Sevelamer hydrochloride: A novel treatment of hyperphosphatemia associated with tumor lysis syndrome in children

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Etat: Public
Version: Final published version
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ID Serval
serval:BIB_41E43DE5FBF7
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Institution
Titre
Sevelamer hydrochloride: A novel treatment of hyperphosphatemia associated with tumor lysis syndrome in children
Périodique
Pediatric Blood and Cancer
Auteur⸱e⸱s
Abdullah  Shaker, Diezi  Manuel, Sung  Lillian, Dupuis  L. Lee, Geary  Denis, Abla  Oussama
ISSN
0008-5472
Statut éditorial
Publié
Date de publication
2008
Volume
51
Numéro
1
Pages
59-61
Langue
anglais
Résumé
Background. Sevelamer is a phosphate-binder used effectively for the treatment of hyperphosphatemia in patients treated with dialysis. Objectives. To describe the safety of sevelamer in children with hyperphosphatemia secondary to tumor lysis syndrome and the serum phosphate concentrations observed following its administration. Procedure. A retrospective chart review of all children with leukemia/lymphoma diagnosed between November 2002 and April 2004 who received sevelamer during their initial admission was conducted. We monitored the effects of sevelamer on serum phosphate concentration, calcium/phosphate product and renal function at hours 24, 48, and 72 from sevelamer initiation. Results. Thirteen patients received sevelamer during the Study period. Their median age was 13 years (range 2.7-17.9) and eight were boys. Nine children had acute lymphoblastic leukemia, one had acute myeloid leukemia and 3 had non-Hodgkin's lymphoma. The most frequently used dose of sevelamer was 400 mg orally twice daily. The median duration of sevelamer therapy was 2 days (range 1 -7). Two children were excluded from the efficacy analysis due to concurrent use of dialysis. Mean serum phosphate levels decreased after sevelamer administration, in eleven patients, from a baseline 2.2 mmol/L +/- 0.4 (95% Cl, 1.7-3.1) to 1.1 mmol/L +/- 0.2 at hour 72 (95%Cl, 0.6-1.5). The only toxicity attributed to sevelamer was mild vomiting in three patients. Conclusions. Sevelamer appears to be effective and tolerable for the treatment of hyperphosphatemia associated with tumor lysis syndrome.
Mots-clé
children, hyperphosphatemia, sevelamer, tumor lysis, Free Phosphate Binder, Calcium, Renagel(R)
Web of science
Création de la notice
13/10/2009 15:10
Dernière modification de la notice
20/08/2019 14:43
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