Evidence map›Paper›PMID 42432369›Full record

ArticlePediatric nephrology (Berlin, Germany)2026

Screening of pediatric patients with congenital anomalies of the kidney and urinary tract for associated congenital heart disease in a tertiary care setting.

Sahar S Sheta, Rana Hendawy, Esraa Fathy, Shaimaa Sayed

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Article in Pediatric nephrology (Berlin, Germany), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

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4 authors.

Sahar S ShetaPediatric Department, Faculty of Medicine, Cairo University, Giza, Egypt.
Rana HendawyPediatric Department, Faculty of Medicine, Cairo University, Giza, Egypt.
Esraa FathyPediatric Department, Matarya Teaching Hospital, Cairo, Egypt.
Shaimaa SayedPediatric Department, Faculty of Medicine, Cairo University, Giza, Egypt. shaimaasayed@kasralainy.edu.eg.ORCID http://orcid.org/0000-0002-9009-165X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCongenital anomalies of the kidney and urinary tract (CAKUT) are among the most common birth defects and represent a leading cause of chronic kidney disease (CKD) in children. Congenital heart disease (CHD) is the most frequent severe congenital malformation worldwide. Given the shared mesodermal embryologic origin of both the renal and cardiovascular systems, an association between CAKUT and CHD has been proposed. We aimed to screen pediatric patients diagnosed with CAKUT for the presence of associated CHD.

methodsThis cross-sectional analytical study included 300 pediatric patients with CAKUT. Demographic data, type of CAKUT and kidney function status were collected. All patients underwent cardiac evaluation and echocardiography to detect structural heart defects and assess cardiac function. CAKUT types and their association with CHD were analyzed.

resultsThe mean age of the cohort was 6.42 years, with a male predominance (68.7%). CHD was detected in 7% of patients, with atrial septal defect (33%) and ventricular septal defect (23%) being the most frequent lesions. 28.5% of these patients with CHD needed surgical intervention. The most common CAKUT subtype was vesicoureteral reflux (27.7%), and it was the most common CAKUT subtype associated with CHD. Fractional shortening impairment was strongly associated with advanced CKD.

conclusionsThe coexistence of CHD among children with CAKUT could emphasize the need for cardiac evaluation and consider the echocardiographic screening in this population. Moreover, the observed link between advanced CKD stage and cardiac dysfunction supports the necessity of integrated nephro-cardiac care in these patients.

Indexed as

Chronic kidney diseaseCongenital anomalies of the kidney and urinary tractCongenital heart diseasePediatricsVesicoureteral reflux

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