Anaemia Flashcards

1
Q

What is the main function of red blood cells

A

Circulate oxygen around the body and remove CO2

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2
Q

What is erythropoiesis

A

Synthesis of RBCs

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3
Q

steps of erythropoiesis

A

EPO secrete from kidneys, which stimulates stem cells in bone marrow to develop into a mature erythrocyte

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4
Q

What other things are required for erythropoiesis

A

Fe
Folate(B9- for DNA synthesis to produce cells)

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5
Q

What is anaemia

A
  • Fewer RBCS than normal OR
  • Less haemoglobin than normal in each RBC
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6
Q

What is anaemia in pregnant women reffered to as

A

Dilutational anaemia - as they have an expansion in blood volume and higher oxygen needs

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7
Q

What is the clinical definition of anaemia in quantity of haemoglobin IN MEN

A

Hb < 13g/dL

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8
Q

What is the clinical definition of anaemia in quantity of haemoglobin IN WOMEN

A

Hb <12g/dL
* lower due to menstrual cycle

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9
Q

What are the two main causes of Anaemia

A
  1. Increased haemoglobin loss
  2. reduced haemoglobin synthesis
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10
Q

what conditions cause an Increased haemoglobin loss

A
  1. Hemorrhage - injuries, trauma
  2. haemolysis(splitting of RBCs) - due to infections, medications and cancers, autoimmune disorders
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11
Q

What conditions cause reduced haemoglobin synthesis

A
  1. Reduced proliferation of precursors(i.e iron deficiencies, renal failure, aplastic anaemia)
  2. precursors not maturing effectively(iron. folate defiency, vitamin B12, disorders of globin synthesis/thalassemias )
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12
Q

What are 8 symptoms of anaemia

A

Fatigue
Increased HR
Shortness of breath
Headache
Dizziness
Chest pain
Paleness
Coldness

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13
Q

What is microcytic anaemia

A

Low mean corpuscular volume (smaller red blood cells)

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14
Q

What is the common cause of microcytic anaemia

A

iron deficiency

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15
Q

What 7 blood tests are there for anaemia

A
  1. Haemoglobin
  2. RBC
  3. Mean corpuscular volume
  4. Haematocrit - proportion of RBC in blood
  5. Ferritin (iron stores)
  6. Folate
  7. B12 levels
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16
Q

Where do we get iron from

A

Solely from diet

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17
Q

Where is iron absorbed

A

Duodenum and proximal jejunum

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18
Q

What the 3 causes of iron def anemia

A
  1. inadequate iron absorption (poor diet to malabsorption)
  2. increased blood loss (i.e menstruation, PUD)
  3. Increased requirement (i.e pregnancy)
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19
Q

What pregnancy complications of iron defiency anaemia

A

Pre-term delivery
Maternal post partum fatigue and depression

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20
Q

What would a blood test for iron deficiency anaemia show

A

Low hb
Low MCV
Low ferritin(<30mcg/L confirms diagnosis)
Low mean cell haemoglobin(hypochromia)

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21
Q

What should we exclude in iron deficiency anaemia

A
  1. Other anaemias,
  2. GI bleed,
  3. GI cancer
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22
Q

When should we refer those with iron defiency

A
  1. GI symptoms
  2. FIT test result of 10mcg Hb in feces
  3. Men and post-menoposal women, unless clearing no GI bleeding
  4. Pregnant women with hb<70g/L or advanced gestation 34 weeks+
  5. Unresponsive to tx
  6. positive coeliac seriology
  7. profound anaemia with symptoms of heart failure
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23
Q

What is tx of Iron def anemia

A

One tablet daily of either
- Ferrous sulfate
- Ferrous fumarate
- Ferrous gluconate(exc One tablet BD)

Which=65mg of elemental iron

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24
Q

What should you do initially if ferrous salt not tolerated/causes S/E for iron deficiency anaemia

A

Reduce to alternative daily dosing

or take with/ after food but this reduces efficacy

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25
Q

How long should you continue elemental iron supplementals for iron deficiency anaemia after corrected

A

3 months

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26
Q

How much should Hb rise by after 1 month of iron supplementation

A

20g/L or 10g/L(alternate day dosing)

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27
Q

What are side effects of elemental iron

A

Constipation.
Diarrhoea.
Epigastric pain.
Faecal impaction.
Gastrointestinal irritation.
Nausea.

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28
Q

What are iron rich foods

A

Dark green vegetables
Red meat
Apricots
Prunes
Raisins

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29
Q

When should you review patient on iron supplementation

A

3-4 weeks after initation

If no response(did not rise by 20g/L) then refer.

