Anaemia Flashcards

1
Q

A 50 year old man presents with lethargy and fatigue

DDx?

A
  • Psychological
  • Environmental
  • Endocrine
  • Haematological
  • Rheumatologcal
  • Cardiovascular
  • Respiratory
  • Pharmacological
  • Dietary
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2
Q

What are the (5) broad causes of blood loss?

A
  • Gastrointestinal tract
  • Urinary
  • Menstrual loss
  • Chronic recurrent epistaxis
  • Hereditary AVM
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3
Q

What are the (5) broad causes of decreased production of blood in anaemia?

A

Anaemia of Chronic Disease

  • Chronic renal failure
  • Rheumatological disorders (RA)
  • Malignancy

Bone marrow infiltration (leukaemia, lymphoma, myeloma, myeloproliferative disease, myelodysplastic syndromes, secondary malignancies)

Endocrine – thyroid disorders (hypothyroidism), EPO deficiency (renal failure)

Nutritional Deficiency – B12, folate, iron

Infectious – acute or chronic. (e.g. TB, chronic suppurative disease, HIV, HCV, CMV, EBV, parvovirus)

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4
Q

What should you ask on Hx of possibly anaemic pt?

A
  • blood loss: haematemesis, melaena, change bowel habit, tenesmus, PR bleed, LOW, menstruation Hx
  • chronic disease/inflammation: RA, chronic infection, renal failure, thyroid disease
  • diet: vegan, vego, coeliac, parasite infection
  • bone marrow failure: bleeding, infection, fevers, sweats, LOW, hx of RADIATION!!!, prior malignancy
  • increased destruction: dark urine, jaundice, gall stones, FMHx of splenectomy, cholycystectomy
  • malabsorption
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5
Q

Discuss classifications of anaemia based on MCV & the flowchart for diagnosis

  • microcytic
  • normocytic
  • macrocytic
A

Microcytic (less than 80 MCV): check Fe.

  • if low Fe: establish cause
  • if normal Fe: anaemia of chronic disease or haemoglobinopathy

Normocytic: check reticulocytes

  • if high: haemolysis or blood loss
  • if low: anaemia of chronic disease, renal failure, marrow failure

Macrocytic: measure B12 & folate

  • if normal: consider bone marrow if cause is not obvious
  • if low: establish cause
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6
Q

Describe the iron studies results in:

  • iron deficiency anaemia
  • anaemia of chronic disease
  • thalassaemia trait
A

Iron deficiency anaemia:

  • low serum iron
  • high transferrin/TIBC
  • low serum ferritin!!
  • high soluble transferrin receptor

Anaemia of chronic disease

  • low serum iron
  • low transferrin/TIBC
  • HIGH serum ferritin!!!
  • low or normal soluble transferrin receptor

Thalassaemia trait:

  • normal serum iron
  • normal transferrin/TIBC
  • normal serum ferritin
  • HIGH soluble transferrin receptor
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7
Q

Px of iron deficiency

A
  • anaemia: fatigue, pallor, exertional dyspnoea
  • Koilonychia (spoon-shaped nails)
  • Angular cheilosis
  • Glossitis
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8
Q

Ix of iron deficiency

A
  • Faecal occult blood: screening
  • Gastroscopy
  • Colonoscopy: if symptomatic
  • Tumour markers
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9
Q

Causes of:

  • hypochromic microcytic anaemia
  • normochromic normocytic anaemia
  • macrocytic anaemia
A
  • Hypochromic microcytic: Iron deficiency (pencil cells), thalassemia (target cells), sickle cell, lead poisoning and sideroblastic anaemia. -> iron studies. Ferritin down, sat up in iron deficiency.
  • Normochromic normocytic: Anaemia chronic disease, haemolysis, renal failure, pregnancy dilution
  • Macrocytic: B12 or folate deficiency, alcohol, liver disease, drugs, hypothyroidism, myeloma
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10
Q

