Hematologic And Immunologic Dysfunction Flashcards

1
Q

What information is important to collect when assessing hema?

A
CBC
History and physical 
Comments on lack of energy
Food diary
Frequent infections 
Bleeding
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

What do red blood cells do?

A

Carry O2 via hemoglobin

Release CO2 in lungs and pick up O2

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

What do white blood cells do?

A

Responsible for immune responses

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

What do platelets do?

A

Clotting component

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

What is erythropoiesis?

A

Process of forming new RBCs

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

Where are RBCs formed?

A

Bone marrow

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

What is polycythemia?

A

Above average increase in RBCs

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

What is anemia?

A

A reduction in the number of RBCs

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

What causes anemia?

A

Depletions of RBC, hemoglobin, or both

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

How is anemia diagnosed?

A

Hemoglobin less than 11-10 g/dL

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

How does anemia affect the circulatory system?

A
Hemodilation 
Decreased peripheral resistance
Increased cardiac circulation and turbulence 
Cyanosis
Growth retardation
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

Which two age groups are at high risk for iron deficiency anemia?

A

Infants and adolescents

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

What is sickle cell anemia?

A

Partial or total replacement of normal hgb with abnormal hgb S

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

What is the cause of sickle cell anemia?

A

Autosomal recessive disorder

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

What is the prognosis for sickle cell anemia?

A

No cure

Supportive care/prevention of suckling episodes

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

How long is fetal hemoglobin present for?

A

4-6 months

17
Q

What can precipitate a sickle cell crisis?

A
Anything increasing the body's need for oxygen 
Trauma 
Infection/fever
Physical or emotional stress
Hypoxia
18
Q

How is sickle cell crisis treated?

A
Rest
Hydration 
Electrolyte replacement 
Analgesia
Blood replacement 
Antibiotics
19
Q

What is thalassemia?

A

Genetic disorder of deficiencies of the rate of production of globin chains in the hgb

20
Q

How does thalassemia present?

A

Not until later half of infancy

Severe anemia and growth failure

21
Q

What is the treatment for thalassemia?

A

Blood transfusion for normal hgb levels

Desferal

22
Q

What is pancytopenia?

A

Simultaneous depression of all formed elements of the blood

23
Q

What is hypoplastic anemia?

A

Profound depression of RBCs but normal WBCs and platelets

24
Q

How is aplastic anemia treated?

A

Similar to leukemia

Immunosuppressive therapy and bone marrow transplantation

25
What is hemophilia?
A group of hereditary bleeding disorders that result from deficiencies of specific clotting factors
26
What is hemophilia A?
Classic hemophilia | Deficiency of factor 8
27
What is hemophilia B?
Christmas disease | Deficiency in factor 9
28
What is Von Willebrand disease?
Deficiency of von Willebrand factor and factor 8
29
What is the therapeutic management for hemophilia?
Replace missing clotting factors | Desmopressin (DDAVP) IV or nasal
30
How do you get von Willebrand disease?
Autosomal dominant | On chromosome 12
31
What is von Willebrand factor used for?
Platelet adhesion
32
What are symptoms of von Willebrand disease?
Easy bruising Epistaxis Gingival bleeding Increased bleeding with lacerations
33
How is von Willebrand disease treated?
Infusion of von Willebrand protein concentrate | DDAVP
34
What is immune thrombocytopenia?
An acquired hemorrhagic disorder characterized by thrombocytopenia and purpura
35
How do you manage immune thrombocytopenia?
IV immune globulin | Anti D antibody
36
What is disseminated intravascular coagulation?
Disorder of coagulation that occurs as complication of numerous pathological processes
37
What could epistaxis be a sign of?
Vascular abnormalities Leukemia Thrombocytopenia Clotting factor deficiency diseases
38
How do you manage epistaxis?
Sit up and lean forward | Apply pressure to the soft lower part of the nose
39
What is leukemia?
A broad group of malignant diseases of bone marrow and lymphatic system