Sublingual Tacrolimus as an Alternative to Intravenous Route in Patients With Thoracic Transplant: A Retrospective Study

被引:24
|
作者
Collin, C. [1 ]
Boussaud, V. [2 ]
Lefeuvre, S. [1 ]
Amrein, C. [2 ]
Glouzman, A. S. [3 ]
Havard, L. [3 ]
Billaud, E. M. [1 ]
Guillemain, R. [2 ]
机构
[1] Hop Europeen Georges Pompidou, Dept Pharmacol, F-75908 Paris 15, France
[2] Hop Europeen Georges Pompidou, Dept Cardiovasc Surg, F-75908 Paris 15, France
[3] Hop Europeen Georges Pompidou, Dept Pharm, F-75908 Paris 15, France
关键词
HEALTHY-HUMAN SUBJECTS; LUNG TRANSPLANTATION; CLINICAL PHARMACOKINETICS; IMMUNOSUPPRESSIVE DRUGS; KIDNEY-TRANSPLANTATION; T-LYMPHOCYTES; CALCINEURIN; PHTHALATE; FK-506; FK506;
D O I
10.1016/j.transproceed.2010.09.126
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Tacrolimus (TRL) is an immunosuppressive drug characterized by a narrow therapeutic index, low bioavailability, and pharmacokinetic variability. Intravenous (IV) TRL may be needed whenever the oral route is unavailable. The small amount of infusion formulation (5 mg/mL) results in a large dilution and need for careful technical management of the infusion. This study addressed the feasibility to provide sublingual (SL) as an alternative to IV. TRL for transplanted patients. In a substudy, we performed a retrospective analysis of 17 lung and heart transplant patients using SL TRL. It included therapeutic drug monitoring and 4 area under curve (AUC) measurements. Patients received SL TRL on a dose-to-dose basis from the oral formulation. The mean age of the subjects (14 male, 3 female) was 35.3 +/- 15.6 years; 146 trough (C-0) samples were collected during the SL period (15.8 +/- 20.6 days) showing a conformity level of 90.4%. Mean dose, C-0, and AUC of SL tacrolimus were 0.116 +/- 0.096 mg/kg, 12.9 +/- 5 ng/mL, and 230 +/- 74 ng . h/mL, respectively, with an average 1 hour time to peak concentration. Acute rejection episodes, renal toxicity, and drug interactions were not observed. This study supported the convenience of short-term SL TRL administration, even in unconscious patients. Further investigations are needed to validate the dose range of the SL route.
引用
收藏
页码:4331 / 4337
页数:7
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