L5: Causes of Anaemia Flashcards

1
Q

What is the definition of Anaemia and features of presentation - including those relating to compensation

A

Haemoglobin lower than normal for the age and sex of patient

Compensation for reduced O2 delivery capacity:

-increased cardiac stroke volume and tachycardia
+ right shift in O2 dissociation curve

  • Features:
  • can be assymptomatic however eventually
  • SOB, fatigue, pallor (conjunctiva, palm creases)
  • then congestive HF if severe enough.
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2
Q

How does levels of Hb differ at different stages of life and between f/m

A

Hb is high at birth and then drops off sharply from 3m - 1 yr old, after which it increases until ~15yrold

Men have higher resting Hb than women. Pregnant women have lowest

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3
Q

What are the 2 approaches to classifying anaemia

+ 3 things related to each one

A
  1. Morphological: based on
    - RBC appearance under microscope (blood film)
    - mean (1) cell volume (bigness)
    - mean cell haemoglobin concentration
2. Pathogenetic: 
based on cause: 
- Impaired production
- blood loss
- haemolysis (excess destruction)
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4
Q

What are the other blood tests that help to differentiate anaemias

  1. > low suggests bone marrow deficiency??
A
  1. Hb in g/L ->
  2. Red cell count
  3. Haematocrit/packed cell volume (% of RBC compared to blood volume)
  4. Iron studies
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5
Q

What are the main causes of Impaired production of RBC - and give eg

A
  1. Deficiency of substances essential for RBC production
    - iron, vit B12, folate
  2. Genetic defect in production
    - thalassaemia
  3. Failure of bone marrow: .WBC and platelet count also low
    - eg. infiltration of leukaemia, irradiation or drug damage
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6
Q

What are the main causes of Losing RB ->Haemolysis of RBC / haemolytic anaemia

A
  1. Blood loss: acute from trauma/surgery
  2. Haemolysis: shortened survival within the body,
    - environment/extrinsic: autoimmune destruction of RBC
    - intrinsic problem - eg. inherited defect in RBC structure/ function
    eg. G6PD deficiency, hereditary spherocytosis
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7
Q

What are the 3 morphological anaemias

A
  1. Microcytic hypochromic anaemia (pale=less Hb, MCV <76)
  2. Normochromic normocytic anaemia (normal)
  3. Macrocytic anaemia (MCV>96). most of them normochromic.
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8
Q

What is the 3 main causes of microcytic anaemia

2 is generally mild

A

Anything that reduces RBC production so less Hb

Haem production:
1. Iron deficiency

  1. Chronic illness - eg. rheumatoid arthritis, osteomyelitis.
    - Underlying inflammation/infection causes block of iron release from macrophages to protect against bacteria growth

This is normochromic- mild hypochromic, and only mild anaemia 90-100g/L

Globin production:
3. Genetic: eg. Thalassaemia (no globins)

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9
Q

What is measured to diagnose Iron deficiency

A
  1. Serum iron
  2. Serum ferritin: soluble storage form of iron
  3. Iron binding capacity (transferrin- iron transport protein)
  4. Iron saturation: - amount of iron bound to transferrin
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10
Q

How do you differentiate true iron deficiency from iron block in anaemia of chronic illness using iron measures

A

In true iron deficiency - transferrin/ unbound iron binding capacity is upregulated via loss of negative feedback so

  • high UIBC: serum iron
  • Serum ferritin is also very low

In chronic illness/iron block

  • serum iron is low-normal so can negative feedback to
  • transferrin (low normal) so
  • UIBC: serum iron normal
  • Normal/raised serum ferritin
  • Normal saturation
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11
Q

Is anaemia a late or early stage of iron deficiency

A

late

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12
Q

What are the causes of true iron deficiency and what are the most likely for premenopausal females, children, post menopausal/men

A
  1. Reduced intake from diet: eg. vegetarian
  2. Malabsorption: from proximal small bowel
  3. Increased demands: pregnancy
  4. Chronic blood loss from GI or GU tract

Premenopausal: imbalance between dietary intake and menstrual blood loss

Post/men: occult blood loss from GI tract/ other sites (tumour)

Children: deficient diet

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13
Q

What are the treatments available for iron deficiency and what would the blood film look like in someone on it

A

Replacement therapy
- oral tablet: ferogradumet (Gi toxicity causing diarrhoea/constipation so adherence poor)

IV infusion: ferric carboxymaltose

The Hb conc increases ~20g/L every 3 weeks so blood film would look dimorphic - old bad cells with good new ones + have more reticulocytes

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14
Q

How is thalassaemia diagnosed and what is the difference between minor and major

A
  1. Haemoglobinopathy screen:
    a) blood film: fragmented, irregular shaped, small, microcytic RBC
    & other blood test values for anaemia

b) iron studies
c) phenotypic analysis: splenomegaly, hepatomegaly, expansion of bone marrow, jaundice
2. Genetic testing

Het: mild anaemia which looks like iron deficiency

Homo: severe anaemia bc both alpha or beta chains reduced/absent depending on alpha or b thalassaemia

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15
Q

What are the 6 causes of macrocytic / megaloblastic anaemia - 2 main ones

Why does it cause anaemia?

A
  1. B12 deficiency
  2. Folate deficiency

B12/Folate involved in DNA synthesis causing abnormal maturation and growth of RBC - not Hb deficiency. May affect all cell lineages if severe

Also

  1. liver disease
  2. heavy alcohol abuse
  3. primary bone marrow disorders
  4. hypothyroidism
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16
Q

What are the causes of low vit B12 and why

  • body has stores for 3-4 yrs
A
  1. Diet: vegan (B12 mostly found in meat products)
  2. Malabsorption:
    - gastrectomy : removal of parietal cells that make intrinsic factor that complexes with b 12 to be absorbed
    - terminal ileum disease (where its usually absorbed)
    - immune (pernicious anaemia) : autoimmune against parietal cells or intrinsic factor
17
Q

What are the causes of low folate level

A
  1. Diet: lack of vegetables
  2. Malabsorption: coeliac disease in small bowel
  3. Increased demands due to pregnancy/ haemolytic anaemia (need more for making replacements)
18
Q

What are the clinical features of haemolytic anaemia

A
  • Mildly jaundiced (increased unconjugate bilirubin)
  • pallor
  • Splenomegaly (site of haemolysis)
  • Increased reticulocyte count.
  • Damaged RBCs
  • Haptoglobins