Red cells (anaemia) 2 Flashcards

1
Q

What is the normal haemoglobin range for a healthy:

a) female (12-70)
b) elderly female (>70)
c) male (12-70)
d) elderly male (>70)

A

a) female = 120-160
b) elderly female = 108-143
c) male = 140-180
d) elderly male = 116-156

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2
Q

What clinical features may be seen in patients who are anaemic - related to the underlying cause

A

Evidence of bleeding:

  • menorrhagia
  • dyspepsia, PR bleeding

Symptoms of malabsorption:

  • diarrhoea
  • weight loss

Jaundice

Splenomegaly

Lymphadenopathy

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3
Q

What are the 2 main red cell indices that are used for investigating anaemia?

What are the possible morphological descriptions from these indices?

A

Mean cell haemoglobin (MCH)

Mean cell volume (MCV)

1) Hypochromic microcytic
2) Normochromic normocytic
3) Macrocytic

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4
Q

The morphological description of anaemia (from MCH, MCV measurements) gives an indication of the probable cause of the anaemia - and dictates the next step of investigation

What is the (usual) next step of investigation for:

a) hypochromic microcytic
b) normochromic normocytic
c) macrocytic

A

a) hypochromic microcytic = serum ferritin
* iron deficiency anaemia most common cause of h.m. anaemia*
b) normochromic normocytic = reticulocyte count
* can be elevated (haemolysing causes) or depressed (aplastic anaemia etc)*
c) macrocytic = B12/folate, bone marrow
* B12 & folate deficiency most commo​n cause of macrocytic*

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5
Q

Hypochromic microcytic anaemia is identified on a blood film, so you measure serum ferritin…

What would be indicated by a:

a) Low serum ferritin
b) normal / elevated

A

a) Low serum ferritin:
* = iron deficiency anaemia
b) Normal or elevated serum ferritin:

  • Thalassaemia
  • secondary anaemia
  • sideroblastic anaemia (rare)

Note that ferritin is elevated with inflammation and in some liver diseases

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6
Q

On the topic of iron:

a) how much is in us?
b) where is iron utilized?
c) where is iron stored?

A

a) 4g
b) haemoglobin and myoglobin (muscles)
c) RBCs, reticuloendothelial macrophages, liver

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7
Q

In what formm is dietary iron absorbed most efficiently?

A

In the form of haem (ie from blood)

non-haem iron absorbed less effectively

so up you, vegetarians

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8
Q

go learn the metabolic pathway for iron - roles of ferroportin, transferrin, ferritin, hepcidin

A
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9
Q

What are the causes of iron deficiency anaemia?

A

Insufficient dietary intake (veggies n vegans)

Menstruation (mennorhagia)

Dyspepsia, GI bleeding

Malabsorption - coeliac disease, gastrectomy

Increased requirement (pregnancy, puberty)

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10
Q

How do you correct iron deficiency anaemia?

A

Correct the deficiency:

  • oral iron - usually sufficient
  • IV iron if intolerant to oral
  • transfusion rarely indicated

Correct the cause:

  • diet
  • ulcer therapy
  • gynae interventions
  • surgery
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11
Q

Normochromic normocytic anaemia is identified and investigation of reticulocyte count is carried out

What causes would these results indicate:

a) Increased reticulocyte count
b) Normal or low reticulocyte count

A

a) increased reticulocyte count:

  • acute blood loss
  • haemolysis

b) Normal or low reticulocyte count:

  • Secondary anaemia - eg renal impairment
  • hypoplasia
  • marrow infiltration
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12
Q

What is secondary anaemia?

What morphological appearances of RBCs are seen in secondary anaemias?

A

Anaemias secondary to chronic diseases

70% normochromic normocytic

30% hypochromic microcytic

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13
Q

Another cause of normochromic normocytic anaemia is (abnormal) haemolysis

How do the values for Haemoglobin and reticulocytes change in haemolytic anaemia and why?

A

Accellerated RBC destruction decreases Haemoglobin

Bone marrow compensation for this = High reticulocyte count

The overall level of Hg depends on balance between production and destruction

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14
Q

Haemolysis can happen extravascularly and intravascularly

Which is bad?

A

Extravascular haemolysis occurs normally - but is pathologically elevated in certain conditions

Intravascular haemolysis is pathological and shouldnt happen

In certain haemoglobinopathies it occurs - eg in sickle cell disease

free haemoglobin in the blood is toxic

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15
Q

What are some congenital causes of haemolytic anaemia?

Do these cause intravascular or extravascular haemolysis?

A

Hereditary spherocytosis (HS)

Enzyme deficiencies (eg G6PD)

Haemoglobinopathies (eg HbSS)

These all cause increased extravascular haemolysis but conditions like sickle cell disease (HbSS) and G6PD cause some intravascular haemolysis as well

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16
Q

What are the acquired causes of haemolytic anaemia?

Which of these causes extravascular and intravascular haemolysis?

