Spotlight on Fetal Hydronephrosis During Pregnancy
One of the most frequently observed
conditions during pregnancy ultrasounds is fetalhydronephrosis. It is the oedema or enlargement of the kidneys of an unborn
child as a result of excess urine. Although the diagnosis can be worrying for
expecting parents, in most instances, the condition heals itself and does not
indicate severe complications. Understanding what fetal hydronephrosis is, its
causes, and how it is managed can help guide parents through the process with
clear information and confidence.
What Is Fetal Hydronephrosis?
Fetal
hydronephrosis is a condition that arises when urine
cannot drain out of the kidney into the bladder, leading to swelling of the
kidney. This is normally identified during a routine prenatal ultrasound,
typically between 18 and 22 weeks of pregnancy. The classification depends upon
how much the renal pelvis (the section of the kidney where the urine gathers)
is dilated. Milder cases can either resolve before or after birth, whereas the
severe ones may need medical care following delivery.
Fetal Hydronephrosis Causes
Fetal hydronephrosis can be caused by a
number of factors. The most prevalent reasons are:
●
Ureteropelvic Junction (UPJ) Obstruction: This
occurs when the kidney and the ureter are not properly connected, preventing
normal urine flow.
●
Vesicoureteral Reflux (VUR): A condition in
which urine flows backwards from the bladder into the kidneys.
●
Posterior Urethral Valves (PUV): A condition
that affects male fetuses, involving the growth of abnormal tissues in the
urethra that restricts urine flow.
●
Physiological Hydronephrosis: In most
instances (particularly mild ones), the swelling is temporary and results from
normal changes during fetal development.
How Is It Diagnosed?
Prenatal ultrasound is primarily used to
make the diagnosis. The physician measures the size of the renal pelvis and
monitors it throughout the pregnancy. If the dilation seems significant or
progresses, further ultrasounds or specialised scans may be prescribed to check
kidney function and bladder health.
In some instances, a postpartum
ultrasound helps determine whether the condition has cleared or requires
further management. In certain cases, tests such as a voiding cystourethrogram (VCUG) or a renal scan may be recommended to evaluate urinary flow and kidney
function.
Treatment and Management
The majority of fetal hydronephrosis cases do not necessitate immediate
intervention during pregnancy. Monitoring—particularly through regular
ultrasounds that track kidney development and detect changes—is key. If the
swelling does not disappear after birth or worsens, a pediatric urologist may
recommend additional examinations and treatments.
Treatment varies depending on the cause
and severity. Mild cases often resolve naturally as the baby grows. Moderate to
severe cases may require antibiotics to prevent urinary tract infections, or in
rare situations, surgical procedures to correct obstructions or repair reflux.
Outlook and Prognosis
The outlook for fetal hydronephrosis is generally very good. Most mild cases—around
70–80%—resolve spontaneously without long-term kidney damage. Prenatal
screening allows early detection, enabling healthcare providers to monitor and
manage the condition effectively, minimising risks to the baby’s health.
Final Thoughts
Fetal
hydronephrosis may sound like a frightening condition,
but advancements in prenatal imaging and pediatric care have made it highly
manageable. With consistent monitoring, early assessment, and appropriate
medical treatment, most affected babies go on to lead normal lives with healthy
kidney function. Awareness and education remain essential to reducing parental
anxiety and ensuring the best possible outcomes for both mother and baby.
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