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Antenatally detected urinary tract dilatation: a pediatric nephrologist's point of view
- Source :
- Childhood Kidney Diseases, Vol 28, Iss 1, Pp 1-7 (2024)
- Publication Year :
- 2024
- Publisher :
- Korean Society of Pediatric Nephrology, 2024.
-
Abstract
- Antenatally diagnosed urinary tract dilatation (UTD), previously referred to as antenatal hydronephrosis, is the most commonly detected abnormality by prenatal ultrasonography. Several grading systems have been developed for the classification of antenatal UTD using prenatal and postnatal ultrasonography. UTD comprises a wide variety of congenital abnormalities of the kidney and urinary tract ranging from transient UTD to more significant abnormalities such as vesicoureteral reflux, ureteropelvic junction obstruction, ureterocele, ureterovesical junction obstruction, posterior urethral valves, and non-refluxing megaureter. Optimizing the evaluation of antenatally detected UTD is essential to recognize children with important disorders while avoiding excessive investigations. Conservative approach with close follow-up is increasingly accepted as an appropriate treatment option for patients with asymptomatic vesicoureteral reflux and ureteropelvic junction obstruction in recent years. However, predicting permanent kidney damage in an unselected group of children with antenatal UTD is still challenging. The management and follow-up of children with UTD should be individualized based on recommendations from a pediatric nephrologist, a pediatric urologist, or both. Future research directed at predicting long-term outcomes of children diagnosed with UTD from mild findings to severe disease is needed to refine management for those at higher risk of kidney disease progression.
Details
- Language :
- English
- ISSN :
- 23840242 and 23840250
- Volume :
- 28
- Issue :
- 1
- Database :
- Directory of Open Access Journals
- Journal :
- Childhood Kidney Diseases
- Publication Type :
- Academic Journal
- Accession number :
- edsdoj.7abf761b8411438fa609bd2de16a3971
- Document Type :
- article
- Full Text :
- https://doi.org/10.3339/ckd.24.002