6 - Clotting disorders Flashcards

1
Q

What is the extrinsic pathway?

A

Exposer to tissue factor

F VII –> VIIa

=> activation of the common pathway

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2
Q

What is the intrinsic pathway?

A

Platelets activate FXII

cascade activates XI, IX IXa and VIIIa

activates common pathway

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3
Q

How does warfarin work?

A

Inhibits Vit. K reductase

inhibits protein C and S - inhibits clotting factors and enhances fibrinolysis decreases PT

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4
Q

What is the common pathway?

A

FX become acite and with co FV helps activate FII (to thrombin), which in turn activates fibrin.

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5
Q

How does Heparin?

A

inhibits FII and increase antithrombin activation.

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6
Q

What effects PT?

A

Warfarin

Factor II

Factor V

Factor VI

Factor X

Measures the extrinsic and common pathway

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7
Q

What effects APTT?

A

Heparin

Factor VIII

Factor IX

Factor XI

Factor XII (but no bleeding diathesis)

von Willebrand’s Disease

Measures the intrinxic and common pathway

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8
Q

If APTT and PT are prolonged consider:

A

Vit K deficiency

disseminated intravascular coagulation

rarely vWF deficiency

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9
Q

What are the VIt. K dependent factors?

A

Factor II

Factor VII

Factor IX

Factor X

Protein C

Protein S

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10
Q

What is the 50/50 mixture test?

A

APTT and PT done compared to with 50% normal bloodcontent

same times = factor deficiency

still prolonged times = factor inhibition

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11
Q

What is heamophillia A?

A

X linked disorder

deficiency of F VIII

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12
Q

What is haemophilia B?

A

X linked disorder

deficiency of FIX

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13
Q

What is Von Willibrand’s disease?

A

vWF deficiency which would have stabilised VIII and clotting

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14
Q

Reasons for Vit. K deficiency?

A

1) inadequate stores - malnutrition and haemorrhage disease
2) Vit. K malabsorption - Jaundice (fat soluble)
3) Oral anticoagulants

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15
Q

What is the treatment for haemophilia A?

A

IV FVIII concentrate

DDAVP

Tanexamic acid

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16
Q

What is the treatment for haemophilia B?

A

IV FIX concentrate

17
Q

Which blood thinner can cause thrombocytopenia?

18
Q

Treatment for VTE?

A

Anti-embolism stockings

LMWH and UFH

DOACs

Do not use Wafrin

19
Q

What is Homan’s sign?

A

Tenderness with dorsiflexion of the ankle.

Indicates of DVT

20
Q

Calf has a circumference >3cm compared to other.

What does this indicate?

21
Q

What is Virchows triad?

A

1) Damaged endothelium
2) Blood stasis
3) Hypercoagulopathy

22
Q

What does Tranexamic acid do?

A

Anti-fibrinolytic

23
Q

What can Dessmopressin treat?

A

Haemophilia A and vW disease

24
Q

How is LWMH different?

A

Longer half life greater bio availability Greater activity against Xa than IIa

25
What to ask in a history of bleeding?
bruising epistaxis greater than 30 mins GI tract bleeding menses heamaturia bleeding at dentist, surgery family history
26
How to investigate a clotting disorder?
Thrombocytonpenia? 50/50 mixture test? consider vWF deficeincy?
27
28
Management of PE
Start treatment unless investigations within 1 hour Initially start LMWH before investigations Later add warfarin or replace with DOAC Investigaiton include: CTPA or V/Q scan
29
Diagnosis of PE
Wells score \> 4 Wells score \>4 and + D-dimer Can confirm with CTPA
30
Symptoms of PE
Syncope Tachycardia Hypotension Heamoptysis Dyspnoea pleuritic chest pain
31
What can mangement for recurrent PE/ DVT and not able to anti-coagulate sufficeintly?
IVC filter
32
Risk factors for PE
Stasis recent surgery pregnancy oral contraceptive previous VTE FH malignancy or chemotherapy
33
Diagnosis of DVT
Wells score \>/= 2 and positive USS Wells score = 1 and posotive D dimer
34
Management of DVT
Start LMWH if unless \<4 hours until investigaiton Add warfarin or replace with DOAC
35
What is an advantage of LMWH?
Quick onset Easily stopped with protamine
36
How is anticoagulation via warfarin reversed?
PCC - prothrombine complex concentrate Contains F II, V, VII, IX and X takes 30 mins Used instead of FFP - fresh frosen plasma Vit. K takes 4-6 hours to work
37
PT is prolonged and the patient is not on warfarin. What is the most likley cause?
FVII deficiency
38