Hematologic Emergencies Flashcards

1
Q

A delicate balance of procoagulant and anticoagulant factors in blood is called __

A

Hemostasis

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2
Q

Bleeding controlled by the vasculature and platelets is called __

A

Primary Hemostasis

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3
Q

When plasma coagulation factors are needed to form a clot, this is called __

A

Secondary Hemostasis

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4
Q

The body’s first response to blood vessel injury is ___. It diverts blood glow from an injured area.

A

Vasoconstriction

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5
Q

There are 3 phases of primary hemostasis. These are __

A

Platelet adhesion, Platelet Activation, and Platelet aggregation

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6
Q

When plasma coagulation forms a stable hemostatic plug, this is called __

A

Secondary Hemostasis

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7
Q

Thrombocytopenia, Thrombopathia, and Von Willebrand’s Disease are disorders of __

A

Primary Hemostasis

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8
Q

Low platelet count (< 20,000 – 30,000/microliter) resulting in bleeding when inadequate platelets are available to form a plug is called __

A

Thrombocytopenia

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9
Q

This disease is characterized by immune-mediated destruction of either circulating platelets or, less commonly, marrow megakaryocytes. It can be acute, chronic, or recurrent

A

Immune-mediated thrombocytopenia

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10
Q

A platelet function defect in patients with a normal platelet count and history of surface bleeding is called __

A

Thrombopathia

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11
Q

Significant bleeding caused by thrombocytopenia and thrombopathia warrants a ___ transfusion. This is contraindicated in IMT.

A

Platelet
**This will not increase platelet numbers, but will allow clotting.

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12
Q

If a patient is acutely bleeding into a vital organ or uncontrollable, a __ transfusion is a better option

A

Whole Blood

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13
Q

This is the most common hereditary bleeding defect in dogs, caused by a deficiency in vWF (a large plasma protein). Common in Doberman Pinschers

A

von Willebrand’s Disease

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14
Q

There are three types of vWD - characterized by vWF concentration and multimer pattern:
Type 1 -
Type 2 -
Type 3 -

A

Type 1 – mild to mod dz with all multimer sizes reduced proportionally
Type 2 – mod to severe dz with lack of larger multimers
Type 3 – complete absence of vWFs

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15
Q

One type of therapy for von Willebrand’s Disease patients is a concentrate of vWF, FVIII, fibrinogen, and fibronectin that is derived from FFPt and has a lower risk of transfusion complications that FFP or whole blood. This is called __

A

Cryoprecipitate

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16
Q
A