P17 - Primary Hemostatic Disorders Flashcards

1
Q

primary hemostasis involves

A
  • vasoconstriction

- platelet adhesion

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2
Q

secondary hemostasis involves

A
  • coagulation cascade
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3
Q

tertiary hemostasis involves

A
  • fibrinolysis
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4
Q

thrombocytopenia

A
  • low platelet count (quantity)
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5
Q

pseudothrombocytopenia

A
  • false thrombocytopenia
  • cats (large platelets)
  • horses when blood in EDTA tube
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6
Q

thrombocytosis

A
  • increased platelet count
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7
Q

thrombocytopathy

A
  • loss or impaired platelet function

- think vWD

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8
Q

BMBT

A

buccal mucosal bleeding time

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9
Q

clinical pathology abnormalities in vWD (4)

A
  • Thrombocrit is less than 1%
  • BMBT is prolonged
  • CRT is abnormal (prolonged)
  • Clot lysis is abnormal
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10
Q

hemostasis is an interaction between (4)

A
  • blood vessels
  • platelets
  • coagulation factors
  • fibrinolysis
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11
Q

evaluation of coagulopathies (5)

A
  • onset of bleeding
  • age
  • history
  • environmental evidence
  • coagulation profile
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12
Q

sample collection that test PTT and PT (secondary hemostasis)

A
  • sodium citrate
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13
Q

sample collection that test platelet counts, thrombocrit, MPV (primary hemostasis)

A
  • EDTA
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14
Q

sample collection that test platelet CT, ACT, CRT

A
  • plain tubes
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15
Q

goal of primary hemostasis (2)

A
  • formation of platelet plug

- vasoconstriction

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16
Q

proteins of primary hemostasis (3)

A
  • vWF
  • collagen
  • fibrinogen binds platelets
17
Q

major inhibitor of primary hemostasis (2)

A
  • prostacyclin (prostaglandin P-12)

- Nitric oxide produced by endothelial cells

18
Q

quality of platelets described as

A
  • thrombocytopathy
19
Q

quantity of platelets described as

A
  • thrombocytopenia
20
Q

petechiae

A
  • pinpoint hemorrhages

- indicative of platelet or blood vessel problem

21
Q

test for platelets (5)

A
  • thrombocrit or plateletocrit
  • platelet counts
  • platelet distribution width
  • measurement of anti-platelet antibodies
  • flow cytometry
22
Q

factors that could cause prolonged bleeding time (2)

A
  • vascular or platelet (quantity and quality)

- von Willebrand’s disease

23
Q

clot retraction time (CRT) technique

A
  • red top tube
24
Q

platelet aggregation test measures

A
  • ability of platelets to clot (speed and degree)
25
Q

clinical presentation of vWD

A
  • bleeding in gums, epistaxis, hematuria, melena

- small puppies bleed excessively

26
Q

clinical pathology abnormalities of vWD (7)

A
  • coagulation test are WRI (PTT & PT)
  • thrombocrit is less than 1%
  • platelet count is WRI
  • BMBT is prolonged
  • CRT is abnormal
  • clot lysis is abnormal
  • low vWF
27
Q

reasons for thrombocytopenia (4)

A
  • inadequate production
  • increased utilization
  • increased destruction
  • clinical pathology abnormalities
28
Q

pseudothrombocytopenia due to (3)

A
  • platelet clumping
  • bad sample collection
  • band sample handling
29
Q

naturally susceptible species of pseudothrombocytopenia

A
  • cats and pigs

- horses blood in EDTA

30
Q

thrombocytosis occurs secondary to (4)

A
  • leukoerythroblastic response
  • neoplasia
  • inflammation
  • hemolysis