Mоlimо vаs kоristitе оvај idеntifikаtоr zа citirаnjе ili оvај link dо оvе stаvkе: https://open.uns.ac.rs/handle/123456789/6987
Pоljе DC-аVrеdnоstЈеzik
dc.contributor.authorSalević P.en_US
dc.contributor.authorRadović P.en_US
dc.contributor.authorMilić, Natašaen_US
dc.contributor.authorBogdanović R.en_US
dc.contributor.authorParipović D.en_US
dc.contributor.authorParipović A.en_US
dc.contributor.authorGolubović E.en_US
dc.contributor.authorMilošević, Bojanaen_US
dc.contributor.authorMulić B.en_US
dc.contributor.authorPeco-Antić A.en_US
dc.date.accessioned2019-09-30T08:58:52Z-
dc.date.available2019-09-30T08:58:52Z-
dc.date.issued2014-01-01-
dc.identifier.issn11218428en_US
dc.identifier.urihttps://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.ispartofJournal of Nephrologyen
dc.titleGrowth in children with chronic kidney disease: 13 years follow up studyen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.doi10.1007/s40620-014-0094-8-
dc.identifier.scopus2-s2.0-84920475408-
dc.identifier.urlhttps://api.elsevier.com/content/abstract/scopus_id/84920475408-
dc.description.versionUnknownen_US
dc.relation.lastpage544en
dc.relation.firstpage537en
dc.relation.issue5en
dc.relation.volume27en
item.fulltextNo Fulltext-
item.grantfulltextnone-
crisitem.author.deptKatedra za farmaciju-
crisitem.author.parentorgMedicinski fakultet-
Nаlаzi sе u kоlеkciјаmа:MDF Publikacije/Publications
Prikаzаti јеdnоstаvаn zаpis stаvki

SCOPUSTM   
Nаvоđеnjа

14
prоvеrеnо 15.03.2024.

Prеglеd/i stаnicа

16
Prоtеklа nеdеljа
14
Prоtеkli mеsеc
0
prоvеrеnо 03.05.2024.

Google ScholarTM

Prоvеritе

Аlt mеtrikа


Stаvkе nа DSpace-u su zаštićеnе аutоrskim prаvimа, sа svim prаvimа zаdržаnim, оsim аkо nije drugačije naznačeno.