Publication:
Growth in children with chronic kidney disease: 13 years follow up study

dc.contributor.authorSalević, Petar (56469660900)
dc.contributor.authorRadović, Pavle (56469431600)
dc.contributor.authorMilić, Nataša (7003460927)
dc.contributor.authorBogdanović, Radovan (7004665744)
dc.contributor.authorParipović, Dušan (14621764400)
dc.contributor.authorParipović, Aleksandra (35311948800)
dc.contributor.authorGolubović, Emilija (6602901479)
dc.contributor.authorMilosević, Biljana (22981084000)
dc.contributor.authorMulić, Bilsana (56469655800)
dc.contributor.authorPeco-Antić, Amira (7004525216)
dc.date.accessioned2025-06-12T20:03:49Z
dc.date.available2025-06-12T20:03:49Z
dc.date.issued2014
dc.description.abstractBackground: 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.urihttps://doi.org/10.1007/s40620-014-0094-8
dc.identifier.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-84920475408&doi=10.1007%2fs40620-014-0094-8&partnerID=40&md5=d0072c6cfbb9b2608372ac529989ac39
dc.identifier.urihttps://remedy.med.bg.ac.rs/handle/123456789/8504
dc.subjectChildren
dc.subjectChronic kidney disease
dc.subjectDialysis
dc.subjectGrowth failure
dc.subjectTransplantation
dc.titleGrowth in children with chronic kidney disease: 13 years follow up study
dspace.entity.typePublication

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