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30
Q

What patients can take ongoing iron supplementation for prophylaxis

A

Recurrent anaemia where further investigations not indicated,
Plant-based diet,
Malabsorption disease,
Menorrhagia,
Pregnant women (continue throughout pregnancy)

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31
Q

Should you refer pregnant women with iron deficiency anaemia

A

Yes if they have significant symptoms and or/severe anaemia(Hb<70g/L) OR if pregnancy at advanced gestation(34 weeks)

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32
Q

What level of ferritin would confirm Iron deficiency anaemia diagnosis

A

30mcg/L

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33
Q

When is parenteral iron necessary

A
  1. oral therapy unsucessful
  2. Continuing blood loss or malabsorption
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34
Q

How is parenteral dose calculated

A

According to body weight and iron need(Hb deficit)
Check SPC for products dosing

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35
Q

what is the risk of parenteral iron

A

Iron overload
Severe Hypersensitivity reactions(Anaphylaxis)

36
Q

What is ferinject

A

Parenteral Iron

37
Q

How much ferinject can be given in a single week

38
Q

How do you calculate dose of ferinject?

A
  1. Patient weight and Hb - then look at table for dose
  2. Calculate maximum cumulative dose(to ensure it dose not exceed)
  3. if over 1000mg then split administration by 7 days
  4. how much diluent is need and how long is infusion(check table in SPC)
39
Q

How many tablets of ferrous gluconate should be taken for iron deficiency anaemia

A

Two (300mg) tablets daily

300mg is equivalent to 35mg of elemental iron

40
Q

aside from iron deficiency anaemia, what are two other microcytic anaemias

A
  1. Anaemias of chronic diseases
  2. Sideroblastic anaemia
41
Q

What conditions cause anaemia of chronic disease

A

Inflammatory conditions such as Crohns, UC, Rheumatoid arthritis

Cancers( + cytotoxic agents also impact this)

Renal disease

42
Q

What happens in anaemias of chronic inflammatory diseases

A

Inflammatory cytokines cause the liver to produce hepcidin which decreases iron absorption from the gut and reduces the release of iron from body stores

43
Q

What happens in anaemias of chronic renal disease or heart failure

A

decreased production of EPO –> leads to anaemia

44
Q

How do you treat anemia of chronic disease

A
  • Treat the underlying condition- anaemia should resolve.
  • Do NOT treat these patients with iron – functional disorder, not actual deficiency (and reduced absorption of iron)
45
Q

How do you treat anaemia of chronic kidney disease (Hb falls to <10-11g/dL and patient has symptoms)

A
  1. ESAs (erythropoietic stimulating agents) i.e Epoetin
    - Give SC Once weekly
  2. if they also have iron deficiency give IV iron therapy. Serum ferritin levels should not rise above 800mcg/L
46
Q

What is sideroblastic anaemia caused by

A

abnormal utilisation of iron during heme production in erythropoiesis.

47
Q

Are iron stores(ferritin) low in anaemia of chronic diseases

A

Normal ferritin but iron is not circulation (low serum iron)

48
Q

What are sideroblast

A

Erythroblasts which contain excessive iron granules arranged in a distinct ring around the nucleus

49
Q

Are iron stores low in sideroblastic anaemia

A

No they are normal

50
Q

What causes sideroblastic anaemia

A
  1. myeloproliferative disorders i.e myeloma/leukemia
  2. hereditary
  3. drugs - TB drugs isoniazid/pyrazinamide, Chloramphenicol, alcohol
  4. Copper deficiency
51
Q

Treatment of sideroblastic anaemia

A

Discontinue the drugs/toxins

X-linked sideroblastic anaemia - Trial pyridoxine 50-200mg daily - takes several months to see results, if severe: Blood transfusion may be required to move oxygen around the body.

Idiopathic sideroblastic anaemia - Pyridoxine high dose 100-400mg daily

52
Q

What does megaloblastic anaemias mean

A

They are macrocytic having a raised MCV >100fL

53
Q

what are the two main causes of megaloblastic anaemias

A

Vitamin B12 deficiency
Folate deficiency

54
Q

What is Pernicious Anaemia

A

an Autoimmune condition causing gastric atrophy of parietal cells which secretes intrinsic factor

Intrinsic factor is required for B12 absorption from the gut –> anaemia

55
Q

what is the role of Vitamin B12 and Folate

A

Essential co-factors in the synthesis of DNA precursors purine and pyrimidines.

