Platelets Flashcards

1
Q

Platelets

A

Initial hemostatic plug
Temporary

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2
Q

Coagulation proteins

A

Reinforce the platelet framework and part of definitive hemostatic plug

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3
Q

What is the precursor cell to platelets

A

Megakaryocyte, cytoplasmic fragments

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4
Q

How are platelets released in blood

A

Megakaryocyte in bone marrow and reach out branches into the blood vessel and the sheer flow of blood will cause portions of the cytoplasm to break off

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5
Q

Platelet regulation

A

Thrombopoietin from the liver at a constant rate and removed from blood by circulating platelets. If platelet mass reduces there is an increase in TPO concentration resulting in increased production. Inflammatory cytokines also increase production

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6
Q

Thrombopathia

A

Qualitative disorder of platelets

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7
Q

Extrinsic platelet disorder

A

Platelets are normal but there is some other part of the way the platelets work is not. IE von Willebrand factor missing

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8
Q

Intrinsic platelet disorder

A

Platelets are abnormal

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9
Q

4 categories of platelet disorders

A
  1. Congenital for abnormal conc
  2. Acquired causes for abnormal conc, most common
  3. Congenital functional defect
  4. Acquired functional defect
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10
Q

Platelet type bleeding from thrombocytopenia or thrombopathia

A

Bleeding from mucosal surfaces including: epistaxis, gingival, UT, and GI bleeding. See petechial or ecchymotic hemorrhage on any skin or mucosal surface

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11
Q

At what point can you get spontaneous bleeding due to low platelet conc?

A

<50,000platelets/ul

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12
Q

Mean platelet volume

A

MPV from automated platelet concentration.
Average size of circulating platelets

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13
Q

High MPV with thrombocytopenia

A

Megakaryocytes are trying to respond to low platelet numbers. Not you and will stay that big. Good sign

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14
Q

Low MPV with thrombocytopenia

A

May indicate insufficient number of megakaryocyte present or failure to response

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15
Q

Normal MPV in thrombocytopenia

A

Megakaryocytes not responding or it is too early for response

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16
Q

When do we test platelet function

A

When the concentration is adequate but have platelet type bleed

17
Q

Buccal mucosal bleeding time

A

Indicate primary hemostasis or platelet status. Only use on pt with adequate platelet concentrations. Can’t be used to detect coagulopathies

18
Q

Clot retraction

A

Test platelet function and do not do on pt with medications that affect clotting. Tests to see if blood mixed with thrombin will form a clot retraction. Always do duplicates and with control

19
Q

Platelet aggregometry

A

Gold standard. Highly specialized and not readily available and must be completed quickly

20
Q

Cats and platelets

A

-Tend to be more clumped (reactive)
-Variable size
-See more giant platelets
-Do not use impedance hematology analyzers
-Often have no clinical signs of thrombocytopenia

21
Q

Inherited macrothrombocytopenia signalment

A

Cavalier King Charles are poster child

22
Q

Inherited macrothrombocytopenia

A

Low number but larger so there is no clinical bleeding

23
Q

Immune mediated thrombocytopenia

A

Circulating platelets or megakaryocytes destroyed by immune mediated mechanism

24
Q

Causes of ItP

A
  1. Primary or autoimmune
  2. Secondary to immune complex absorption or neoantigen expression
  3. Incompatible transfusion
25
Rickettsial induced thrombocytopenia
-Erlichia canis -Anaplasma platys and phagocytum -Rickettsia rickettsia Have immune mediated clearance and decreased lifespan as well as vasculitis induced consumption
26
Drug induced thrombocytopenia
-Primary-> destroyed by drug interaction -Secondary immune mediated-> drug dependent (if you stop drug and stops reaction to platelets) or independent -Secondary bone marrow suppression
27
DIC
Pathologic process characterized by widespread activation of clotting cascade and get clots throughout body and use up all the platelets. See if there is massive tissue damage
28
Destruction or crowding of marrow cavity thrombocytopenia
Inflammatory disease Myeloproliferative disease Myelopthsis/myelofibrosis
29
Von Willebrand disease
Most common congenital extrinsic platelet function disorder in dogs. Decreased VW factor reduces platelet adhesion
30
Diagnosis of von Willebrand
ELISA to determine antigen levels using plasma not serum Clot retraction and APTT is normal
31
Diagnosis of von Willebrand
ELISA to determine antigen levels using plasma not serum (EDTA or citrated plasma) DNA test is available Clot retraction and APTT is normal
32
Glanzmann Thrombasthenia
Congenital intrinsic platelet dysfunction. No clot retractions. Defect in GpIIb-IIIa so abnormal fibrinogen binding and unable to aggregate platelets
33
CalDAG-GEFI Thrombopathia
Congenital intrinsic platelet dysfunction. Abnormal signal transduction so decreased binding of platelets to fibrinogen. Normal clot retraction
34
Acquired Qualitative Platelet Function disorders
-FeLV -Drug induced (TXA2)