Red Cells 2 Flashcards

(28 cards)

1
Q

what is the normal haemaglobin range for males 12-70 years old?

A

140-180

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2
Q

what is the normal haemaglobin range for males > 70 years old?

A

116-156

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3
Q

what is the normal haemaglobin range for females aged 12-70?

A

120-160

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4
Q

what is the normal haemaglobin range for females > 70 years old?

A

108-143

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5
Q

what does MCH stand for?

A

mean cell haemaglobin

low would mean hypochromic

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6
Q

what does MCV stand for?

A

mean cell volume (cell size)

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7
Q

what would be the next investigation if red cell indices and blood film showed hypochromic microcytic anaemia?

A

serum ferritin

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8
Q

what would be the next investigation if red cell indices and blood film showed normochromic normocytic anaemia?

A

reticulocyte count

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9
Q

what would be the next investigation if red cell indices and blood film showed macrocytic anaemia?

A

B12/folate levels
bone marrow biopsy

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10
Q

what type of anaemia is shown by the blood film on the right?

A

hypochromic, microcytic anaemia

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11
Q

A blood film shows hypochromic microcytic anaemia. A serum ferritin is taken and is found to be low. What could this indicate as the cause for anaemia?

A

iron deficiency

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12
Q

A blood film shows hypochromic microcytic anaemia. A serum ferritin is taken and is found to be normal/increased. What could this indicate as the possible causes for anaemia?

A
  • thalassaemia
  • secondary anaemia
  • sideroblastic anaemia
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13
Q

total body iron in g

A

4g
- lose on average 1-2mg per day
- dietary intake balanced by loss

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14
Q

how is iron absorbed and what happens next?

A
  • absorbed in duodenum: Fe2+ > Fe3+
  • transported from enterocytes and macrophages by ferroportin
  • transported in plasma bound to transferrin
  • stored in cells as ferritin
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15
Q

what is the role of Hepcidin?

A

Hepcidin synthesised in hepatocytes in response to increased iron levels and inflammation.
- block ferroportin so reduces intestinal iron absorption and mobilisation from reticuloendothelial cells

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16
Q

what are some causes of iron deficiency?

A
  • malnutrion
  • GI blood loss
  • mennorhagia
  • malabsorption e.g. gastrectomy or coeliac disease
17
Q

Iron deficiency management

A

Correct the deficiency:
- oral iron usually sufficient
- IV iron if tolerant of oral
- blood transfusion rarely indicated

Correct the cause:
- diet
- ulcer therapy
- gynae interventions
- surgery

18
Q

A blood film shows normochromic normocytic anemia. A reticulocyte count is also increased. What could be the possible causes for this?

A
  • acute blood loss
  • haemolysis
19
Q

A blood film shows normochromic normocytic anemia. A reticulocyte count is taken and is normal/low. What could be the possible causes for this?

A
  • secondary anaemia (of chronic disease)
  • hypoplasia
  • marrow infiltration
20
Q

Describe secondary anaemia

A
  • ‘anaemia of chronic disease’
  • 70% normochromic normocytic, 30% hypochromic microcytic
  • defective iron utilisation: increased hepcidin in inflammation, ferritin normal or elevated (an acute phase reactant)
  • identifiable underlying disease e.g. infection, inflammarion, malignancy, renal impairment (role of erythropoietin)
21
Q

what are some causes for haemolytic anaemia?

congenital and acquired

A

congenital:
- hereditary sperocytosis (HS)
- enzyme deficiency (G6PD deficiency)
- haemoglobinopathy (HbSS)

acquired:
- auto-immune haemolytic anaemia, DAT+ (extravascular)
- mechanical e.g. artificial valve (intravascular)
- severe infection/DIC (intravascular)
- PET/HUS/TTP (intravascular)

22
Q

describe a direct antiglobulin test

A
  • detects antibody or complement on red cell membrane
  • reagent contains either anti-human IgG or anti-complement
  • reagent binds to Ab (or complement) on red cell surface and causes agglutination in vitro
  • implies immune basis for haemolysis
23
Q

haemolytic anaemia diagnostic investigations

A

Is patient haemolysing?
- FBC, reticulocyte count, blood film
- serum bilirubin (unconjugated/indirect), LDH
- serum haptoglobin

What is the mechanism?
- history and exam
- blood film
- direct antiglobulin test (Coombs’ test)
- urine for haemosiderin/urobilinogen

24
Q

Haemolytic anaemia management

A
  • Support marrow function > folic acid
  • immunosuppression if autoimmune > steroids, treat trigger e.g. CLL, lymphoma
  • remove site of red cell destruction > splenectomy
  • treat sepsis, leaky prosthetic valve, malignancy etc. if intravascular
  • consider transfusion
25
describe vitamin B12 absorption
- dietary B12 binds to intrinsic factor, secreted by gastric parietal cells - B12-IF complex attaches to specific IF receptors in distal ileum - vitamin B12 bound by transcobalamin II in portal circulation for transport to marrow and other tissues.
26
describe pernicious anaemia
- most common cause of B12 deficiency in western populations - autoimmune disease - antibodies against intrinsic factor (diagnostic) and gastric parietal cells (less specific) - malabsorption of dietary B12, symptoms take 1-2 years to develop (stores last a long time)
27
Megaloblastic anaemia treatment
- replace vitamin B12 deficiency: B12 intramuscular injection, oral if not pernicious anaemia, loading dose then 3 monthly maintenance folate deficiency: oral folate replacement, ensure B12 normal if neuropathic symptoms
28
what are some causes of non-megaloblastic macrocytic anaemia?
- alcohol - drugs e.g. methotrexate, antiretrovirals, hydroxycarbamide - disordered liver function - hypothyroidism - myelodysplasia