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Cinacalcet for Severe Secondary Hyperparathyroidism in Children with End-stage Kidney Disease.
Sheerah, Areej Adel; Al-Ahmed, Rafif Ali; El-Desoky, Sherif M; Alhasan, Khalid Abdulaziz; Albanna, Amr S; Shalaby, Mohamed A; Kari, Jameela Abdulaziz.
Afiliação
  • Sheerah AA; Department of Pediatrics, Pediatric Nephrology Unit, King Abdulaziz University Hospital, Jeddah, Saudi Arabia.
  • Al-Ahmed RA; Department of Pediatrics, Pediatric Nephrology Unit, King Abdulaziz University Hospital, Jeddah, Saudi Arabia.
  • El-Desoky SM; Department of Pediatrics, Pediatric Nephrology Unit; Faculty of Medicine, King Abdulaziz University, Jeddah, Saudi Arabia.
  • Alhasan KA; Department of Pediatrics, College of Medicine, King Saud University; Division of Pediatric Kidney Transplant, Organ Transplant Center, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
  • Albanna AS; King Abdullah International Medical Research Center, King Saud Bin Abdulaziz University for Health Sciences, Jeddah, Saudi Arabia.
  • Shalaby MA; Department of Pediatrics, Pediatric Nephrology Unit; Faculty of Medicine, King Abdulaziz University, Jeddah, Saudi Arabia.
  • Kari JA; Department of Pediatrics, Pediatric Nephrology Unit; Faculty of Medicine, King Abdulaziz University, Jeddah, Saudi Arabia.
Saudi J Kidney Dis Transpl ; 32(6): 1628-1636, 2021.
Article em En | MEDLINE | ID: mdl-35946275
ABSTRACT
Advanced chronic kidney disease with mineral and bone disorder have a significant obstacles to control serum bone profile [serum intact parathyroid hormone (iPTH), calcium and phosphorus] which subsequently have major effect on optimal bone strength, final adult height, and cardiovascular health. A retrospective, observational study, including a total of 36 children with end-stage kidney disease (ESKD). Fourteen children who were prescribed cinacalcet had been compared with the remaining 22 children who were managed with standard care. We report the efficacy and safety of cinacalcet for treatment of refractory secondary hyperparathyroidism (SHPT) in children with ESKD. After 6 months of cinacalcet treatment, the mean level of iPTH serum level decreased by 56% from 202 pmol/L [95% confidence interval (CI) 150-253] to 88 pmol/L (95% CI 41-136), compared to the change observed in the control group (P <0.001). None of our patients reported serious adverse effects or developed hypocalcemia. Cinacalcet could be an effective and safe alternative to treat severe SHPT in children with ESKD. Further long-term and large-scale studies are necessary to confirm its safety and efficacy.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Hiperparatireoidismo Secundário / Falência Renal Crônica Tipo de estudo: Diagnostic_studies / Etiology_studies / Observational_studies / Risk_factors_studies Limite: Adult / Child / Humans Idioma: En Revista: Saudi J Kidney Dis Transpl Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Hiperparatireoidismo Secundário / Falência Renal Crônica Tipo de estudo: Diagnostic_studies / Etiology_studies / Observational_studies / Risk_factors_studies Limite: Adult / Child / Humans Idioma: En Revista: Saudi J Kidney Dis Transpl Ano de publicação: 2021 Tipo de documento: Article