Anemia Flashcards

(35 cards)

1
Q

Causes of decreased production of RBC x2

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

Causes of ineffective erythropoiesis x5

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

Causes of red cell aphasia x6

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

Causes of iron deficiency anemia x3

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

What is red cell aplasia

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

Daily requirement for iron in infants

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

Causes of RBC destruction x6

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

Causes of blood loss x3

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

How does JIA cause anemia

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

Causes of microcytic anemia x3

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

Which micronutrient helps with iron absorption

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

Immune causes of RBC destruction x2

A
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

Causes of normocytic anemia without bone marrow failure

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

Causes of bone marrow failure resulting in normocytic anemia

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

Diagnostic clues for hemolysis x5

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

Vaccines needed before splenectomy x3 and life long prophylactic drug x1

A

Meningitis
Hemophilus influenza
Streptococcus pneumoniae

Penicillin prophylaxis

17
Q

Clinical features of hereditary spherocytosis x5

18
Q

Proteins in for RBC membrane x3

A

Spectrin
Ankyrin
Band 3

19
Q

Function of G6PD enzymes

A

Prevent oxidative damage to RBC

20
Q

Drugs inducing hemolysis in G6PD Deficiency x5

21
Q

Signs of acute hemolysis x3

A

Pallor
Jaundice
Dark urine

22
Q

Pathophysiology of sicke cell disease

23
Q

Triggers of vasooclussive crisis x5

24
Long term problems of SCD x5
25
Describe hyposplenism and autosplenectomy in SCD
Reduced splenic function due to spleen infarction and chronic sickling Autosplenectomy- infarction, scarring causes atrophy of the spleen
26
Clinical manifestations of SCD x5
27
Prophylaxis in SCD x3
Penicillin Folic acid Hydroxyurea
28
Management of acute crisis in SCD x5
Fluids Oxygen Pain control Antibiotic cover Exchange transfusion
29
Indications for exchange transfusion in SCD x3
Stroke Priaprism Acute chest syndrome
30
Describe B thalassemia and its types x2
Reduced production of HbA due to mutations on the B globin gene 1. B thalassemia major- no HbA production 2. B thalassemia intermedia- some HbA production
31
Manifestation of extramedullary hemopoiesis x2
Hepatosplenomegaly Bone marrow expansion
32
Complications of chronic iron overload x5 and organs affected
33
Causes of anemia of prematurity x4
34
Acquirec causes of bone marrow failure x4
Hepatic viruses Chemotherapy Sulphonamides Toxins