Evidence map›Paper›PMID 40342889›Full record

ArticleFrontiers in pediatrics2025

Clinical outcomes and risk factors in pediatric patients with solitary functioning kidney: a comparative analysis of congenital and acquired etiologies.

Hülya Gözde Önal, Yonca Semet

Abstract read
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Article in Frontiers in pediatrics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

The trial behind it

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Review
4 · The record

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5 · Who and what money

Authors and funding

2 authors.

Hülya Gözde ÖnalDepartment of Pediatric Nephrology, Samsun Training and Research Hospital, Samsun, Türkiye.
Yonca SemetDepartment of Pediatric Nephrology, Faculty of Medicine, Samsun University, Samsun, Türkiye.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: This study aims to assess the clinical outcomes and kidney function in pediatric patients with a solitary functioning kidney (SFK) due to various causes. It focuses on evaluating the glomerular filtration rate (GFR) across five groups: renal agenesis, multicystic dysplastic kidney (MCDK), atrophic kidney, hypoplastic kidney, and patients who underwent nephrectomy due to bleeding, stones, infection, or tumor without having progressed to renal failure. Methods: A retrospective chart review was conducted on single kidneys of 396 patients seen at the pediatric nephrology clinic from January 2011 to June 2024. Descriptive statistics were used to summarize the data, with chi-square tests employed for categorical variables and Results: Baseline and final GFR values showed significant differences between the groups in the pre- and post-tests. The MCDK group had significantly lower GFR than the renal agenesis group and the remaining etiologies. Albumin levels were decreased in MCDK patients, whereas neutrophil levels were elevated in patients with renal agenesis. Hypertension or proteinuric activity did not exhibit significant variations in the frequency across these groups. Discussion: This study highlights the importance of a personalized management approach for pediatric patients with an SFK, specifically those with MCDK, who are more likely experience early loss of kidney function. Minimizing the risks and improving the outcomes would require a routine, topical course of monitoring, along with appropriate treatment.

Indexed as

multicystic dysplastic kidneynephrectomypediatric nephrologyrenal agenesissolitary functioning kidney

Identifiers

PMID40342889
PMCPMC12058790

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