coagulation disorders Flashcards

(34 cards)

1
Q

haemostasis

A

arrest of bleeding

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2
Q

thrombosis

A

inappropriate formation of clots within vascular system

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3
Q

bleeding

A

failure of blood to clot in response to appropriate stimulus

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4
Q

stages of haemostasis

A
  1. vessel spasm
  2. formation of platelet plug
  3. blood coagulation or development of insoluble fibrin clot
  4. clot restriction
  5. clot dissolution
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5
Q

requirements of blood clotting process

A

platelets (produced in bone marrow)
Von Willebrand factor (generated in vessel endothelium)
clotting factors (synthesised in liver using Vit K)

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6
Q

clotting factor I

A

fibrinogen

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7
Q

clotting factor II

A

prothrombin

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8
Q

clotting factor III

A

thromboplastin

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9
Q

clotting factor IV

A

calcium

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10
Q

clotting factor VIII

A

anti-hemophilic factor

if don’t have = haemophilia A

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11
Q

intrinsic blood clotting pathway

A

disease within body triggers clot formation, vitamin K dependent

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12
Q

extrinsic blood clotting pathway

A

external stimulus triggers blood clot

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13
Q

terminal steps of blood clotting process

A
  1. calcium, factors V and X, platelet phospholipids combine to form prothrombin activator
  2. prothrombin activator converts prothrombin to thrombin
  3. this causes the conversion of fibrinogen to fibrin strands which create the insoluble clot
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14
Q

hypercoagulability states

A

increase risk of clot or thrombus formation in the arterial or venous circulations

caused by accelerated activity of coagulation system or increased platelet function

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15
Q

conditions that create increased platelet function

A

atherosclerosis, diabetes, smoking, elevated blood lipids and cholesterol, increased platelet levels

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16
Q

conditions that cause accelerated activity of coagulation system

A

pregnancy, peurperium (6 weeks after delivery), oral contraceptives, post-surgical state, immobility, congestive heart failure, malignant diseases

17
Q

arterial thrombi

A

associated with conditions that produce turbulent blood flow and platelet adherence

18
Q

venous thrombi

A

associated with conditions that cause stasis of blood flow with increased concentrations of coagulation factors

19
Q

coagulation defects

A

impaired synthesis of coagulation factors

hereditary disorders - hemophilia A and Von Willebrand disease

20
Q

conditions associated with disseminated intravascular coagulation

A

obstetric conditions, cancer, infections, shock, trauma and surgery, hematologic conditions

21
Q

disseminated intravascular coagulation

A

plenty of blood clots and blockages = tissue and organ death, but some bleeding occurring too

22
Q

hemophilia

A

inherited bleeding disorder in which there is a deficiency or lack of factor VIII (A) or IX (B)

23
Q

detection of hemophilia

A

family history, symptoms (bruising, bleeding after minor surgery, muscle/joint/soft tissue bleeding), lab testing, hemostatic challenges (surgery, dental work, trauma)

24
Q

types of bleeds

A

joint bleeding, muscle hemorrhage, soft tissue, life threatening and other

25
Von Willebrand disorder
bleeding disorder - hereditary pseudohemophilia prolonged bleeding despite normal platelet count - VW factor deficiency
26
platelet function
formation of mechanical plug during normal hemostatic response to vascular injury adhesion, activation and release, aggregation
27
normal platelet count
250 000 uL life span 7-10 days
28
platelet adhesion
platelet adheres to sub-endothelial collagen dependent on VW factor and glycoproteins
29
platelet activation
changes shape and release chemical signals (ADP, serotonin, prostaglandins)
30
platelet aggregation
stick to cells going past to form the plug
31
causes of bleeding
decrease in number of circulating platelets or impaired platlet function
32
scurvy causing bleeding
poor collagen synthesis and failure of endothelial cells to cement together = fragile wall
33
cushing's disease causing bleeding
protein wasting and loss of vessel tissue support because of excess cortisol
34
VW factor
role in anchoring platelets to site of injury and links exposed collagen to platelets function in hemostasis - protects factor VIII from proteolytic degradation and localised it to site of injury