Haematology: Anaemia in children; Bruising Flashcards

(29 cards)

1
Q

What are anaemia thresholds for:
* Neonates
* Infants
* Child
* Teenagers

A

Neonates:
- < 140

Infants:
- < 110

Child:
< 115

Teenagers:
< 120

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2
Q

Describe what is meant by physiological anaemia of infancy [1]

A

Foetus naturally has high fetal Hb (causes O2 dissociation curve to go to left) so can maximise O2 from mother

Fetal Hb is gradually lost throughout first 6 months of life

Which is why settles at 110 g/dl at 6-9months of age

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3
Q

When / why might a baby be suffering from IDA? [1]

A

If they are exclusively milk feeding (bottle / breastfeeding) at ~ 1 year age

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4
Q

What are common causes of reduced red cell production causing anaemia in children [4]

A

Common:
- Nutritional causes - iron,
B12, folate deficiency
- Reduced intake
- Malabsorption - e.g. coeliac
- Increased requirement (growth)

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5
Q

What are more rare causes of reduced rbc production in children [4]

A

Rare:
- Bone marrow failure
- Malignancy & chemo
- Diamond Blackfan anaemia (genetic syndrome w reduced bone morrow production of rbc)
- Aplastic anaemia

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6
Q

What are the causes of infant IDA [6]

A

Maternal IDA
Premature / LBW
Multiple pregnancy
Exclusively breast-fed after 6 months
Late or insufficient introduction of iron rich solid
XS cow’s milk consumption

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7
Q

What causes IDA in children / adolescents? [5]

A

Vegan / vegetarian diet
GI disorders (Mecke’s diverticulum, coeliac, IBD, gastric surgery)
Extreme athletes
Heavy menstruation
Other chronic blood loss

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8
Q

What are the three overall causes of haemolysis causing anaemia (in children) [3]

A

3 Is:
Immune
Intracellular red cell defects
Infections

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9
Q

What are causes for immune haemolysis anaemia (in children) [2]

A

Anti-Rh antibodies
Anti ABO antibodies

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10
Q

A baby has rhesus incompatibility. How would they present [4] due to which condition? [1]

How might you treat? [4]

A

Hydrops fetalis
- Skin oedema, pericardial effusions, ascites, secondary jaundice

Treatment:
- Phototherapy, IV IG, Blood transfusion, exchange transfusion

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11
Q

What are the most common causes of intracellular red defects [6]

Describe their presentations [+]

A

Sickle cell disease

Thalassemias

Hereditary spherocytosis
- Hereditary spherocytosis is a condition where the red blood cells are sphere shaped, making them fragile and easily destroyed when passing through the spleen. It is the most common inherited haemolytic anaemia in northern Europeans. It is an autosomal dominant condition.
- splenomegaly
- risk of aplastic, haemolytic or megaloblastic crisis (causing acute exacerbation of anaemia)

Hereditary eliptocytosis

G6PD deficiency
- bite cells and heinz bodies
- avoid triggers

Pyruvate kinase defiency

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12
Q

Which infections would most likely cause haemolysis [3]

A

Parvovirus
Malaria
HUS

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13
Q

Describe the presentation of parvovirus b19 infection [+]

A
  • causes transient aplastic anaemia, temporary suspension of erythropoeisis - risk in SCA or hereditary spherocytosis
  • mild feverish illness which can be hardly noticeable
  • cheeks appear bright red, hence the name ‘slapped cheek syndrome
  • child begins to feel better as the rash appears and the rash usually peaks after a week and then fades
  • the rash is unusual in that for some months afterwards, a warm bath, sunlight, heat or fever will trigger a recurrence of the bright red cheeks and the rash itself
  • causes aplastic crisis in SCA ptx
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14
Q

Why does malaria cause anaemia? [3]

A

Increased splenic activity
Bone marrow suppression
Increased haemolysis of rbc

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15
Q

Which causes of anaemia in children would be due to blood loss? [5]

A

Blood loss
* Gastric ulcers
* Milk intolerance
* Hereditary
haemorrhagic telangiectasia
* Meckels diverticulum
* IBD
* Epistaxis

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16
Q

How would you determine if a microcytic anaemia is due to IDA or thalassemia minor on initial investigation? [1]
How would you then determine if a patient has Beta thalassaemia minor / alpha thalassaemia minir? [2]

A

Look at ferritin level
- if low = IDA
- if normal = thal. minor

Then do Hb electrophoresis
- Elevated HbA2 = beta thal. minor
- Normal HbA2 = alpha thal. minor

17
Q

Normocytic MCV:

  • How would you determine if a child is suffering from haemolytic cause / blood loss? [1]
  • How would you determine if is from marrow hypoplasia / leukaemia
A

Reticulocytes increased

18
Q

What are red flags for anaemia in children? [5]

A

Red flags in anaemia
* Hb < 60g/L
* Tachycardia, cardiac murmur or signs of cardiac failure
* Features of haemolysis (dark urine, jaundice, scleral icterus)
* Associated reticulocytopenia (low reticulocyctes)
* Presence of nucleated red blood cells on blood film
* Associated thrombocytopenia or neutropenia
* Severe vitamin B12 or folate deficiency - associated w failure to thrive / neurodevelopment problems

Where possible defer transfusion until a definitive diagnosis is made

19
Q

Why is associated reticulocytopenia (low reticulocyctes) in anaemia a red flag? [1]

A

Should have increased reticulocytes to correct for anaemia

20
Q

Which drugs should children with ITP avoid? [1]

A

NSAIDs / Ibuprofen - can disrupt platelet count

21
Q

add haemophilia notes
add scd notes
add leukaemia notes

22
Q

Which conditions have increased platelet destruction? [4]

A

ITP
DIC
HUS (microangipathic)
Hypersplenism

23
Q

What is the basic pathophysiology of ITP? [1]

A

Production of antibodies to platelets which are then destryed in liver and spleen

24
Q

What advice would you give ITP patients when platelet count is low? [3]

A

Avoid antiplatelets, anticoagulants and IM Injections

25
Describe the treatment ladder for ITP [3]
**Cutaneous symptoms only:** * Watchful waiting **Mucosal bleeding:** - Steroids/ IVIG/ topical or oral TXA **Chronic ITP**: - TPO agonists, MMF, rituximab, splenectomy
26
What is the most serious complication of ITP that should be worried about? [1]
**Intraventricular haemorrhage**
27
Large platelets but low count = [] syndrome
**Bernard-Soulier syndrome**
28
Eczema x immunodeficiency x small platelets and low count = [] syndrome
**Wiskott-Aldrich syndrome**
29
What are red flags for features in bleeding or brusing? [5]
* Unexplained bruising or inconsistent history * Unprovoked or severe bleeding * Fever & unwell appearance * Associated pallor, lymphadenopathy, hepatosplenomegaly * Family history of unusual bleeding