Dextranomer/hyaluronic acid for pediatric vesicoureteral reflux: systematic review

Jonathan C Routh1, Brant A Inman, Yuri Reinberg

  • 1Children's Hospital Boston, Department of Urology, Boston, MA 02115, USA. jon.routh@gmail.com

Pediatrics
|April 7, 2010
PubMed

Insights

Dextranomer/hyaluronic acid (Dx/HA) injection for pediatric vesicoureteral reflux (VUR) shows a 77% success rate, but outcomes vary. Higher VUR grade negatively impacts success, while other factors like age and COI disclosure are not significant. Further research is needed.

Area of Science:

  • Pediatric Urology
  • Minimally Invasive Surgery
  • Medical Device Technology

Background:

  • Pediatric vesicoureteral reflux (VUR) is a common condition requiring effective treatment.
  • Dextranomer/hyaluronic acid (Dx/HA) injection is a minimally invasive option for VUR.
  • Reported success rates for Dx/HA injection vary significantly across studies.

Purpose of the Study:

  • To investigate the heterogeneity in published success rates of Dx/HA injection for pediatric VUR.
  • To identify patient and study-level factors contributing to the variability in Dx/HA treatment outcomes.

Main Methods:

  • Comprehensive literature search of multiple databases (1990-2008).
  • Duplicate assessment and data abstraction of identified studies.
  • Meta-regression analysis to adjust for confounding variables including VUR grade and conflict of interest (COI) disclosure.

Main Results:

  • A total of 47 studies with 7303 ureters were included in the pooled analysis.
  • The overall per-ureter success rate for Dx/HA injection was 77% at 3 months.
  • Preoperative VUR grade was the primary factor influencing success rates; COI disclosure, patient age, and Dx/HA volume were not significant after adjustment.

Conclusions:

  • Dx/HA injection demonstrates a 77% success rate for pediatric VUR, but significant heterogeneity exists.
  • Higher VUR grade is associated with lower success rates.
  • Improved reporting standards and comparative studies are necessary for VUR treatments.
Abstract

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