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Durasphere® EXP: a non-biodegradable agent for treatment of primary Vesico-Ureteral reflux in children
Ozkuvanci, Unsal; Donmez, Muhammet Irfan; Ozgor, Faruk; Erbin, Akif; Pasin, Özge; Muslumanoglu, Ahmet Yaser.
  • Ozkuvanci, Unsal; Haseki Training and Research Hospital. Department of Urology. Fatih. TR
  • Donmez, Muhammet Irfan; Istanbul University. Istanbul Faculty of Medicine. Department of Urology. Fatih. TR
  • Ozgor, Faruk; Haseki Training and Research Hospital. Department of Urology. Fatih. TR
  • Erbin, Akif; Haseki Training and Research Hospital. Department of Urology. Fatih. TR
  • Pasin, Özge; Istanbul University. Istanbul Faculty of Medicine. Department of Biostatistics. Fatih. TR
  • Muslumanoglu, Ahmet Yaser; Haseki Training and Research Hospital. Department of Urology. Fatih. TR
Int. braz. j. urol ; 44(3): 585-590, May-June 2018. tab, graf
Artículo en Inglés | LILACS | ID: biblio-954059
ABSTRACT
ABSTRACT

Introduction:

Durasphere® EXP (DEXP) is a compound of biocompatible and non--biodegradable particles of zirconium oxide covered with pyrolytic carbon. The aim of this study is to evaluate the durability of off-label use of DEXP in the treatment of primary vesicoureteral reflux in children. Materials and

Methods:

Patients who underwent subureteric injection of DEXP for the correction of primary VUR were retrospectively reviewed. Patients aged >18 years as well as those who had grade-I or -V VUR, anatomic abnormalities (duplicated system, hutch diverticulum), neurogenic bladder or treatment refractory voiding dysfunction were excluded. Radiologic success was defined as the resolution of VUR at the 3rd month control. Success was radiographically evaluated at the end of the first year.

Results:

Thirty-eight patients (9 boys, 29 girls; mean age, 6.3±2.7 years) formed the study cohort. Forty-six renal units received DEXP (grade II 22; grade III 18; grade IV 6). Mean volume per ureteric orifice to obtain the mound was 0.70±0.16mL. First con- trol VCUG was done after 3 months in all patients. After the first VCUG, 6 patients had VUR recurrence. Short-term radiologic success of DEXP was 84.2%. Rate of radiologic success at the end of the first year was 69.4% (25/32). Lower age (p0.006) and lower amount of injected material (p0.05) were associated with higher success rates at the end of 1 year.

Conclusion:

This is the first study to assess the outcomes of DEXP for treatment of primary VUR in children. After 1 year of follow-up, DEXP had a 69.4% success rate.
Asunto(s)


Texto completo: Disponible Índice: LILACS (Américas) Asunto principal: Reflujo Vesicoureteral / Circonio / Materiales Biocompatibles / Glucanos Tipo de estudio: Estudios de evaluación / Estudio observacional / Factores de riesgo Límite: Niño / Child, preschool / Femenino / Humanos / Masculino Idioma: Inglés Revista: Int. braz. j. urol Asunto de la revista: Urología Año: 2018 Tipo del documento: Artículo País de afiliación: Turquía Institución/País de afiliación: Haseki Training and Research Hospital/TR / Istanbul University/TR

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Texto completo: Disponible Índice: LILACS (Américas) Asunto principal: Reflujo Vesicoureteral / Circonio / Materiales Biocompatibles / Glucanos Tipo de estudio: Estudios de evaluación / Estudio observacional / Factores de riesgo Límite: Niño / Child, preschool / Femenino / Humanos / Masculino Idioma: Inglés Revista: Int. braz. j. urol Asunto de la revista: Urología Año: 2018 Tipo del documento: Artículo País de afiliación: Turquía Institución/País de afiliación: Haseki Training and Research Hospital/TR / Istanbul University/TR