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

CONTEXT: A congenital solitary functioning kidney (cSFK) is a common developmental defect that predisposes to hypertension and chronic kidney disease (CKD) as a consequence of hyperfiltration. Every urologist takes care of patients with a cSFK, since some will need lifelong urological care or will c...

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Autores principales: Groen in 't Woud, Sander, Westland, Rik, Feitz, Wout F.J., Roeleveld, Nel, van Wijk, Joanna A.E., van der Zanden, Loes F.M., Schreuder, Michiel F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8317823/
https://www.ncbi.nlm.nih.gov/pubmed/34337499
http://dx.doi.org/10.1016/j.euros.2021.01.003
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author Groen in 't Woud, Sander
Westland, Rik
Feitz, Wout F.J.
Roeleveld, Nel
van Wijk, Joanna A.E.
van der Zanden, Loes F.M.
Schreuder, Michiel F.
author_facet Groen in 't Woud, Sander
Westland, Rik
Feitz, Wout F.J.
Roeleveld, Nel
van Wijk, Joanna A.E.
van der Zanden, Loes F.M.
Schreuder, Michiel F.
author_sort Groen in 't Woud, Sander
collection PubMed
description CONTEXT: A congenital solitary functioning kidney (cSFK) is a common developmental defect that predisposes to hypertension and chronic kidney disease (CKD) as a consequence of hyperfiltration. Every urologist takes care of patients with a cSFK, since some will need lifelong urological care or will come with clinical problems or questions to an adult urologist later in life. OBJECTIVE: We aim to provide clear recommendations for the initial clinical management and follow-up of children with a cSFK. EVIDENCE ACQUISITION: PubMed and EMBASE were searched to identify relevant publications, which were combined with guidelines on related topics and expert opinion. EVIDENCE SYNTHESIS: Initially, cSFK diagnosis should be confirmed and risk factors for kidney injury should be identified using ultrasound. Although more research into early predictors of kidney injury is needed, additional congenital anomalies of the kidney or urinary tract and absence of compensatory kidney hypertrophy have repeatedly been associated with a worse prognosis. The role of voiding cystourethrography and antibiotic prophylaxis remains controversial, and is complicated by the exclusion of children with a cSFK from studies. A yearly follow-up for signs of kidney injury is recommended for children with a cSFK. As masked hypertension is prevalent, annual ambulatory blood pressure measurement should be considered. During puberty, an increasing incidence of kidney injury is seen, indicating that long-term follow-up is necessary. If signs of kidney injury are present, angiotensin converting enzyme inhibitors are the first-line drugs of choice. CONCLUSIONS: This overview points to the urological and medical clinical aspects and long-term care guidance for children with a cSFK, who are at risk of hypertension and CKD. Monitoring for signs of kidney injury is therefore recommended throughout life. Large, prospective studies with long-term follow-up of clearly defined cohorts are still needed to facilitate more risk-based and individualized clinical management. PATIENT SUMMARY: Many children are born with only one functioning kidney, which could lead to kidney injury later in life. Therefore, a kidney ultrasound is made soon after birth, and other investigations may be needed as well. Urologists taking care of patients with a solitary functioning kidney should realize the long-term clinical aspects, which might need medical management.
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spelling pubmed-83178232021-07-29 Clinical Management of Children with a Congenital Solitary Functioning Kidney: Overview and Recommendations Groen in 't Woud, Sander Westland, Rik Feitz, Wout F.J. Roeleveld, Nel van Wijk, Joanna A.E. van der Zanden, Loes F.M. Schreuder, Michiel F. Eur Urol Open Sci Review – Pediatric Urology CONTEXT: A congenital solitary functioning kidney (cSFK) is a common developmental defect that predisposes to hypertension and chronic kidney disease (CKD) as a consequence of hyperfiltration. Every urologist takes care of patients with a cSFK, since some will need lifelong urological care or will come with clinical problems or questions to an adult urologist later in life. OBJECTIVE: We aim to provide clear recommendations for the initial clinical management and follow-up of children with a cSFK. EVIDENCE ACQUISITION: PubMed and EMBASE were searched to identify relevant publications, which were combined with guidelines on related topics and expert opinion. EVIDENCE SYNTHESIS: Initially, cSFK diagnosis should be confirmed and risk factors for kidney injury should be identified using ultrasound. Although more research into early predictors of kidney injury is needed, additional congenital anomalies of the kidney or urinary tract and absence of compensatory kidney hypertrophy have repeatedly been associated with a worse prognosis. The role of voiding cystourethrography and antibiotic prophylaxis remains controversial, and is complicated by the exclusion of children with a cSFK from studies. A yearly follow-up for signs of kidney injury is recommended for children with a cSFK. As masked hypertension is prevalent, annual ambulatory blood pressure measurement should be considered. During puberty, an increasing incidence of kidney injury is seen, indicating that long-term follow-up is necessary. If signs of kidney injury are present, angiotensin converting enzyme inhibitors are the first-line drugs of choice. CONCLUSIONS: This overview points to the urological and medical clinical aspects and long-term care guidance for children with a cSFK, who are at risk of hypertension and CKD. Monitoring for signs of kidney injury is therefore recommended throughout life. Large, prospective studies with long-term follow-up of clearly defined cohorts are still needed to facilitate more risk-based and individualized clinical management. PATIENT SUMMARY: Many children are born with only one functioning kidney, which could lead to kidney injury later in life. Therefore, a kidney ultrasound is made soon after birth, and other investigations may be needed as well. Urologists taking care of patients with a solitary functioning kidney should realize the long-term clinical aspects, which might need medical management. Elsevier 2021-02-03 /pmc/articles/PMC8317823/ /pubmed/34337499 http://dx.doi.org/10.1016/j.euros.2021.01.003 Text en © 2021 The Author(s) https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review – Pediatric Urology
Groen in 't Woud, Sander
Westland, Rik
Feitz, Wout F.J.
Roeleveld, Nel
van Wijk, Joanna A.E.
van der Zanden, Loes F.M.
Schreuder, Michiel F.
Clinical Management of Children with a Congenital Solitary Functioning Kidney: Overview and Recommendations
title Clinical Management of Children with a Congenital Solitary Functioning Kidney: Overview and Recommendations
title_full Clinical Management of Children with a Congenital Solitary Functioning Kidney: Overview and Recommendations
title_fullStr Clinical Management of Children with a Congenital Solitary Functioning Kidney: Overview and Recommendations
title_full_unstemmed Clinical Management of Children with a Congenital Solitary Functioning Kidney: Overview and Recommendations
title_short Clinical Management of Children with a Congenital Solitary Functioning Kidney: Overview and Recommendations
title_sort clinical management of children with a congenital solitary functioning kidney: overview and recommendations
topic Review – Pediatric Urology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8317823/
https://www.ncbi.nlm.nih.gov/pubmed/34337499
http://dx.doi.org/10.1016/j.euros.2021.01.003
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