bleeding disorders Flashcards

1
Q

what happens in the common pathway?

A

10 converted to thrombin (2) using 5

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2
Q

extrinsic pathway involves

A

10 - 10a in the presence of factor 7 and TF

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3
Q

the intrinsic/propagation pathway involves

A

12-11-9-10 with the help of 8

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4
Q

what 2 factors help activate factor 12

A

prekallikrein and HMWK

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5
Q

Do you need PK and HMWK or factor 12 to control bleeding?

A

NO

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6
Q

PTT assesses

A

intrinsic (inside) and common pathway (have to get to the end)

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7
Q

PT assesses

A

extrinsic and common

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8
Q

Protein C and S (cofactor)

antithrombin

A

degrade 5 and 8

preferentially neutralizes 10 and 10a

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9
Q

INR is

A

PT in sec/ geo mean in sec

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10
Q

non-enzymatic co factors include

A

5, 8, TF

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11
Q

which factors are NOT made in the liver

A
  • tPA
  • VWF
  • thrombomodulin
  • factor 8 made by endoth as well
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12
Q

Factors with the shortest half life

A

7

5 and 8

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13
Q

VWF is synthesized by

A

endothelial cells and megs

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14
Q

VWF extends the half life of

A

factor 8

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15
Q

Primary hemostatic disease is

A

VWF disease

can impact secondary hemostasis because less factor 8 around

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16
Q

3 clinical components of VWF disease

A

1 - mucocutaneous bleed
2- autosomal inheritance
3- CBC INR/PTT often normal

17
Q

how do we treat mild VWF disease

A
  • DDAVP - desmopressin- increase hemostasis - due to stress

-

18
Q

more moderate severe VWF - how do you treat

A
  • give VWF/Factor 8 concentrate
  • humate - wilate
  • OCP
19
Q

In Hemophilia A and B which lab finding is commonly found

A

Prolonged PTT -

intrinsic pathway is delayed

20
Q

treating hemophilia –>

A

TREAT IMMEDIATED

then scan

21
Q

Severe hemophilia how do you treat?

A
  • factor 8 or 9 concentrate can be given
    or
    DDAVP if moderate- mild
22
Q

in patients with liver disease most commonly present with

A
  • esophageal/GI varices
    gastritis
    ulcers
    risk for bleeding and clotting
23
Q

Clues that a patient has liver disease from lab tests include

A
  • Thrombocytopenia
  • prolngation of INR and PTT
  • decreased factors except factor 8
24
Q

treating coagulopathy of liver disease -

A

treat liver disease
vitamin K not effective
DDAVP
anti fibrinolytics

25
Q

Features of DIC

A
  • prolonged INR PTT
  • Thrombocytopenia
  • Low fibrinogen
26
Q

Uncontrolled generation of what 2 factors results in DIC

A
  • thrombin

- plasmin

27
Q

with DIC you can get excessive release of what factor

A

tissue factor release

28
Q

how do you treat DIC

A

treat the underlying cause -

protein C and antithrombin may help

29
Q

what are some causes of a vitamin K deficiency

A
  • nutritional deficiency
  • warfarin
  • Antibiotics
  • Biliary obstruction/malabsorption
  • hemorrhagic disease of newborn
30
Q

what lab tests will you find with a vitamin K deficiency?

A
  • prolonged PT/INR
  • PTT prolonged in more severe cases
    reduced factors 2,7,9,10
31
Q

INR/PTT for following diseases

VWF
Factor 8 or 9 or 12 deficiency
Drug induced heparin, thrombin inhibitor
Inherited/acquired factor 7 deficiency
vitamin k deficiency/early liver disease
Severe vitamin K deficiency
Severe liver disease
A
INR/PTT often normal
Isolated PTT deficiency normal INR
Isolated PTT deficiency normal INR
prolonged INR/normal PTT
prolonged INR/normal PTT
Prolonged INR and PTT
Prolonged INR and PTT