Chapter 17: Blood Flashcards

(154 cards)

1
Q

<p>What type of tissue is blood?</p>

A

<p>Connective Tissue</p>

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2
Q

<p>What is the approximate blood volume in adults? Males and Females</p>

A

<p>Male 5-6L, Female 4-5L</p>

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3
Q

<p>What are the 2 main components of blood (liquid and non-liquid)?</p>

A

<p>Plasma (liquid) and Formed Elements (what's being carried around)</p>

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4
Q

<p>What % of blood is plasma?</p>

A

<p>55%</p>

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5
Q

<p>What are the 3 categories of formed elements?</p>

A

<p>Erythrocytes, Leukocytes, Platelets</p>

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6
Q

<p>What are Erythrocytes</p>

A

<p>Red blood cells</p>

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7
Q

<p>What are Leuokocytes</p>

A

<p>white blood cells</p>

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8
Q

<p>What are Platelets</p>

A

<p>Thrombocytes/fragments of cells; less than 1% of blood</p>

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9
Q

<p>5 Types of Leuokocytes</p>

A

<p>Neutrophils, Eosinophils, Basophils, Lymphocytes, Monocytes</p>

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10
Q

<p>What is in the "buffy coat?"</p>

A

<p>Leukocytes and Platelets</p>

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11
Q

<p>What are the functions of blood?</p>

A

<p>Distribution, Regulation, Protection</p>

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12
Q

<p>In blood, what is being distributed?</p>

A

<p>O2 & nutrients to body cells, remove metabolic waste to lungs and kidneys for elimination, transports hormones from endocrine to target organs</p>

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13
Q

<p>In blood, what is being regulated?</p>

A

<p>Body temp, blood ph, blood volume</p>

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14
Q

<p>How does blood protect?</p>

A

<p>Hemostasis and Prevents Infections</p>

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15
Q

<p>What is hemostasis? How does it work?</p>

A

<p>Protects against blood loss; plasma protein and platelets initiate clot</p>

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16
Q

<p>How does blood help prevent infection?</p>

A

<p>Antibodies, compliment proteins, WBC defend against foreign invaders</p>

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17
Q

<p>What color is plasma? Is it thick or thin?</p>

A

<p>Straw/pale yellow in color, viscous</p>

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18
Q

<p>What is the composition of plasma?</p>

A

<p>90% Water, 10% solute</p>

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19
Q

<p>What things are dissolved in plasma?</p>

A

<p>nutrients, gases, salts, hormones, proteins</p>

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20
Q

<p>Where do most formed elements come from?</p>

A

<p>Bone marrow, they do not divide</p>

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21
Q

<p>How long do mot formed elements last in the blood stream?</p>

A

<p>only a few days, except rbc's</p>

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22
Q

<p>What are the 3 classes of formed elements?</p>

A

<p>Erythrocytes (RBC), Leukocytes (WBC), Platelets (thrombocytes)</p>

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23
Q

<p>What are erythrocytes</p>

A

<p>Also known as RBC's, bag of hemoglobin</p>

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24
Q

<p>Characteristics of erythrocytes</p>

A

<p>Biconcave, anucleate, hemoglobin (Hb)</p>

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25

What is the main function of erythrocytes?

respiratory gas transport

26

What is the name of the molecule that binds oxygen?

Hemoglobin

27

Hemoglobin

Made up of heme, globin and iron. 4 globin chains containing heme, which contain iron, iron binds to O2

28

Hematopoesis

blood cell formation

29

Where does hematopoiesis occur?

red bone marrow of axial skeleton, girdles and proximal epiphyses of humor and femur

30

What is the name for the formed element stem cell?

Hemocytoblasts

31

What determines the pathway for further differentiation for formed element stem cells?

hormones and growth factors

32

What is erythropoiesis?

red blood cell formation

33

What signals the start of erythropoiesis?

Erythropoietin (released by kidney in response to Hypoxia)

34

Why is the regulation of erythropoiesis so important?

Tissue hypoxia, blood viscosity

35

How is erythropoiesis controlled?

balance between production and destruction by hormones and adequate supply of iron, amino acids and b vitamins

36

What is hypoxia?

Low oxygen

37

What causes hypoxia?

hemorrhage or increased RBC destruction, iron deficiency/low hemoglobin, reduced O2 availability in high altitudes

38

What does hypoxia cause the kidney to release? And why?

erythropoietin to stimulate red bone marrow to produce rbc

39

What is the lifespan of RBC?

100-120 days

40

What happens to RBC's as they deteriorate?

They become fragile, hemoglobin degenerate

41

Who eats RBC's and where are they doing it?

Macrophage engulf RBC in spleen and liver

42

What is a leukocyte and what % of blood volume does it make up?

White blood cell, makes up 1% of total blood volume

43

What do leukocyte's leave behind during diapedesis?

capillaries (small blood vessels)

44

What is diapedesis?

blood cells moving out of blood vessels into tissue

45

What are the 2 main classes of leukocytes? And what are they based off of?

