<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Shroff R</submitter><funding>Kidney Research UK</funding><funding>National Institute for Health Research (NIHR)</funding><funding>NIH</funding><pagination>1114-1127</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5837664</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>32(7)</volume><pubmed_abstract>In patients with chronic kidney disease (CKD), renal synthesis of active vitamin D [1,25-dihydroxyvitamin D (1,25(OH)2D)] declines and is associated with hypocalcaemia, secondary hyperparathyroidism and the spectrum of CKD-mineral and bone disorder (MBD). In advanced CKD, active vitamin D analogues, including alfacalcidol, calcitriol and paricalcitol, are routinely administered. There are few studies on the use of vitamin D analogues in children with CKD and on dialysis. It is difficult to define bone-specific outcomes that can guide treatment with active vitamin D analogues in children with CKD-MBD. A core working group (WG) of the European Society for Paediatric Nephrology (ESPN) CKD-MBD and Dialysis WGs has developed recommendations for the use of active vitamin D therapy in children wi</pubmed_abstract><journal>Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association</journal><pubmed_title>Clinical practice recommendations for treatment with active vitamin D analogues in children with chronic kidney disease Stages 2-5 and on dialysis.</pubmed_title><pmcid>PMC5837664</pmcid><funding_grant_id>RP39/2013</funding_grant_id><funding_grant_id>CDF-2016-09-038</funding_grant_id><funding_grant_id>KKR/Paed2017/01</funding_grant_id><funding_grant_id>ICA-CDRF-2016-02-057</funding_grant_id><pubmed_authors>Bacchetta J</pubmed_authors><pubmed_authors>Bakkaloglu S</pubmed_authors><pubmed_authors>European Society for Paediatric Nephrology Chronic</pubmed_authors><pubmed_authors>Stefanidis CJ</pubmed_authors><pubmed_authors>Wan M</pubmed_authors><pubmed_authors>Ariceta G</pubmed_authors><pubmed_authors>Klaus G</pubmed_authors><pubmed_authors>Nagler EV</pubmed_authors><pubmed_authors>Edefonti A</pubmed_authors><pubmed_authors>Schmitt CP</pubmed_authors><pubmed_authors>Cozzolino M</pubmed_authors><pubmed_authors>Shroff R</pubmed_authors><pubmed_authors>Haffner D</pubmed_authors><pubmed_authors>Vande Walle J</pubmed_authors></additional><is_claimable>false</is_claimable><name>Clinical practice recommendations for treatment with active vitamin D analogues in children with chronic kidney disease Stages 2-5 and on dialysis.</name><description>In patients with chronic kidney disease (CKD), renal synthesis of active vitamin D [1,25-dihydroxyvitamin D (1,25(OH)2D)] declines and is associated with hypocalcaemia, secondary hyperparathyroidism and the spectrum of CKD-mineral and bone disorder (MBD). In advanced CKD, active vitamin D analogues, including alfacalcidol, calcitriol and paricalcitol, are routinely administered. There are few studies on the use of vitamin D analogues in children with CKD and on dialysis. It is difficult to define bone-specific outcomes that can guide treatment with active vitamin D analogues in children with CKD-MBD. A core working group (WG) of the European Society for Paediatric Nephrology (ESPN) CKD-MBD and Dialysis WGs has developed recommendations for the use of active vitamin D therapy in children wi</description><dates><release>2017-01-01T00:00:00Z</release><publication>2017 Jul</publication><modification>2025-04-04T14:48:41.472Z</modification><creation>2025-04-04T14:48:41.472Z</creation></dates><accession>S-EPMC5837664</accession><cross_references><pubmed>28873971</pubmed><doi>10.1093/ndt/gfx080</doi></cross_references></HashMap>