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Status: Bibliographieeintrag

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Verfasst von:Bacchetta, Justine [VerfasserIn]   i
 Schmitt, Claus P. [VerfasserIn]   i
 Ariceta, Gema [VerfasserIn]   i
 Bakkaloglu, Sevcan A. [VerfasserIn]   i
 Groothoff, Jaap [VerfasserIn]   i
 Wan, Mandy [VerfasserIn]   i
 Vervloet, Marc [VerfasserIn]   i
 Shroff, Rukshana [VerfasserIn]   i
 Haffner, Dieter [VerfasserIn]   i
Titel:Cinacalcet use in paediatric dialysis
Titelzusatz:a position statement from the European Society for Paediatric Nephrology and the Chronic Kidney Disease-Mineral and Bone Disorders Working Group of the ERA-EDTA
Verf.angabe:Justine Bacchetta, Claus Peter Schmitt, Gema Ariceta, Sevcan A. Bakkaloglu, Jaap Groothoff, Mandy Wan, Marc Vervloet, Rukshana Shroff, and Dieter Haffner, on behalf of the European Society for Paediatric Nephrology and the Chronic Kidney Disease-Mineral and Bone Disorders and Dialysis Working Group of the ERA-EDTA
E-Jahr:2020
Jahr:22 October 2019
Jahr des Originals:2019
Umfang:18 S.
Fussnoten:Gesehen am 29.10.2020
Titel Quelle:Enthalten in: Nephrology, dialysis, transplantation
Ort Quelle:Oxford : Oxford Univ. Press, 1986
Jahr Quelle:2020
Band/Heft Quelle:35(2020), 1, Seite 47-64
ISSN Quelle:1460-2385
Abstract:Secondary hyperparathyroidism (SHPT) is an important complication of advanced chronic kidney disease (CKD) in children, which is often difficult to treat with conventional therapy. The calcimimetic cinacalcet is an allosteric modulator of the calcium-sensing receptor. It has proven to be effective and safe in adults to suppress parathyroid hormone (PTH), but data on its use in children are limited. To date, studies in children only consist of two randomized controlled trials, nine uncontrolled interventional or observational studies, and case reports that report the efficacy of cinacalcet as a PTH-lowering compound. In 2017, the European Medical Agency approved the use of cinacalcet for the treatment of SHPT in children on dialysis in whom SHPT is not adequately controlled with standard therapy. Since evidence-based guidelines are so far lacking, we present a position statement on the use of cinacalcet in paediatric dialysis patients based on the available evidence and opinion of experts from the European Society for Paediatric Nephrology, Chronic Kidney Disease-Mineral and Bone Disorder and Dialysis Working Groups, and the ERA-EDTA. Given the limited available evidence the strength of these statements are weak to moderate, and must be carefully considered by the treating physician and adapted to individual patient needs as appropriate. Audit and research recommendations to study key outcome measures in paediatric dialysis patients receiving cinacalcet are suggested.
DOI:doi:10.1093/ndt/gfz159
URL:Bitte beachten Sie: Dies ist ein Bibliographieeintrag. Ein Volltextzugriff für Mitglieder der Universität besteht hier nur, falls für die entsprechende Zeitschrift/den entsprechenden Sammelband ein Abonnement besteht oder es sich um einen OpenAccess-Titel handelt.

Volltext ; Verlag: https://doi.org/10.1093/ndt/gfz159
 Volltext: https://academic.oup.com/ndt/article-lookup/doi/10.1093/ndt/gfz159
 DOI: https://doi.org/10.1093/ndt/gfz159
Datenträger:Online-Ressource
Sprache:eng
Sach-SW:Calcimimetic Agents
 Child
 Chronic Kidney Disease-Mineral and Bone Disorder
 cinacalcet
 Cinacalcet
 CKD-MBD
 consensus statement
 dialysis
 Evidence-Based Medicine
 Humans
 Hyperparathyroidism, Secondary
 paediatrics
 Practice Guidelines as Topic
 Renal Dialysis
K10plus-PPN:1737358336
Verknüpfungen:→ Zeitschrift

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