean corpuscular Hgb concentration (MCHC)

A

concentration of Hgb (color)

72
Q

Mean cell Hgb (MCH)

A

Mass of RBC

73
Q

What does a BMP look at?

A

Sodium (Na)
Potassium (K)
Chloride (Cl)
CO2
BUN/ creatinine
Glucose
EGFR
Anion gap

74
Q

What is the anion gap?

A

Related to acid-base balance of electrolytes

75
Q

What does a CMP include?

A

Same as BMP
Plus:
-AST (SGOT)
-ALT (SGPT)
-Alkaline phosphatase
-Total protein
-Albumin
-Bilirubin

76
Q

List the different iron studies

A

Iron level
Ferritin
Transferrin
Total iron binding capacity (TIBC)

77
Q

Iron level:

A

Measures amount of iron bound to Hgb
Not helpful alone

78
Q

Ferritin:

A

Measure of iron stores
Inflammation may cause levels to increase

79
Q

Transferrin:

A

Iron transport protein takes Fe back to the BM

80
Q

List 4 other lab studies to look at

A

Vitamin B12
Folic acid
Hgb electrophoresis
Comprehensive metabolic profile (CMP)

81
Q

Hgb electrophoresis

A

Looks at the globin chains

82
Q

CMP measures…

A

14 proteins, electrolytes, enzymes, & minerals in the blood

83
Q

CMP is a BMP plus

A

Calcium
Albumin
Total protein
Liver function studies (AST, ALT, ALP, Bili)