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Published on: October 12, 2017
The relationship between dysfunctional voiding and congenital vesicoureteral reflux
1Department of Pediatric Urology, Children's Hospital of Buffalo, New York 14222, USA.
Insights
Voiding dysfunction is linked to congenital vesicoureteral reflux in children. Early recognition and treatment of aberrant lower urinary tract function are crucial to prevent infections and renal scarring.
Area of Science:
- Pediatric Urology
- Nephrology
- Developmental Biology
Background:
- Congenital vesicoureteral reflux (VUR) in children may be associated with voiding dysfunction.
- Aberrant lower urinary tract function and structural deficiencies of the ureterovesical junction are implicated in VUR etiology.
- Voiding dysfunction can be congenital or acquired during toilet training.
Purpose of the Study:
- To explore the etiological role of voiding dysfunction in congenital vesicoureteral reflux.
- To highlight the association between lower urinary tract dysfunction and VUR in infants and children.
- To emphasize the clinical significance of recognizing and managing voiding dysfunction in VUR patients.
Main Methods:
- Review of existing evidence linking voiding dysfunction and VUR.
- Analysis of the developmental and acquired aspects of lower urinary tract dysfunction.
- Discussion of clinical outcomes associated with undiagnosed/untreated voiding dysfunction.
Main Results:
- Voiding dysfunction is increasingly recognized as a factor in congenital VUR.
- Both structural and functional abnormalities of the lower urinary tract contribute to VUR.
- Undiagnosed voiding dysfunction correlates with higher rates of breakthrough infections, renal scarring, and surgical failure.
Conclusions:
- Voiding dysfunction plays a significant etiological role in congenital VUR.
- Recognition and management of lower urinary tract dysfunction are vital for improving outcomes in children with VUR.
- Further research is needed to clarify the roles of urodynamics and anticholinergic therapy.
Abstract:
Voiding dysfunction may play an etiological role in congenital vesicoureteral reflux in otherwise normal children. There is increasing evidence to suggest that in some infants and older children, vesicoureteral reflux is associated with congenital structural deficiency of the trigonal ureterovesical junction valve mechanism as well as aberrant lower urinary tract function. In the youngest infants this abnormal function can be present at birth, whereas in older children it may be acquired and learned during the toilet training years, if it is not already present. Voiding dysfunction may spontaneously improve or require additional therapy. Increased rates of breakthrough infection, renal scarring and surgical failure have been associated with undiagnosed and untreated lower urinary tract dysfunction, emphasizing the importance of its recognition. Controversy remains regarding the role of invasive urodynamics and anticholinergic medication, and further large-scale prospective studies are necessary before either modality becomes routine when assessing and treating these children.
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