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Congenital anomalies of the kidney and urinary tract (CAKUT) in critically ill infants: a multicenter cohort study.

Publication ,  Journal Article
Leow, EH; Lee, JH; Hornik, CP; Ng, YH; Hays, T; Clark, RH; Tolia, VN; Greenberg, RG
Published in: Pediatr Nephrol
January 2023

BACKGROUND: The aim of the study was to determine the prevalence of congenital anomalies of the kidney and urinary tract (CAKUT) in the neonatal intensive care unit (NICU) and to evaluate risk factors associated with worse outcomes. We hypothesized that infants with CAKUT with extra-renal manifestations have higher mortality. METHODS: This is a cohort study of all inborn infants who were diagnosed with any form of CAKUT discharged from NICUs managed by the Pediatrix Medical Group from 1997 to 2018. Logistic and linear regression models were used to analyze risk factors associated with in-hospital mortality. RESULTS: The prevalence of CAKUT was 1.5% among infants hospitalized in 419 NICUs. Among the 13,383 infants with CAKUT analyzed, median gestational age was 35 (interquartile range [IQR] 31-38) weeks and median birth weight was 2.34 (IQR 1.54-3.08) kg. Overall in-hospital mortality for infants with CAKUT was 6.8%. Oligohydramnios (adjusted odds ratio [aOR] 4.5, 95% confidence interval [CI] 2.2-9.1, p < 0.001), extra-renal anomalies (aOR 2.5, 95% CI 2.0-3.1, p < 0.001), peak SCr (aOR 1.02, 95% CI 1.01-1.03, p < 0.001) and exposure to nephrotoxic medications (aOR 1.4, 95% CI 1.1-1.7, p = 0.01) were associated with increased mortality, while a history of urological surgery or intervention was associated with lower mortality (aOR 0.6, 95% CI 0.4-0.7, p < 0.001). CONCLUSIONS: Infants hospitalized in the NICU who have CAKUT and the independent risk factors for mortality (e.g., oligohydramnios and presence of extra-renal anomalies) require close monitoring, minimizing of exposure to nephrotoxic drugs, and timely urological surgery or intervention. A higher resolution version of the Graphical abstract is available as Supplementary information.

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Published In

Pediatr Nephrol

DOI

EISSN

1432-198X

Publication Date

January 2023

Volume

38

Issue

1

Start / End Page

161 / 172

Location

Germany

Related Subject Headings

  • Urology & Nephrology
  • Urogenital Abnormalities
  • Urinary Tract
  • Pregnancy
  • Oligohydramnios
  • Kidney
  • Infant, Newborn
  • Infant
  • Humans
  • Female
 

Citation

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Leow, E. H., Lee, J. H., Hornik, C. P., Ng, Y. H., Hays, T., Clark, R. H., … Greenberg, R. G. (2023). Congenital anomalies of the kidney and urinary tract (CAKUT) in critically ill infants: a multicenter cohort study. Pediatr Nephrol, 38(1), 161–172. https://doi.org/10.1007/s00467-022-05542-0
Leow, Esther Huimin, Jan Hau Lee, Christoph P. Hornik, Yong Hong Ng, Thomas Hays, Reese H. Clark, Veeral N. Tolia, and Rachel G. Greenberg. “Congenital anomalies of the kidney and urinary tract (CAKUT) in critically ill infants: a multicenter cohort study.Pediatr Nephrol 38, no. 1 (January 2023): 161–72. https://doi.org/10.1007/s00467-022-05542-0.
Leow EH, Lee JH, Hornik CP, Ng YH, Hays T, Clark RH, et al. Congenital anomalies of the kidney and urinary tract (CAKUT) in critically ill infants: a multicenter cohort study. Pediatr Nephrol. 2023 Jan;38(1):161–72.
Leow, Esther Huimin, et al. “Congenital anomalies of the kidney and urinary tract (CAKUT) in critically ill infants: a multicenter cohort study.Pediatr Nephrol, vol. 38, no. 1, Jan. 2023, pp. 161–72. Pubmed, doi:10.1007/s00467-022-05542-0.
Leow EH, Lee JH, Hornik CP, Ng YH, Hays T, Clark RH, Tolia VN, Greenberg RG. Congenital anomalies of the kidney and urinary tract (CAKUT) in critically ill infants: a multicenter cohort study. Pediatr Nephrol. 2023 Jan;38(1):161–172.
Journal cover image

Published In

Pediatr Nephrol

DOI

EISSN

1432-198X

Publication Date

January 2023

Volume

38

Issue

1

Start / End Page

161 / 172

Location

Germany

Related Subject Headings

  • Urology & Nephrology
  • Urogenital Abnormalities
  • Urinary Tract
  • Pregnancy
  • Oligohydramnios
  • Kidney
  • Infant, Newborn
  • Infant
  • Humans
  • Female