Cyclosporine pharmacokinetics and blood pressure responses after conversion to once-daily dosing in maintenance liver transplant patients
: In this six‐month randomized multicenter trial, we characterized cyclosporine pharmacokinetics and blood pressure profiles in maintenance liver transplant patients converting from twice‐daily to once‐daily cyclosporine dosing. A total of 60 patients were randomized as follows: group A (n = 14) ma...
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Published in | Clinical transplantation Vol. 22; no. 1; pp. 68 - 75 |
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Main Authors | , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Oxford, UK
Blackwell Publishing Ltd
01.01.2008
Blackwell |
Subjects | |
Online Access | Get full text |
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Summary: | : In this six‐month randomized multicenter trial, we characterized cyclosporine pharmacokinetics and blood pressure profiles in maintenance liver transplant patients converting from twice‐daily to once‐daily cyclosporine dosing. A total of 60 patients were randomized as follows: group A (n = 14) maintained twice‐daily dosing; group B (n = 24) converted to once‐daily dosing at the same total daily dose as pre‐conversion; and group C (n = 22) was treated the same as group B but with a 25% reduction in dose and C2 at two to three wk post‐conversion. After conversion to once‐daily dosing in groups B and C, trough blood levels (C0) did not change; whereas, C2 nearly doubled. The total daily area under the concentration–time curve AUC(0–24) increased by 29%. After the dose reduction in group C, the AUC(0–24) was similar to the pre‐conversion value. Hence, a 25–30% dose reduction can be considered after conversion to once‐daily dosing. In the study observation period in weeks 4–15, the median (25–75 percentile) C2 was 568 (469–750) ng/mL for group A; 1055 (840–1224) ng/mL for group B; and 764 (575–959) ng/mL for group C. Conversion to once‐daily dosing was associated with a decrease in nighttime mean arterial blood pressure. |
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Bibliography: | ArticleID:CTR747 istex:FE8B1837CABAF14FB13EF1766B47FCC6B40ED34C ark:/67375/WNG-B0XQ9NP5-0 Study sponsored by Novartis Pharmaceuticals ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-News-2 ObjectType-Feature-3 content type line 23 |
ISSN: | 0902-0063 1399-0012 |
DOI: | 10.1111/j.1399-0012.2007.00747.x |