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Updated: May 28, 2026

Vessel-sparing Excision and Primary Anastomosis
Published on: January 7, 2019
Long-term risk of end stage renal disease in patients with posterior urethral valves
Jukka Heikkilä1, Christer Holmberg, Lauri Kyllönen
1Department of Pediatric Surgery, Hyvinkää Hospital, Hyvinkää, Finland.
Insights
Patients with posterior urethral valves face a significant lifetime risk of end-stage renal disease (ESRD). However, this risk appears to decrease after age 34, with early kidney function being a key prognostic factor.
Area of Science:
- Pediatric Urology
- Nephrology
- Public Health
Background:
- Congenital obstructive uropathy, such as posterior urethral valves (PUV), can lead to end-stage renal disease (ESRD).
- While childhood progression to ESRD is documented, long-term adult outcomes remain less understood.
- Understanding long-term renal prognosis in adults with PUV is crucial for effective management.
Purpose of the Study:
- To evaluate the long-term risk of ESRD in adult patients previously treated for PUV.
- To identify factors associated with the progression of renal disease in this cohort.
Main Methods:
- A cohort of 200 male patients treated for PUV between 1953 and 2003 was retrospectively analyzed.
- Renal outcomes, including progression to ESRD, dialysis, and transplantation, were tracked for 193 patients.
- Data were collected from patient records, national registries, and hospital archives.
Main Results:
- Of 193 patients followed, 44 (22.8%) progressed to ESRD.
- The estimated lifetime risk of ESRD was 28.5%.
- No ESRD occurred after age 34. Factors like early presentation, pneumothorax, reflux, and recurrent UTIs were linked to increased ESRD risk. Lower serum creatinine in the first postoperative year correlated with faster progression.
Conclusions:
- Congenital obstructive uropathy can lead to ESRD in childhood and young adulthood.
- The risk of ESRD appears to diminish with age, suggesting a potential stabilization of renal function.
- Initial kidney function is a critical predictor of long-term renal prognosis in patients with PUV.
Purpose:
Congenital obstructive uropathy can lead to end stage renal disease. Progression to end stage renal disease in childhood is well described but long-term prognosis in adulthood has not been thoroughly investigated. In this study we evaluated the risk of end stage renal disease in patients with posterior urethral valves.
Materials And Methods:
During 1953 to 2003 a total of 200 male patients were treated for posterior urethral valves at our institution and of these 193 could be followed for renal outcome. Followup data on patients treated with dialysis or kidney transplantation were collected from patient records and the Finnish Kidney Transplantation Registry, and data on deceased patients were collected from hospital records and the Finnish Population Register Centre.
Results:
Median patient age at evaluation was 31 years (range 6 to 69). Of the 193 patients followed 44 (22.8%) had progression to end stage renal disease. According to a Kaplan-Meier analysis the lifetime risk of end stage renal disease was 28.5% (SE 3.8%). No patient had end stage renal disease after the age of 34 years. The lowest serum creatinine value during postoperative year 1 was associated with speed of progression to end stage renal disease. Early presentation, pneumothorax, bilateral vesicoureteral reflux and recurrent urinary tract infections after the abolition of urethral obstruction were associated with an increased risk of end stage renal disease at followup.
Conclusions:
Congenital obstructive uropathy can lead to end stage renal disease during childhood or young adulthood. However, the risk of end stage renal disease seems to decrease eventually. Poor kidney function at presentation is associated with worse renal prognosis.
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