Using known drug interactions to manage supratherapeutic calcineurin inhibitor concentrations

Clin Transplant. 2017 Nov;31(11). doi: 10.1111/ctr.13098. Epub 2017 Sep 18.

Abstract

Objectives: To summarize the available body of evidence guiding the management of supratherapeutic concentrations of calcineurin inhibitors (CNI) using cytochrome P450 (CYP450) enzyme inducers.

Methods: A nondate restricted literature search within MEDLINE, Embase, and Scopus was performed using the terms "cyclosporine," "tacrolimus," "calcineurin inhibitor," "toxicity," "pharmacokinetics," "carbamazepine," "rifampin," "phenytoin," and "phenobarbital." Additional references were identified from a review of all included citations. All English-language reports that describe the management of supratherapeutic CNI concentrations with interventions targeting metabolic induction using CYP450 enzyme inducers were evaluated.

Results: A total of 10 publications were identified in which a CYP450 enzyme inducer was utilized intentionally to enhance CNI clearance in the setting of supratherapeutic concentrations; 7 case reports describe the use of phenytoin and 3 case reports describe the use of phenobarbital. Patient demographics, dosing strategies employed, and reported efficacy across this series of publications are heterogeneous; however, both agents appear to be well-tolerated when used in this setting.

Conclusions: There is a paucity of published data on the use of CYP450 enzyme inducers for the management of supratherapeutic CNI concentrations. While routine use of this approach cannot be recommended, thorough risk-benefit analyses should be performed in the management of each such clinical scenario.

Keywords: calcineurin inhibitor; complication; immunosuppressant; pharmacokinetics/pharmacodynamics; side effects.

Publication types

  • Review

MeSH terms

  • Calcineurin Inhibitors / therapeutic use*
  • Drug Interactions*
  • Graft Rejection / drug therapy*
  • Graft Rejection / etiology
  • Humans
  • Kidney Transplantation / adverse effects*

Substances

  • Calcineurin Inhibitors