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Indexed/Abstracted in: CAB, EMBASE, PubMed/MEDLINE, Science Citation Index Expanded (SciSearch), Scopus
Impact Factor 0,532
Online ISSN 1827-1715
Özdemir K. 1, Yilmaz E. 1, Dincel N.1, Bozabali S. 2, Apaydın S. 1, Gun Z. H. 1, Sozeri B. 1, Mir S. 1
1 Ege University School of Medicine, Department of Pediatric Nephrology, İzmir, Turkey;
2 Ege University School of Medicine, Department of Pediatric Cardiology, İzmir, Turkey
AIM: The prominent cause of mortality in children receiving dialysis treatment is cardiovascular diseases. Risk factors related to chronic renal disease, are effective in the development of cardiovascular diseases. The aim of study was to investigate cardiovascular system (CVS) involvement for functional and structural alterations in children receiving dialysis, and display any association between cardiovascular morbidity and uremic toxins.
METHODS: 20 dialysis patients and 20 healthy controls were included to the study. Clearance of small, middle and large molecularweight uremic toxins was evaluated in blood samples collected 30 minutes before(D0) and 2 hour after dialysis(D2), and change value was calculated as; D0-D2/ D0. Cardiovascular involvement was determined by comparing arterial stiffness, Carotid intimamedia thickness (CIMT) and left ventricular mass index (LVMI) with the control group.
RESULTS: Four patients receiving hemodialysis and two patients in continuous ambulatory peritoneal dialysis (CAPD) group who have significant differences in all functional and structural parameters were detected. 4 dialysis-patients with detected cardiovascular disease have distinctively lower beta-2 micro globulin and homocysteine clearances compared to the patients with no CVS involvement.
CONCLUSION: The clearance of middle and large molecular-weight substances should be closely monitored in children receiving dialysis.