hemostasis Flashcards

1
Q

hemostasis

A

bodys ability to maintain integrity of blood and blood vessels

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2
Q

how does body maintain hemostasis

A

interaction between vessels, platelets, and coag factors

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3
Q

primary hemostasis

A

vascular response (vessels contract due to injury) and platelet response (become sticky using von Willebrand’s) platelet plug

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4
Q

secondary hemostasis

A

coag cascade (made in liver, forms fibrin clot)

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5
Q

fibrinolysis

A

dissolves clot, activation of plasminogen into plasmin

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6
Q

primary hemostasis is the

A

interaction between platelets and vessel wall

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7
Q

circulating blood contacts the

A

subendothelial (connective tissue)

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8
Q

vascular spasm

A

immediate but temporary closure of blood vessel by contraction stimulated by nervous system response

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9
Q

platelet plug formation

A

stimulated by vWF

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10
Q

adhesion of platelets

A

platelets stick to connective tissue

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11
Q

aggregation of platelets

A

forms plug, thromboxane stimulates platelets to join, only in small vessels

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12
Q

secretion of platelets

A

vasoconstriction and further aggregation

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13
Q

acquired primary hemostasis disease

A

vasculitis, collagen deficiency, extensive vascular injury

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14
Q

inherited primary hemostasis disease

A

von Williebrands

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15
Q

most common cause of bleeding disorders

A

thrombocytopenia

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16
Q

von Willibrands disease

A

lack of vWF (dobies)

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17
Q

clinical signs of vWD

A

spontaneous hemorrhage from nose, vagina, urinary bladder, mucous membranes, prolonged bleeding time

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18
Q

treatment of vWF

A

transfusion of dog blood products, suture bandage or wound glue, should not be given drugs

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19
Q

dogs having low plasma below 50%…

A

may be as risk of expressing vWF

20
Q

dogs having low plasma below 25%…

A

severely affected by vWF

21
Q

secondary hemostasis requires

A

coagulation (clotting) factors

22
Q

cascade

A

conversion of inactive factors to active factors (domino effects)

23
Q

fibrin clot is….

A

long lasting (minutes to hours)

24
Q

coag factor substances are made in the

25
factors for intrinsic pathway
12, 11, 9, 8 (XII, XI, IX, VIII)
26
intrinsic pathway
all factors required for pathway is already available in the blood
27
extrinsic pathway
requires tissue factor for activation (thromboplastin)
28
factor for extrinsic pathway
7 (VII)
29
the liver synthesizes...
all pathways
30
vitamin K dependent factors
II, VII, IX, X (2, 7, 9, 10)
31
hemostasis defects may be
acquired or hereditary
32
most common inherited blood clotting disorder in dogs
hemophilia A
33
what causes hemophilia
mutation of specific gene causing a deficiency in factor VIII which interferes with clotting factors
34
Dx of hemophilia
APTT and measuring factor VIII
35
deficiency of vitamin K
rodenticide poisoning
36
disseminated intravascular coagulopathy (DIC)
secondary to heat stroke, endotoxemia, massive necrosis, trauma, septicemia
37
clinical signs of hemostasis defects
hematomas, hemorrhaging, bleeding into muscles, joints, and cavities, delayed clotting, petechiae
38
fibrinolysis
break down of fibrin clot
39
lysis of clot through activation of...
plasminogen into plasmin
40
breakdown of fibrin produces...
fibrinogen degradation products (FDP)
41
FDPs
have anticoagulant activity; block thrombin & inhibit platelets
42
excessive FDP
DIC, liver failure, heat stroke, trauma, necrosis
43
DIC
Excessive activation of clotting mechanism results in fibrin clot formation throughout microcirculation
44
primary hemostasis in house tests
platelet count and BMBT
45
secondary hemostasis in house tests
ACT and APTT
46
what tests for fibrinogen
thromboplastin time