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Diagnostic efficiency of truncated area under the curve from 0 to 2 h (AUC0-2) of mycophenolic acid in kidney transplant recipients receiving mycophenolate mofetil and concomitant tacrolimus
被引:2
|作者:
Lampon, Natalia
[1
]
Tutor-Crespo, Maria J.
[1
]
Romero, Rafael
[2
]
Tutor, Jose C.
[1
]
机构:
[1] Hosp Clin Univ, Cent Lab, Unidad Monitorizac Farma, Inst Invest Sanit IDIS, Santiago De Compostela 15706, Spain
[2] Hosp Clin Univ, Serv Nefrol, Santiago De Compostela, Spain
关键词:
mycophenolic acid;
renal transplantation;
therapeutic drug monitoring;
truncated area under the curve;
LIMITED SAMPLING STRATEGY;
RENAL-TRANSPLANT;
PHARMACOKINETICS;
DRUG;
CYCLOSPORINE;
D O I:
10.1515/CCLM.2011.191
中图分类号:
R446 [实验室诊断];
R-33 [实验医学、医学实验];
学科分类号:
1001 ;
摘要:
Background: Recently, the use of the truncated area under the curve from 0 to 2 h (AUC(0-2)) of mycophenolic acid (MPA) has been proposed for therapeutic monitoring in liver transplant recipients. The aim of our study was the evaluation of the clinical usefulness of truncated AUC(0-2) in kidney transplant patients. Methods: Plasma MPA was measured in samples taken before the morning dose of mycophenolate mofetil, and one-half and 2 h post-dose, completing 63 MPA concentration-time profiles from 40 adult kidney transplant recipients. The AUC from 0 to 12 h (AUC(0-12)) was calculated using the validated algorithm of Pawinski et al. The truncated AUC(0-2) was calculated using the linear trapezoidal rule, and extrapolated to 0-12 h (trapezoidal extrapolated AUC(0-12)) as previously described. Results: Algorithm calculated and trapezoidal extrapolated AUC(0-12) values showed high correlation (r=0.995) and acceptable dispersion (ma68=0.71 mu g.h/mL), median prediction error (6.6%) and median absolute prediction error (12.6%). The truncated AUC(0-2) had acceptable diagnostic efficiency (87%) in the classification of subtherapeutic, therapeutic or supratherapeutic values with respect to AUC(0-12). However, due to the high inter-individual variation of the drug absorption-rate, the dispersion between both pharmacokinetic variables (ma68=6.9 mu g.h/mL) was unacceptable. Conclusions: The substantial dispersion between truncated AUC(0-2) and AUC(0-12) values may be a serious objection for the routine use of MPA AUC(0-2) in clinical practice.
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页码:1167 / 1170
页数:4
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