Thrombocytopenia Flashcards

(28 cards)

1
Q

What is thrombocytopenia?

A

Low platelet count

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2
Q

What is the normal platelet count?

A

150-450 x 10^9/L

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3
Q

How can the causes of low platelet count be split?

A

Problems with production or destruction

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4
Q

What can reduced platelet production occur with?

A

Certain viral infections (EBC, CMV, HIV), B12 deficiency, folic acid deficiency, liver failure, leukaemia, myelodysplastic syndrome, chemotherapy

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5
Q

What can increased platelet destruction occur with?

A

Medications (eg. sodium valproate and methotrexate), alcohol, ITP, thrombotic thrombocytopenic purpura, heparin-induced thrombocytopenia, haemolytic uraemic syndrome

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6
Q

How can it be diagnosed?

A

Mild thrombocytopenia can be asymptomatic and found incidentally on a FBC

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7
Q

How does thrombocytopenia present?

A

Platelet counts below 50x10^9 ⇒ easy bruising and prolonged bleeding times, nosebleeds, bleeding gums, heavy periods, easy bruising, haematuria, rectal bleeding

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8
Q

What can platelet count below 10x10^9 lead to?

A

They’re at high risk of spontaneous bleeding, particularly concerning are: intracranial haemorrhage, GI bleeding

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9
Q

What are some differentials for abnormal or prolonged bleeding?

A

Thrombocytopenia, Von Willebrand disease, haemophilia A and B, DIC (usually secondary to sepsis)

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10
Q

What is ITP also called?

A

Autoimmune thrombocytopenic purpura, idiopathic thrombocytopenia purpura, and primary thrombocytopenia purpura

These all refer to the same condition

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11
Q

What is ITP?

A

A condition where antibodies are created against platelets, leading to their destruction and a low platelet count (thrombocytopenia), isolated low platelet count with normal bone marrow in the absence of other causes of low platelets

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12
Q

How does ITP characteristically present?

A

Purpura, which are non-blanching skin lesions caused by bleeding under the skin, petechiae, bleeding (eg. epistaxis)

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13
Q

Difference between timing of presentation in children and adults?

A

Children: acute thrombocytopenia that may follow infection or vaccination; adults tend to have a more chronic condition

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14
Q

Investigations for ITP?

A

Blood film

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15
Q

What does the care for ITP involve?

A

Monitoring platelet count, controlling BP, suppressing menstrual periods

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16
Q

Management options for ITP?

A

Oral prednisolone first line, IV immunoglobulins, thrombopoietin receptor agonists (eg. avatrombopag), Rituximab (MCA that targets B cells), splenectomy (less commonly used)

17
Q

How does Rituximab work?

A

Rituximab is a MCA that targets the CD20 proteins on the surface of B cells, by attacking B cells and reducing their numbers, it reduces the production of the antibodies that are responsible for autoimmune disease

18
Q

What is TTP?

A

Condition where tiny thrombi develop throughout the small vessels, using up platelets, described as a microangiopathy

19
Q

What does TTP cause?

A

Thrombocytopenia, purpura, tissue ischaemia and end organ damage

20
Q

Features of TTP?

A

Fever, neurological signs (microemboli), MAHA, renal failure, thrombocytopenia

21
Q

Why do thrombi develop in TTP?

A

Due to a problem with a specific protein called ADAMTS13

22
Q

What does the ADAMTS13 protein normally do?

A

Inactivate VWB factor, reduces platelet adhesion to vessel walls, reduces clot formation

23
Q

What can deficiency in the ADAMTS13 protein be due?

A

An inherited genetic mutation (hereditary), autoimmune disease, where antibodies are created against the protein (acquired)

24
Q

Treatment for TTP?

A

Guided by haematologist, plasma exchange, steroids, rituximab

25
What is HIT?
Involves the development of antibodies against platelets in response to heparin, heparin induced antibodies target a protein on platelets called platelet factor 4 (PF4)
26
How does HIT present?
Around 5-10 days after starting treatment with heparin, HIT antibodies bind to platelets and activate the clotting system, causing a hyper coagulable state and thrombosis (eg. DVT), they also breakdown platelets and cause thrombocytopenia
27
Diagnosis of HIT?
By testing for HIT antibodies on a blood sample
28
Management of HIT?
Stopping heparin and using an alternative anticoagulant eg. fondaparinux or argatroban