OBJECTIVE: To report an interaction between tacrolimus and the protease inhibitor combination lopinavir/ritonavir in a liver transplant patient. CASE SUMMARY: A 48-year-old white male liver transplant recipient receiving tacrolimus 5 mg twice daily for immunosuppression started highly active antiretroviral therapy for his HIV-positive status. Three days after initiation of lopinavir/ritonavir, the tacrolimus concentration rose sharply to toxic levels. Subsequent tacrolimus doses were withheld until tacrolimus concentrations normalized over 15 days. The tacrolimus dose was reestablished at a much lower dose, 0.5 mg once weekly. An objective causality assessment revealed that the adverse event was highly probable. DISCUSSION: Tacrolimus is metabolized in the liver via CYP3A4. Protease inhibitors are known to inhibit CYP3A4 and have been documented to increase tacrolimus concentrations, putting the patient at risk of developing nephrotoxic and/or neurotoxic symptoms. In this case, concomitant use of lopinavir/ritonavir caused tacrolimus concentrations to rise more dramatically than had been previously reported in the literature for other protease inhibitors. CONCLUSIONS: Extreme caution must be used when administering tacrolimus concomitantly with lopinavir/ritonavir. Therapeutic concentrations of tacrolimus can be maintained with tacrolimus doses that are far below standard dosages.
OBJECTIVE: To report an interaction between tacrolimus and the protease inhibitor combination lopinavir/ritonavir in a liver transplant patient. CASE SUMMARY: A 48-year-old white male liver transplant recipient receiving tacrolimus 5 mg twice daily for immunosuppression started highly active antiretroviral therapy for his HIV-positive status. Three days after initiation of lopinavir/ritonavir, the tacrolimus concentration rose sharply to toxic levels. Subsequent tacrolimus doses were withheld until tacrolimus concentrations normalized over 15 days. The tacrolimus dose was reestablished at a much lower dose, 0.5 mg once weekly. An objective causality assessment revealed that the adverse event was highly probable. DISCUSSION: Tacrolimus is metabolized in the liver via CYP3A4. Protease inhibitors are known to inhibit CYP3A4 and have been documented to increase tacrolimus concentrations, putting the patient at risk of developing nephrotoxic and/or neurotoxic symptoms. In this case, concomitant use of lopinavir/ritonavir caused tacrolimus concentrations to rise more dramatically than had been previously reported in the literature for other protease inhibitors. CONCLUSIONS: Extreme caution must be used when administering tacrolimus concomitantly with lopinavir/ritonavir. Therapeutic concentrations of tacrolimus can be maintained with tacrolimus doses that are far below standard dosages.
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Authors: Antonio Franco; Patricio Más-Serrano; Yussel González; Noelia Balibrea; David Rodríguez; María Isabel López; Francisco Javier Pérez Contreras Journal: Nefrologia (Engl Ed) Date: 2019-08-12
Authors: Verónica López; Teresa Vázquez; Juana Alonso-Titos; Mercedes Cabello; Angel Alonso; Isabel Beneyto; Marta Crespo; Carmen Díaz-Corte; Antonio Franco; Francisco González-Roncero; Elena Gutiérrez; Luis Guirado; Carlos Jiménez; Cristina Jironda; Ricardo Lauzurica; Santiago Llorente; Auxiliadora Mazuecos; Javier Paul; Alberto Rodríguez-Benot; Juan Carlos Ruiz; Ana Sánchez-Fructuoso; Eugenia Sola; Vicente Torregrosa; Sofía Zárraga; Domingo Hernández Journal: Nefrologia (Engl Ed) Date: 2020-04-03
Authors: Yaerim Kim; Ohyun Kwon; Jin H Paek; Woo Y Park; Kyubok Jin; Miri Hyun; Ji Y Lee; Hyun A Kim; Seungyeup Han Journal: Am J Transplant Date: 2020-05-16 Impact factor: 8.086