Impact of direct-acting antivirals for hepatitis C virus therapy on tacrolimus dosing in liver transplant recipients

被引:7
作者
Bixby, Alexandra L. [1 ]
Fitzgerald, Linda [1 ]
Leek, Rachael [2 ]
Mellinger, Jessica [3 ]
Sharma, Pratima [3 ]
Tischer, Sarah [1 ]
机构
[1] Michigan Med, Dept Pharm, Ann Arbor, MI USA
[2] Vanderbilt Univ, Med Ctr, Dept Pharm, Nashville, TN USA
[3] Michigan Med, Dept Internal Med, Ann Arbor, MI USA
关键词
direct-acting antiviral; hepatitis C virus; liver transplantation; tacrolimus; DOSE RATIO; INFECTION; SOFOSBUVIR; DYSFUNCTION; ADULTS; RISK;
D O I
10.1111/tid.13078
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Introduction Direct-acting antivirals (DAAs) have transformed hepatitis C virus (HCV) management post-liver transplant. As HCV clears during DAA treatment, hepatic metabolism improves, resulting in decreased tacrolimus concentrations that may require dose adjustment. The purpose of this study was to determine appropriate management of immunosuppression in liver transplant recipients during and following treatment of HCV. Methods This study was a single-center retrospective analysis of 71 liver transplant recipients who were treated for HCV with DAAs. The primary outcome was change in dose-normalized tacrolimus concentrations from the start of DAA treatment to 12 weeks following therapy. Results The mean change in log-transformed dose-normalized tacrolimus concentrations was a reduction of 0.43 ng/mL/mg (95% CI; 0.26-0.60, P < 0.0001). The greatest decrease occurred in the first 4 weeks of treatment, after which levels stabilized. The overall mean tacrolimus concentration was 4.8 ng/mL (+/- 2.5). Two patients (3%) developed acute cellular rejection and two patients (3%) had graft loss and died. Conclusion From the start of treatment to 12 weeks post-DAA therapy, liver transplant recipients experienced a significant decrease in dose-normalized tacrolimus concentrations. In conclusion, close monitoring of tacrolimus concentrations is warranted during and following treatment with DAAs, as dose increases may be indicated in order to maintain therapeutic concentrations to prevent graft rejection.
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页数:6
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