Approach to the bleeding patient Flashcards

1
Q

When approaching the bleeding patient, the first thing to do is to identify life threatening situations. Give examples of these situations

A

Hypovolaemic shock
Severe anaemia
Brain haemorrhage
Pulmonary haemorrhage

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2
Q

How can you stabilise a bleeding patient?

A

Control haemorrhage with wound pressure
Blood transfusion
Volume replacement wuith IVFT

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3
Q

After stabilising a bleeding patient, what is the next thing to do?

A
Collect blood samples:
Full blood count (EDTA) 
Coagulation profile
Biochem 
PCV/total protein
Blood smear
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4
Q

When examining a bleeding patient, what should you consider?

A

Signalment
History - when started, any recent trauma, medications
Is bleeding local or systemic

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5
Q

Describe basically how a blood vessel responds to injury

A

Vessel injury causes vessel contraction
Primary haemostasis - primary plug
Secondary haemostasis - coagulation cascade and fibrin
Tertiary haemostasis - fibrinolysis

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6
Q

Primary haemostasis involves creating a primary plug within seconds/minutes of vessel injury. What substances/factors are involved?

A

Endothelium collagen
Platelets
Von Willebrand factor

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7
Q

Tertiary haemostasis involves fibrin. What is fibrin?

A

Insoluble protein

Forms fibrous mesh that impedes blood flow (aids clotting)

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8
Q

What is fibrin formed from?

A

Fibrinogen

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9
Q

What is fibrinogen?

A

Glycoprotein circulating in blood

Converted to fibrin during injury

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10
Q

What happens during primary haemostasis?

A

Formation of primary plug by Von Willebrand factor and platelets

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11
Q

What cells make von Willebrand factor?

A

Megakaryocytes

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12
Q

What happens during secondary haemostasis?

A

Coagulation cascade
Extrinsic activated by tissue factor, intrinsic activated by exposure of damaged endothelium
Results in fibrinogen –> Fibrin

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13
Q

What is the third stage of haemostasis?

A

Fibrinolysis

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14
Q

How does the size of an injury/defect alter haemostasis?

A

Small defect = primary haemostasis only

Large defect = requires platelets and stabilisation of clot by cross-linked fibrin

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15
Q

What are primary haemostasis disorders?

A

Disorders caused by platelet disorders or vasculopathies

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16
Q

What are the clinical signs of primary haemostatic disorders?

A

Ooze from small wounds
Petechia and ecchymoses
Bleeding from mms (epistaxis, melaena)
Signs of underlying disease

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17
Q

What is the most common cause of abnormal bleeding in dogs?

A

Thrombocytopenia

18
Q

What are some causes of thrombocytopenia?

A

Increased platelet destruction - immune mediated (common), primary, or secondary
Increased platelet consumption
Platelet sequestration
NOT caused by platelet loss from haemorrhage

19
Q

What are some differentials for thrombocytopenia?

A
Neoplasia
DIC (platelet consumption)
Infectious disease
Immune mediated
Breed related - may not be pathological
20
Q

What is the most common cause of marked thrombocytopenia in dogs?

A

Immune mediated thrombocytopenia (IMTP)

21
Q

Immune-mediated thrombocytopenia (IMTP) is common in dogs. Primary IMPT is usually seen in which dogs?

A

Females

Spaniels

22
Q

Immune-mediated thrombocytopenia (IMTP) is common in dogs. What can cause secondary IMTP?

A

Drug reactions - cephalosporins
Neoplasia
Viral disease
Ehrlichia or the vaccine (live virus)

23
Q

What are patients with IMTP at risk of? How can this be reduced?

A

Spontaneous haemorrhage

Reduce risk of trauma, reduce activity

24
Q

What is the treatment of IMTP?

A

If secondary treat underlying disease
Supportive
Immunosuppressives

25
What immunosuppressive drugs can be given for IMTP? (Similar to IMHA)
Corticosteroids | Azathioprine
26
What is von Willebrand disease?
Acquired or inherited deficiency of von Willebrand factor
27
Von Willebrand disease can be acquired or inherited. What condition can cause it to be acquire?
Severe aortic stenosis
28
Where is Von Willebrand factor synthesised and stored?
Endothelial cells
29
Von Willebrand disease can be acquired (severe aortic stenosis) or inherited. Which breed is predisposed to this disease?
Dobermanns
30
What tests can be used to diagnose Von Willebrand disease?
BMBT (buccal mucosal bleed time) Antigenic test vWF function assays Genetic testing to detect carriers
31
What is the treatment for von Willebrand disease?
Cryoprecipitate (from frozen blood plasma) | Whole blood or plasma therapy
32
What are 3 types of Von Willebrand disease? Which is most common?
Type 1 - most common Type 2 Type 3
33
Briefly explain the 3 types of Von Willebrand disease
Type I - partial quantitive deficiency Type 2 - qualitative deficiency Type 3 - severe quantitative deficiency
34
What are some symptoms of type I von Willebrand disease?
Bleeding from mucous membranes | Excessive bleeding/haemorrhage during surgery
35
Von Willebrand disease can be inherited. What type of inheritance is it?
Autosomal recessive
36
Platelet dysfunctions can be associated with many conditions and drugs. What group of drugs in particular?
NSAIDs | E.g. aspirin
37
How can platelet function be tested?
Buccal mucosal bleeding time (BMBT) Clot retraction Platelet function tests (usually not available, must be carried out within 4hrs)
38
Disorders of secondary haemostasis are either inherited or acquired. Which is more common?
Acquired
39
What is haemophilia A?
Genetic disorder | Deficiency of Factor VIII
40
What is haemophilia B?
Genetic disorder | Deficiency of Factor IX
41
What causes extrinsic pathway defects?
Hepatic/hepatoiliary diseae | OR early vitamin K antagonism/deficiency