Objectives: To determine if prenatal identification of significant ren
al duplication anomalies affects the management of the patient or the
clinical outcome. Methods: This is a retrospective review of 79 consec
utive children with severe hydronephrosis involving a duplex renal col
lecting system, identified by either prenatal ultrasound (asymptomatic
), or symptoms, most. often urinary tract infection, but also includin
g abdominal mass, hematuria, or incontinence. An individualized combin
ation of voiding cystourethrogram, ultrasound, intravenous urogram, an
d nuclear renal scan was used to assess anatomy and function. Ablation
of the involved segment was carried out if no or extremely poor funct
ion was identified; a definitive reconstructive procedure was elected
in the face of easily measureable function. Outcome was determined cli
nically and by repeat imaging. Results: There was no difference in the
rate of renal segment salvage between the prenatally and clinically d
iagnosed groups. Of the cases analyzed, 20/79 were prenatally identifi
ed, of which 13/20 (65%) were reconstructed; 59/79 were identified on
clinical grounds, of which 34/59 (58%) were reconstructed. One patient
in the prenatal salvage group underwent removal of the affected kidne
y 5 years later. Another, in the clinical salvage group, underwent a s
uccessful secondary procedure for closure of a ureteral fistula. All o
thers have shown improved function, drainage, or both in follow-up. No
secondary procedures have been required for the ablation group to dat
e. Follow-up ranges from 4 months to 12 years. Conclusions: Prenatal i
dentification of significant duplex system hydronephrosis does not imp
rove the rate of renal segment salvage, as determined by standard radi
ographic means, compared to later identification an clinical grounds.
The decision for reconstruction versus ablation in significant duplex
system hydronephrosis can be made on the basis of function alone. (C)
1998, Elsevier Science inc. All rights reserved.