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1.
Int. braz. j. urol ; 44(3): 585-590, May-June 2018. tab, graf
Artículo en Inglés | LILACS | ID: biblio-954059

RESUMEN

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 (p:0.006) and lower amount of injected material (p:0.05) 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)
Humanos , Masculino , Femenino , Preescolar , Niño , Reflujo Vesicoureteral/tratamiento farmacológico , Circonio/uso terapéutico , Materiales Biocompatibles/uso terapéutico , Glucanos/uso terapéutico , Recurrencia , Reflujo Vesicoureteral/cirugía , Índice de Severidad de la Enfermedad , Reproducibilidad de los Resultados , Estudios Retrospectivos , Dextranos/uso terapéutico , Resultado del Tratamiento , Estadísticas no Paramétricas , Endoscopía/métodos , Ácido Hialurónico/uso terapéutico , Inyecciones
2.
Int Braz J Urol ; 44(3): 585-590, 2018.
Artículo en Inglés | MEDLINE | ID: mdl-29522294

RESUMEN

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 control 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 (p:0.006) and lower amount of injected material (p:0.05) 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)
Materiales Biocompatibles/uso terapéutico , Glucanos/uso terapéutico , Reflujo Vesicoureteral/tratamiento farmacológico , Circonio/uso terapéutico , Niño , Preescolar , Dextranos/uso terapéutico , Endoscopía/métodos , Femenino , Humanos , Ácido Hialurónico/uso terapéutico , Inyecciones , Masculino , Recurrencia , Reproducibilidad de los Resultados , Estudios Retrospectivos , Índice de Severidad de la Enfermedad , Estadísticas no Paramétricas , Resultado del Tratamiento , Reflujo Vesicoureteral/cirugía
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