Literature DB >> 9160170

The use of other drugs to allow a lower dosage of cyclosporin to be used. Therapeutic and pharmacoeconomic considerations.

T E Jones1.   

Abstract

Since its discovery in 1970, and introduction into clinical practice in 1978, cyclosporin has become the most important immunosuppressive drug used to prevent organ transplant rejection. This has been achieved by virtue of the improved graft survival rates and adverse effect profiles in patients when compared with that of the older agents. Cyclosporin is substantially more expensive (both to provide and to monitor) however, and the magnitude of these costs may preclude its use, particularly where the transplant recipient is required to pay. Cyclosporin has a complex pharmacokinetic profile with poor absorption, extensive metabolism to more than 30 metabolites and considerable inter- and intrapatient variability. Many transplant centres routinely use drugs ("cyclosporin-sparing agents') to allow a reduction in the dosage of cyclosporin while maintaining therapeutic blood cyclosporin concentrations. The use of a second drug to affect the pharmacokinetic profile of a primary drug is not new, but the use of cyclosporin-sparing agents is a departure from previous practices in that this coprescription is primarily for economic reasons. The decision to use these agents (and the choice of agent) is based upon economic and other factors including the extent of the cyclosporin-sparing effect, the potential for additional therapeutic benefit and/or adverse effects. The coprescription of cyclosporin-sparing agents is ethically more acceptable where the transplant recipient is the economic beneficiary but where the savings accrue to a third party it is more difficult. Benefits to the community at large must be balanced against the risk of adverse effects to the patient. The use of cyclosporin-sparing agents may reduce compliance and hence, jeopardise transplant and/or recipient outcomes. The transplant recipient must be informed about the reasons for their use and advised to consult an experienced physician or pharmacist before altering the established drug regimen.

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Year:  1997        PMID: 9160170     DOI: 10.2165/00003088-199732050-00002

Source DB:  PubMed          Journal:  Clin Pharmacokinet        ISSN: 0312-5963            Impact factor:   6.447


  95 in total

1.  Survey of cyclosporine therapeutic ranges, assay methodology, and use of 'sparing agents' in Australasian transplant centers.

Authors:  T E Jones; R G Morris
Journal:  Ther Drug Monit       Date:  1997-12       Impact factor: 3.681

2.  Cost-containment strategies in transplantation: the utility of cyclosporine-ketoconazole combination therapy.

Authors:  O Odocha; B Kelly; S Trimble; C Murigande; R M Toussaint; C O Callender
Journal:  Transplant Proc       Date:  1996-04       Impact factor: 1.066

3.  Ketoconazole, cyclosporin metabolism, and renal transplantation.

Authors:  R M Ferguson; D E Sutherland; R L Simmons; J S Najarian
Journal:  Lancet       Date:  1982-10-16       Impact factor: 79.321

4.  Diltiazem and economic use of cyclosporin.

Authors:  H H Neumayer; K Wagner
Journal:  Lancet       Date:  1986-08-30       Impact factor: 79.321

5.  A double-blind randomized study of Sandimmun Neoral versus Sandimmun in new renal transplant recipients: results after 12 months. The International Sandimmun Neoral Study Group.

Authors:  D Niese
Journal:  Transplant Proc       Date:  1995-04       Impact factor: 1.066

6.  Diltiazem does not always increase blood cyclosporin concentration.

Authors:  T E Jones; R G Morris
Journal:  Br J Clin Pharmacol       Date:  1996-11       Impact factor: 4.335

7.  Diltiazem improves cyclosporine dosage in cystic fibrosis lung transplant recipients.

Authors:  H Shennib; J L Auger
Journal:  J Heart Lung Transplant       Date:  1994 Mar-Apr       Impact factor: 10.247

8.  Interpatient heterogeneity in expression of CYP3A4 and CYP3A5 in small bowel. Lack of prediction by the erythromycin breath test.

Authors:  K S Lown; J C Kolars; K E Thummel; J L Barnett; K L Kunze; S A Wrighton; P B Watkins
Journal:  Drug Metab Dispos       Date:  1994 Nov-Dec       Impact factor: 3.922

9.  Beneficial effects of conversion from cyclosporin to azathioprine after kidney transplantation.

Authors:  A A Hollander; J L van Saase; A M Kootte; W T van Dorp; H J van Bockel; L A van Es; F J van der Woude
Journal:  Lancet       Date:  1995-03-11       Impact factor: 79.321

10.  Cyclosporine pharmacokinetics in nephrotic and kidney-transplanted children.

Authors:  E Jacqz-Aigrain; C Montes; P Brun; C Loirat
Journal:  Eur J Clin Pharmacol       Date:  1994       Impact factor: 2.953

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  16 in total

Review 1.  Effects of the antifungal agents on oxidative drug metabolism: clinical relevance.

Authors:  K Venkatakrishnan; L L von Moltke; D J Greenblatt
Journal:  Clin Pharmacokinet       Date:  2000-02       Impact factor: 6.447

2.  Impact of the cyclosporine-ketoconazole interaction in children with steroid-dependent idiopathic nephrotic syndrome.

Authors:  Amr El-Husseini; Fathy El-Basuony; Ihab Mahmoud; Ahmed Donia; Hussein Sheashaa; Alaa Sabry; Nabil Hassan; Nagy Sayed-Ahmad; Mohamed Sobh
Journal:  Eur J Clin Pharmacol       Date:  2005-12-23       Impact factor: 2.953

Review 3.  Inhibition and induction of cytochrome P450 and the clinical implications.

Authors:  J H Lin; A Y Lu
Journal:  Clin Pharmacokinet       Date:  1998-11       Impact factor: 6.447

Review 4.  Clinically relevant drug-drug interactions in oncology.

Authors:  H L McLeod
Journal:  Br J Clin Pharmacol       Date:  1998-06       Impact factor: 4.335

Review 5.  Cytochrome P450 3A: ontogeny and drug disposition.

Authors:  S N de Wildt; G L Kearns; J S Leeder; J N van den Anker
Journal:  Clin Pharmacokinet       Date:  1999-12       Impact factor: 6.447

6.  Prevalence and nature of potential drug-drug interactions among kidney transplant patients in a German intensive care unit.

Authors:  Julia Amkreutz; Alexander Koch; Lukas Buendgens; Anja Muehlfeld; Christian Trautwein; Albrecht Eisert
Journal:  Int J Clin Pharm       Date:  2017-08-19

7.  Cyclosporin therapeutic drug monitoring--an established service revisited.

Authors:  Raymond G Morris
Journal:  Clin Biochem Rev       Date:  2003-05

Review 8.  Pharmacogenomics: a new paradigm to personalize treatments in nephrology patients.

Authors:  G Zaza; S Granata; F Sallustio; G Grandaliano; F P Schena
Journal:  Clin Exp Immunol       Date:  2009-11-24       Impact factor: 4.330

9.  Diltiazem co treatment with cyclosporine for induction of disease remission in sight-threatening non-infectious intraocular inflammation.

Authors:  Usama Shalaby
Journal:  Jpn J Ophthalmol       Date:  2016-12-10       Impact factor: 2.447

10.  Co-administration of cyclosporine and ketoconazole in idiopathic childhood nephrosis.

Authors:  Amr el-Husseini; Fathy el-Basuony; Ihab Mahmoud; Ahmed Donia; Nabil Hassan; Nagy Sayed-Ahmad; Mohamed Sobh
Journal:  Pediatr Nephrol       Date:  2004-07-06       Impact factor: 3.714

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