Efficacy and safety of Hyadex for treatment of vesicoureteral reflux: a multicenter experience

J Int Med Res. 2023 Aug;51(8):3000605231195165. doi: 10.1177/03000605231195165.

Abstract

Objective: This study was performed to evaluate the efficacy and safety of dextranomer/cross-linked hyaluronic acid (Hyadex) in patients with a clinical diagnosis of vesicoureteral reflux (VUR).

Methods: In this cross-sectional multicenter observational study, Hyadex was used in four different centers for the endoscopic treatment of VUR from 2020 to 2022. The study involved 74 patients (93 renal units) who were diagnosed with VUR according to voiding cystourethrography (VCUG) findings and were considered suitable for subureteric endoscopic treatment. The follow-up time (control VCUG time) was 3 months.

Results: In the VCUG evaluation, grade I VUR was found in 13 renal units, grade II in 23 renal units, grade III in 42 renal units, and grade IV in 12 renal units. The success rates of Hyadex treatment according to the degree of VUR were as follows: 84.6% for grade I, 82.6% for grade II, 71.4% for grade III, and 66.0% for grade IV. No major complications were observed.

Conclusion: Endoscopic subureteric Hyadex injection had high success rates in appropriately selected patients with VUR and may be used as the first-line treatment for children with VUR.

Keywords: Hyadex; Vesicoureteral reflux; cross-linked hyaluronic acid; dextranomer; subureteric injection; voiding cystourethrography.

Publication types

  • Observational Study
  • Multicenter Study

MeSH terms

  • Child
  • Cross-Sectional Studies
  • Humans
  • Hyaluronic Acid / adverse effects
  • Kidney
  • Vesico-Ureteral Reflux* / drug therapy

Substances

  • Hyaluronic Acid