General concepts
Coagulation stuff
More coagulation stuff
Clotting Disorders
Stick to the Status Quo
100

Name of the process of RBC production

Erythropoiesis

100

Which lab value would be drawn to assess the status of the extrinsic pathway within the clotting cascade?

PT- Prothrombin Time.

100

Which coagulation factor is obtained from the diet?

Calcium 

100

What are the three major factors involved with Virchow's Triad?

1. Endothelial Injury

2. Venous Stasis

3. Hypercoagulability. 

100

Genetic hemoglobinopathy in which the production of either alpha and/or beta chains from hemoglobin molecules are either reduced or absent 

Thalassemia 

200

Glycoprotein synthesized and secreted by the kidneys. In cases of CKD there is a reduction of it causing anemia 

Erythropoietin

200

Unconjugated bilirubin needs to bind to this in order to become water soluble conjugated bilirubin so that it can be excreted in the bile

Albumin

200

Derived from arachidonic acid, this lipid mediator is continuously produced by healthy endothelial cells and it functions to reduce platelet adherence and promote vasodilation. 

Prostacyclin 

200

A young healthy patient presents with an unexplained/unprovoked PE. What autosomal dominant clotting disorder will they likely be tested for?

Factor V Lieden 

(mutation of F5 gene)

200

Extrinsic causes of hemolytic anemia include immune, mechanical, clotting disorders, and meds. What are some intrinsic causes?

Abnormal HgB

Membrane or enzyme defects 

300

___ and ____ are required for a high rate of DNA synthesis needed to produce RBCs & WBCs. 

Vitamin B12; Folate 

300

Endothelial cells release this as an inhibitor of platelet activation/aggregation 

nitric oxide - NO

300

which clotting factors are associated with the intrinsic pathway?

VIII, IX, XI, XII

300

There are 3 types of hemophilia with type A being the most common. Which factor is associated with it?

Factor VIII 

(Ate=8) 

Hemophilia B- IX (B-nine, benign) 

Hemophilia C- XI (IDK) 

300

Name of enzyme that supports rapid platelet aggregation (Thromboxane A2) and Vasoconstriction when activated. 

Cyclooxgenase 

400

T/F- The majority of our iron is obtained from our diet

False:

95%- is recycled from breakdown of RBCs in spleen

5%- From dietary absorption 

400

The very first step of achieving hemostasis is what?

Vasoconstriction

400

Protein C binds to Protein S in order to inactivate which cofactors?

VIII, V

400

In type 1 von willebrand factor disease, the treatment of choice is DDAVP which is a synthetic antidiuretic hormone. Which specific receptor does this act on? 

Type 2 vasopressin receptor 

(increases VWF and Factor VIII) 

400

What protein found on endothelial cells binds to thrombin in order to activate protein C?

Thrombomodulin

500

Name for process that occurs during sickle cell disease in which there is an increased removal rate of RBCs within the spleen. This may lead to the need for a splenectomy 

Extravascular hemolysis

500

Which enzyme is essential for converting fibrinogen into fibrin?

Thrombin

500

Which protease factors are reliant on Vit K? 

II

VII

IX

X

(2+7=9 and then if you add one more you get 10!)

500

T/F- Gerontological considerations for blood and clotting include 

1. Increased incidence of anemia

2. Alterations in bone marrow

3. Decreased coagulability 

False-

#3 should be Increased Hypercoagulability. 

500

This condition is common in pediatrics and can result in hearing loss, intellectual disability, and encephalopathy if left untreated.

Hyperbilirubinemia 

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