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dc.contributor.authorDrube, Jens
dc.contributor.authorWan, Mandy
dc.contributor.authorBonthuis, Marjolein
dc.contributor.authorWuhl, Elke
dc.contributor.authorBacchetta, Justine
dc.contributor.authorSantos, Fernando
dc.contributor.authorGrenda, Ryszard
dc.contributor.authorEdefonti, Alberto
dc.contributor.authorHarambat, Jerome
dc.contributor.authorShroff, Rukshana
dc.contributor.authorTonshoff, Burkhard
dc.contributor.authorHaffner, Dieter
dc.contributor.authorSchnabel, D.
dc.contributor.authorLinglart, A.
dc.contributor.authorRees, L.
dc.contributor.authorCochat, P.
dc.contributor.authorBrauner, C.
dc.contributor.authorRenault, D.
dc.contributor.authorRomano, L. N.
dc.contributor.authorColling, G.
dc.contributor.authorPrytula, A.
dc.contributor.authorLeifheit-Nestler, M.
dc.contributor.authorKlaus, G.
dc.contributor.authorSchmitt, C. P.
dc.contributor.authorStabouli, S.
dc.contributor.authorReusz, G.
dc.contributor.authorVerrina, E.
dc.contributor.authorGroothoff, J.
dc.contributor.authorAnton-Gamero, M.
dc.contributor.authorPetrosyan, E.
dc.contributor.authorBakkaloglu, S. A.
dc.contributor.authorDursun, I.
dc.contributor.authorBooth, C.
dc.contributor.authorAufricht, C.
dc.contributor.authorVande Walle, J.
dc.contributor.authorVondrak, K.
dc.contributor.authorHoltta, T.
dc.contributor.authorRanchin, B.
dc.contributor.authorFischbach, M.
dc.contributor.authorSchmitt, C. P.
dc.contributor.authorKlaus, G.
dc.contributor.authorStefanidis, C.
dc.contributor.authorKyriakou, A.
dc.contributor.authorStabouli, S.
dc.contributor.authorPrintza, N.
dc.contributor.authorPaglialonga, F.
dc.contributor.authorVerrina, E.
dc.contributor.authorVidal, E.
dc.contributor.authorAllinovi, M.
dc.contributor.authorJankauskiene, A.
dc.contributor.authorZurowska, A.
dc.contributor.authorFaria, M. Do Sameiro
dc.contributor.authorAriceta, G.
dc.contributor.authorSartz, L.
dc.contributor.authorBakkaloglu, S.
dc.contributor.authorBayazit, A. K.
dc.contributor.authorDuzova, A.
dc.contributor.authorKnops, N.
dc.contributor.authorRaees, A.
dc.contributor.authorZieg, J.
dc.contributor.authorPape, L.
dc.contributor.authorMelk, A.
dc.contributor.authorDello, L.
dc.contributor.authorGuzzo, I.
dc.contributor.authorGhio, L.
dc.contributor.authorMurer, L.
dc.contributor.authorPeruzzi, L.
dc.contributor.authorBouts, A.
dc.contributor.authorCornelissen, M.
dc.contributor.authorPetrosyan, E.
dc.contributor.authorLopez-Baez, Victor
dc.contributor.authorAriceta, G.
dc.contributor.authorSoylemezoglu, O.
dc.contributor.authorTopaloglu, R.
dc.contributor.authorBayazit, A. K.
dc.contributor.authorDuzova, A.
dc.contributor.authorChristian, M.
dc.contributor.authorMarks, S.
dc.contributor.authorNephrology, European Soc Paediat
dc.contributor.authorD, Chronic Kidney Dis Mineral Bone
dc.contributor.authorWorkin, Dialysis & Transplantat
dc.date.accessioned2021-06-03T05:20:10Z
dc.date.available2021-06-03T05:20:10Z
dc.date.issued2019
dc.identifier.issn1759-5061
dc.identifier.urihttp://dx.doi.org/10.1038/s41581-019-0161-4
dc.identifier.urihttp://hdl.handle.net/11655/23995
dc.description.abstractAchieving normal growth is one of the most challenging problems in the management of children with chronic kidney disease (CKD). Treatment with recombinant human growth hormone (GH) promotes longitudinal growth and likely enables children with CKD and short stature to reach normal adult height. Here, members of the European Society for Paediatric Nephrology (ESPN) CKD-Mineral and Bone Disorder (MBD), Dialysis and Transplantation working groups present clinical practice recommendations for the use of GH in children with CKD on dialysis and after renal transplantation. These recommendations have been developed with input from an external advisory group of paediatric endocrinologists, paediatric nephrologists and patient representatives. We recommend that children with stage 3-5 CKD or on dialysis should be candidates for GH therapy if they have persistent growth failure, defined as a height below the third percentile for age and sex and a height velocity below the twenty-fifth percentile, once other potentially treatable risk factors for growth failure have been adequately addressed and provided the child has growth potential. In children who have received a kidney transplant and fulfil the above growth criteria, we recommend initiation of GH therapy 1 year after transplantation if spontaneous catch-up growth does not occur and steroid-free immunosuppression is not a feasible option. GH should be given at dosages of 0.045-0.05 mg/kg per day by daily subcutaneous injections until the patient has reached their final height or until renal transplantation. In addition to providing treatment recommendations, a cost-effectiveness analysis is provided that might help guide decision-making.
dc.language.isoen
dc.relation.isversionof10.1038/s41581-019-0161-4
dc.rightsAttribution 4.0 United States
dc.rightsinfo:eu-repo/semantics/openAccess
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.titleClinical Practice Recommendations For Growth Hormone Treatment In Children With Chronic Kidney Disease
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion
dc.relation.journalNature Reviews Nephrology
dc.contributor.departmentİç Hastalıkları
dc.identifier.volume15
dc.identifier.issue9
dc.description.indexWoS


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Attribution 4.0 United States
Aksi belirtilmediği sürece bu öğenin lisansı: Attribution 4.0 United States