Pathophysiology, 5th Edition By Lee-Ellen C. Copstead
Pathophysiology, 5th Edition By Lee-Ellen C. Copstead
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Chapter 14: Alterations in Hemostasis and Blood Coagulation
Complete Chapter Questions With Answers
Sample Questions Are Posted Below
MULTIPLE CHOICE
| a. | vitamin K deficiency. |
| b. | hemophilia B. |
| c. | hemophilia A. |
| d. | idiopathic thrombocytopenia. |
ANS: A
Vitamin K deficiency should be considered as the cause for bleeding when the PT and INR are increased but other coagulation studies are normal. Hemophilia B results from factor deficiency or the abnormal function of factor IX. Hemophilia A results from factor deficiency or the abnormal function of factor VIII. In idiopathic thrombocytopenia, a decreased platelet count is seen in prolonged bleeding times.
REF: Pg. 306
| a. | conversion of prothrombin to thrombin. |
| b. | platelet degranulation and adhesion. |
| c. | conversion of fibrinogen to fibrin. |
| d. | clot retraction. |
ANS: D
Clot retraction, the final stage of clot formation, occurs when the components of the fibrin clot are compressed or contracted to form a firm clot. Platelets serve as a catalyst in accelerating the conversion of prothrombin to thrombin. Platelet degranulation is not involved in clot formation. The formation of a fibrin clot occurs when fibrinogen is converted to fibrin, usually at the site of an injury.
REF: Pg. 295
| a. | Liver |
| b. | Kidney |
| c. | Spleen |
| d. | Pancreas |
ANS: A
The liver is responsible for the synthesis of coagulation factors. A clotting factor deficiency is the result of liver dysfunction. Coagulation does not occur in the kidneys. About 25% of the total number of platelets can be found in the spleen. The pancreas is not a location where coagulation occurs.
REF: Pg. 295
| a. | clot retraction. |
| b. | fibrinolysis. |
| c. | platelet aggregation. |
| d. | activation of thrombin. |
ANS: B
Fibrinolysis is the process of clot dissolution and occurs when plasminogen activators cleave plasminogen to plasmin. Clot retraction occurs when the components of the fibrin clot are compressed or contracted to form a clot. Factors released from platelets contribute to hemostasis by enhancing vasoconstriction, platelet aggregation, and vessel repair. Platelet aggregation is not the result of plasmin conversion. Thrombin cleaves fibrinogen to form a fibrin clot.
REF: Pg. 297 | Pg. 299
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