Prenatal complicated duplex collecting system and ureterocele-Important risk factors for urinary tract infection

Sofia Visuri1, Timo Jahnukainen2, Seppo Taskinen1

  • 1Department of Pediatric Surgery, Helsinki University Hospital, Helsinki, Finland.

Insights

Infants with prenatally detected complicated urinary tract issues like ureterocele or duplex collecting system face a high risk of urinary tract infections (UTIs). Early endoscopic perforation may be considered for ureteroceles to reduce infection rates.

Area of Science:

  • Pediatric Urology
  • Nephrology
  • Medical Diagnostics

Background:

  • Prenatal detection of urinary tract abnormalities is crucial for early intervention.
  • Complicated duplex collecting systems (CDS) and ureteroceles are associated with potential urinary tract complications.

Purpose of the Study:

  • To evaluate the risk of urinary tract infections (UTIs) in infants diagnosed with prenatally detected complicated duplex collecting system (CDS) or ureterocele.

Main Methods:

  • Retrospective analysis of patients with prenatally detected CDS or single system ureterocele (2003-2013).
  • Complicated cases included ureterocele, vesicoureteral reflux (VUR), or nonrefluxing megaureter.
  • UTI prevalence was compared between affected patients and 66 controls.

Main Results:

  • 44% of patients experienced at least one UTI compared to 5% of controls (p<0.001).
  • UTIs occurred prior to surgery in 31% with ureterocele and 57% with both ureterocele and VUR.
  • Postoperative UTIs were observed in 29% of girls, with a 14% incidence after ureterocele perforation.

Conclusions:

  • Children with prenatally detected ureterocele or CDS with nonrefluxing megaureter have a high risk of UTI, even with prophylactic antibiotics.
  • Early endoscopic perforation of prenatally detected ureteroceles is suggested to mitigate UTI risk.
Abstract

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