A

Extravascular:

  • autoimmune haemolytic anaemia

Intravascular:

  • mechanical destruction - ie leaky artificial valves
  • severe infections, DIC
  • pre-eclampsia (PET)
  • haemolytic uraemic syndrome (HUS)
  • Thrombotic thrombocytopenic purpura (TTP)

Immune - extravascular. Non-immune - intravascular

17
Q

How do you test for immune causes of haemolytic anaemia

A

Direct antiglobulin test - aka Coomb’s test

this detects any antibodies or compliment on RBC membrane

Contains either:

  • anti-human IgG
  • anti-compliment

If positive (ie immune haemolytic anaemia) then reagant causes agglutination in vitro

18
Q

What appearance (shape) do RBCs have on blood films in immune haemolytic anaemia?

Why?

A

Spherical appearance - spherocytes

This is because:

1) RBCs with auto-antibodies attached enter spleen
2) Spleen recognises antibodies and is like nah not tonight mate - so removes the antibodies and a wee bit of RBC membrane
3) Damaged RBC membrane causes them to take up this spherical shape

19
Q

On a blood film, what would be the appearance of RBCs seen with intravascular haemolysis?

A

Schistocytes

Fragmented RBCs sort of all mashed up

20
Q

Summarise what investigations would tell if you if a patient was haemolysing abnormally?

A

FBC, Reticulocyte count, blood film

High bilirubin

High LDH

Low haptoglobin

21
Q

What tests would you do to determine the mechanism causing haemolytic anaemia?

A

History and examination

Blood film

Coomb’s test (DAT)

Urine for haemosiderin/urinobilinogen

22
Q

Describe the management of haemolytic anaemia

A

Support marrow function:

  • Folic acid - people with H anaemia use up lots of folate

Correct the cause:

  • Immunosuppression if autoimmune:
    • steroids
    • treat causes such as CLL, lymphoma etc
  • Remove site of RBC destruction
    • splenectomy
  • Treat sepsis, leaky valves, malignancy etc

Transfusion if required

23
Q

What is the primary investigation for someone who has macrocytic anaemia and why?

A

B12 / Folate assay

Deficiency in these is the most common cause of macrocytic anaemia. Macrocytic anaemia caused by this are called Megaloblastic

24
Q

If a patient has macrocytic anaemia that is non-megaloblastic, what investigations are indicated and what are the potential causes?

A

Blood film

Bone marrow

Potential causes - myelodysplasia, marrow infiltration, certain drugs (methotrexate etc)

25
Q

Megaloblastic anaemia is caused by deficiency in folate and/or B12

What are the:

a) symptoms of B12/folate deficiency
b) causes of B12 deficiency
c) causes of Folate deficiency

A

a) symptoms of b12/folate deficiency:

  • sx of anaemia (breathlessness and all that pish)
  • neurological symptoms
    • esp peripheral neuropathy
    • ‘subacute combined degeneration of the cord in B12 deficiency’

b) causes of B12 deficiency:

  • pernicious anaemia (malabsorption of B12 in GI tract)
  • gastric/ileal disease

c) causes of folate deficiency:

  • dietary
  • increased requirements - eg haemolysis
  • GI pathology - eg coeliac disease
26
Q

How and where is vitamin B12 absorbed

(in more detail in GI physiology)

A

Intrinsic factor

which is secreted by gastric parietal cells

absorbed in ileum

27
Q

What will blood tests show for a patient with megaloblastic anaemia?

A

Blood tests will show elevated bilirubin and LDH

Elevated bilirubin because the red cells are ‘friable’ (big flabby structurally poor) and haemolyse a bit in the circulation

28
Q

On a blood film, megaloblastic anaemia has effects on the morphology of other blood cells as well

Which other blood cells show a characteristically different appearance in megaloblastic anaemia?

A

Neutrophils - hypersegmented appearance

B12 and folate are essential for DNA synthesis in blood cells - so deficiencies will affect white cells too - esp neutrophils

29
Q

What causes pernicious anaemia?

(malabsorption of B12)

A

Autoimmune disease - the patient develops antibodies against intrinsic factor

(identification of these antibodies is diagnostic)

Some patients also develop antibodies against gastric parietal cells

30
Q

How is pernicious anaemia treated?

A

IM Vitamin B12 injection

  • loading dose then 3 monthly maintenance -

If dietary cause of B12 deficiency (so not the autoimmune stuff) then oral B12 suffice

31
Q

How is folate deficiency treated?

There is a common problem encountered with treatment of folate deficiency. What is this and how is it corrected?

A

Oral folic acid

If a patient is also B12 deficient, then folic acid treatment can precipitate/exacerbate neuropathic symptoms

This is corrected by giving B12 as well as folic acid

32
Q

What are the other causes of macrocytosis?

A

Alcohol

Drugs - Methotrexate, Antiretrovirals, hydroxycarbamide

Disordered liver function

Hypothyroidism

Myelodysplasia

Marrow infiltration

33
Q

To summarise - identify the investigations associated with each morphological appearance of red blood cells

A