500 likes | 992 Views
Improving Management of Secondary Hyperparathyroidism (SHPT) in Non-Dialysis Patients. CKD Is a Global Burden With Major Implications. CKD-MBD. Pathophysiology of CKD-MBD. Biochemical Phenotype of Disordered Mineral Metabolism in CKD. SHPT Is a Component of CKD-MBD Pathophysiology.
E N D
Improving Management of Secondary Hyperparathyroidism (SHPT) in Non-Dialysis Patients
Biochemical Phenotype of Disordered Mineral Metabolism in CKD
Vitamin D Metabolism: 1,25(OH)2 D Levels Are Tightly Regulated
Low Levels Of 25(OH)D (Calcifediol) Increase the Risk of Disease Progression and Mortality in Patients With CKD
Relationship Between 25(OH)D and PTH Before and After Treatment With Vitamin D and Calcium for 8 Weeks
Management of Bone Mineral Parameters Remains the Therapeutic Goal
Vitamin D Receptor Activators Did Not Improve CV Outcomes but Increased Hypercalcemia Risk
Ergocalciferol vs Paricalcitol for SHPT in CKD Stages 3 and 4
Calcifediol ER Increases 25(OH)D Levels And Reduces iPTH in Patients With Non-Dialysis CKD
Calcifediol ER Increased Serum Total 25-Hydroxyvitamin D: 1-Year Results
Calcifediol ER Has an Inconsequential Impact on Serum Calcium and Phosphorus