Literature DB >> 25255780

Selection of infants who potentially have congenital anomalies of the kidney and urinary tract from a large cohort for a more thorough examination.

Atsunori Yoshino1, Masataka Honda, Naomi Sasaki, Hiroshi Hataya, Kenji Ishikura, Satoru Sakazume, Yuriko Tanaka, Toshiro Nagai.   

Abstract

BACKGROUND: Although congenital anomalies of the kidney and urinary tract (CAKUT) are the most common cause of pediatric end-stage renal disease (ESRD), little is known about the characteristics exhibited in the infantile period by CAKUT patients who develop ESRD. Further, an efficient screening method for CAKUT diagnosis is not available currently. In the present study, we aimed to develop a method to select infants who potentially have CAKUT from a large group of infants.
METHODS: We retrospectively investigated the clinical characteristics of CAKUT patients in the infantile period. The medical records of 101 patients with CAKUT who had undergone dialysis or renal transplantation were reviewed. The data of gestational age, birth weight, oligohydramnios, poor body weight gain, asphyxia, and jaundice were recorded. We attempted to determine the ideal characteristics that could be used to select infants who potentially have CAKUT.
RESULTS: 14 % of patients were born prematurely, 18 % had low birth weight, 79 % had poor body weight gain, 18 % had asphyxia, 8 % had oligohydramnios, and 12 % had jaundice. We found that 82 % of patients had poor body weight gain or oligohydramnios among our patients and regarded these two symptoms as ideal markers for selecting those who potentially have CAKUT (specificity, 95 %; efficacy, 95 %). Further, the age of ≤ 7 months was the most appropriate time for the selection.
CONCLUSIONS: For timely diagnosis of CAKUT, we recommend that ultrasound examination and the serum creatinine test be conducted for infants showing poor body weight gain or oligohydramnios at age ≤ 7 months.

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Year:  2014        PMID: 25255780     DOI: 10.1007/s10157-014-1036-4

Source DB:  PubMed          Journal:  Clin Exp Nephrol        ISSN: 1342-1751            Impact factor:   2.801


  16 in total

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2.  Cardiovascular risk reduction in high-risk pediatric populations.

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Authors:  H Wong; K Mylrea; J Feber; A Drukker; G Filler
Journal:  Kidney Int       Date:  2006-06-21       Impact factor: 10.612

5.  Carotid intima-media thickness in children with CKD: results from the CKiD study.

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6.  Pre-dialysis chronic kidney disease in children: results of a nationwide survey in Japan.

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Journal:  Nephrol Dial Transplant       Date:  2013-07-03       Impact factor: 5.992

7.  The 1998 report of the Japanese National Registry data on pediatric end-stage renal disease patients.

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8.  Renal outcome in patients with congenital anomalies of the kidney and urinary tract.

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Journal:  Kidney Int       Date:  2009-06-17       Impact factor: 10.612

9.  Chronic renal insufficiency in children: the 2001 Annual Report of the NAPRTCS.

Authors:  Mouin G Seikaly; P L Ho; Lea Emmett; Richard N Fine; Amir Tejani
Journal:  Pediatr Nephrol       Date:  2003-06-14       Impact factor: 3.714

10.  Cardiovascular mortality in children and young adults with end-stage kidney disease.

Authors:  R S Parekh; C E Carroll; R A Wolfe; F K Port
Journal:  J Pediatr       Date:  2002-08       Impact factor: 4.406

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  1 in total

1.  Early detection of congenital anomalies of the kidney and urinary tract: cross-sectional results of a community-based screening and referral study in China.

Authors:  Yinv Gong; Ying Zhang; Qian Shen; Liping Xiao; Yihui Zhai; Yunli Bi; Jian Shen; Hong Chen; Yun Li; Hong Xu
Journal:  BMJ Open       Date:  2018-05-30       Impact factor: 2.692

  1 in total

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