Week 7- Approach to Coagulopathies Flashcards

1
Q

What are the three phases of clotting?

A
  • Initiation
  • Amplification
  • Propagation
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2
Q

What is DIC

A

when you stop clotting (clotting factors used up)

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3
Q

What is the clinical presentation of a bleeding patient?

blood disorder

A
  • lethargy
  • collapse
  • tachycardia
  • excessive bleeding
  • pale mucous membranes
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4
Q

What does a secondary haemostasis bleed look like?

A
  • Bigger bleed s
  • Usually in body cavities
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5
Q

What is fibrinolysis?

A
  • Fibrin breakdown
  • Fibrin stabilises clot
  • Mediated by plasmin
  • release of FDP’s
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6
Q

What is Primary Hyperfibrinolysis

A

Delayed bleeding post trauma or minor
procedures
* 36-48 hours after the incident * Greyhounds
* Normal coagulation parameters

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7
Q

What is secondary hyperfibrinolysis?

A

Due to systemic hypercoagulability –
first stages of DIC

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8
Q

What is secondary hypofibrinolysis?

A

Late DIC
* Impaired fibrin structure
(dysfibrinogenaemia) * Impaired fibrinogen production – liver * Congenital fibrinogen deficiency
* Excessive fibrinogen loss – large blood
loss
* Iatrogenic – anti-fibrinolytic therapy

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9
Q

Why does heat stroke cause bleeding disorders?

A

they go into DIC due to the inflammatory process that has been triggered

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10
Q

What in house diagnostic tests might you do?

A
  • Blood smear
  • PCV/TS
  • BMBT
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11
Q

What out of house diagnostic tests might you do?

A

Haematology
* Serum chemistry – may include liver function tests
* Clotting times (coagulation profiles)
* FDPs; D-dimers; fibrinogen levels

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12
Q

What specific tests might you do?

A

Hereditary conditions (ELISA for vWF)
* SNAP 4DX – anaplasmosis, ehrlichiosis,
dirofilariasis, borreliosis

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13
Q

What platelet counts should you be seeing?

A

look for > 10 platelets per field of monolayer cells under 100x oil immersion (Dog 8-15; Cat 10-12)
* Count 10 fields and get average per field
* < 2-3 per field = thrombocytopaenia and spontaneous bleeding
* Estimated count/μL = average x 15 000
* < 20 000 – 50 000/μL = spontaneous bleed

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14
Q

What is Buccal mucosal bleeding time (BMBT)

A

Test of platelet and vessel function
* Indicated if suspect primary haemostatic defect despite normal platelet number
* Normal: 2 - 4 min dog / 1 - 2.5 min cat

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15
Q

What is the procedure for buccal mucousal bleeding time

A

Conscious animal (may need sedation)
* Lateral recumbency, minimal restraint
* Upper lip folded back and held with gauze bandage
* Incision in non-vascular area
* Filter paper used to absorb the blood
* Time from incision to cessation of bleeding recorded

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16
Q

What are the platelet tests?

A

Blood smear with platelet count and evaluation
* PCV/TP
* Maybe BMBT
* (Thrombocytopaenia, thrombocytopathy, von Willebrand’s disease)

17
Q

What are the clotting tests?

A

Prothrombin time (PT) – Extrinsic and common pathway – Factor VII
* Activated Partial thromboplastin time (aPTT) – Intrinsic and common
pathway – XII, XI, IX,VIII
* (Liver disease, Vit K antagonism, Haemophilia, DIC)

18
Q

What tests would you do if fibrinolysis is suspected?

A

FDPs (DIC, blood clots, liver not clearing FDPs)
* D-dimer (DIC, recent blood clots – within previous 5h, neoplasia)

19
Q

What factor has the shortest half life

A
  • factor 7
  • will most likely run out first

also has no storage pools

20
Q

What tube is used for the blood?

A

Citrate tube- blue- avoids TF from tissue

21
Q

What is vascular endothelium disorder?

A

Rare
* Vasculitis; vascular fragility (due to hyperadrenocorticism)

22
Q

What are the 4 types of thrombocytopenia?

A

Decreased production – bone marrow disease, ehrlichiosis, drug
reactions, oestrogen toxicity, myelofibrosis
* Increased consumption – bleeding, thrombosis, DIC
* Destruction – immune-mediated thrombocytopaenia (ITP)
* Splenic sequestration – torsion, neoplasia, sepsis

23
Q

What may cause thrombopathia?

A

Hereditary or acquired
* vWF deficiency (vWD) – Some DOG breeds
* Glanzmann’s thrombasthaenia
* Chediak-Higashi syndrome – CAT
* NSAIDs, DIC, liver failure, uraemia

24
Q

When does hypercoagulation occur?

A

Increased platelet or coagulation factor activity. * Deficient anticoagulation factors or decreased fibrinolysis. * Vascular stasis or vascular damage.

25
Q

How would you treat vitamin K antagonism?

A

Subcutaneous injection q 12h until PCV is stable and active bleeding
decreased
* Followed by oral Vit K1 q 12h for 2 weeks
* Can taper every 2 weeks and continue for 6-8 weeks
* Monitor with PT and aPTT 48 hours after last dose

26
Q

How would youi treat hypercoagulation?

A

Low dose aspirin or clopidogrel

27
Q

How would you treat hyperfibrinolysis?

A

Tranexamic acid – decreases fibrinolysis and increases clot strength

28
Q

How would you treat immunosuppression?

A

Prednisolone; azathioprine, cyclosporine, mycophenolate mofetil,
leflunomide