Red cells 3 (anaemia) Flashcards

(38 cards)

1
Q

Factors influencing the normal range for haemoglobin

A
  • Age
  • Sex
  • Ethnicity
  • Time of day sample is taken
  • Time to analysis
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2
Q

Normal haemglobin range for males

A
  • 12-70 = 140-180

- >70 = 116-156

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3
Q

Normal haemoglobin range for females

A
  • 12-70 = 120-160

- >70 = 108-146

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4
Q

Clinical features of anaemia due to reduced O2 delivery to tissues

A
  • Tiredness/pallor
  • Breathlessness
  • Ankle oedema
  • Dizziness
  • Chest pain
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5
Q

Clinical features of anaemia related to underlying cause

A

-Evidence of bleeding
Menorrhagia, PR bleeding, Dyspepsia

-Symptoms of malabsorption
Diarrhoea, Weight loss

  • Jaundice
  • Splenomegaly/Lymphadenopathy
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6
Q

What causes destruction/loss of blood leading to anaemia

A
  • Haemorrhage (blood loss)
  • Haemolysis
  • Hypersplenism (overactive spleen)
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7
Q

What problems with RBCs themselves can lead to anaemia

A
  • Membrane
  • Haemoglobing
  • Enzymes
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8
Q

What is MCV + MCH

A
  • MCV = Mean Cell Volume (size)
  • MCH = Mean Cell Haemoglobin
  • Can give morphological discription of anaemia
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9
Q

3 types of anaemia

A
  • Hypochromic Microcytic Anaemia
  • Normochromic Normocytic Anaemia
  • Macrocytic Anaemia
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10
Q

What investigations are used to distinguish between types of anaemia

A
  • Red cell indices

- Blood film

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11
Q

What investigation is done when Hypochromic Microcytic anaemia is diagnosed

A

Serum ferritin

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12
Q

What investigation is done when Normochromic Normocytic anaemia is diagnosed

A

Reticulocyte count

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13
Q

What investigation is done when Macrocytic anaemia is diagnosed

A
  • Serum B12 + Folate assay

- ?Bone marrow biospy?

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14
Q

If serum ferritin is high or low in Hypochromic Microcytic anaemia what is the cause

A
  • Low = Iron deficiency

- High = Thalassaemia/Secondary anaemia/?sideroblastic anaemia?

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15
Q

How does Iron move around the blood

A
  • In haemoglobin

- Bound to Transferrin

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16
Q

How is iron stored in most cells

17
Q

How is iron transported from enterocytes + macrophages

18
Q

What is hepcidin and where is it made

A
  • Synthesised in Hepatocytes
  • Responds to inflammation (and increased Fe levels)
  • Blocks ferroportin, so reduces intestinal Fe absorption
19
Q

What do high + low levels of hepcidin cause

A
  • High = Anaemia

- Low = Haemochromatosis

20
Q

What is ferroportin

A
  • Transmembrane portein

- Transports iron from inside a cell to outside (i.e. out of gut cells into blood)

21
Q

Commonest cause of anaemia worldwide

A

Iron deficiency anaemia

DISCRIPTION, NOT A DIAGNOSIS, MUST ESTABLISH A CAUSE

22
Q

Hx for iron deficiency anaemia

A
  • Dyspepsia, GI bleeding
  • Other bleeding, e.g. menorrhagia
  • Diet (N.B. children + elderly)
  • Increased requirement e.g. pregnancy
23
Q

Signs of iron deficiency

A
  • Koilonychia
  • Angular stomatitis
  • Atrophic tongue (smooth + glossy can be tender/painful)
24
Q

Causes of iron deficiency anaemia

A
  • GI blood loss (worms)
  • Menorrhagia
  • Malabsorption (Gastrectomy, coeliac disease)
25
Management of iron deficiency anaemia
Correct cause - Diet - Ulcer therapy - Surgery if bleeding - ?COC pill if menorrhagia? Correct anaemia - Oral iron supplement ussually adequate - Possible need of transfusion
26
If reticulocyte count is high or low in Normochromic Normocytic anaemia what is the cause
- High = Acute blood loss or Haemolysis | - Low = Secondary anaemia, hypoplasia, marrow infiltration
27
Causes of haemolytic anaemia
Congenital - Hereditary spherocytosis (HS) - G6PD deficiency Acquired -Auto-immune haemolytic anaemia (extravascular) Intravascular (also acquired) - Mechanical (artificial valve) - Severe infection - Drugs
28
2 ways of categorising acquired haemolytic anaemia
- Immune (mostly extravascular) | - Non-mmune (mostly intravascular)
29
How to test for auto-immune haemolytic anaemia
- Direct antiglobin test - Casuses agglutination in vitro (if -ve suggests the haemolytic anaemia is not immune mediated)
30
What is seen on a blood film in intravascular haemolysis
Shcistocytes (red cell fragments)
31
Management of haemolytic anaemia
-Folic acid (support marrow function) Correct cause -Immunosupression if autoimmune (?Prednisolone?)(treat trigger CLL, lymphoma) -Remove site of destruction (splenectomy) -Treat sepsis, leaky prosthetic valce, malignancy etc -Consider transfusion
32
Describe secondary anaemia
- "Anaemia of chronic disease" - 70% normochromic normocytic, 30% hypochromic microcytic - Defective iron utilisation - Identifiable underlying disease (infection, inflammation, malignancy)
33
If there is megaloblastic changes or no megaloblastic changes in bone marrow in Macrocytic anaemia what is the cause
- Megaloblastic change = B12 + Folate deficiency | - Non-megaloblastic = Marrow infiltration, Myelodysplasia, Drugs
34
Causes of B12 deficiency
- Pernicious anaemia | - Gastric/ileal disease
35
Causes of folate deficiency
- GI disease (coeliac disease) - Increased requirement (haemolysis) - Dietary
36
What happens to the skin in megaloblastic anaemia
Lemon yellow tinge
37
What causes pernicious anaemia
Antibodies against intrinsic factor (auto-immune)
38
Rx for megaloblastic anaemia
Replace vitamin - B12 deficiency = B12 IM injection, loading dose then 3 monthly maintenance - Folate deficiency = Oral folate replacement