Chapter 14 Study Guide Flashcards

1
Q

what is hemostasis?

A

hemostasis = the process to stop bleeding and prevent further blood loss

  • hemostasis fails = bleeding continues
  • excessive hemostasis = blood clotting
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2
Q

different stages of hemostasis

A

primary hemostasis
1. vasoconstriction = injured blood vessel constricts to reduce blood loss
2. platelet plug = complex of platelets and von Willebrand factor (VWF) → platelets stick to VWF

secondary hemostasis
3. coagulation cascade = formation of fibrin clot → fibrinogen is converted to fibrin
4. clot retraction = components of fibrin clot (platelet plug, fibrin, RBCs) get compacted to form a firm clot

after clot is not needed, it will be broken down
5. fibrinolysis = releases tpa (tissue plasminogen activator)

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3
Q

explain fibrinolysis

A

fibrinolysis = breaking down the blood clot/fibrin by releaseing tpa (tissue plasminogen activator)

plasminogen → plasmin → plasmin breaks down blood clot → D-dimers

  • plasmin breaks down blood clot into D-dimers
  • D-dimers = small pieces of broken down blood clot
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4
Q

what are D-dimers?

  • what do high amount of D-dimers mean?
  • what do low amount of D-dimers mean?
A

D-dimers = small pieces of broken down blood clot → it was broken down by plasmin

  • high amount of D-dimers = there must be a blood clot in the body → bc body is trying to break it down
  • low amount of D-dimers = no blood clots → this is normal
    normally, we should have a very low amount of D-dimers in the body
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5
Q

what organ produces many of the coagulation factors?

A

liver produces many of the coagulation factors

  • if a person has liver cirrhosis → they are unable to make coagulation factors
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6
Q

are clotting factors active or inactive?

A

clotting factors are always inactive by default

  • clotting factors must be activated by the previous factor before them
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7
Q

what are 2 things that are a must need for hemostasis = coagulation cascade?

A

calcium and vitamin K = are critical for hemostasis / coagulation cascade

  • vitamin K = makes a lot of clotting factors
  • calcium = activates a lot of clotting factors
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8
Q

what pathways does calcium and vitamin K work on?

A

calcium and vitamin K work on all the pathway = intrinsic (platelet) pathway, extrinsic (tissue) pathway, and common pathway

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9
Q

how do we diagnose the pathways?

A

intrinsic (platelet) pathway = aPTT
- aPTT = activated partial prothromblastin time

extrinsic (tissue) pathway = PT/INR
- PT/INR = prothrombin time/international normalized ratio

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10
Q

what are main points of intrinsic vs extrinsic coagulation

A

intrinsic (platelet) pathway = contact activation → blood clot is activated from inside of cell = aPTT

extrinsic (tissue) pathway = cell injury from external trauma = PT/INR

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11
Q

what is the common pathway?

A

intrinsic and extrinsic pathway will both lead to the common pathway

common pathway = prothrombin → thrombin → fibrinogen → fibrin

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12
Q

what drug prolongs bleeding time?

A

aspirin

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13
Q

dysfunction of what organ can lead to clotting factor deficiency?

A

dysfunction of the liver can lead to clotting factor deficiency

  • this is because the liver makes a lot of coagulation factors
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14
Q

hemophilia (2 types)

A

hemophilia = inherited (X-linked recessive) disease → male dominant disease

  • hemophilia A = factor VIII deficiency
    hemophilia A = factor 8 deficiency
  • hemophilia B = Christmas disease = factor IX deficiency
    hemophilia B = Christmas disease = factor 9 deficiency

factor 8 and 9 are part of intrinsic (platelet) pathway = aPTT will be prolonged
- prolonged aPTT
- prolonged bleeding time
- normal platelet count

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15
Q

hemophilia

  • bleeding time
  • aPTT
  • platelet count
A

hemophilia → intrinsic pathway deficiency

  • aPTT = prolonged
  • bleeding time = prolonged
  • platelet count = normal → hemophilia doesn’t affect platelets
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16
Q

what causes thrombocytopenia?

A

thrombocytopenia = low platelets

  1. chemotherapy = bone marrow suppression
  2. alcohol ingestion
  3. recent immunizations
17
Q

what is included in bleeding time?

A

bleeding time = platelet plug and all 3 pathways → intrinsic (platelet) pathway, extrinsic (tissue) pathway, common pathway

remember…
- intrinsic (platelet) pathway = aPTT
- extrinsic (tissue) pathway = PT/INR

18
Q

vitamin K deficiency

  • platelet count
  • aPTT
  • PT/INR
  • bleeding time (BT)
A

vitamin k deficiency = less vitamin K → less clotting factors
- vitamin K is needed in both intrinsic (platelet) pathway and extrinsic (tissue) pathway

  • normal platelet count
  • prolonged/extended aPTT
  • prolonged PT/INR
  • prolonged bleeding time
19
Q

vitamin k deficiency in newborn

A

newborn has melena, bleeding from umbilicus, and hematuria
- melena = black feces made of digested blood
- hematuria = blood in urine

20
Q

DIC = disseminated intravascular coagulation

  • platelet count
  • aPTT
  • PT/INR
  • BT
  • D-dimer
A

DIC = clotting and bleeding occur simultaneously
- there is too much coagulation (blood clot)
- too much bleeding

  • DIC patients will have a very high amount of D-dimers
  • low platelet count
  • prolonged aPTT
  • prolonged PT/INR
  • prolonged BT
  • increased D-dimers
21
Q

if a patient has a lot of D-dimers in blood, what does that indicate?

A

very high amount of d-dimers = patient had DIC (disseminated intravascular coagulation)

  • the patient has a blood clot
22
Q

von Willebrand disease (vWD)

A

von Willebrand disease = inherited defect in von Willebrand factor → leads to excessive bleeding

  • autosomal dominant = equal in male and demale population
  • prolonged/extended aPTT
  • extended bleeding time
  • normal platelet count
  • normal PT/INR