Hemophilia
Sickle Cell Disease
Anemia
ITP
Thalassemia
100

What are some clinical manifestations of hemophilia?  

Excessive bleeding, hematomas, joint pain 

100

What is the shape of a sickle cell

"C" shape 

100

What are the three types of anemia?

hyperproliferative 

bleeding

hemolytic 

100

ITP is what type of disorder? 

autoimmune 

100

What kind of blood disorder is thalassemia? 

Inherited hemolytic anemia (genetic disorder) 

200

Where is bleeding most likely to occur in patients with hemophilia?  

The joints- knees, elbows, ankles, shoulders, wrists and hips 

200

What is the most common symptom of a sickle cell crisis ? 

Pain 

200

What are risk factors of anemia? 

rapid metabolic activity, diet, age 

200

In this bleeding disorder what is decreased to cause the bleeding 

platelets 

200

What supplements are contraindicated with thalassemia? 

iron supplements 

300

what component of the blood is missing in hemophilia that causes bleeding? 

Factor VIII and/or factor IX 

300

How is sickle cell diagnosed? 

Blood test, genetic testing 

300

What lab values would be low with anemia? 

Decrease iron, vit B12, folate, erythropoietin, RBC, H&H  

300

ITP can result in a sever hemorrhage following what event(s)?

laceration / cesarean birth 

300

What are the main manifestations of thalassemia? 

anemia, bone deformities, jaundice, enlarged spleen, problems with liver growth, weakness and fatigue 

400

What nursing education should be provided to parents of children with hemophilia? 

Administration techniques of factor VIII and/or IX Prophylactically 3-4 times a week

avoid heat during bleeding episodes, wear medical alert bracelet, avoid roughhousing or contact sports.     

400

What triggers a sickle cell crisis? (what should be avoided?) 

Cold 
400

What is an example of inherited hemolytic anemia? 

Sickle cell 

400

This procedure will be preformed if the body does not respond to medical management.  

splenectomy

400

Which finding is most concerning for a patient with beta-thalassemia? 

Iron overload (joint pain, weakness, liver dysfunction, cardiac dysfunctions 

500

What sever complications can result from recumbent factor therapy? 

Development of neutralizing antibodies to factor concentrates 

500

What are treatment option for  sickle cell crisis? 

Pain management,  RBC transfusion, hematopoietic stem cell transplant (HSCT)   

500

What complications can anemia lead to? 

heart failure, confusion, injury f/t falls 

500

What is one of the medication used to treat ITP that can cause side effects and list the side effects of this medication? 

Corticosteroids SE: infection, increased BS, osteoporosis 

500

What is the rationale behind chelation therapy 

to remove excess iron caused by frequent blood transfusions.  

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