Paediatric Haematology Flashcards

1
Q

What are the differences in red blood cells in children?

A
  • site of haematopoiesis varies
  • haemoglobin switching - at birth 55-65% is HbF
  • difference in red cell structure and metabolism
  • larger red blood cells
  • higher haematocrit
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2
Q

What is meant by haematocrit?

A

the ratio of the volume of red blood cells to the total volume of blood

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3
Q

How does the site of haematopoiesis change in children?

A
  • occurs in the yolk sac up to 2 ½ months
  • at 1 month, the liver starts producing red cells
  • this peaks at 5 months and ends at 9 months
  • the spleen starts at around 2 ½ months, peaks at 5 months and ends at 7 months
  • the bone marrow starts at 4 ½ months and takes over
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4
Q

What is the purpose of haemoglobin switching?

A

to bind oxygen with greater affinity so that it can be taken from the mother

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5
Q

What are the 3 different types of embryonic haemoglobin?

A

Hb Gower-1:

  • consists of 2 zeta chains and 2 epsilon chains

Hb Gower-2:

  • consists of 2 alpha chains and 2 epsilon chains

Hb Portland:

  • consists of 2 zeta chains and 2 gamma chains
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6
Q

What are the embryonic haemoglobin chains?

Which chromosome do they originate from?

A

zeta:

  • originates from chromosome 16
  • this codes for the 2 alpha chains

epsilon:

  • originates from chromosome 11
  • this codes for the 2 beta chains
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7
Q

What happens in haemoglobin switching after 14/40?

A

Hb Portland and Hb Gower-2 switch to become HbF

this consists of 2 alpha and 2 gamma chains

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8
Q

What happens to haemoglobin switching at the neonatal stage?

A

Hb F switches to Hb A

this consists of 2 alpha and 2 beta chains

it may also convert to Hb A2

this consists of 2 alpha and 2 delta chains

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9
Q

What is the difference in white blood cell numbers in children and adults?

A

they have similar numbers of white blood cells

children have higher lymphocyte counts

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10
Q

How does the immune system progress in childhood?

When can a child start making satisfactory immune responses?

A
  • IgG crosses the placenta
  • breast milk contains IgA, IgD, IgE, IgG, IgM which provide passive immunity
  • antibody production starts between 2/3 - 12 months
  • satisfactory immune responses are produced between 6 - 12 months
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11
Q

Why does ABO incompatibility produce less severe haemolytic disease of the newborn than Rhesus group?

A

most antibodies to A and B antigens on the blood cells are IgM

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12
Q

Why are babies not vaccinated at birth?

A

for the first 6-12 months of life, the baby receives passive immunity from maternal antibodies

if you were to vaccinate a young baby with a virus, the mother’s antibodies would stick to the virus and try to eliminate it, so the vaccination would not work

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13
Q

How do platelets vary in children?

A
  • adult numbers are reached by 18/40 gestation
  • platelets initially larger but they slim down to adult size
  • functionally different at birth
  • hyporesponsive to certain agonists
  • hyperresponsive to vWF
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14
Q

Why is the highest rate of thrombosis seen in neonates compared to all paediatrics?

A

hyper-responsiveness to vWF enhances the platelet - blood vessel wall interaction

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15
Q

What is haemostasis like at birth?

When does it reach adult values?

A

coagulation proteins do not cross the placenta effectively

only fibrinogen, FV, FVIII, FXIII are normal at birth

most haemostatic parameters reach adult values by 6 months

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16
Q

Which clotting factors are vitamin K dependent?

Where does the foetus receive its vitamin K from?

A

FII, FVII, FIX, FX, protein C, protein S

the placental gradient means fetal vitamin K is 10% mother

17
Q

How can haemorrhagic disease of the newborn be prevented?

What is it?

A

rare form of bleeding disorder that affects newborns and young infants due to low stores of vitamin K at birth

commonly presents with intracranial haemorrhage and risks of brain damage / death

prevented by routine neonatal vitamin K injection

18
Q

What maternal medications can exacerbate haemolytic disease of the newborn?

A
  • anti-convulsants - the mother needs oral vitamin K
  • warfarin is teratogenic
19
Q

Which procoagulant proteins are reduced at birth?

A
  • FII
  • FVII
  • FIX
  • FX
  • ​FXI
  • FXII
  • prekallikrein
  • high molecular weight kininogens
20
Q

Which coagulation inhibitors are there a reduced concentration of at birth?

A
  • antithrombin III
  • heparin cofactor 2
  • protein C
  • protein S
  • tissue factor pathway inhibitor (TFPI)
21
Q

What are other differences present in neonatal haemostasis?

A
  • unique forms of fibrinogen and plasminogen
  • raised D-Dimers and vWF
  • platelet aggregation differs
22
Q

What are the congenital reasons for anaemia in childhood?

A
  • haemoglobinopathy - problem with haemoglobin synthesis
  • bone marrow failure syndromes
  • bone marrow infiltration
  • peripheral destruction
  • blood loss
23
Q

What are examples of haemoglobinopathies?

How can they be prevented?

A

thalassaemia and sickle cell disease

prevented through antenatal screening (before birth, during pregnancy)

24
Q

What is a haemoglobinopathy?

A

a hereditary condition involving an abnormality in the structure of haemoglobin

5% of the worldwide population carry an abnormal gene

25
Q

During haemoglobin switching at the neonatal stage, how can sickle cell or beta thalassaemia arise?

A

sickle cell:

  • single base change resulting in defective beta chain

beta thalassaemia:

  • reduced or absent beta chains
26
Q

What condition is shown here?

A

sickle cell anaemia

27
Q

What 3 factors influence the global distribution of haemoglobinopathies?

A
  • malaria benefit
  • genetic drift
  • population mixing
28
Q

What can lead to peripheral destruction, resulting in anaemia?

A
  • Rh / ABO or other incompatibility
  • infection
  • membrane defect - hereditary spherocytosis
  • enzyme defect
  • G6PD deficiency
  • PK deficiency
29
Q

What type of anaemia results from peripheral destruction?

A

increased destruction of red blood cells in the peripheral blood without evidence of ineffective erythropoiesis

this is haemolytic anaemia

30
Q

What is shown here?

A

hereditary spherocytosis

caused by mutations which lead to defects in RBC membrane proteins

the microspherocyte results from the loss of RBC membrane surface area

31
Q

What procedures are performed when there is blood loss after birth?

A
  • twin to twin transfusion
  • fetomaternal haemorrhage
32
Q

What are the causes of acquired anaemia in childhood?

A
  • nutritional deficiency - iron, B12, folate
  • bone marrow failure
  • bone marrow infiltration
  • peripheral destruction - haemolysis
  • blood loss
33
Q

What are congenital causes of bleeding and bruising in childhood?

A
  • platelet problem
  • clotting factor problem
  • connective tissue disorder
34
Q

What are the acquired causes of bleeding and bruising in childhood?

A
  • trauma
  • tumour
  • infection (acute - meningococcus or chronic - HIV)
  • immune disorder
  • primary - immune thrombocytopenia, TTP
  • secondary - SLE, ALPS
  • bone marrow failure
  • drug related
35
Q

What is meant by epigenetics?

A

the same child behaves differently in different situations

e.g. in school and at home

this is applied to genes