1
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      Is the interaction between ticlopidine and cyclosporin dose related? Report of three cases

      letter

      Read this article at

      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          Ticlopidine is an effective anti-platelet agent used for prevention of thrombosis (1–3). It was reported that treatment with ticlopidine at the dose of 250 mg daily in kidney transplant patients caused significant reduction of cyclosporin A (CsA) blood levels (4, 5). In heart transplant patients treated with higher doses of ticlopidine 500mg daily, it was found to cause significant decrease of cyclosporine concentration but not in those treated with only 250mg daily (1, 2). It was thought that ticlopidine interacts with cyclosporine metabolism at cytochrome P450 (1–3). We report three living kidney donor recipients whose blood level of cyclosporine decreased significantly under treatment with a very low dose of ticlopidine of 100 mg daily. The patients were on immunosuppressive treatment with steroids, CsA, and mycophenolate mofetil (MMF) or azathioprin. The total daily CsA dose was 125–150 mg. The patients developed severe hypertension 15 days to 4 months after kidney transplantation. Serum creatinine was normal except in patient number 2 (Table 1). Doppler ultrasonography confirmed significant stenosis of at least 70% degree in the artery of the transplanted kidney. Percutanuous transluminal angioplasty (PTA) with stent placement was performed. Anti-platelet treatment with aspirin (160mg/day) and ticlopidine (100mg/day) were given to prevent thrombosis. CsA blood levels were monitored by C0 (before morning dose) (Fig. 1). Under ticlopidine treatment, CsA blood levels decreased in patient 1 from 137 to 112 ng/ml, in patient 2 it decreased from 120 to 100 ng/ml, and in patient 3 it decreased from 131 to 106 ng/ml. Consequently CsA dose had been increased by 50–75 mg/day. No signs of acute kidney transplant rejection were observed. Fig. 1 Cyclosporin A blood levels (C0) and doses during 60 days of ticlopidine therapy: follow of blood CsA levels and doses in the three patients. Table 1 Characteristic of three patients with kidney transplantation and renal artery stenosis Characteristics Patient 1 Patient 2 Patient 3 Age (years) 18 26 20 Gender F M F HLA mismatch 3 3 3 Serum creatinine (mg/l) 8.5 15.4 7.1 Number of anti-hypertensive drugs 3 4 3 Diagnosis of stenosis after transplantation 2 months 15 days 4 months Date of PTA 2 months after the diagnosis 14 months after diagnosis 2 months after the diagnosis Note: PTA, percutanuous transluminal angioplasty. In summary: In kidney transplant patients, ticlopidine can cause a significant decrease in CsA blood level even at a low dose of ticlopidine. The interaction of ticlopidine with CsA seems to be not related to the doses. We recommend careful monitoring of CsA blood level in patients treated with ticlopidine.

          Related collections

          Most cited references5

          • Record: found
          • Abstract: found
          • Article: not found

          Clinically significant drug interactions with cyclosporin. An update.

          Since its approval in 1983 for immunosuppressive therapy in patients undergoing organ and bone marrow transplants, cyclosporin has had a major impact on organ transplantation. It has significantly improved 1-year and 2-year graft survival rates, and decreased morbidity in kidney, liver, heart, heart-lung and pancreas transplantation. Several studies have supported the efficacy of cyclosporin in preventing graft-versus-host disease in bone marrow transplantation. Cyclosporin is also possibly effective in treating diseases of autoimmune origin and as an antineoplastic agent. The introduction of therapeutic drug monitoring of cyclosporin was extremely useful because of the wide inter- and intraindividual variability in the pharmacokinetics of cyclosporin after oral or intravenous administration. Optimal long term use of cyclosporin requires careful monitoring of the blood (or plasma) concentrations. Sustained and clinically significant drug-drug interactions can occur during long term therapy with cyclosporin. The coadministration of multiple drugs with cyclosporin could result in graft rejection, renal dysfunction or other undesirable effects. Any interaction that leads to modified cyclosporin concentrations is of potential clinical importance. Cyclosporin itself may have significant effects on the pharmacokinetics and/or pharmacodynamics of coadministered drugs, such as digoxin, HMG-CoA reductase inhibitors and antineoplastic drugs affected by multidrug resistance. Many drugs have been shown to affect the pharmacokinetics and/or pharmacodynamics of cyclosporin. Interactions between cyclosporin and danazol, diltiazem, erythromycin, fluconazole, itraconazole, ketoconazole, metoclopramide, nicardipine, verapamil, carbamazepine, phenobarbital (phenobarbitone), phenytoin, rifampicin (rifampin) and cotrimoxazole (trimethoprim/sulfamethoxazole) are well documented in a large number of patients. Other interactions (such as those with aciclovir, estradiol and imipenem) are documented only in isolated case studies.
            Bookmark
            • Record: found
            • Abstract: not found
            • Article: not found

            Drug points. Probable interaction between cyclosporin A and low dose ticlopidine.

              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              A drug interaction study between ticlopidine and cyclosporin in heart transplant recipients.

              Previous uncontrolled studies have suggested an interaction between ticlopidine, a major antiplatelet agent, and cyclosporin in heart- and kidney-transplant recipients. The aims of this study were to examine in a randomised, double-blind fashion, the possible interaction between cyclosporin A and ticlopidine (250 mg per day) and the tolerability of this combination in heart-transplant recipients. Twenty heart-transplant recipients were randomised into either a treated or a placebo group. Blood samples were drawn for time-course evaluation of cyclosporin blood levels over a period of 12 h, following the morning intake of cyclosporin and, for platelet aggregation studies, before and after 14 days of ticlopidine administration. Twenty four-hour urine samples were collected for 6-beta-hydroxycortisol measurements, before and after 14 days of ticlopidine. Although given at half the recommended daily dosage, ticlopidine significantly reduced platelet aggregation. Pharmacokinetic parameters indicate that the bioavailability of cyclosporin A was not significantly modified by ticlopidine. However, one patient in the ticlopidine group was withdrawn because of a major fall in cyclosporin blood level within 3 days of treatment. Urinary excretion of 6-beta-hydroxycortisol was augmented after treatment in the ticlopidine group compared with the placebo group, suggesting that induction of drug metabolism might have occurred. Data also show quite a large intra-individual variability in cyclosporin bioavailability in the placebo group, suggesting that poor absorption of the drug formulation and/or poor compliance might have contributed to the decreased cyclosporin blood levels in the patient withdrawn from this study and in previous uncontrolled studies. Cyclosporin bioavailability was not clearly modified by a half dosage of ticlopidine in this study. We, however, recommend closely monitoring cyclosporin blood levels when prescribing ticlopidine. Further studies will be needed with new formulations of cyclosporin or when using the full dosage of ticlopidine.
                Bookmark

                Author and article information

                Journal
                Libyan J Med
                LJM
                The Libyan Journal of Medicine
                CoAction Publishing
                1993-2820
                1819-6357
                01 July 2010
                2010
                : 5
                : 10.3402/ljm.v5i0.5334
                Affiliations
                Nephrology department, Ibn Sina University Hospital, Rabat, Morocco
                Author notes
                Article
                LJM-5-5334
                10.3402/ljm.v5i0.5334
                3066751
                21483566
                ad9691c6-3fb9-4d0d-93ac-af3f425e590e
                © 2010 Tarik Sqalli Houssaïni et al.

                This is an Open Access article distributed under the terms of the Creative Commons Attribution-Noncommercial 3.0 Unported License, permitting all non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                Categories
                Letter to the Editor

                Medicine
                Medicine

                Comments

                Comment on this article