Tacrolimus-Related Neurologic and Renal Complications in Liver Transplantation: A Single-Center Experience

Among 71 patients, 19 (26.7%) experienced tacrolimus-related complications including 15 neurologic reactions and four problems with nephrotoxicity. Seven of these patients received grafts from cadaveric donors and 12 from living donors. Nine patients were children. The cohort included 5 female and 1...

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Published inTransplantation proceedings Vol. 38; no. 2; pp. 619 - 621
Main Authors Emiroglu, R., Ayvaz, I., Moray, G., Karakayali, H., Haberal, M.
Format Journal Article Conference Proceeding
LanguageEnglish
Published New York, NY Elsevier Inc 01.03.2006
Elsevier Science
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Abstract Among 71 patients, 19 (26.7%) experienced tacrolimus-related complications including 15 neurologic reactions and four problems with nephrotoxicity. Seven of these patients received grafts from cadaveric donors and 12 from living donors. Nine patients were children. The cohort included 5 female and 14 male subjects of mean age 26 ± 20 (min 6, max 65) years. The common indications for the liver transplantation were cholestatic and metabolic diseases in pediatric patients, and viral hepatitis in adult patients. Blood tacrolimus levels were within the normal range. All patients with neurologic complications received antiepileptic therapy and drug conversion to rapamycin in 4 cases and to cyclosporine (CsA) in 11 cases. Six cases with Wilson disease and all cases with tyrosinemia experienced neurologic complications, which reversed in all but one case. In four cases with nephrotoxicity, we switched to rapamycin. Renal function improved in all cases. Patients with Wilson disease and tyrosinemia were more susceptible to the neurologic side effects of tacrolimus. In these cases we recommend the use of drugs with fewer neurologic side effects. Tacrolimus also has nephrotoxic effects, which can be reversed by converting to rapamycin.
AbstractList Among 71 patients, 19 (26.7%) experienced tacrolimus-related complications including 15 neurologic reactions and four problems with nephrotoxicity. Seven of these patients received grafts from cadaveric donors and 12 from living donors. Nine patients were children. The cohort included 5 female and 14 male subjects of mean age 26 +/- 20 (min 6, max 65) years. The common indications for the liver transplantation were cholestatic and metabolic diseases in pediatric patients, and viral hepatitis in adult patients. Blood tacrolimus levels were within the normal range. All patients with neurologic complications received antiepileptic therapy and drug conversion to rapamycin in 4 cases and to cyclosporine (CsA) in 11 cases. Six cases with Wilson disease and all cases with tyrosinemia experienced neurologic complications, which reversed in all but one case. In four cases with nephrotoxicity, we switched to rapamycin. Renal function improved in all cases. Patients with Wilson disease and tyrosinemia were more susceptible to the neurologic side effects of tacrolimus. In these cases we recommend the use of drugs with fewer neurologic side effects. Tacrolimus also has nephrotoxic effects, which can be reversed by converting to rapamycin.
Among 71 patients, 19 (26.7%) experienced tacrolimus-related complications including 15 neurologic reactions and four problems with nephrotoxicity. Seven of these patients received grafts from cadaveric donors and 12 from living donors. Nine patients were children. The cohort included 5 female and 14 male subjects of mean age 26 ± 20 (min 6, max 65) years. The common indications for the liver transplantation were cholestatic and metabolic diseases in pediatric patients, and viral hepatitis in adult patients. Blood tacrolimus levels were within the normal range. All patients with neurologic complications received antiepileptic therapy and drug conversion to rapamycin in 4 cases and to cyclosporine (CsA) in 11 cases. Six cases with Wilson disease and all cases with tyrosinemia experienced neurologic complications, which reversed in all but one case. In four cases with nephrotoxicity, we switched to rapamycin. Renal function improved in all cases. Patients with Wilson disease and tyrosinemia were more susceptible to the neurologic side effects of tacrolimus. In these cases we recommend the use of drugs with fewer neurologic side effects. Tacrolimus also has nephrotoxic effects, which can be reversed by converting to rapamycin.
Author Moray, G.
Haberal, M.
Emiroglu, R.
Ayvaz, I.
Karakayali, H.
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  email: rektorluk@baskent-ank.edu.tr
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Issue 2
Keywords Center
Calcineurin inhibitor
Digestive system
Liver
Lactone
Homotransplantation
Macrolide
Kidney
Immunomodulator
Medicine
Experience
Treatment
Urinary system
Tacrolimus
Surgery
Complication
Graft
Immunosuppressive agent
Antibacterial agent
Kidney transplantation
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PublicationTitle Transplantation proceedings
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Elsevier Science
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Snippet Among 71 patients, 19 (26.7%) experienced tacrolimus-related complications including 15 neurologic reactions and four problems with nephrotoxicity. Seven of...
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SubjectTerms Antibacterial agents
Antibiotics. Antiinfectious agents. Antiparasitic agents
Biological and medical sciences
Cyclosporine - therapeutic use
Fundamental and applied biological sciences. Psychology
Fundamental immunology
Hepatolenticular Degeneration - surgery
Humans
Immunosuppressive Agents - adverse effects
Kidney Transplantation - adverse effects
Kidney Transplantation - immunology
Liver Transplantation - adverse effects
Liver Transplantation - immunology
Medical sciences
Nervous System Diseases - chemically induced
Nervous System Diseases - epidemiology
Pharmacology. Drug treatments
Postoperative Complications - epidemiology
Postoperative Complications - immunology
Psychotic Disorders - etiology
Retrospective Studies
Risk Factors
Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases
Surgery of the urinary system
Tacrolimus - adverse effects
Tissue, organ and graft immunology
Title Tacrolimus-Related Neurologic and Renal Complications in Liver Transplantation: A Single-Center Experience
URI https://dx.doi.org/10.1016/j.transproceed.2005.12.114
https://www.ncbi.nlm.nih.gov/pubmed/16549190
Volume 38
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