SECTION ON UROLOGY 1996 ANNUAL MEETING PROGRAM

PEDIATRICS ◽  
1996 ◽  
Vol 98 (3) ◽  
pp. 591-647

Background: In boys with posterior urethral valves (PUV's), nonfunctioning and poorly functioning kidneys are frequently removed early in life to improve voiding dynamics when associated with vesicoureteral reflux (VUR) and for control of infections. We have encountered boys with PUV's and unilateral poorly functioning kidneys usually associated with varying degrees of VUR and have managed these patients with nephrectomy, reimplantation and/or observation. We analyzed the eventual outcome of these patients in terms of clinical and urodynamic (UD) parameters in order to make some recommendations regarding their management. Methods: Over a 5 year period, we studied 33 patients with PUV's after valve ablation with serial multichannel urodynamic (UD) studies. Fourteen (42%) patients had unilateral poorly functioning kidneys (<10% of total renal function on nuclear renal scans) (8 left. 6 right), 12 of whom had VUR upon initial presentation Only these 14 patients were included in this report. Six of the 14 (43%) had been initially treated with transurethral valve ablation (TURV). 6 (43%) by vesicostomy followed by closure and TURV, and 2 (14%) by pyelostomy followed by closure and TURV. The 12 patients with ipsilateral VUR on initial presentation includes 7 grade 5, 2 grade 4 and 3 grade 3 VUR. All patients were followed as closely as possible with serial UD studies and aggressive medical management (anticholinergics, CIC, timed voiding, etc.) of abnormal UD parameters. Results: There were no clinical sequelae from not removing 11 of 14 kidneys with poor function. Three of 14 boys (21%), all initially treated with vesicostomy, required nephrectomy at a mean age of 21 months after a mean period of observation of 20 months because of recurrent infections and ipsilateral grade 5 VUR.

2016 ◽  
Vol 46 (10) ◽  
pp. 1418-1423 ◽  
Author(s):  
Véronique Hochart ◽  
Annie Lahoche ◽  
René-Hilaire Priso ◽  
Véronique Houfflin-Debarge ◽  
Alfred Bassil ◽  
...  

1997 ◽  
Vol 158 (3) ◽  
pp. 1004-1007 ◽  
Author(s):  
Peter M. Cuckow ◽  
M.D. Dinneen ◽  
R.A. Risdon ◽  
P.G. Ransley ◽  
P.G. Duffy

2006 ◽  
Vol 34 (5) ◽  
Author(s):  
Stefanie Kleppe ◽  
Joachim Schmitt ◽  
Annegret Geipel ◽  
Ullrich Gembruch ◽  
Manfred Hansmann ◽  
...  

2019 ◽  
Vol 6 (2) ◽  
pp. 545
Author(s):  
Ravindra G. Khasnis ◽  
Rajshankar S.

Background: It is important to detect and manage hydronephrosis early for improved clinical outcomes. The objective of this study is to detect and manage the hydronephrosis which occurs antenatally.Methods: Hospital based cross sectional study was carried out in 20 cases of hydronephrosis in pregnant women as per the inclusion and exclusion criteria laid down for the present study. Patients with mild hydronephrosis were observed. Patients with PUJ obstruction underwent pyeloplasty. Patients with posterior urethral valves underwent cystoscopic dilatation. Patients with VUR were put on prophylactic antibiotic and observed. The patients were followed up post operatively with USG and DTPA scan as indicated.Results: Among the 20 cases with hydronephrosis, majority were males. All cases in terms of side affected were found to be equally distributed. Hydronephrosis was found to be mild in seven (35%) of the cases. Renal dysplasia and bilateral hydronephrosis were found to be the predictors of post natal pathology. Grade 3 and grade 4 were 40% each. There was no persistent case. The most common cause of hydronephrosis was transient hypertension in 5 (33.3%) of the cases.Conclusions: Mild hydronephrosis resolves early and there is no persistence. Renal dysplasia and bilateral hydronephrosis are the important predictors of the post natal hydronephrosis.


2004 ◽  
Vol 171 (6 Part 1) ◽  
pp. 2409-2412 ◽  
Author(s):  
MAZEN A. GHANEM ◽  
KATJA P. WOLFFENBUTTEL ◽  
ANN DE VYLDER ◽  
RIEN J.M. NIJMAN

2006 ◽  
Vol 175 (5) ◽  
pp. 1894-1897 ◽  
Author(s):  
Orhan Ziylan ◽  
Tayfun Oktar ◽  
Haluk Ander ◽  
Esat Korgali ◽  
Hasan Rodoplu ◽  
...  

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