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Published on: July 8, 2025
Postnatal management of infants with antenatally detected hydronephrosis
Nejat Aksu1, Onder Yavaşcan, Murat Kangin
1Department of Pediatric Nephrology, Yenişehir, SSK Tepecik Teaching Hospital, Izmir, Turkey.
Insights
All infants with antenatal hydronephrosis measuring 5 mm or greater require postnatal investigation. A normal postnatal ultrasound does not rule out urinary tract abnormalities, emphasizing the need for thorough follow-up.
Area of Science:
- Pediatric Nephrology
- Fetal Medicine
- Diagnostic Imaging
Background:
- Antenatal sonography increasingly detects fetal hydronephrosis, leading to management controversies.
- Postnatal evaluation and treatment guidelines for fetal renal pelvis enlargement lack consensus.
Purpose of the Study:
- To prospectively investigate the postnatal management and outcomes of infants with prenatally diagnosed hydronephrosis.
- To establish management guidelines based on postnatal findings.
Main Methods:
- Prospective study of neonates with fetal renal pelvis measurements >= 5 mm on antenatal ultrasound.
- Postnatal investigations included ultrasound (US), voiding cystourethrography, isotope studies, and intravenous urograms as indicated.
- Follow-up duration averaged 26.3 months.
Main Results:
- 156 neonates (193 kidney units) were evaluated; 145 units showed abnormalities.
- Ureteropelvic junction obstruction (62.7%) and vesicoureteral reflux (16.6%) were the most common diagnoses.
- A normal initial postnatal US did not exclude urinary tract abnormalities in 45% of cases.
- Larger antenatal renal pelvis anteroposterior diameter (APPD) correlated with lower spontaneous resolution and higher surgery rates (P<0.01).
Conclusions:
- Antenatal hydronephrosis (AH) with APPD >= 5 mm requires postnatal investigation, as no normal upper limit exists.
- Management guidelines should be based on postnatal findings.
- A normal postnatal US does not rule out significant urinary tract abnormalities.
Abstract:
With the increasing use of antenatal sonography, fetal hydronephrosis has been reported more frequently. Because of the lack of consensus regarding treatment of these infants, the postnatal approach toward fetal renal pelvis enlargement remains controversial. The aim of this prospective study is to demonstrate the postnatal investigation, treatment, and outcome of infants with prenatally diagnosed hydronephrosis. Infants whose antenatal ultrasound scan showed a fetal renal pelvis of 5 mm or greater were investigated postnatally using ultrasound (US) and voiding cystourethrography. When indicated, isotope studies and intravenous urograms were also performed. We followed prospectively neonates with antenatally diagnosed hydronephrosis and recommended management guidelines on the basis of our findings. In 156 neonates (193 kidney units) that were found to have hydronephrosis, the average gestational age at which the diagnosis was made was 32.94+/-5.10 weeks. The mean duration of postnatal follow-up was 26.3+/-13.56 months (range 3-60 months). The mean APPD of the fetal renal pelvis was 10.35+/-3.24 mm (5-9 mm in 84 kidneys, 10-14 mm in 96 kidneys and > or =15 mm in 13 kidneys). Of the 193 kidney units, 145 units were found to be pathological. The most common detected underlying abnormalities were ureteropelvic junction obstruction (in 91 kidneys; 62.7%) and vesicoureteral reflux (in 24 kidneys; 16.6%). Postnatally, 23 (45%) of 51 patients whose first US was normal were diagnosed postnatally as having urinary tract abnormality. There was a negative correlation between APPD and the rate of spontaneous resolution and positive correlation between APPD and the rate of surgery (P<0.01). In conclusion, because it is not possible to determine an upper limit of normal for the antenatal renal pelvis, any baby with AH should not be considered clinically insignificant. Infants with antenatal renal pelvis measurements > or =5 mm should be investigated postnatally. A normal postnatal ultrasound scan does not preclude the presence of urinary tract abnormality.
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