Ch. 18 Flashcards

Blood

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1
Q

What is the average blood volume in humans?

A

70 mL per kg of body weight

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2
Q

What is the between plasma and serum?

A

Serum lacks fibrinogen and other coagulation factors

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3
Q

What is the normal amount of hematocrit in men vs women?

A

Women: 38-42%

Men: 40-44%

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4
Q

Calculate Hematocrit

A

Hematocrit = height of RBCs/ total height

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5
Q

What is the source of most blood cells?

A

Bone Marrow

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6
Q

What cells are produced from megakaryocyte-erythroid progenitor cells?

A

Megakaryocyte, platelets, and RBCs

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7
Q

What is necessary for the production of RBCs?

A

EPO

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8
Q

What is necessary for the production of platelets?

A

TPO and IL11 are required to produce megakaryocytes, which produce platelets

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9
Q

How does renal failure effect RBC development?

A

JG (which senses oxygen) does not function, so EPO levels don’t rise correctly in response to low O2 levels; results in anemia

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10
Q

Coagulation

A

the cessation of bleeding

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11
Q

Anticoagulation

A

limiting the extent of coagulation so you don’t get blood clots

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12
Q

Fibrinolysis

A

clot lysis

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13
Q

What are the 4 methods by which hemostasis can be achieved?

A
  1. Vasoconstriction
  2. Increased tissue pressure
  3. Formation of a platelet plug in the case of capillary bleeding
  4. Coagulation or clot formation
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14
Q

What are the 3 A’s of Platelet Function?

A

Adhesion
Activation
Aggregation

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15
Q

How are platelets involved in primary hemostasis?

A

At the site of vessel injury, they adhere by GP1b and vWF (Adhesion). They get activated by a number of receptors that leads to signaling for recruitment of other platelets, then form complexes on their surfaces to have platelet-platelet interactions that causes aggregation (Activation). Eventually they form a big glob of platelets that forms a platelet thrombus.

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16
Q

Know the Coagulation Cascade

A

How’d you do?

17
Q

Disorders of the intrinsic system

A

Associated with bleeding: VIII, IX, XI

Not Associated with Bleeding: XII, HMWK, Prekallikren

18
Q

Surface Bound Zymogens

A

Factor XII, Prekallikrein, Factor XI

19
Q

Phospholipid Bound Zymogens

A

Factors II, VII, IX, and X

20
Q

Cofactors/Substrates

A

HMWK, Factors V and VIII, Tissue Factor, and Fibrinogen

21
Q

Activated Partial Thromboplastin Time (APTT)

A

Measures intrinsic and common pathways

22
Q

Prothrombin Time

A

measures extrinsic and common pathways

23
Q

Thrombin Time

A

measures transition from fibrinogen to fibrin

24
Q

Tenase

A

necessary to make factor Xa

25
Q

Prothrombinase

A

necessary to convert prothrombin (II) to thrombin (IIa)

26
Q

Protein C/Protein S System

A

inactivates factors Va and VIIIa (cofactors for prothrombinase and tenase, respectively)

27
Q

Antithrombin

A

inhibits many factors, but main effect is on IIa and Xa

28
Q

Tissue Factor Pathway

A

inhibits VIIa and Xa

29
Q

What are 3 high risk defects associated with Venous Thrombosis?

A

Protein C, Protein S, and Antithrombin