Should I Be Worried That My Unborn Baby Has Hydronephrosis?

Baby Hydronephrosis

With many pregnant women routinely getting ultrasounds, their fetuses are more frequently being diagnosed with a condition known as hydronephrosis. That literally translates to “water on the kidneys,” but it refers to a dilation of the kidney. This is actually quite common, occurring in as many as 5% of all pregnancies. If you’ve been told your baby has hydronephrosis, you probably have many questions: What does that mean? Is it serious? Should I be worried?

Some Basic Anatomy

Let’s start with the basics. All of us should have two kidneys and a ureter or tube coming from each kidney to the bladder. The kidneys filter toxins from our blood, and produce urine, which travel through the ureters to the bladder. When we urinate, the urine travels from the bladder through the urethra and out of our body. Even your baby inside of you makes urine, which is what makes up most of the amniotic fluid your baby is floating in.

Hydronephrosis specifically denotes a dilation of the renal pelvis, the central part of the kidney where urine is collected after it is made and before it makes its way through the ureters to the bladder. To be exact, ultrasonographers measure the anterior-posterior diameter (APD) of the renal pelvis. Hydronephrosis in a fetus is defined as an APD equal to or greater than 4mm before 33 weeks gestation, or equal to or greater than 7mm after 33 weeks gestation.

What Causes Hydronephrosis?

There are many reasons why the kidneys may be dilated in a fetus, but as many as 64-94% of fetuses who have hydronephrosis will NOT have any significant urological problems after they are born. In these patients, the hydronephrosis resolves on follow-up studies or becomes clinically insignificant. For these infants, the hydronephrosis is termed idiopathic, meaning there is no cause identified for it.

For the others, there are multiple causes, most of them related to some sort of obstruction of the urinary system causing an excess of urine to back up into the kidneys. A few of these causes are listed below:

  • Ureteropelvic junction (UPJ) obstruction: a complete or partial blockage of urine at the point where the ureter exits the kidney.
  • Posterior urethral valves: tiny valves with very small openings in the urethra.
  • Vesicoureteral reflux: the abnormal, backwards flow of urine from the bladder up the ureters towards and sometimes into the kidney.
  • Megaureter: a large, dilated ureter that does not function properly and therefore doesn’t drain the kidney as it should.
  • Duplicating collecting system: two ureters draining a single kidney, and this is often associated with a ureterocele or thin-walled ballooning of the ureter as it enters the bladder.

These and other obstructions can cause hydronephrosis, and if severe enough, can lead to kidney damage or failure, which is why it is important to identify and monitor hydronephrosis in fetuses and infants. If one of these causes is identified, it will need to be treated.

Not All Hydronephrosis is Created Equal

For the patients who have hydronephrosis but don’t have an identifiable reason for it, the severity of the condition determines the prognosis. As mentioned above, measuring the APD is how hydronephrosis is defined, and the larger the diameter, the more severe the hydronephrosis is considered.

But there is another way to measure the severity of hydronephrosis, and that is by a grading system designed by the Society for Fetal Urology (SFU) based on the ultrasound appearance of the kidneys. Normal kidneys get an SFU grade of 0, and hydronephrotic kidneys are graded 1-4, with the most severe at Grade 4.

Several studies have demonstrated that the higher the APD (the larger the dilation of the kidney) and the higher the SFU grade (the more severe the hydronephrosis), then the worse the prognosis.

One study of 690 affected fetal kidneys demonstrated that no kidneys with an APD of less than 15mm or a SFU Grade 2 or less required treatment after birth.1 Similarly, another study of 308 fetal kidneys revealed that no kidney with an APD less than 10mm or an SFU Grade of 2 or less required treatment after birth.

What Happens After Birth?

If your baby has hydronephrosis, after she is born, there will probably be further testing. Often, a post-natal ultrasound in performed to look at the kidneys and bladder again, usually in the first week of life. Up to 25% of all cases of prenatal hydronephrosis will resolve on the first ultrasound. However, another ultrasound may be required about a month later, even if the first one is normal, just to confirm the normal results.

If a true urinary obstruction is suspected, then further testing and referral will probably occur. One common test is known as a VCUG: voiding cystourethrogram. The VCUG consists of putting dye into the bladder through a catheter in the urethra and watching what happens when the bladder constricts to urinate. This test can identify if the baby has vesicoureteral reflux or other problems.

Remember, in most cases, the hydronephrosis will simply resolve, and there will be no treatment, and your infant will experience nothing worse than an ultrasound or two. But in some cases, an antibiotic is prescribed to prevent urinary tract infections. And in some cases of urinary obstruction, you may be referred to a pediatric urologist and surgery may be needed.

In summary, most cases (as many as 94%) of hydronephrosis identified in fetuses will result in no significant urological problem. Prognosis is determined by the size and severity of the dilation: the more dilated the kidney and the more severe the hydronephrosis, the more likely it is to result in post-natal problems. Some infants with hydronephrosis are followed by urologists. And a minority of patients will require some treatment, including medicine or surgery.

Helpful resources for parents:

  1. Urine Blockage in Newborns from the National Institute of Diabetes and Digestive and Kidney Diseases
  2. Pediatric Hydronephrosis from the Children’s National Health System
Ruben Rucoba
Dr. Rucoba has over 25 years of experience as a primary care pediatrician after completing medical school at the University of California, San Francisco. His clinical areas of expertise include caring for children with special health care needs and assisting families with international adoption. He has been a freelance medical writer since 2010, writing for health websites, continuing medical education providers, and various print outlets. He currently works at Wheaton Pediatrics in the suburbs of Chicago, where he lives with his wife and four daughters, including a set of twins.

Leave a Reply