Haem Flashcards

(36 cards)

1
Q

Define microcytic anaemia

A

Anaemia associated with a decreased MCV
Microcytic (MCV <80 fL).

Haemoglobin (Hb) level <120 g/L in females and <140 g/L in males

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2
Q

Explain the aetiology / risk factors of microcytic anaemia

A
Iron-deficiency:
- Blood loss
Anaemia of chronic disease:
- Usually normocytic, but can be microcytic
Thalassaemia
Sideroblastic anaemia:
- Abnormal haem synthesis
Lead poisoning:
- Globin and haem synthesis interference
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3
Q

Summarise the epidemiology of microcytic anaemia

A

most common cause is iron deficiency anaemia

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4
Q

Recognise the presenting symptoms of microcytic anaemia

A

Anaemia: lethargy, tiredness, dyspnoea, pallor, weakness

Lead poisoning: anorexia, nausea, vomiting, abdominal pain

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5
Q

Recognise the signs of microcytic anaemia on physical examination

A

Anaemia: pallor, brittle nails and hair, conjunctival pallor
Tachycardia in severe cases?
Glossitis, cheilitis
Lead poisoning: blue gum line, peripheral nerve lesions, encephalopathy

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6
Q

Identify appropriate investigations for microcytic anaemia and interpret the results

A

Bloods: FBC, serum iron, iron-binding capacity, serum ferritin, serum lead
Blood film:
- Iron-deficiency: microcytic, hypochromic, anisocytosis, poikilocytosis
- Sideroblastic anaemia: dimorphic blood film
- Lead poisoning: basophilic stripping
If >40/menopausal women:
- Upper GI endoscopy, colonoscopy

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7
Q

Generate a management plan for microcytic anaemia

A

Iron deficiency: iron supplements, consider parenteral if doesn’t work
Sideroblastic anaemia: treat cause (drugs), pyridoxine in inherited forms
Lead poisoning: remove source of poison, dimercaprol

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8
Q

Identify the possible complications of microcytic anaemia and its management

A

High-output cardiac failure, complications of cause

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9
Q

Summarise the prognosis for patients with microcytic anaemia

A

Depends on underlying cause

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10
Q

Define macrocytic anaemia

A

Anaemiais defined as Hb <120 g/L in females and <140 g/L in males
Macrocytic (MCV >100 fL)

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11
Q

Explain the aetiology / risk factors of macrocytic anaemia

A

Megaloblastic:
• B12 deficiency (Crohn’s, metformin, omeprazole)
• Folate deficiency (alcoholics, phenytoin)
• Drugs: methotrexate
Non-megaloblastic:
• Alcohol excess, liver disease

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12
Q

Summarise the epidemiology of macrocytic anaemia

A

More common in elderly and females

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13
Q

Recognise the signs of macrocytic anaemia on physical examination

A

Anaemia: pallor, tachycardia
Pernicious anaemia: lemon-tinted skin, glossitis, weight loss
B12 deficiency: peripheral neuropathy, ataxia

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14
Q

Recognise the presenting symptoms of macrocytic anaemia

A

Anaemia: tiredness, lethargy, dyspnoea

Family history of autoimmune disease

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15
Q

Identify appropriate investigations for macrocytic anaemia and interpret the results

A

Blood: FBC, LFTs, ESR, TFTs, B12, folate
Blood film: large erythrocytes
Schilling’s: radiolabelled B12 measured in urine

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16
Q

Generate a management plan for macrocytic anaemia

A

Pernicious anaemia: IV hydroxycobalamin

Folate deficiency: oral folic acid (treat B12 deficiency first, folate can worsen neuropathy)

17
Q

Identify the possible complications of macrocytic anaemia and its management

A

Risk of gastric cancer, pregnancy + folate deficiency predisposes to spinal cord abnormalities

18
Q

Summarise the prognosis for patients with macrocytic anaemia

A

Majority are treatable

19
Q

Define normocytic anaemia

A

Anaemia associated with a normal MCV

Anaemiais defined as Hb <120 g/L in females and <140 g/L in males
Normocytic (MCV 80-100 fL

20
Q

Explain the aetiology / risk factors of normocytic anaemia

A
Loss of blood cells: 
	• Blood loss (peptic ulcers, oesophageal varices, trauma)
	• Hypersplenism (RBCs pool in the spleen)
	• Haemolytic disorders 
Reduced blood cell formation: 
	• Myelopathies 
	• Renal failure (secondary)
Plasma expansion: 
Pregnancy/overhydration
21
Q

Summarise the epidemiology of normocytic anaemia

A

Most common anaemia

22
Q

Recognise the presenting symptoms of normocytic anaemia

A

Anaemia: pallor, fatigue, dyspnoea

Anorexia, headache, bowel disturbances

23
Q

Recognise the signs of normocytic anaemia on physical examination

A

Koilonychia (iron deficiency), pallor, glossitis, tachycardia, wide pulse pressure, systolic ejection murmur

24
Q

Identify appropriate investigations for normocytic anaemia and interpret the results

A

Bloods: FBC, U&Es, eGFR, clotting screen

Pregnancy test

25
Generate a management plan for normocytic anaemia
Treat underlying cause | Erythropoietin administration
26
Identify the possible complications of normocytic anaemia and its management
Fatigue
27
Summarise the prognosis for patients with normocytic anaemia
Dependant on cause
28
Define aplastic anaemia
Diminished haematopoietic precursors in the bone marrow, and a deficiency of all blood cells (pancytopaenia)
29
Explain the aetiology / risk factors of aplastic anaemia
Idiopathic (>40%): destruction due to autoimmune mechanisms Acquired: drugs (chloramphenicol, gold), chemicals, radiation Inherited: Fanconi’s anaemia
30
Summarise the epidemiology of aplastic anaemia
Rare, 2-4:1,000,000
31
Recognise the presenting symptoms of aplastic anaemia
Slow or rapid onset | Anaemia: lethargy, tiredness, dyspnoea Thrombocytopaenia: easy bruising, bleeding gums Leukopenia: increased infections
32
Recognise the signs of aplastic anaemia on physical examination
Anaemia: pallor Thrombocytopaenia: bruises, petechiae Leukopenia: multiple infections
33
Identify appropriate investigations for aplastic anaemia and interpret the results
Bloods: FBC (everything lowered, normal MCV) Blood film: exclude leukaemia Bone marrow trephine biopsy: for diagnosis and exclusion Criteria for severe aplastic anaemia (AA) - Marrow with <25% normal cellularity - Neutrophils <0.5 x 109/L - Platelets <20 x 109/L - Reticulocytes <40 x 109/L
34
Define haemolytic anaemia
Shortened erythrocyte life span, due to premature breakdown (<120 days), with anaemia
35
Explain the aetiology / risk factors of haemolytic anaemia
``` Hereditary: - Membrane defects - Metabolism defects - Haemoglobinopathies (sickle cell, thalassaemia) Acquired: - Autoimmune - Isoimmune (transfusion reactions) - Drugs (penicillin) - Trauma - Infection (malaria) - Paroxysmal nocturnal haemoglobinuria ```
36
Summarise the epidemiology of haemolytic anaemia
Common