
Haemolytic disease of the fetus and newborn (HDFN) can happen when you have a certain blood type (D negative) that's different to your baby's blood type (D positive).
This may mean you have antibodies that can break down your baby's red blood cells.
You might have antibodies if you've come into contact with D positive blood before, for example during:
Haemolytic disease of the fetus and newborn (HDFN) is routinely screened for during pregnancy. You'll be offered a blood test at your first antenatal appointment at 8 to 12 weeks.
If the results of the blood test show your blood type is:
If the results show your baby’s blood type is:
If there's a risk of haemolytic disease of the fetus and newborn (HDFN) during pregnancy, you’ll usually be offered injections to stop you developing antibodies.
If these injections do not help and you develop antibodies, then there are extra scans and blood tests to help monitor your baby.
After they're born, your baby will continue to be monitored, to look for signs of jaundice and anaemia.
Symptoms of jaundice include:
Symptoms of anaemia include:
You've been told your baby may have HDFN and:
If your baby is diagnosed with haemolytic disease of the fetus and newborn (HDFN), your midwife or doctor will discuss the treatment options with you. They'll explain what will happen, as well as the benefits and risks.
Treatment during pregnancy includes:
If your baby develops anaemia later on in the pregnancy, you may need to have a C-section before your due date.
Treatment for newborns includes:
The risk of complications is low because the treatments are usually very effective.
But if your baby is very unwell, they may need to be treated in a neonatal intensive care unit.