Hemostasis Flashcards

1
Q

what are the 3 basic mechanisms of anemia

A

red cell loss
red cell destruction / lysis
lack of marrow production

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2
Q

what is something that could cause red cell loss

A

hemorrhage

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3
Q

what is something that can cause red cell destruction / lysis

A

hemolysis

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4
Q

what is something that can cause a lack of marrow production

A

bone marrow disease or suppression

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5
Q

what is the result of a lack of marrow production

A

limits the production of RBCs

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6
Q

if the bone marrow is normal, what would you expect to see with anemia

A

the body actively trying to correct the loss of RBCs through regenerative efforts

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7
Q

what type(s) of anemia are seen with regenerative anemias

A

hemorrhage
hemolysis

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8
Q

what is typically seen on a blood smear of a regenerative anemia

A

increase in reticulocytes present

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9
Q

which type of anemia is non-regenerative

A

bone marrow disease or suppression

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10
Q

what can be used to determine if the regenerative anemia is from blood loss or hemolysis

A

serum protein

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11
Q

why is low serum proteins indicative of a hemorrhage anemia

A

loss of RBCs and plasma proteins because it is leaking out of the capillaries

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12
Q

why is normal serum protein indicative of hemolysis anemia

A

the RBCs and plasma proteins will still be present within the circulatory system

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13
Q

what type of cell will stain blue

A

polychromasia

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14
Q

what causes polychromasia

A

recently released cells still with mRNA from the bone marrow (reticulocytes)

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15
Q

other than blue stain, what type of stain can be used to identify reticulocytes

A

vital stain

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16
Q

describe the cells when they first leave the bone marrow

A

larger
not fully hemoglobinized
blue in color

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17
Q

what is platelet adhesion

A

when a platelet adheres to the subendothelium

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18
Q

what protein is responsible for starting platelet adhesion

A

Von Willebrand Factor

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19
Q

what is formed through platelet - platelet adhesion

A

platelet plug

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20
Q

what process is done to form the platelet plug

A

platelet aggregation

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21
Q

what protein is responsible for platelet aggregation

A

fibrinogen

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22
Q

what are the differential diagnoses with primary hemostasis

A

platelet number
platelet function
Von Willebrand Disease

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23
Q

what is platelet number in clinical terms

A

thrombocytopenia

24
Q

what acts as a catalyst for fibrin formation

25
what are the coagulation factors of the intrinsic pathway
XII (12) XI (11) IX(9) VIII (8) *X (10)
26
what are the coagulation factor(s) of the extrinsic pathway
VII (7) *X(10)
27
what are the coagulation factors of the common pathway
X (10) V(5) II(2) I (1)
28
what protein is factor 1
fibrinogen
29
what does fibrinogen turn into? what is its use?
fibrinogen --> fibrin clot formation
30
which coagulation factor has the shortest half life
VII (7)
31
what is secondary hemostasis
formation of the fibrin clot
32
what is the differential diagnosis list for secondary hemostasis problems
reduction in one or more of the factors presence of an anticoagulant (rare)
33
what are some defects of primary hemostasis
petechiae eccyhmoses epistaxis
34
what are some defects of secondary hemostasis
hematoma formation hemothorax hemoabdomen
35
what is not significant in determining primary or secondary defects
excessive bleeding due to trauma
36
what "older" test can be done to test all primary hemostatic defects
buccal mucosal bleeding time
37
what "emergency" test could be done to screen for secondary hemostatic defects
Activated Clotting Time (ACT)
38
what are 2 routine coagulation tests used now
PT (Prothrombin time) PTT (Partial thromboplastin time)
39
which routine coagulation test is used to activate/ evaluate the extrinsic pathway
PT (prothrombin time)
40
which routine coagulation test is used to activate/ evaluate the intrinsic pathway
PTT (partial thromboplastin time)
41
what is used in the PT test to activate the clotting cascade
factor 7
42
what is used in the PTT test to activate the clotting cascade
factor 12
43
which tube is used to run a PT or PTT test
blue top tube
44
what is used in a blue top tube which makes it ideal for PT and PTT tests
citrate -- reacts with Ca which is needed to clot
45
true or false: factors must generally be increased by 30% of normal to prolong times
false decreased to prolong times
46
what is the ideal way to handle a PT / PTT test to ensure the best / most accurate results
separate plasma within 1 hour run test within 4 hours
47
what are the 4 top secondary hemostatic diseases
vitamin K antagonism / deficiency severe hepatic disease consumptive coagulopathy inherited coagulation factor deficiency
48
what are the 2 main consumptive coagulopathy disorders
disseminated intravascular coagulation (DIC) localized consumption
49
what is the most common secondary hemostatic disease
vitamin K deficiency / antagonism
50
what factors is vitamin K necessary for activation
II VII IX X
51
what are the 2 ways for vitamin K deficiency
absence (uncommon) antagonism (rodenticide poisoning)
52
why is liver disease often seen with vitamin K issues
vitamin K is fat soluble and needs bile for transportation / breakdown and often blocks the bile ducts
53
how long does it take for an animal with vitamin K antagonism to respond to treatment with vitamin K
a few hours
54
why is knowing the half life of vitamin K important when treating a rodenticide patient
will determine how long you need to treat an animal
55
what are 2 ways liver disease impacts hemostasis
makes coagulation factors -- damage would decrease the amount made colistatic liver disease-- bile issues
56
what would you expect to see on test results of and animal with liver disease causing secondary hemostatic disease
increased PT increased PTT *history and clinical signs are important