Cyclosporine Monitoring

Author:

Taylor William J.1,Robinson J. Daniel2,Burckart Gilbert J.3,Canafax Daniel M.4,Yee Gary C.5

Affiliation:

1. Neurology, College of Medicine, University of South Alabama, Mobile, AL 36688

2. Center for Computer Applications in Pharmacy, University of Florida, Gainesville, Fl. 32601

3. Pharmacy and Pediatrics, Clinical Pharmacokinetics Laboratory, 807 Salk Hall, University of Pittsburgh, Pittsburgh, PA 15261

4. Organ Transplant Pharmacist, University of Minnesota, Minneapolis, MN

5. Clinical Pharmacology, Division of Clinical Research, Fred Hutchinson Cancer Research Center, 1124 Columbia Street, Seattle, WA.

Abstract

Cyclosporine is an important immunosuppressive agent in organ and bone marrow transplantation. The pharmacokinetics of cyclosporine are quite complex and are complicated by the availability of two assay systems that yield differing results. This article summarizes the views from two major solid organ transplant centers and one bone marrow transplant center on important cyclosporine monitoring questions. A general consensus exists in the four areas discussed that: (1) cyclosporine concentrations must be monitored due in part to the extreme variability in kinetics, (2) either blood or plasma can be used in monitoring programs, (3) the radioimmunoassay or high pressure liquid chromatography can be used in routine monitoring, and (4) the interpretation of cyclosporine concentrations must be performed in relation to patient variables that affect drug response and toxicity.

Publisher

SAGE Publications

Subject

Pharmacology (medical)

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