Publication: Growth in children with chronic kidney disease: 13 years follow up study
| dc.contributor.author | Salević, Petar (56469660900) | |
| dc.contributor.author | Radović, Pavle (56469431600) | |
| dc.contributor.author | Milić, Nataša (7003460927) | |
| dc.contributor.author | Bogdanović, Radovan (7004665744) | |
| dc.contributor.author | Paripović, Dušan (14621764400) | |
| dc.contributor.author | Paripović, Aleksandra (35311948800) | |
| dc.contributor.author | Golubović, Emilija (6602901479) | |
| dc.contributor.author | Milosević, Biljana (22981084000) | |
| dc.contributor.author | Mulić, Bilsana (56469655800) | |
| dc.contributor.author | Peco-Antić, Amira (7004525216) | |
| dc.date.accessioned | 2025-06-12T20:03:49Z | |
| dc.date.available | 2025-06-12T20:03:49Z | |
| dc.date.issued | 2014 | |
| dc.description.abstract | Background: Growth retardation is one of the most visible comorbid conditions of chronic kidney disease (CKD) in children. To our knowledge, published data on longitudinal follow-up of growth in pediatric patients with CKD is lacking from the region of South-East Europe. Herein we report the results from the Serbian Pediatric Registry of Chronic Kidney Disease.; Methods: The data reported in the present prospective analysis were collected between 2000 and 2012. A total of 324 children with CKD were enrolled in the registry.; Results: Prevalence of growth failure at registry entry was 29.3 %. Mean height standard deviation scores (HtSDS) in children with stunting and those with normal stature were −3.00 [95 % confidence interval (CI) −3.21 to −2.79] and −0.08 (95 % CI −0.22 to 0.05) (p < 0.001), respectively. Children with hereditary nephropathy had worse growth at registration (−1.51; 95 % CI −1.97 to −1.04, p = 0.008). Those with CKD stages 4 and 5 before registration had more chance to have short stature at registration than those with CKD stages 2 and 3 [odds ratio (OR) = 0.458, CI 0.268–0.782, p = 0.004]. Dialysis was an independent negative predictor for maintaining optimal stature during the follow-up period (OR = 0.324, CI = 0.199–0.529, p < 0.001), while transplantation was an independent positive predictor for improvement of small stature during follow-up (OR = 3.706, CI = 1.785–7.696, p < 0.001).; Conclusion: Growth failure remains a significant problem in children with CKD, being worst in patients with hereditary renal disease. Growth is not improved by standard dialysis, but transplantation has a positive impact on growth in children. © 2014, Italian Society of Nephrology. | |
| dc.identifier.uri | https://doi.org/10.1007/s40620-014-0094-8 | |
| dc.identifier.uri | https://www.scopus.com/inward/record.uri?eid=2-s2.0-84920475408&doi=10.1007%2fs40620-014-0094-8&partnerID=40&md5=d0072c6cfbb9b2608372ac529989ac39 | |
| dc.identifier.uri | https://remedy.med.bg.ac.rs/handle/123456789/8504 | |
| dc.subject | Children | |
| dc.subject | Chronic kidney disease | |
| dc.subject | Dialysis | |
| dc.subject | Growth failure | |
| dc.subject | Transplantation | |
| dc.title | Growth in children with chronic kidney disease: 13 years follow up study | |
| dspace.entity.type | Publication |
