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https://open.uns.ac.rs/handle/123456789/6987
Pоljе DC-а | Vrеdnоst | Јеzik |
---|---|---|
dc.contributor.author | Salević P. | en_US |
dc.contributor.author | Radović P. | en_US |
dc.contributor.author | Milić, Nataša | en_US |
dc.contributor.author | Bogdanović R. | en_US |
dc.contributor.author | Paripović D. | en_US |
dc.contributor.author | Paripović A. | en_US |
dc.contributor.author | Golubović E. | en_US |
dc.contributor.author | Milošević, Bojana | en_US |
dc.contributor.author | Mulić B. | en_US |
dc.contributor.author | Peco-Antić A. | en_US |
dc.date.accessioned | 2019-09-30T08:58:52Z | - |
dc.date.available | 2019-09-30T08:58:52Z | - |
dc.date.issued | 2014-01-01 | - |
dc.identifier.issn | 11218428 | en_US |
dc.identifier.uri | https://open.uns.ac.rs/handle/123456789/6987 | - |
dc.description.abstract | © 2014, Italian Society of Nephrology. 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. | en |
dc.relation.ispartof | Journal of Nephrology | en |
dc.title | Growth in children with chronic kidney disease: 13 years follow up study | en_US |
dc.type | Journal/Magazine Article | en_US |
dc.identifier.doi | 10.1007/s40620-014-0094-8 | - |
dc.identifier.scopus | 2-s2.0-84920475408 | - |
dc.identifier.url | https://api.elsevier.com/content/abstract/scopus_id/84920475408 | - |
dc.description.version | Unknown | en_US |
dc.relation.lastpage | 544 | en |
dc.relation.firstpage | 537 | en |
dc.relation.issue | 5 | en |
dc.relation.volume | 27 | en |
item.fulltext | No Fulltext | - |
item.grantfulltext | none | - |
crisitem.author.dept | Katedra za farmaciju | - |
crisitem.author.parentorg | Medicinski fakultet | - |
Nаlаzi sе u kоlеkciјаmа: | MDF Publikacije/Publications |
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