This is essential for rapidly dividing cells such as red blood cells

56
Q

What drugs can cause megaloblastic anaemias

A

Medications which modulate purine metabolism (e.g. azathioprine, MMF, allopurinol) or interfere with pyrimidine synthesis (e.g. hydroxyurea, trimethoprim), or both (e.g. MTX)

57
Q

What food contain B12

A

animal products such as fish, eggs and dairy products

58
Q

What the Blood tests results indicative of megaloblastic anaemia

A

Hb reduced,
MCV Increased,
Bilirubin increased – as cells haemolyse,
Serum B12 (cobalamin) and Folate will be reduced (One or both are low),
Serum autoimmune antibodies (parietal cell and IF),
Bone marrow examination
LFTs, TFTs to identify underlying cause

59
Q

What the further features of megaloblastic anaemias

A

Glossitis(smooth/ pale tongue)
Anorexia
Mild jaundice
Sterility
Altered bowel habits

60
Q

What is a serious distinctive feature of B12 deficiency

A

neurological involvement
- Loss of sensation(symmetrical neuropathy)
- Visual disturbances
- Muscle weakness
- Loss of mental or physical drive

61
Q

What is the level of folate described in folate deficiency

62
Q

what causes folate defiency

A
  • deficient intake of folate foods
  • Alcoholism
  • GI disorders (i.e coeliac disease impairs absorption)
  • Pregnancy (preferential to foetus- deficiency in utero increases risk of neural tube defects in child)
  • Haematological disorders
  • Medications
63
Q

What foods contain folate

A

leafy geen vegetables(spinach, cabbage, kale)
Beans and legumes
Fortified breads and cereals

64
Q

What drugs cause folate deficiency

A

Phenytoin
Barbiturates
Sulfasalazine
Oral contraceptives
Methotrexate
Trimethoprim

65
Q

How do you manage folate deficiency

A
  1. Assess their dietary intake
  2. Check for coeliac disease(antibodies)
  3. Replace with folic acid - 5mg daily
  4. Replace B12 deficiency first or concurrently(check B12 in patients with folate deficiency as folate can mask symptoms of B12 deficiency)
66
Q

What level is B12 deficiency diagnosed

67
Q

What drugs cause B12 deficiency

A

Tb drugs
Metformin
5-ASAs
Colchicine
PPI

68
Q

What drug treatment should you use for unknown cause of B12 deficiency without neurological involvement

A

IM hydroxocobalamin 1mg every 2-3 months for life

PO cyanocobalamin large doses 500-1000mcg daily

69
Q

How is B12 given

A
  1. Initial replacement
  2. Maintenance doses
70
Q

if there is neurological involvement in B12 deficiency what should you do

A

Start IV hydroxycolabalamin
Refer to specialist

71
Q

Treatment for B12 deficiency of a dietary cause

A
  1. Dietary advice
  2. Oral Cyanocobalamin between meals
  3. if poor adherence(IM hydroxocobalamin 1mg/3 weeks)
  4. Stop tx when corrected or possibly life long if vegan diet
72
Q

What are the 4 haemolytic anaemias

A
  1. Autoimmune
    1. Sickle cell
    2. Thalassemia
    3. G6PD deficiency
73
Q

What is sickle cell anaemia

A

Structural abnormality of red blood cells, resulting in deformed sickle shaped cells.

These cells cannot pick up oxygen well or flow through the body well

74
Q

Is haemoglobin low in sickle cell anaemia

75
Q

What is a sickle cell crisis

A
  • blood vessels to part of body become blocked due to sickle shape.
  • Extremely severe pain lasting days or weeks
76
Q

Why might sickle cell patients also be on folic acid 5mg

A

Increased cell breakdown, so compensatory increased erythropoiesis (overactive bone marrow), increased demand for folate

77
Q

What other treatments are sickle cell patients on

A
  • Blood transfusions or hydroxycarbamide(specialist)
  • Iron transfusion
  • Prophylactic antibiotics (spleen damage)
78
Q

How do they treat sickle cell crisis

A

IV fluids, Analgesia, antibiotics if infection

79
Q

What is G6PD?

A

Glucose 6-phosphate dehydrogenase is an enzyme helps protect RBC from damage and premature destruction.

80
Q

what is G6PD deficiency and its relevance to anaemia

A

without the enzyme, these patients have a susceptibility to develop acute haemolytic anaemia when taking certain drugs, when they have infection or when eating fava beans.

81
Q

What drugs have a definite risk of causing haemolytic anemia in someone with G6PD deficiency

A

Nitrofurantoin
Fluroquinolones (ciprofloxacin)
Rasburicase
Sulfonamides

82
Q

What drugs have a possible risk of causing haemolytic anemia in someone with G6PD deficiency

A

Aspirin(acceptable up to 1g daily)
Chloroquine (acceptable for malaria)
Menadione(vit K3)
Quinine - (acceptable for acute malaria)
Sulfonylureas

83
Q

What is thalassaemias

A

it is an inherited autoimmune recessive disorder in which there is little to no haemoglobin production.

84
Q

What is the most severe type of thalassaemias and what can it cause

A

Beta-thalassaemia and can serious organ damage/ life-threatening complications.

85
Q

How do you manage thalassemias

A

Manage with regular blood transfusions.

86
Q

What is the cure of thalassaemias

A

Stem cell or bone marrow transplant