Effect of diltiazem on the pharmacokinetics of microemulsion cyclosporine A in renal transplantation

Objective: Diltiazem might be used as a cyclosporine A (CsA)-sparing agent. There is evidence that CsA (C 2) level is the best single point blood sampling for monitoring the CsA level. The authors, therefore, studied the effect of diltiazem on the pharmacokinetics (PK) of CsA, including C 2, in rena...

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Main Authors: Sakarn Bunnag, Kriengsak Vareesangthip, Leena Ong-ajyooth
Other Authors: Rajavithi Hospital
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Published: 2018
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Online Access:https://repository.li.mahidol.ac.th/handle/123456789/23656
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spelling th-mahidol.236562018-08-20T14:13:43Z Effect of diltiazem on the pharmacokinetics of microemulsion cyclosporine A in renal transplantation Sakarn Bunnag Kriengsak Vareesangthip Leena Ong-ajyooth Rajavithi Hospital Mahidol University Medicine Objective: Diltiazem might be used as a cyclosporine A (CsA)-sparing agent. There is evidence that CsA (C 2) level is the best single point blood sampling for monitoring the CsA level. The authors, therefore, studied the effect of diltiazem on the pharmacokinetics (PK) of CsA, including C 2, in renal transplant patients. Material and Method: Twenty-five CsA-treated renal transplant patients, with neither diseases nor agents that alter the PK of CsA, were enrolled in the present study. The PK of CsA was studied in all patients before and 2 weeks after taking diltiazem. Results: The area under the concentration-time curve (AUC) of CsA was obtained by 2 methods, AUC 0-4 and AUC 0-12. Before taking diltiazem, the correlation (r) between C 0 with AUC 0-4 and C 0 with AUC 0-12 were 0.799 and 0.871, respectively (p = 0.01), r between C 2 with AUC 0-4 and C 2 with AUC 0-12 were 0.988 and 0.956, respectively (p = 0.01). Time to maximum concentration (Tmax) of CsA was at 1.5 hr (1.5-4.0 hr) [median (range)]. After two weeks of taking diltiazem, r between C 2 with AUC 0-4 and C 0 with AUC 0-12 were 0.577 and 0.784, respectively (p = 0.01), r between C 2 with AUC 0-4 and C 2 with AUC 0-12 were 0.988 and 0.896, respectively (p = 0.01). Tmax of CsA was at 1.5 hr (1.5-4.0 hr) [median (range)]. The dosage of CsA could be reduced by 25.8% to maintain the same levels of C 0 and C 2 in the same patients after taking diltiazem. Conclusion: Diltiazem slightly altered the correlation between C 2 with AUC of CsA. This indicates that C 2 is the best single point blood sampling to monitor the therapeutic levels of CsA in renal transplant patients who are taking diltiazem. 2018-08-20T07:13:43Z 2018-08-20T07:13:43Z 2006-08-01 Article Journal of the Medical Association of Thailand. Vol.89, No.SUPPL. 2 (2006) 01252208 01252208 2-s2.0-33845439899 https://repository.li.mahidol.ac.th/handle/123456789/23656 Mahidol University SCOPUS https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=33845439899&origin=inward
institution Mahidol University
building Mahidol University Library
continent Asia
country Thailand
Thailand
content_provider Mahidol University Library
collection Mahidol University Institutional Repository
topic Medicine
spellingShingle Medicine
Sakarn Bunnag
Kriengsak Vareesangthip
Leena Ong-ajyooth
Effect of diltiazem on the pharmacokinetics of microemulsion cyclosporine A in renal transplantation
description Objective: Diltiazem might be used as a cyclosporine A (CsA)-sparing agent. There is evidence that CsA (C 2) level is the best single point blood sampling for monitoring the CsA level. The authors, therefore, studied the effect of diltiazem on the pharmacokinetics (PK) of CsA, including C 2, in renal transplant patients. Material and Method: Twenty-five CsA-treated renal transplant patients, with neither diseases nor agents that alter the PK of CsA, were enrolled in the present study. The PK of CsA was studied in all patients before and 2 weeks after taking diltiazem. Results: The area under the concentration-time curve (AUC) of CsA was obtained by 2 methods, AUC 0-4 and AUC 0-12. Before taking diltiazem, the correlation (r) between C 0 with AUC 0-4 and C 0 with AUC 0-12 were 0.799 and 0.871, respectively (p = 0.01), r between C 2 with AUC 0-4 and C 2 with AUC 0-12 were 0.988 and 0.956, respectively (p = 0.01). Time to maximum concentration (Tmax) of CsA was at 1.5 hr (1.5-4.0 hr) [median (range)]. After two weeks of taking diltiazem, r between C 2 with AUC 0-4 and C 0 with AUC 0-12 were 0.577 and 0.784, respectively (p = 0.01), r between C 2 with AUC 0-4 and C 2 with AUC 0-12 were 0.988 and 0.896, respectively (p = 0.01). Tmax of CsA was at 1.5 hr (1.5-4.0 hr) [median (range)]. The dosage of CsA could be reduced by 25.8% to maintain the same levels of C 0 and C 2 in the same patients after taking diltiazem. Conclusion: Diltiazem slightly altered the correlation between C 2 with AUC of CsA. This indicates that C 2 is the best single point blood sampling to monitor the therapeutic levels of CsA in renal transplant patients who are taking diltiazem.
author2 Rajavithi Hospital
author_facet Rajavithi Hospital
Sakarn Bunnag
Kriengsak Vareesangthip
Leena Ong-ajyooth
format Article
author Sakarn Bunnag
Kriengsak Vareesangthip
Leena Ong-ajyooth
author_sort Sakarn Bunnag
title Effect of diltiazem on the pharmacokinetics of microemulsion cyclosporine A in renal transplantation
title_short Effect of diltiazem on the pharmacokinetics of microemulsion cyclosporine A in renal transplantation
title_full Effect of diltiazem on the pharmacokinetics of microemulsion cyclosporine A in renal transplantation
title_fullStr Effect of diltiazem on the pharmacokinetics of microemulsion cyclosporine A in renal transplantation
title_full_unstemmed Effect of diltiazem on the pharmacokinetics of microemulsion cyclosporine A in renal transplantation
title_sort effect of diltiazem on the pharmacokinetics of microemulsion cyclosporine a in renal transplantation
publishDate 2018
url https://repository.li.mahidol.ac.th/handle/123456789/23656
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