Postnatal management of infants with antenatally detected hydronephrosis
- 16 July 2005
- journal article
- Published by Springer Nature in Pediatric Nephrology
- Vol. 20 (9) , 1253-1259
- https://doi.org/10.1007/s00467-005-1989-3
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 ≥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 ≥5 mm should be investigated postnatally. A normal postnatal ultrasound scan does not preclude the presence of urinary tract abnormality.Keywords
This publication has 33 references indexed in Scilit:
- Antenatal hydronephrosis: changing concepts in diagnosis and subsequent managementBJU International, 2000
- Clinical relevance and implications of antenatal hydronephrosisArchives of Disease in Childhood: Fetal & Neonatal, 1997
- Primary vesicoureteric reflux--how useful is postnatal ultrasound?Archives of Disease in Childhood, 1996
- Minimal Hydronephrosis in the Fetus: Clinical Significance and Implications for ManagementJournal of Urology, 1996
- Correlation of Prenatal Renal Pelvic Anteroposterior Diameter with Outcome in InfancyJournal of Urology, 1996
- Outcome of Urological Abnormalities Prenatally Diagnosed by UltrasoundFetal Diagnosis and Therapy, 1996
- Fetal pelvi‐ureteric junction obstruction: predictors of outcomeBritish Journal of Urology, 1995
- Prenatal diagnosis of urinary tract anomalies: The value of two ultrasound examinationsActa Obstetricia et Gynecologica Scandinavica, 1994
- In UteroUltrasonography: Impact on UrologyJournal of Endourology, 1992
- Management of fetal urinary tract anomalies detected by prenatal ultrasonography.Archives of Disease in Childhood, 1984