Primary haemostasis Flashcards

1
Q

List the 3 steps of haemostasis

A

Primary= platelet plug
Secondary= fibrin plug that requires the coagulation cascade
Tertiary= Clot lysis

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2
Q

List the clinical signs of dysfunction of primary coagulation

A

Petechiae/ ecchymoses common
bleeding from mucous membranes
often more than one site of bleeding
Haematomas rare

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3
Q

List the clinical signs of dysfunction of secondary coagulation

A

Petechiae/ ecchymoses rare
Deep or cavity bleeds
can bleed from mucous membranes
sometimes single sites of bleeding
Haematomas common

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4
Q

What is needed to make a platelet clot

A

cells
protein (vWF and others)
Facilitators
Physiological inhibitors

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5
Q

What cells are the source of von Willebrand factors

A

Endothelial cells

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6
Q

What is diascopy and what does it test

A

Does the lesion blanch under a glass slide
Yes= vascular vasodilation
No= Petechiae

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7
Q

List 3 reasons why primary haemostasis be dysfunctional

A

Thrombocytopaenia
Thrombocytopathia
vWBF deficiency

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8
Q

What is Thrombocytopathia

A

platelet dysfunction

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9
Q

Describe how primary haemostatic disorders are investigated

A

Signalment
Platelet count and morphology
Buccal mucosal bleeding time
vWF assay
Platelet function assays

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10
Q

List 3 causes of thrombocytopaenia

A

defective platelet production
Accelerated platelet removal (IMTP)
Platelet sequestration or loss (haemorrhage)

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11
Q

What is the most common acquired cause of primary haemostatic defects in dog

A

IMTP- immune-mediated thrombocytopaenia

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12
Q

What is Evans syndrome

A

IMHA + IMTP

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13
Q

Describe how is IMTP treated

A

treat any underlying disease
Immunosuppression

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14
Q

What are the negative prognostic indicators in IMTP

A

melaena
high BUN (blood urea nitrogen)

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15
Q

List 3 causes of thrombocytopathia

A

Inherited
drug induced defects (NSAIDs)
platelet dysplasia

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16
Q

DEcsribe how you diagnose a thrombocytopathia

A

normal platelet count but prolonged BMBT
normal levels of vWF
platelet function tests
to a degree often a diagnosis of exclusion

17
Q

Describe how thrombocytopathia is treated

A

no specific therapy
platelet transfusion not possible
withdraw any drug use (NSAID)
treat symptomatically- blood transfusion if marked anaemia

18
Q

What is the most common inherited bleeding disorder in dogs

A

vWD- Von Willebrans disease

19
Q

List te differences between the 3 types of vWD

A

1= abnormally low concentrations of structurally normal vWF
2= structurally abnormal vWF
3= Essentially no plasma vWF, diagnosed by ELISA

20
Q

What breed of dog is most prone to vWD

A

Dobermans

21
Q

What are the clinical signs of vWD

A

mucosal haemorrhage
cutaenous bleeding
prolonged bleeding from wound

22
Q

Describe the diagnostic testing used for vWD

A

platelet count will be normal
BMBT screening test
Diagnosis is confirmed by demonstration of low vWF antigen concentrations
Genetic testing can be performed

23
Q

How is vWD treated in severe cases

A

plasma - in severe cases
stabilisation
cessation of active haemorrhage
red cells if O2 carrying capacity compromised

24
Q

Describe how type 1 vWD is treated

A

Desmopressin - acts by causing release of vWF from endothelial cells

25
Q

below what platelet concentration does spontaneous bleeding occur

A

50 x 10^9