Approach to the bleeding patient Flashcards

(43 cards)

1
Q

In ml/Kg what is the total blood volume of:

  • dogs
  • cats
A

80/90ml/Kg

60-70ml/Kg

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2
Q

When there is blood loss which 3 life threatening situations need to be considered?

A
  • Hypovolaemic shock
  • Severe anaemia
  • Brain or pulmonary haemorrhage
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3
Q

In a patient, what samples would you want to collect?

A
  • Blood smear
  • Full blood count (EDTA)
  • Coagulation profile (Citrate)
  • Biochemistry (heparinised plasma)
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4
Q

What are the steps when approaching a bleeding pateint?

A
  • Attempt to quantify blood loss
  • Identify life threatening situations
  • Establish venous access and take samples
  • Control haemorrhage
  • Fluid replacement
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5
Q

What fluids should be given if a patient is hypovolaemic?

A

Crystalloids

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6
Q

“Shock rates”: recommend a bolus of fluids of?

A

1/4 of the animals normal blood volume

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7
Q

What are the 5 stages of haemostasis?

A
  • Vessel injury
  • Vascular contraction
  • Primary haemostasis
  • Secondary haemostasis
  • Tertiary haemostasis
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8
Q

Describe primary haemostasis

A

Formation of the primary plug:
- Von Willebrand factor attached to the walls of vessels interacts with platelets and allows them to bind to each other and the vessel wall

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9
Q

What does secondary haemostasis involve?

A

Coagulation cascade resulting in the generation of thrombin

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10
Q

Compare when primary vs primary and secondary haemostasis is needed

A
  • Small defect: platelet only (primary haemostasis)

- Large defect: requires platelets and stabilisation of the clot by cross-linked fibrin (secondary haemostasis)

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11
Q

What does tertiary haemostasis involve?

A

Fibrinolysis - plasmin

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12
Q

What are the clinical signs of secondary haemostasis defects?

A
  • Deficiency in clotting factors
  • Present more acutely with life-threatening blood loss
  • subcutaneous or cavity bleeding e.g. haemothorax
  • haematoma formation
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13
Q

Which vessel must you not sample from if a bleeding disorder is suspected and why?

A

Jugular vein

- it will be very hard to stop the bleeding and a pressure bandage cant be used on the neck

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14
Q

Which in house labs tests are used to differentiate 1 vs 2 coagulopathy

A

Primary coagulopathy (test of platelet function or number)

  • Manual platelet count
  • Buccal Mucosal Bleeding Time
  • Von Willebrand factor

Test of Coagulation

  • Prothrombin Time (PT)
  • Activated Partial Thromboplastin Time (APTT)
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15
Q

In which situation should you use a buccal mucosal bleeding time test?

A

Should only be performed in a situation of a normal platelet count & normal clotting (PT/APTT) times – assessing platelet function

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16
Q

Give examples of disorders of primary haemostasis

A
  • Thrombocytopenia
  • Inherited thrombocytopenia
  • Immune mediated thrombocytopenia
  • Platelet dysfunction
  • Von Willebrand disease
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17
Q

What is thrombocytopenia?

A

a condition in which you have a low blood platelet count

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18
Q

What are the causes of a thrombocytopenia?

A
  • Lack of platelet production
  • Increased platelet consumption
  • Increased platelet destruction
  • Splenic torsion
19
Q

What can cause a lack of production of platelets?

A
  • Bone marrow disorder

- Drug toxicosis

20
Q

What can cause an increase in platelet consumption?

A
  • Disseminated Intravascular Coagulation

- Acute severe haemorrhage

21
Q

What causes a primary immune mediated thrombocytopenia?

A

IgG binding to platelets, resulting in their destruction

22
Q

What causes a secondary immune mediated thrombocytopenia?

A

Secondary to drugs, infectious disease or neoplasia

- 5-7d of exposure of drug required to produce sensitisation and onset of thrombocytopenia

23
Q

How would you treat an Immune Mediated Thrombocytopaenia?

A

If 1° treat with glucocorticoids, eg Prednisolone or Dexamethasone.

If 2° treat underlying disease of discontinue drug

24
Q

What is the name given to decreased platelet function?

A

Thrombocytopathia

25
Which test is used to assess platelet function?
Buccal mucosal bleeding time
26
Describe Von Willebrand disease
Deficiency of von Willebrand factor
27
How is von Willebrand factor normally synthesised, stored and used?
By endothelial cells - vital for platelet adherence - Binds to factor VIII and prolongs its half life
28
Which situation should prompt evaluation of von Willebrand factor?
Mucosal surface bleeding or excessive bleeding following surgery or trauma in a dog with a normal platelet count, prothrombin time (PT), and activated partial thromboplastin time (aPTT)
29
Disorders of secondary haemostasis are inherited or quired disorders of ...?
Clotting factors
30
Give examples of acquired secondary disorders of haemostasis
- vitamin K deficiency - liver disease - DIC
31
Vitamin K deficiency is most commonly caused by?
Ingestion of vitamin K antagonist rodenticides
32
Vitamin K is involved in the production/activation of which clotting factors?
II VII IX X
33
What are the clinical signs of a vitamin K deficiency?
- observed 2-5 days after ingestion - epistaxis, melaena (black stool), haemoptysis, haematoma, ecchymoses, haematuria, gingival bleeding, haemoabdomen, haemothorax
34
Which breeds are pre-disposed to von Willebrand disease?
Doberman pinschers
35
What is haemophilia A? What is haemophilia B?
Deficiency of factor VIII | Deficiency of factor IX
36
Disseminated Intravascular Coagulation (DIC) is related to which part of haemostasis?
Tertiary haemostasis - problems with the breakdown of the clot
37
How does DIC first present?
As a thromboembolic disease so there are clots everywhere
38
How does DIC progress leading to organ failure?
Bleeding begins as clotting factors are exhausted - widespread activation of coagulation and thrombosis - microthrombi in organs - ischaemia and necrosis
39
What are some of the underlying causes of DIC?
- infectious disease - immune mediated disease - neoplasia - trauma - heat stroke - cardiac disease
40
What lab abnormalities are seen with acute DIC?
- prolonged clotting times - thrombocytopenia (low platelet blood count) - decreased fibrinogen
41
When are fibrin degradation products formed?
During degradation of both fibrin (fibrinolysis) and fibrinogen (fibrinogenolysis)
42
When are fibrin degradation elevated?
- DIC | - Thrombotic disease
43
What are D-dimers specific for?
Breakdown of cross linked fibrin