Morphofunctional disorders of the cardiovascular system in cakutsyndrome in children

Author:

Umalatova M. I.1ORCID,Letifov G. M.2,Makhachev B. P.3ORCID

Affiliation:

1. Children's Clinic No. 3

2. Rostov State Medical University

3. Dagestan State Medical University

Abstract

BACKGROUND. Congenital abnormalities of the kidneys and urinary tract in children are included in the concept of CAKUT (con­genital anomalies of the kidney and urinal tract) - a syndrome and are often accompanied by changes in the cardiovascular system, which requires an interdisciplinary approach when observing them. THE AIM: to evaluate the nature and frequency of morphofunctional disorders ofthe cardiovascular system in children with CAKUT syndrome and optimize their medical follow-up. PATIENTS AND METHODS. 120 children were examined-90 with CAKUT syndrome (group 1) (24 - the doubling of the urinary tract, 36 - with congenital hydronephrosis, 30 - with polycystic kidney disease), and 30 practically healthy children (group 2). In group 1, there were 38 (42.2%) boys and 52 (57.8%) girls aged 4 to 16 years (average age 8±5.82 years), in group 2-13 (43.3%) boys and 17 (56.7%) girls aged 4 to 15 years (average age 6±6.73 years). A comprehensive examination of the urinary and cardiovascular systems was performed using ultrasound diagnostics and Holter monitoring of ECG and blood pressure. Statisti­cal processing was performed using the program "Statistica 8.0"("Stat Soft Inc., USA"). RESULTS. In CAKUT syndrome, often chronic infection was registered in children with a doubling of MVP (91.7%), hydronephrosis (88.9%). Persistent and increased crystalluria was observed in every third patient (33.3%) with a doubling of MVP, in 47.2% of children with hydronephrosis, and in almost 2/3 of patients (73.3%) with the polycystic disease. In children with CAKUT syndrome, congenital heart disease was de­tected in 15.0% of cases, with a high frequency of small heart abnormalities with a predominance ofthe left ventricular false chord (38.9%) and mitral valve prolapse (33.6%). CONCLUSION. The data obtained by us justify the need to include in the standard of dispensary observation of children with urinary tract congenital malformation examination by a pediatric cardiologist 1 -2 times a year with additional examination ofthe cardiovascular system (ECG, heart ultrasound, and daily blood pressure monitoring).

Publisher

Non-profit organization Nephrology

Subject

Nephrology

Reference26 articles.

1. Vemulakonda V, Yiee J, Wilcox DT. Prenatal hydroneph­rosis: postnatal evaluation and management. Curr Urol Rep 2014;15(8):430. doi: 10.1007/s11934-014-0430-5

2. Chugunova OL, Cherkasova SV, Tumanova EL et al. Polycystic kidney disease in infants and young children: problems of diag­nosis, management and treatment. Pediatrics 2015;94(3):88-94 (In Russ.)

3. Narayanan R, Shankar B, Kulkarni CD. Localized renal cystic disease. Indian JUro/2015;31:146-147. doi: 10.4103/0970­1591.152923

4. Averyanova Nl, Dolotkazina EV, Shirinkin AB, Balueva LG. Analysis ofthe frequency and nature of congenital pathology of the kidneys in children according to postnatal ultrasound screening. Modern problems of science and education 2017;6. URL: http://science-education.ru/ru/article/view?ld=27306 (In Russ.)

5. Ignatova MS, Morozov SL, Kryganova ТА et al. Modern ideas about congenital anomalies of the organs of the urinary system (CAKUT syndrome) in children. Clinical Nephrology 2013;2:58-64 (In Russ.)

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