Haematology in the Neonate Flashcards

1
Q

Why is vitamin K a problem in the neonate?

A

This occurs as there are no enteric bacteria in the gut to make vitamin K. The baby will usually be well in itself but have bruising and increased PT and PTT as well as deranged platelets.

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2
Q

How do we prevent vitamin k deficient bleeding in the neonate?

A

To prevent give Vit K IM or mixed colloidal phytomenadione. Repeat in 7 days, if breast fed repeat again at one month if bottle fed then no need as it is already fortified.

For active bleeding give plasma and vit K

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3
Q

What usually causes DIC in the neonate?

A

Secondary to sepsis or necrotising enterocolitis

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4
Q

How does DIC present in the neonate?

A

Clinical features – septic, petechiae, oozing wounds and GI bleeding

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5
Q

How should DIC be investigated in the neonate?

A

Investigations – reduced platelets, schistocytes, increased INR, decreased fibrinogen, increased PT and PTT and increased D dimer.

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6
Q

How is DIC managed in the neonate?

A

Management – treat cause, give vit k and platelets, fresh plasma and cryoprecipitate, heparin and protein C. If bleeding continues consider exchange transfusion.

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7
Q

What is autoimmune thrombocytopenia?

A

Can occur randomly but 10% of babies born to a mother with ITP will also develop it. There is also something called alloimmune thrombocytopenia where the mothers antibodies attach the foetal platelets leading to a deranged platelet count in the baby.

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8
Q

How is ITP managed in utero?

A

If this occurs in utero it can cause CNS problems. Treat with compatible platelets or irradiated maternal platelets. Steroids may also help. Platelet transfusion via cordocentesis from 24 weeks may be needed in later pregnancies.

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9
Q

How is a diagnosis of ITP made in utero?

A

Diagnosis made by detecting maternal platelet allo-antibodies against father’s platelets.

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10
Q

What is rhesus haemolytic disease?

A

A conditions that occurs after the mother develops an immune response to rhesus positive babies.

This becomes progressively worse with each Rh+ baby that is born to a sensitised mother.

Note ABO incompatibility can occur as well but treatment is the same.

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11
Q

How does a baby with Rhesus disease of the newborn present?

A

Clinical presentation of the baby varies with severely ill babies termed foetal hydrops due to oedematous stiff lungs occurring due to anaemia induced congestive cardiac failure as well as hypoalbuminaemia as the liver becomes preoccupied with producing RBCs.

Jaundice
Yellow vernix
CCF – Oedema and ascites
Hepatosplenomegaly 
Progressive anaemia 
Bleeding 
CNS signs 
Kernicterus
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12
Q

When does a Rhesus -ve mother receive her doses of Anti D?

A

All mothers are tested for D antibodies when booked and at 28 and 34 weeks. Doses of Anti-D less than 4u/ml are unlikely to cause any disease

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13
Q

How are foetuses monitored for Rhesus disease?

A

Foetuses can be monitored by US (and amniocentesis if >4u/ml) to detect oedema, cardiomegaly, pericardial effusion, hepatosplenomegaly and ascites).

Monitoring should occur 10weeks prior to event in the previous pregnancy.

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14
Q

How is Rhesus disease managed?

A

Prevention – Anti-D immunoglobulin to all Rh- mothers at 28 and 34 weeks
Exchange transfusion – indicated with foetal Hb <7
Phototherapy may be all that is needed if jaundice is the only symptom

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15
Q

What is hydrop fetalis?

A

Serious foetal conditions defined as abnormal accumulation of fluid in two or more foetal compartments including ascites, pleural effusion, pericardial effusion and skin oedema. This occurs as the liver fails to produce enough albumin or as a result of other fluid management issues secondary to an underlying condition. It is rare for this to occur as a result of Rhesus or ABO incompatibility but can happen, this is termed immune hydrops. Nonimmune hydrops is more common and occurs as a result of anaemia, infection, heart, liver or lung defects and chromosomal abnormalities.

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16
Q

How should a baby suspected of having hydrops fetalis be investigated at birth?

A

At birth – cord blood for Hb, haematocrit, bilirubin (both conjugated and unconjugated), blood group, Coomb’s test, protein, LFT and infection screen to find cause (anything that can cause anaemia can cause foetal hydrops).

17
Q

How is hydrops fetalis managed?

A

Expect to require ventilation with high inspiratory peak pressure and positive end pressure.
Monitor plasma glucose 2-4hourly.
Drain ascites and pleural effusion.
Give vitamin K IM to reduce risk of haemorrhage
If CCF then give furosemide
Limit IV fluids

18
Q

What are the risk factors for neonatal hypoglycaemia?

A
Hypothermia
Acidosis
Infants of diabetic mothers as they produce higher levels of insulin but less sugar intake
Infection and sepsis
Prolonged labour
Preterm (fewer reserves laid down)
Feeding issues both maternal and neonatal (e.g. maternal mental health and vomiting)
Growth restricted baby
19
Q

What complications can occur from neonatal hypoglycaemia?

A

Complications - seizures causing long term brain injuries

20
Q

What blood glucose levels are acceptable in a neonate?

A

3-5 is a roughly normal glycaemia
A new-born can tolerate slightly lower 2.5 cut off for neonates
2 is potentially acceptable if asymptomatic
Dropping below 2 could be transient but should start to get worried

21
Q

How does a neonate with hypoglycaemia present?

A

Drowsy
Jittery (can see clonus) can distinguish from seizures by if it stops when you grab the limb
Irritability
Seizures

22
Q

How should hypoglycaemia be managed in a neonate?

A

Manage by giving titrated sugar whilst you wait for insulin to come down
This can be oral feeds or mucosal glucose gels
Avoid invasive management as much as possible
NG tube
IV dextrose (+/- bolus of 2.5-3ml/kg of 10% dextrose)