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NUR 529 Exam 2 2026 | Hemodynamics, Hemostasis, Cardiovascular & Blood Coagulation Questions with Verified Answers

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This NUR 529 Exam 2 study guide provides fully verified questions and answers for advanced nursing students, updated for 2026. It covers cardiovascular and hematologic concepts including systemic arterial pressure, left ventricular afterload, and detailed stages of hemostasis. Key content includes vessel spasm as the first stage of hemostasis, formation of the platelet plug involving platelet adhesion, activation, aggregation, and the role of von Willebrand factor. Platelet morphology changes from smooth disks to spiny spheres during hemostasis. This resource is ideal for exam preparation, clinical review, and understanding hemodynamic and coagulation mechanisms.

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NUR 529 Exam 2 Set Test Questions and
Revised Correct Answers | Already
Passed|| GRADED A+


Systemic arterial pressure -CORRECTANSWER is the main source of afterload on the

left heart, Left ventricle afterload is increased with narrowing (stenosis) of the aortic

valve



Stages of Hemostasis -CORRECTANSWER Vessel Spasm, formation of the platelet

plug, blood coagulation (clot retraction, clot dissolution)



Vessel Spasm -CORRECTANSWER First stage of hemostasis, constricts the vessel

and reduces blood flow. It is a transient event that usually lasts minutes or hours.



Formation of the platelet plug -CORRECTANSWER Second stage of hemostasis, 1.

platelets are attracted to damaged vessel wall. 2. activation by sub-endothelial tissue. 3.

change from smooth disks to spiny spheres. 4. exposing glycoprotein receptors on their

surfaces. This step requires a protein molecule called von Willebrand factor that leaks

into the injured tissue from the plasma. (adhesion, activation, aggregation)



During Hemostasis, platelets change from ..... -CORRECTANSWER Smooth disks to

spiny spheres

,von Willebrand factor -CORRECTANSWER Formation of the platelet plug requires a

protein molecule called (helps platelets stick together)



Glycoprotein Receptors -CORRECTANSWER Exposed during the formation of the

platelet plug when platelets change from smooth disks to spiny spheres



1.Blood coagulation or development of an insoluble fibrin clot -CORRECTANSWER

Third step of hemostasis: stabilization of the plug occurs as the coagulation pathway is

activated on the platelet surface, and fibrinogen is converted to fibrin.



Thrombocytopenia -CORRECTANSWER Results from a decrease in platelet

production, increased sequestration of platelets in the spleen, or decreased platelet

survival



Drug induced thrombocytopenia -CORRECTANSWER can be from aspirin, atorvastatin,

antibiotics and of course Heparin.



Clot retraction -CORRECTANSWER the consolidation or tightening of the fibrin clot

pulls the edges of the damaged vessel close together, allowing for repair of the vessel

lining.

,Clot dissolution -CORRECTANSWER fibrinolysis occurs through conversion of

plasminogen to plasmin by tissue plasminogen activator (tPA), which is released from

damaged endothelial cells. This conversion results in digestion of fibrin fibers within the

clot and the production of fibrin degradation products.... Clot dissolves.



Immune thrombocytopenia -CORRECTANSWER was formally called idiopathic

thrombocytopenia purpura. ITP is the most common thrombocytopenic disorder among

children and often follows an upper respiratory infection.



Thrombotic Thrombocytopenic -CORRECTANSWER rare and caused by a deficiency

of the gene responsible for severing large von Willebrand factor proteins. The

unchecked platelet aggregation results in microvascular occlusions...end organ failure



Spontaneous bleeding from platelet disorders -CORRECTANSWER Most often involves

small vessels of mucous membranes and skin, common sites are nose, mouth, GI,

uterine



Cutaneous bleeding -CORRECTANSWER seen as pinpoint hemorrhages (petechiae),

or purple areas of bruising (purpura)



Petechiae -CORRECTANSWER Occur almost exclusively in conditions of platelet

deficiency, not dysfunction

, 120 days -CORRECTANSWER RBC lifespan



Spleen -CORRECTANSWER Breaks down RBC



5 years -CORRECTANSWER Almost all bones produce RBCS to maintain growth rate

until this age



Red bone marrow -CORRECTANSWER RBCS produced here after birth



20 years -CORRECTANSWER Age when red cell production takes place mainly in the

membranous bones of the vertebrae, sternum, ribs, and pelvis and red marrow changes

to fatty yellow due to decreased activity



Iron and amino acids -CORRECTANSWER Degradation products recycled when RBCS

are broken down



Hematocrit -CORRECTANSWER Measures the volume of red cell mass in 100 mL of

plasma volume



Transfusion reaction symptoms -CORRECTANSWER •Sensation of heat along the vein

where the blood is being infused

•Flushing of the face

•Urticaria/rash, headache, pain in the lumbar area

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