Granulocytes and Agranulocyte; presence of granules in cytoplasm

46

Types of Granulocytes and their percent abundance in WBC

Neutrophils 50-70% (most abundant)
Eosinophils 2-4%
Basophils .5-1% (Rarest)

47

Types of agranulocytes and their percent abundance in WBC

Lymphocytes (25-45%, 2nd most common), Monocytes (3-8%, 3rd most common)

48

What do granulocytes have?

Cytoplasmic granules that stain in characteristic colors with a wright's stain

49

3 types of granulocytes

Neutrophils, Basophils, Eosinophils

50

What are neutrophils? And what is another name for them?

Fine granules that take up both acidic and basic dyes (pale staining), most numerous, very phagocytic, Also called PMN's (polymorphonuclear leukocytes)

51

What does polymorphonuclear leukocytes mean?

many shapes

52

What do neutrophil/pmn granules contain?

hydrolytic enzymes or defensins

53

What does an increase in neutrophil's indicate?

Body is fighting bacterial infection

54

5 Eosinophils Characteristics

Nucleus is bilobed, granules stain pink, granules are similar to lysosomes, digests parasitic worms, regulates immune response

55

3 Basophils characteristics

Rarest of WBC, granules are purple-black and contain histamine

56

What does histamine do?

Anti-inflammatory chemical that attracts other WBC to inflamed sites

57

What are agranulocytes?

Lack granules and nuclei are either spherical or kidney shaped

58

Describe Lymphocytes

large, dark purple nucleus with thin layer of cytoplasm

59

Where are lymphocytes found?

Lymphoid tissue, few in blood

60

What is the job of a lymphocyte?

immunity

61

What are the 2 types of lymphocytes?

B and T cells

62

What are monocytes?

largest of the WBCs, they leave blood circulation and enter tissues where they then turn into macrophage; actively phagocytic

63

Why are monocytes important?

Fight against viruses, intracellular bacterial parasites and chronic infection; can activate lymphocytes

64

Leukopoesis is the production of what?

wbc

65

What is leukopoesis stimulated by?

chemical messengers from bone marrow and mature wbc

66

All leukocytes originate rom what type of stem cell?

Hemocytoblasts

67

What is another name for platelets?

Thrombocytes

68

What is thrombopoiesis?

platelet formation

69

What is the job of thrombopoetin?

stimulate platelet creation

70

What are platelets?

Small fragments of a parent cell called a mega kerocyte (cell with big nucleus)

71

Platelets have granules that contain?

serotonin, calcium, enzymes, ADP, platelet derived growth factor (PDGF)

72

What is hemostasis?

Reactions to prevent blood loss/bleeding; goal is to stop bleeding

73

Three phases of hemostasis

Vascular spasm, platelet plug formation, coagulation

74

3 phases of coagulation

prothrombin activator is formed, prothrombin converted into thrombin, thrombrin triggers fibrinogen to create fibrin

75

What are 2 ways to form prothrombin during coagulation?

Intrinsic (vessel ruptures) and extrinsic (happens in tissue)

76

What happens after hemostasis and clot formation?

clot retraction and repair where actin and myosin retract within 30-60 minutes, platelets pull fibrin strands loose to leak serum

77

Two types of clot repair

PDGF (platelet derived growth factor) and VEGF (vascular endothelial growth factor)

78

Platelet Derived Growth Factor (PDGF)

Stimulates division of smooth muscle cells and fibroblasts to rebuild blood vessel wall

79

Vascular Endothelial Growth Factor (VEGF)

Stimulate endothelial cells to multiply and restore endothelial lining

80

What is fibrinolysis and when does it start?

the breakdown of fibrin, begins within 2 days

81

During fibrinolysis, what is going on with plasminogen and plasmin?

Plasminogen in clot converted to plasmin by the tissue plasminogen activator, factor XII and thrombrin

82

What controls the size of a blood clot?

Swift removal and dilution of clotting factors

83

What 3 things inhibit the activation of clotting factors?

Antithrombin III, protein c, heparin

84

What is a bad clot?

A clot forming that is not needed

85

What prevents bad clots from forming/platelet adhesion?

smooth endothelial lining of blood cells, antithrombic substances, vitamin E

86

Why is restoring blood volume important?

Required to deliver important nutrients to brain (o2)

87

In order to restore blood volume, what can blood be replaced by?

normal saline or electrolyte solution, plasma expanders (may cause complications)

88

When does a whole blood transfusion occur?

When there has been substantial blood loss

89

What are packed RBC used for?

Restore oxygen-carrying capacity (removed plasma from blood)

90

Plasma alone can be used for what?

Restoring blood volume

91

What can happen if blood between a donor and recipient is incompatible?

Can be fatal

92

What are antigens? How many are there?

identifiers on cell membranes that are glycoproteins; 30 different antigens, unique to each individual

93

What happens if blood is mismatched?

Body recognizes it as foreign and then destroys rbc

94

How is blood classified into groups?

Presence of an antigen on the RBC plasma membrane

95

What are the most common blood types?

A, B, AB, O

96

When do anti-A or anti-B antibodies form?

About 2 months of age

97

What does it mean to have Type B blood?

