EXAM #1: THROMBOCYTOPENIA Flashcards

(32 cards)

1
Q

What is the definition of thrombocytopenia?

A

Platelet count less than 150,000/microliter

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2
Q

Describe the appearance of platelets on PBS.

A
  • Round- oval
  • Blue-gray
  • 1/3 the size of a RBC
  • Anuclear
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3
Q

Where are platelets produced? What are they released from?

A
  • Produced in the bone marrow

- Megakaryocytes

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4
Q

What regulates platelet production? Where is this factor synthesized?

A

Thrombopoietin, which is synthesized in the liver

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5
Q

What receptor is activated after binding of Gp1b to vFW?

A

GpIIb/IIIa, which binds fibrin

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6
Q

What are the three underlying causes of thrombocytopenia?

A

1) Underproduction
2) Destruction
3) Sequestration

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7
Q

What are some of the infectious causes of platelet underproduction?

A

1) HIV

2) Parvovirus B19

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8
Q

What is the most common cause of underproduction of platelets from the bone marrow?

A
  • Chemotheraputic agents

- Alcohol

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9
Q

If the MCV is greater than 115 or more, what should you think?

A

Megaloblastic anemia i.e. B12 or Folate

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10
Q

What is the mechanism of thrombocytopenia in pernicious anemia?

A

B12 is necessary to DNA synthesis, i.e. synthesis of platelet precursors

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11
Q

What will the megakaryocyte levels be in pernicious anemia?

A

Normal to increased numbers for megakaryocytes

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12
Q

What cancer is associated with pernicious anemia?

A

Gastric carcinoma

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13
Q

How is pernicious anemia managed?

A

B12 supplementation

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14
Q

What is pseudothrombocytopenia?

A

Platelet aggregation or clumping in vitro leads to a low count

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15
Q

What triggers pseudothrombocytopenia? How do you correct for it?

A
  • EDTA

- Recheck with citrated or heparanized blood tube i.e. purple tube

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16
Q

What is ITP?

A

Idiopathic or Immune Thrombocytopenic Purpura

17
Q

Describe the pathology of ITP.

A
  • Accelerated destruction of platelets b/c antibody coated platelets are destroyed by macrophages in spleen
  • GpIIb/IIIa
  • Normal or increased megakaryocytes
  • Diagnosis of exclusion*
18
Q

What is the typical clinical presentation of ITP?

A

Often asymptomatic with SEVERE thrombocytopenia

Some have purpura, petechiae…etc. but LIFE-THREATENING bleeding is RARE

19
Q

What is the treatment for ITP?

A
  • Observation
  • Steroids
  • IVIG–coat receptors with something other than antiplatelet antibody
  • Rituximab
  • Thrombopoetin
  • Splenectomy
20
Q

What are the two classes of platelet destruction?

A
  • Immune-mediated

- Nonimmune-mediated

21
Q

List the causes of immune-mediated platelet destruction.

A
  • ITP
  • HIT
  • Post transfusion purpura
  • Medications
  • Antiphospholipid antibody syndrome
22
Q

List the causes of nonimmune-mediated platelet destruction.

A
  • DIC
  • TTP/HUS
  • HELLP Syndrome
  • Gestational Thrombocytopenia
  • Mechanical Destruction
  • Localized intravascular coagulopathy
23
Q

What is HIT?

A

Heparin Induced Thrombocytopenia

  • Immune mediated destruction of platelets
  • Antibodies to heparin AND platelet-specific PF4 complex
  • Activates platelets and leads to thrombosis
24
Q

What form of Heparin has a lower risk of HIT associated?

25
How is HIT managed?
1) STOP heparin | 2) Use alternative anti-coagulant
26
Can you use Heparin again in a patient that has developed HIT?
Yes, if they have been Heparin free for 6 months
27
What does jaundice not involving the sclera indicate?
NOT hyperbilirubinemia
28
What causes sequestration of platelets?
Splenomegaly leads to splenic sequestration - Portal HNT - Hereditary spherocytosis - CML - Hairy cell leukemia - MALT lymphoma
29
How do you evaluate thrombocytopenia?
1) HIP and PE 2) Lab eval 3) Bone marrow biopsy
30
When is bone marrow indicated?
1) Multiple cell lines involved 2) Greater than 60 with isolated thrombocytopenia 3) When empiric therapy is unsuccessful
31
What is the formula for platelet transfusion?
1 unit= increase in 5,000 Normal 6-pack is 30,000
32
When is platelet transfusion a BAD idea?
ITP | HIT