2004Therapeutic Drug MonitoringRequires access

Using Established Immunosuppressant Therapy Effectively

Leslie M. Shaw, Arthur Nawrocki, Magdalena Korecka, Sandra Solari, Ju‐Seop Kang

Open publisher page 48 citations

Abstract

Getting the most effective use of immunosuppressant medications in transplant patients continues to be a major challenge in clinical practice. This need applies to established immunosuppressants just as it does to new agents. In this review this principle is illustrated for mycophenolic acid, the active metabolite of mycophenolate mofetil, the most commonly used immunosuppressant, in various combinations with other immunosuppressants, in current clinical practice. Defining, as rigorously as possible, the requirements for effective therapeutic monitoring of MPA is an important goal given all of the changes in immunosuppressive drug regimens. This review will focus on the major factors known to influence MPA clearance including: UDP-glucuronyltransferases, enterohepatic circulation, MPA free fraction, the effect of time posttransplantation, concomitant administration of immunosuppressant drugs. The significant variability of MPA pharmacokinetics and the need to deepen our understanding of the influence of these factors on MPA clearance are strong reasons why additional clinical trials are needed to define best practice therapeutic drug monitoring of this drug.

About this research paper

What this paper is about

Getting the most effective use of immunosuppressant medications in transplant patients continues to be a major challenge in clinical practice. This need applies to established immunosuppressants just as it does to new agents. In this review this principle is illustrated for mycophenolic acid, the active metabolite of mycophenolate mofetil, the most commonly used immunosuppressant, in various combinations with other immunosuppressants, in current clinical practice. Defining, as rigorously as possible, the requirements for effective therapeutic monitoring of MPA is an important goal given all of the changes in immunosuppressive drug regimens. This review will focus on the major factors known to influence MPA clearance including: UDP-glucuronyltransferases, enterohepatic circulation, MPA free fraction, the effect of time posttransplantation, concomitant administration of immunosuppressant drugs. The significant variability of MPA pharmacokinetics and the need to deepen our understanding of the influence of these factors on MPA clearance are strong reasons why additional clinical trials are needed to define best practice therapeutic drug monitoring of this drug.

Why it matters

OpenAlex reports 48 citations for this work. Citation counts describe recorded attention and do not establish research quality.

Key contribution

A contribution statement is not available in the OpenAlex record.

Method / approach

Method details are not available in the OpenAlex metadata.

Main findings

Findings are not separately available in the OpenAlex metadata.

Limitations

Limitations are not available in the OpenAlex metadata.

Applications

Application details are not available in the OpenAlex metadata.

Available abstract

Getting the most effective use of immunosuppressant medications in transplant patients continues to be a major challenge in clinical practice. This need applies to established immunosuppressants just as it does to new agents. In this review this principle is illustrated for mycophenolic acid, the active metabolite of mycophenolate mofetil, the most commonly used immunosuppressant, in various combinations with other immunosuppressants, in current clinical practice. Defining, as rigorously as possible, the requirements for effective therapeutic monitoring of MPA is an important goal given all of the changes in immunosuppressive drug regimens. This review will focus on the major factors known to influence MPA clearance including: UDP-glucuronyltransferases, enterohepatic circulation, MPA free fraction, the effect of time posttransplantation, concomitant administration of immunosuppressant drugs. The significant variability of MPA pharmacokinetics and the need to deepen our understanding of the influence of these factors on MPA clearance are strong reasons why additional clinical trials are needed to define best practice therapeutic drug monitoring of this drug.

Key concepts: Mycophenolic acid, Medicine, Therapeutic drug monitoring, Mycophenolate, Pharmacology, Active metabolite, Drug, Pharmacokinetics

Related papers

Back to paper searchBrowse research topicsOriginal source
Using Established Immunosuppressant Therapy Effectively — Research Paper | ScholarLens