Iron deficiency and overload Flashcards

1
Q

when iron deficiency is developing, anaemia occurs before the reticuloendothelial stores become completely depleted. T or F.

A

False
it’s the other way around

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2
Q

what are the clinical features of iron deficiency anaemia?

A
  • general signs & symptoms of anaemia (pale & tired, headache, sometimes angina)
  • painless glossitis
  • angular stomatitis
  • brittle, ridged or spoon nails (koilonychia)
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3
Q

what type of anaemia is iron deficiency anaemia?

A

hypochromic, microcytic

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4
Q

what are the causes of iron deficiency anaemia?

A
  • chronic blood loss: uterine, gastrointestinal (peptic ulcer, hookworm etc.)
  • increased demands: pregnancy, growth, prematurity
  • malabsorption: gluten-induced enteropathy, gastrectomy, autoimmune gastritis, poor diet
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5
Q

what does the blood film show in iron deficiency anaemia?

A

hypochromic, microcytic cells with occasional target cells and pencil-shaped poikilocytes

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6
Q

the reticulocyte count is low in relation to the degree of the iron deficiency anaemia. T or F.

A

True

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7
Q

when does a dimorphic film occur with iron deficiency anaemia?

A
  1. 2.
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8
Q

what happens to the serum iron and total iron-binding capacity (TIBC)?

A

serum iron falls and the TIBC rises so that the TIBC is less than 20% saturated

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9
Q

what happens to the serum ferritin in iron deficiency anaemia?

A

its low in iron deficiency

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10
Q

what does a raised serum ferritin indicate?

A

iron overload or excess release of ferritin from damaged tissues or acute phase response
note: serum ferritin is normal or raised in anaemia of chronic disorders

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11
Q

how is iron deficiency anaemia treated?

A

the underlying cause is treated and iron is given to correct the anaemia and replenish iron stores

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12
Q

what are the different kinds of parenteral iron given?

A
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13
Q

what are the different kinds of oral iron given?

A
  • ferrous sulphate (best one)
  • ferrous fumarate
  • ferrous gluconate
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14
Q

what are the indications for parenteral iron?

A
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15
Q

what causes the failure of iron therapy (Hoff says failure of oral iron)?

A
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16
Q

what happens to the bone marrow iron stores and erythroblast iron in iron deficiency anaemia?

A

they’re both absent duhh

17
Q

what happens to there reticulocyte count in iron deficiency?

A

its low

18
Q

Hepcidin decreases iron absorption and decreases release from macrophages. T or F.

A

True
note: its trying to prevent iron overload

19
Q

in iron deficiency what happens to the hepcidin levels?

A

hepcidin decreases
note: I think its trying to fix the iron deficiency by increasing iron absorption

20
Q

what causes iron overload?

A
  • increased iron absorption: hereditary haemochromatosis, ineffective erythropoiesis- myelodysplastic syndromes, chronic liver disease
  • increased iron intake: African siderosis
  • repeated red cell transfusions: transfusion siderosis
21
Q

what method is most widely used to assess iron overload and for monitoring its treatment?

A

serum ferritin
note: it can be increased in inflammation too tho

22
Q

what happens to the serum ferritin in iron overload?

A

serum ferritin greater than 1000 μg/L

23
Q

what is the initial clinical presentation of iron overload often like?

A

non-specific symptoms like fatigue, arthralgia or loss of libido

24
Q

how is hereditary haemochromatosis diagnosed?

A
  • it’s suspected in the presence of increased levels of serum iron, serum transferrin saturation and ferritin
  • its confirmed by testing for HFE mutation
    note: negative test doesn’t exclude the disease
  • liver biopsy is also useful and MRI can be used
25
Q

hereditary haemochromatosis pts may present in adult life with which features?

A
26
Q

what causes African iron overload?

A

combination of iron absorption due to genetic defect and consumption of beverages brewed in iron pots

27
Q

Moderately severe forms of thalassaemia may lead to increased iron levels. T or F.

A

True
in thalassaemia intermedia; this is due to increased iron absorption and may lead to increased levels of iron in the liver

28
Q

the heart is spared from iron loading in thalassaemia intermedia. T or F.

A

True

29
Q

how does transfusional iron overload develop?

A

develops in pts with chronic severe anaemia who have regular blood transfusions.
note: Each 500 mL of transfused blood contains approximately 250 mg iron

30
Q

chronic transfusion

A

aplastic anaemia, Beta thalassemia major, SCD, congenital sideroblastic anemia, B-thal Hb E disease, congenital dyserythropoietic anaemia, red cell aplasia, acute leukemias, MDS, MF

31
Q

Cardiac damage due to iron is a dominant problem in transfusional iron overload. T or F.

A

True

32
Q

what is a valuable measure of cardiac and liver iron loading?

A

T2*MRI

33
Q

how is hereditary haemochromatosis treated?

A

venesection/phlebotomy
note: Treatment is with regular venesection, initially at 1–2 week intervals, with each unit of blood removing 200–250 mg of iron

34
Q

what is used to treat transfusional iron overload?

A

iron chelation therapy

35
Q

what are the drugs used in iron chelation therapy?

A
  • desferasirox: oral
  • deferiprone: oral
  • deferoxamine: parenteral