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| Title: | Cyclosporine short infusion and C2 monitoring in haematopoietic stem cell transplant recipients. |
| Author(s): | Hendriks, M.P. Blijlevens, N.M.A. (277354617) Schattenberg, A.V.M.B. (104035919) Burger, D.M. (119962306) Donnelly, J.P. (107876701) |
| Publication year: | 2006 |
| Document type: | Article / Letter to editor |
| Journal: | Bone Marrow Transplantation |
| ISSN: | 0268-3369 |
| Volume: | vol. 38 |
| Issue: | iss. 7 |
| Start page: | p. 521 |
| End page: | p. 525 |
| Abstract: | Blood concentrations of cyclosporine A (CsA) >or=800 microg/l measured 2 h post-dosing, the C2 concentration, is necessary to obtain a maximal pharmacological effect and correlates well with transplant-related complications such as transplant rejection and toxicity. In an open crossover study CsA blood levels were measured during 24 h to generate a pharmacokinetic profile on days 1, 8 and 15 after starting CsA infusion in 21 haematopoietic allogeneic stem cell transplant recipients who were receiving intravenously CsA 3 mg/kg/day either by continuous infusion or by 2 h infusion given every 12 h. C2 levels after the 2 h infusion correlated better than C1 or C3 levels with the area under the concentration-time curve from 0 to 4 h (r2=0.62). C2 levels >or=800 microg/l were also achieved for 20 out of 24 (83%) of cases after the 2 h infusion of CsA without any increase of CsA-related toxicity but for only three of the 23 patients (13%) after continuous infusion. Therefore, we recommend CsA infusions in 2 h during transplant and perform C2 monitoring to obtain therapeutic C2 levels >or=800 microg/l. |
| Subject: | CTR 2: Clinical Pharmacology and physiology NCMLS 1: Immunity, infection and tissue repair UMCN 3.2: Cognitive neurosciences UMCN 4.1: Microbial pathogenesis and host defense |
| Organization: | UMCN Extern Haematology Clinical Pharmacy |
| Appears in Collections: | Academic bibliography
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Please use this identifier to cite or link to this item:
http://hdl.handle.net/2066/50227
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