B-antigen, A antibody; can give to B and AB, can receive from O, B; 12%of population

98

What does it mean to have Type O blood?

Neither A or B antigen, A and B antibody, can give to anyone, can only receive from O. "universal donor" 45% of population

99

What does it mean to have Type A blood?

A antigen, anti-B, can give to A and AB can receive from A and O; 39% of population

100

What does it mean to have type AB blood?

A and B Antigen, Neither a or b antibodies, can give to AB, can receive from A, B, AB, and O; 4% of population; "universal recipient"

101

How do you blood type?

Serum containing anti-A or anti B antibodies is added to blood, if the matching antigen is present, blood will clump creating a positive reaction

102

What type of blood is this?

Type AB

103

What type of blood is this?

Type B

104

What type of blood is this?

Type A

105

What type of blood is this?

Type O

106
How many different Rh blood groups are there? What are the most common?
45, C, D,E
107
What does Rh+ indicate?
D
108
What happens if a person lacking the Rh antigens (Rh-) receives blood from an Rh+ donor?
They form anti Rh antibodies
109
What are two things that can happen when donor blood is mismatched?
Agglutinate - clotting or lack of O2, blood cells rupture and release hemoglobin into bloodstream
110
what is anemia?
Blood has abnormally low O2 carrying capacity; cells can not thrive
111
Is anemia a sign or a disease?
More a sign than disease
112
What are the common symptoms associated with anemia?
fatigue, paleness, shortness of breath
113
What are the 3 common causes of anemia?
insufficient rbc (erythrocytes), low Hb, abnormal Hb
114
What can cause insufficient RBC?
hemorrhagic anemia, hemolytic anemia, aplastic anemia
115
What is hemorrhagic anemia?
acute or chronic loss of rbc
116
What is hemolytic anemia?
rupture or loss of RBC
117
What is aplastic anemia?
Destruction of red bone marrow
118
What can cause low Hb in RBC?
iron deficiency, pernicious anemia
119
What are the 3 causes of an iron deficiency?
lack of iron in diet, impaired iron deficiency, hemorrhagic anemia
120
What is pernicious anemia? How is it treated?
deficiency of vitamin B12 caused by lack of intrinsic factor need to absorb B12; treated with B12 injection or spray
121
What is abnormal Hb and what its causes?
abnormal looking and easily destroyed RBC caused by Thalassemias and sickle-cell anemia
122
What is thalassemias?
absent or faulty globin chain
123
What is sickle-cell anemia?
Mistake in genetic code for Hb, causing sickle shaped RBC
124
What is polycythemia?
excess RBC that increase blood viscosity
125
What are the 3 causes of polycythemia?
polycythemia vera, secondary polycythemia, blood doping
126
What is polycythemia vera?
bone marrow cancer
127
What is secondary polycythemia?
less o2 available or when EPO production increases
128
What is blood doping?
Taking medicine that increases RBC count
129
What are the 2 leukocyte disorders?
Leukopenia and leukemia
130
What is leukopenia?
Abnormally low WBC, drug induced
131
What is leukemia?
increase in WBC count, cancer in bone marrow
132
What does myelocytic leukemia involve?
myeloblasts
133
What does lymphocytic leukemia involve?
lymphocytes
134
What type of cells does acute leukemia involve? Who is it most prevalent in?
blast-type cells, occurs primarily in children
135
Chronic leukemia is more prevalent in?
older people
136
What happens to the bone marrow in leukemia?
overtaken by cancerous leukocytes, where immature/non-functional WBC are released into the blood stream
137
How can leukemia cause death?
internal hemorrhage and overwhelming infections
138
How is leukemia treated?
Irradiation, anti leukemia drugs, stem cell transplant
139
How are the leukemia's named?
According to the WBC precursor clone involved
140
In bone marrow transplants, what the timeline to know if it worked? And success rates
If no engraftment by 42 days, failure; if engrafted then can go home after 100 days; siblings 55-90%, unrelated 25-65%
141
What is thromboembolic and what are the two types?
blood clotting disorder, Thrombus and Embolus
142
What are Thrombus clots?
Undesirable clot formation, stationary, clot develops in unbroken vessel, can lead to death
143
What are Embolus clots?
Thrombus is freely floating in the bloodstream
144
How can you prevent thromboembolic conditions?
asprin, heparin, warfarin
145
What is Heparin commonly used for?
Anticoagulant used for pre and post operative cardiac care
146
What is warfarin commonly used for?
Used for those prone to fibrillation
147
What are 2 bleeding disorders?
Thrombocytopenia and Hemophillia
148
What is thrombocytopenia? Common symptons?
deficient # of circulating platelets; petechiae, low platelet count (less than 50k)
149
What is hemophilia? What are the 3 types?
hereditary bleeding disorder; hemophilia A, B and C
150
What is hemophilia A?
def. of factor VIII, most common
151
What is hemophilia B?
Def of factor IX
152
What is hemophilia C?
Mild, def of factor XI
153
What are the symptoms of hemophilia?
prolonged bleeding, especially into join cavities
154
How do you treat hemophillia?
plasma transfusions, injection of missing factors