2021
DOI: 10.1007/s00467-021-05145-1
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Epidemiology of pediatric chronic kidney disease/kidney failure: learning from registries and cohort studies

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Cited by 73 publications
(39 citation statements)
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“…There is no comprehensive epidemiological data regarding the prevalence of CKD in children due to the different classification and diagnostic definitions for CKD in children. [ 1 2 ] It is estimated that it ranges between 15 and 74.7 per one million of the age-related population (pmarp). [ 3 ]…”
Section: Introductionmentioning
confidence: 99%
“…There is no comprehensive epidemiological data regarding the prevalence of CKD in children due to the different classification and diagnostic definitions for CKD in children. [ 1 2 ] It is estimated that it ranges between 15 and 74.7 per one million of the age-related population (pmarp). [ 3 ]…”
Section: Introductionmentioning
confidence: 99%
“…Congenital anomalies of the kidney and urinary tract (CAKUT) are the leading cause of kidney failure in children and one of the most common indications for kidney transplantation. 1 Morphologic phenotypes vary, ranging from severe malformations such as bilateral kidney agenesis to milder conditions such as urinary tract dilation. 2 The overall prevalence of CAKUT is estimated at 4 to 60 events per 10 000 births.…”
mentioning
confidence: 99%
“…Etiologies are multifactorial and include familial, genetic, epigenetic, and environmental factors. 1 As survival of extremely preterm infants born prior to 28 weeks' gestation continues to improve, the ability to diagnose and manage associated comorbidities becomes increasingly essential to improving patient outcomes. Over the last decade, efforts to prevent and recognize acute kidney injury (AKI; a common comorbidity in infants with CAKUT) in extremely preterm infants have quickly transformed research and bedside care as pharmacists, clinicians, and nurses have begun to scrutinize nephrotoxic medication use while seeking to identify the earliest warning signs of kidney disease.…”
mentioning
confidence: 99%
“…Среди хромосомных аномалий и пороков, по данным различных авторов, от 20 до 50% приходится на врожденные аномалии развития органов мочевой системы (ВАРМС) [2][3][4]. Большинство вовремя не диагностированных ВПР органов мочевой системы (ОМС) долгое время не имеют клинической симптоматики, при этом у части пациентов (от 30 до 60%) они приводят к развитию хронической болезни почек (ХБП) и хронической почечной недостаточности (ХПН) [2][3][4][5].…”
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