Children under continuous kidney replacement therapy have higher risk of vitamin D deficiency, finds research
A new study by Peace Dorothy Imani and team found that children who need continuous kidney replacement therapy (CKRT) are more likely to have osteopenia, fractures, and/or vitamin D deficiency. The findings of this study were published in the journal of BMC Nephrology. A typical feature of chronic kidney disease (CKD) is altered calcium and phosphate balance. The dysregulation of phosphate metabolism, parathyroid hormone (PTH), fibroblast growth factor (FGF)-23, expression of Klotho, and 1,25-dihydroxyvitamin D (1, 25 di-(OH)2D) causes this. The ensuing metabolic abnormalities are linked to both mineral bone disease (MBD) and an elevated risk of cardiovascular disease, which is a primary cause of morbidity and death in people with chronic kidney disease (CKD).
In critically unwell children with acute kidney injury (AKI), continuous kidney replacement therapy is used to manage hemodynamics and gradually remove fluid while permitting nutritional assistance. Recent consensus from the Acute Disease Quality Initiative (ADQI) defines acute kidney disease (AKD) as AKI lasting more than 7 days but less than 90 days. This study was to characterize the bone and metabolic results of juvenile AKD patients who needed more than 28 days of CKRT combined with localized citrate anticoagulation.
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