Antenatal hydronephrosis tests before birth
In antenatal hydronephrosis, the part of the kidney that swells is the renal pelvis. The 20 week antenatal ultrasound scan looks at the baby growing in the womb and measures the size of the renal pelvis.
What the ultrasound can tell us
The ultrasound cannot give precise information about the problem or what is causing it. Although your doctor will not always know how your baby will be affected at birth, he or she is less likely to have serious problems if:
- he or she is growing well in the womb
- no other problems have been found
- the amount of amniotic fluid (or liquor), which is the liquid that the baby is floating in, is normal.
Often, the expectant mother will need more ultrasound scans during her pregnancy. These will check whether the problem goes away or gets worse.
Referral
Your obstetrician may refer you to specialist healthcare professionals, such as a paediatric nephrologist (a doctor who treats children with kidney problems) or a paediatric urologist (a surgeon who treats children with problems of the urinary system).
You can speak with these doctors about possible complications and their management.
Antenatal hydronephrosis tests after birth
You may need to come back to the hospital for your baby to have imaging tests (scans). These use special scanners that take pictures of the inside of his or her body.
Ultrasound scan
The first test is normally an ultrasound scan, which is similar to the scan mothers have in pregnancy. It looks at the shape and size of the kidneys and other parts of the urinary system. A small handheld device is moved around your baby's skin. A machine attached to the probe directs sound waves into his or her body – your child cannot feel these. These sound waves are turned into pictures that can be seen on a screen.
Other tests
- Your doctor may also arrange a DMSA scan, which checks for any damage in the kidneys, and/or a MAG3 scan, which shows whether blood is going into the kidneys and whether there is a blockage in the urinary system. These are normally done when a baby is some weeks old. In each test, a chemical that gives out a small amount of radiation (energy) is injected into one of your baby’s blood vessels – a special gel or cream can be used to stop your baby feeling any pain. A special camera takes images (pictures) of your baby’s kidneys.
- An MCUG (sometimes called a VCUG) checks how your baby is passing urine, and whether there is any reflux (when urine passes back up towards the kidneys). A thin flexible tube called a catheter is passed through your baby’s urethra and a dye is put through to reach the bladder – this does not hurt your baby. A special X-ray machine takes a series of images of your baby’s bladder while it is emptying.
Antenatal hydronephrosis treatment before birth
Treatment before birth is very rare. It is normally only recommended when there is little or no amniotic fluid (or liquor), the liquid that surrounds the baby growing in the womb. Your healthcare team will speak with you about this.
Antenatal hydronephrosis treatment after birth
Many babies do not need treatment after birth. This depends on findings from the antenatal ultrasound scans and tests after birth. In most cases, babies can be discharged home a short time after birth.
Rarely, babies are born with complications and need to be moved to a neonatal unit, an area of the hospital for newborn babies, for monitoring and treatment.
Preventing and treating UTIs
Some babies are at higher risk of urinary tract infections (UTIs). If they keep coming back, they may cause damage to a kidney. To protect your child’s kidneys, it is important to prevent UTIs, and treat them quickly when they do happen.
- Your baby may need to take a small dose of antibiotic medicine each day – this is called a prophylactic antibiotic. Antibiotics kill the bacteria (germs) that cause UTIs, and so help prevent these infections.
- Sometimes UTIs can happen even when your child is taking these antibiotics. It is important that UTIs are diagnosed and treated quickly to try to prevent them causing kidney damage. If you think your child has a UTI, contact your doctor or local NHS services.
It is important to follow your doctor’s instructions about when and how much to give. Continue to give the antibiotics to your baby as your doctor has told you.
Surgery
A small number of babies who had antenatal hydronephrosis in the womb have complications after birth. These babies may be monitored or treated in a neonatal unit, a special area of the hospital for newborn babies.
Occasionally, a baby needs an operation to correct the problem that is causing the hydronephrosis.
About the future
In most cases, antenatal hydronephrosis does not cause any problems for the pregnancy or childbirth, and the baby and mother will not have any long-term problems. Some cases continue through pregnancy, and a few cause problems after birth.
Your child will be able to do all of the things that other children their age do. He or she can go to nursery and school, and can play with other children and stay active.
Your healthcare team will speak with you and your family about any long-term effects. This depends on the severity of the hydronephrosis and the cause.
Follow up
All babies with antenatal hydronephrosis need follow-up. This may be for the first year of your child’s life or until he or she goes to school. You will need to go back to the clinic or hospital for more tests and to see the doctor.
Preventing UTIs
Some children may be at higher risk of urinary tract infections (UTIs). If your child is taking antibiotics once a day to prevent UTIs, it is important that you continue giving the medicines. Speak with your doctor if you have any concerns.
If you think your child has a UTI, seek medical advice.
Long-term effects
A small number of children who had antenatal hydronephrosis caused by other problems have long-term problems with their bladder or kidneys. Your doctor will give you more information.
Further support
This may be a difficult and stressful experience for you and your family.
If you have any concerns or need additional support, speak with your doctor or nurse.