Literature DB >> 28554812

Outcomes of a Cohort of Prenatally Diagnosed and Early Enrolled Patients with Congenital Solitary Functioning Kidney.

Pierluigi Marzuillo1, Stefano Guarino2, Anna Grandone2, Allegra Di Somma2, Nicoletta Della Vecchia2, Tiziana Esposito2, Giulia Macchini2, Rosaria Marotta2, Andrea Apicella2, Mario Diplomatico2, Pier Francesco Rambaldi3, Laura Perrone2, Emanuele Miraglia Del Giudice2, Angela La Manna2, Cesare Polito2.   

Abstract

PURPOSE: We evaluated the clinical course of patients prenatally diagnosed and enrolled early with congenital solitary functioning kidney, and identified the risk factors for renal injury.
MATERIALS AND METHODS: We retrospectively evaluated 322 patients with congenital solitary functioning kidney according to the inclusion criteria of 1) prenatal diagnosis of solitary kidney; 2) first evaluation at 1 to 3 months of life with confirmation of congenital solitary functioning kidney, and evaluation of possible associated congenital anomalies of the kidney and urinary tract by abdominal ultrasound, renal scintigraphy and cystography; and 3) absence of any condition potentially affecting renal function in the neonatal period as well as absence of renal injury at enrollment (1 to 3 months of life) confirmed by a normal estimated glomerular filtration rate, lack of proteinuria and hypertension. Followup of 306 patients was evaluated.
RESULTS: Median followup was 7.2 years (range 1 to 23) and 1 or more signs of renal injury were found in 12 of 306 patients (3.9%). Considering the entire population the cumulative proportion of patients free from renal injury at 17 years old was 93.7%, vs 81.3% and 95.9% for subjects with and those without congenital anomalies of the kidney and urinary tract of congenital solitary functioning kidney (p <0.001), respectively. Of congenital anomalies of the kidney and urinary tract, congenital solitary functioning kidney resulted in significant risk factors for renal injury (HR 8.75, 95% CI 2.77-27.65).
CONCLUSIONS: In an evaluation of a large cohort of patients enrolled early with congenital solitary functioning kidney with a prenatal diagnosis, excluding those with neonatal onset of renal damage, the prevalence of renal damage was 3.9%. Among congenital anomalies of the kidney and urinary tract, congenital solitary functioning kidney represented the major risk factor.
Copyright © 2017 American Urological Association Education and Research, Inc. Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  CAKUT; child; hypertension; kidney; proteinuria

Mesh:

Year:  2017        PMID: 28554812     DOI: 10.1016/j.juro.2017.05.076

Source DB:  PubMed          Journal:  J Urol        ISSN: 0022-5347            Impact factor:   7.450


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2.  Congenital solitary kidney in childhood: not so bad.

Authors:  Pierluigi Marzuillo; Cesare Polito
Journal:  Pediatr Nephrol       Date:  2017-07-07       Impact factor: 3.714

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5.  Early Renal Ultrasound in Patients with Congenital Solitary Kidney Can Guide Follow-Up Strategy Reducing Costs While Keeping Long-Term Prognostic Information.

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6.  Prevalence of reflux nephropathy in Iranian children with solitary kidney: results of a multi-center study.

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8.  Is the prognosis of congenital single functioning kidney benign? A population-based study.

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9.  Cardiovascular risk assessment in children and adolescents with congenital solitary kidneys.

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Review 10.  Clinical Management of Children with a Congenital Solitary Functioning Kidney: Overview and Recommendations.

Authors:  Sander Groen In 't Woud; Rik Westland; Wout F J Feitz; Nel Roeleveld; Joanna A E van Wijk; Loes F M van der Zanden; Michiel F Schreuder
Journal:  Eur Urol Open Sci       Date:  2021-02-03
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