(5) Expected key Ix results of haemolytic anaemia

A
  • elevated LDH
  • elevated unconjugated bilirubin
  • low haptoglobin (carries free Hb)
  • blood film: spherocytes (AIHA or hereditary), bite cells (oxidative injury), fragments (microangiopathy)
  • direct Coombs test: to r/o AIHA
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11
Q

Compare features of intravascular vs. extravascular haemolytic anaemia

A

Intravascular:

  • Blood film fragmentation
  • Haemoglobinuria
  • Haemoglobinaemia
  • Haemosidinuria

Extravascular:

  • Spherocytes
  • Bite cells
  • Sickle cells
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12
Q

Causes of intravascular haemolysis

A
  • DIC
  • Sepsis
  • Cardiac valvular disease
  • PNH (Paroxsymal haemoglobinuria)
  • Extracorporeal circulation
  • TTP/HUS
  • Disseminated malignancy
  • Arteriovenous malformations
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13
Q

Causes of extravascular haemolysis

A

Non-immune causes:

  • Hypersplenism
  • Immune mediated
  • Red cell membrane disorders
  • Red cell enzyme disorders

Immune causes: AIHA

  • Cold Agglutinin- IgM Ab (EBV, mycoplasma pneumoniae, lymphoma)
  • Warm Agglutinin- IgG Ab (drug induced, lymphoproliferative disorder, SLE, RA, idiopathic AIHA, transfusion reaction)
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14
Q

Describe autoimmune haemolytic anaemia

A

2 types: warm & cold

Warm:

  • IgG, agglutinate at 37’C
  • Positive Direct Coombs’ test for IgG +/- C’
  • idiopathic, 2’ to lymphoproliferative disorder/autoimmune disease. Drug induced
  • Blood film: spherocytes
  • Mx: treat underlying cause, corticosteroids, immunosuppression, splenectomy, folic acid

Cold:

  • IgM, agglutinate at 4-21’C
  • positive for complement on Direct Coomb’s test
  • idiopathic, 2’ to infection (mycoplasma pneumoniae)/lymphoproliferative disorder
  • Blood film: agglutination
  • Mx: treat underlying cause, warm pt, immunosuppression, plasmapharesis, folic acid.
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15
Q

Where are iron, folate & B12 absorbed in the GIT?

A

Iron - duodenum
Folate - jejunum
B12 - ileum

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16
Q

Pencil cells (elongated cells) on blood film indicates what:

A

Iron deficiency (c.f. thalassaemia)

This will be in conjunction with microcytic anaemia

17
Q

Iron studies result in: iron deficiency anaemia

A

Iron deficiency anaemia:

  • low serum iron
  • high transferrin/TIBC
  • low serum ferritin!!
  • high soluble transferrin receptor
  • low saturation
18
Q

Iron studies results in: anaemia of chronic disease/inflammation

A

Anaemia of chronic disease

  • low serum iron
  • low transferrin/TIBC
  • HIGH serum ferritin!!!
  • low or normal soluble transferrin receptor
19
Q

Ix Thalassaemia

A
  • haemoglobin electrophoresis

Serum iron levels is not as useful

20
Q

Is bilirubin unconjugated or conjugated in haemolytic anaemia?

A

Unconjugated (pre-hepatic). Possibly no dark urine

21
Q

What would you see in blood film of haemolysis? (the key Ix after finding out a normocytic anaemia)

A

3 types of morphology

  • fragments & schistocytes: microangiopathy
  • bite cells/blister cells: oxidative injury
  • spherocytes (look smaller, no pale centre): hereditary spherocytosis, warm autoimmune haemolytic anaemia. -> key next Ix: Direct Coomb’s test (+ve in AIHA but -ve in hereditary spherocytosis).
22
Q

Change in biochemistry with blood infusion in an iron deficiency anaemia in the order of fastest to slowest

A

Reticulocyte, Hb, MCV in the order (fastest -> slowest)

23
Q

In women over 50 years old, What is the most common cause of iron-deficiency anemia?

A

Chronic gastrointestinal bleeding from nonparasitic causes, such as gastric ulcers, duodenal ulcers or gastrointestinal cancer