Tacrolimus-related adverse effects in liver transplant recipients: Its association with trough concentrations
Autor: | Gomathy Narasimhan, Joy Varghese, Olithselvan Arikichenin, Rajasekhar Perumalla, Vijaya Srinivasan, Mohamed Rela, Naresh Shanmugam, Venkataraman Jayanthi, Mettu Srinivasa Reddy, Vivekanandan Shanmugam, Kota Venugopal |
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Rok vydání: | 2014 |
Předmět: |
Adult
Graft Rejection Male medicine.medical_specialty Adolescent medicine.medical_treatment chemical and pharmacologic phenomena Pharmacology Liver transplantation Gastroenterology Tacrolimus Young Adult Seizures Internal medicine Tremor medicine Humans Trough Concentration Renal Insufficiency Chronic Confusion Adverse effect Aged Retrospective Studies Dose-Response Relationship Drug medicine.diagnostic_test business.industry Headache Retrospective cohort study Immunosuppression Middle Aged Hepatology Liver Transplantation surgical procedures operative Psychotic Disorders Therapeutic drug monitoring Female Drug Monitoring business Immunosuppressive Agents |
Zdroj: | Indian Journal of Gastroenterology. 33:219-225 |
ISSN: | 0975-0711 0254-8860 |
DOI: | 10.1007/s12664-014-0456-0 |
Popis: | Tacrolimus is an important immunosuppressant administered to patients following liver transplantation (LT), with a recommended trough concentration of 8 to 11 ng/mL to prevent allograft rejection. We retrospectively examined our data to identify the tacrolimus trough concentration that combined efficacy with minimal adverse effects.The case records of LT recipients, who were nondiabetic, nonhypertensive, and with normal renal parameters prior to LT were retrospectively examined for acute cellular rejection (ACR) episodes and three major adverse effects of tacrolimus, i.e. neurotoxicity, nephrotoxicity, and new onset diabetes mellitus (NODM).Thirty-two LT recipients fulfilled the criteria for the study. The mean (±SD) tacrolimus level for the 290 troughs (after 10 days) was 8.5 ± 3.8 ng/mL. At 10 days, 1 month, 3 months, and 6 months, the trough values were 7.3 ± 2.9, 9.7 ± 3.4, 7.9 ± 3.3, and 7.6 ± 2.6 ng/mL, respectively. The mean time taken for stabilization of the blood pressure and biochemical parameters was 7 ± 2 days. Overall, a trough window with the least adverse effect was 7 to 7.9 ng/mL. Neurotoxicity was least in the trough range 5 to8 ng/mL. Symptoms included headache in four, tremors in three, seizure in one, confusion and psychosis in two, and combination in three. Nephrotoxicity was least in trough 8 to11 ng/mL. One patient progressed to chronic kidney disease at 6 months. NODM was present in 11 % to 18 % across the various trough range, including the extremes (mean trough level, 8.4 ± 4.4 ng/dL). At 6 months, five recipients were on treatment for NODM. Three recipients developed ACR, two within the first month and one at 7 weeks. The trough levels were 8.5, 9, 15.2 ng/mL, respectively. All recovered with three pulse doses of methylprednisolone.Tacrolimus concentration of 5 to8 ng/mL was associated with least overall toxicity, neurotoxicity, and ACR. |
Databáze: | OpenAIRE |
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