Bleeding Flashcards

1
Q

how can infection lead to multi-organ failure

A
  • infection
  • sepsis-systemic infection
  • intravascular TF exposure
  • systemic coagulation –> microvascular clots
  • consumption of clottign factors –> bleeding
  • multiple organ failure
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2
Q

what causes intravascular activation of coagulation

A

loss of localisation

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3
Q

why uncontrolled bleeding can’t stop

A
  • coagulation factors consumed at faster rate than produced

- platelets consumed at faster rate than produced

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4
Q

what factors does vitamin K help

A
  • factor ii
  • factor vii
  • factor ix
  • factor x
  • protein c
  • protein s
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5
Q

what do completed forms of factors ii, vii, ix, x and proteins c & s do

A
  • more effective binding of Ca2+ and phospholipids on platelet surface
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6
Q

what are VKA monitored by

A
  • INR –> based on PT assay

- keep blood levels within therapeutic window

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7
Q

what are circulating anticoagulants and what types are they split into

A
  • antibodies that neutralise clotting factors activity

- lupus & factor viii antibodies

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8
Q

what are lupus anticoagulants

A
  • antibodies to phospholipid binding sites on clotting Fs

- prevent factors accumulating on phospholipid surfaces

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9
Q

what are factor viii anticoagulants

A
  • antibodies

- same profile as haemophilia A

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10
Q

Defects in platelet-vessel wall interaction

A

Von Willebrand syndrome.​

Bernard–Soulier syndrome.​

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11
Q

Defects in platelet-platelet interaction

A

Glanzmann thrombasthenia.​

Congenital afibrinogenemia.​

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12
Q

Defects in platelet granules, secretion and signal transduction.​

A

Wiskott-Aldrich Syndrome

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13
Q

what is haemophilia

A
  • X-linked disease
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14
Q

how many cases of haemophilia are mutations

A
  • 30%
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15
Q

what does haemophilia result in

A

insufficient thrombin generation

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16
Q

what factor is deficient in haemophilia A

A
  • Factor VIII
17
Q

what factor is deficient in haemophilia B

A
  • Factor IX
18
Q

what are normal levels of factors VIII & IX

A
  • 50-150%
19
Q

what are the levels of factors VIII & IX at different stages of haemophilia

A
  • mild: 6-50%
  • moderate: 1-5%
  • severe: <1%
20
Q

what are the consequences of haemophilia

A
  • bruising

- joint bleeding & destruction

21
Q

how is clotting time restored

A
  • mixing with normal plasma

- replacement of VIII

22
Q

what factor affect PT (prothrombin)

A

Factor VII

23
Q

what factors affect APTT (Activated partial thermoplastin time)

A
  • factor XII
  • factor PK
  • factor XI
  • factor IX
  • factor VIII
24
Q

what factors affect TT (thrombin time)

A
  • factor X
  • factor V
  • factor II
  • factor I