Bleeding disorders Flashcards

1
Q

Three main possible reasons for failure of the platelet plug (primary haemostasis)

A

Vascular disease
Reduced platelet number/function
Von Willbrand factor deficiency

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2
Q

What causes Henoch-Schonlein purpura?

A

IgA-mediated vasculitis following an infection

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3
Q

Features of HSP (4)

A

Palpable purpuric rash over buttocks and extensor surfaces
Polyarthritis
Abdominal pain
Possibly nephropathy

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4
Q

Causes of acquired thrombocytopenia (4)

A

Marrow failure
Disseminated intravascular coagulation
Immune thrombocytopenic purpura
Hypersplenism

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5
Q

Common causes of acquired reduced platelet function (2)

A
Antiplatelet drugs
Renal failure (uremic platelet failure)
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6
Q

Most common inherited bleeding disorder, and its inheritance pattern

A

von Willebrand disease

Usually autosomal dominant

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7
Q

Why is coagulation affected by liver failure?

A

All clotting factors are synthesised by the liver

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8
Q

Causes of multiple clotting factor deficiencies (3)

A

Liver failure
Vitamin K deficiency/warfarin
DIC

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9
Q

Excessive and inappropriate activation of the haemostatic system

A

Disseminated intravascular coagulation

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10
Q

What does an elevated D-dimer suggest and which conditions have this as a feature?

A

Suggests there is active clotting happening in the body but does not indicate location or cause; DIC and VTE (such as DVT/PE) have this as a feature

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11
Q

Causes of DIC (4)

A

Sepsis
Obstetric emergencies
Malignancy
Hypovolaemic shock

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12
Q

Treatment of DIC (2)

A

Treat the underlying cause

Replace platelets/plasma

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13
Q

Cause of

a) haemophilia a
b) haemophilia b

A

a) factor VIII deficiency

b) factor IX deficiency

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14
Q

Clinical features of severe haemophilia (3)

A

recurrent haemarthroses
recurrent soft tissue bleeds
prolonged bleeding after dental extractions, surgery and invasive procedures

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15
Q

What measure of blood clotting is deranged in the haemophilias and why?

A

APTT.
Because APTT is affected by the intrinsic pathway, which is mediated by factors VIII (deficiency in haemophilia A) and IX (deficient in haemophilia B)

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16
Q

How does hypersplenism cause deranged blood clotting?

A

Increased destruction of platelets leading to primary haemostatic deficiency

17
Q

Contrast bleeding patterns seen in primary and secondary bleeding disorders

A

Primary- mucosal bleeding, purpura

Secondary- haemarthroses, intra-muscle bleeding