Literature DB >> 34515945

Long-term follow-up of congenital anomalies of the kidney and urinary tract diagnosed in utero: a longitudinal study.

Talia Israel1,2, Weissbach Tal2,3, Yael Pasternak1,2, Alina Weissmann-Brenner4,5.   

Abstract

BACKGROUND: Congenital-anomalies of the kidney-and-urinary-tract (CAKUT) are diagnosed in 3-6 per 1000 live-births. The objective of the current study was to examine the short and long-term outcomes of children diagnosed prenatally with CAKUT.
METHODS: A retrospective study was performed in 2018 on all pregnancies diagnosed with CAKUT between 2004 and 2008 at our hospital. Pregnancy outcomes and long-term morbidity were evaluated. Comparison was made between mild and severe forms of CAKUT and between unilateral and bilateral anomalies.
RESULTS: Ninety-eight children were included in the study. Most of them were born with an adequate weight for gestational-age, and were born at term by vaginal-deliveries. Children with major renal anomalies suffered significantly more frequently from recurrent UTIs (33.3% vs. 8.4%), needed more preventive antibiotics (50% vs. 20.5%), and had more renal surgeries (75% vs. 28%) than those with milder forms of CAKUT. Significantly more children with polycystic/multicystic kidney disease had recurrent UTIs (50% compared to 25% of the children with renal agenesis, and 5.6% of the children with hydronephrosis/hydroureter). There were no significant differences in the need for neurodevelopmental follow-up between the different groups of severity. Unilateral CAKUT patients required longer periods of nephrologist follow-up and repeated sonographic exams compared to bilateral CAKUT patients. Children with bilateral CAKUT more often needed special educational support than peers with unilateral disease (29.4% vs. 11.1%, P = 0.03).
CONCLUSIONS: Pregnancies whose children are diagnosed with CAKUT in utero usually deliver at term, with adequate-weight for gestational-age. The most common long-term comorbidities in children were recurrent UTIs and the use of preventive antibiotics was often needed. Expecting couples can be reassured of a generally good outcome of their children, at least during the first decade of life.
© 2021. Italian Society of Nephrology.

Entities:  

Keywords:  CAKUT; Congenital renal anomalies; Neurodevelopment; Urinary tract infection

Mesh:

Year:  2021        PMID: 34515945     DOI: 10.1007/s40620-021-01142-7

Source DB:  PubMed          Journal:  J Nephrol        ISSN: 1121-8428            Impact factor:   3.902


  2 in total

1.  The congenital and acquired solitary kidney.

Authors:  Ellen Shapiro; David A Goldfarb; Michael L Ritchey
Journal:  Rev Urol       Date:  2003

2.  Long-term clinical outcome of infants with mild and moderate fetal pyelectasis: validation of neonatal ultrasound as a screening tool to detect significant nephrouropathies.

Authors:  Khalid Ismaili; Fred E Avni; K Martin Wissing; Michelle Hall
Journal:  J Pediatr       Date:  2004-06       Impact factor: 4.406

  2 in total

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