z-logo
Premium
A clinical assessment of mycophenolate drug monitoring after liver transplantation
Author(s) -
Hwang Shin,
Lee SungGyu,
Ahn ChulSoo,
Kim KiHun,
Moon DeokBog,
Ha TaeYong,
Song GiWon,
Jung DongHwan,
Choi NamKyu,
Kim KwanWoo,
Yu YoungDong,
Park GilChun,
Park PyoungJae,
Choi YoungIl
Publication year - 2010
Publication title -
clinical transplantation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.918
H-Index - 76
eISSN - 1399-0012
pISSN - 0902-0063
DOI - 10.1111/j.1399-0012.2009.01166.x
Subject(s) - tacrolimus , medicine , mycophenolate , therapeutic drug monitoring , mycophenolic acid , liver transplantation , transplantation , urology , gastroenterology , pharmacokinetics , pharmacology
Hwang S, Lee S‐G, Ahn C‐S, Kim K‐H, Moon D‐B, Ha T‐Y, Song G‐W, Jung D‐H, Choi N‐K, Kim K‐W, Yu Y‐D, Park G‐C, Park P‐J, Choi Y‐I. A clinical assessment of mycophenolate drug monitoring after liver transplantation.
Clin Transplant 2010 DOI: 10.1111/j.1399‐0012.2009.01166.x
© 2010 John Wiley & Sons A/S. Abstract: Background:  Recent findings have suggested the clinical utility of therapeutic drug monitoring (TDM) in patients treated with mycophenolate mofetil (MMF). Aim:  To assess whether routine mycophenolic acid (MPA) TDM is beneficial and how to utilize it. Methods:  A series of short‐term prospective studies on TDM for MPA and/or tacrolimus was performed at a large‐volume center. Results:  The 673 adult liver transplants were divided into four groups based on immunosuppressive regimens as tacrolimus monotherapy (n = 369), tacrolimus–MMF therapy (n = 270), MMF‐minimal tacrolimus therapy (n = 17), and MMF monotherapy (n = 17). There was a significant difference of tacrolimus concentration between the groups receiving tacrolimus monotherapy and tacrolimus–MMF therapy during the first two yr (at two yr: 8.4 ± 2.7 vs. 6.3 ± 2.6 ng/mL; p ≤ 0.002). MMF‐minimal tacrolimus therapy and MMF monotherapy were applied after first three months and MPA levels ranged from 1.8 to 5.3 μg/mL. Correlation between MMF dosage and MPA concentration showed wide interindividual variations (n = 304, r 2  = 0.271, p < 0.001), in which r 2 was fluctuating from 0.056 to 0.213 according to the post‐transplant period over five yr; wide intraindividual variation was also observed during the first two months (n = 12, r 2  < 0.2, p > 0.195). About 10% of patients were classified as poor MMF absorber and excluded from MMF usage. Mean MPA level leading to successful MMF monotherapy or MMF‐minimal tacrolimus therapy was ≥1.0 μg/mL in 87% and >2.0 μg/mL in 56.5%. Conclusion:  MPA TDM‐based MMF dosage adjustment enabled us to administer MMF more confidently than categorical dosing. MPA TDM appears to be a useful tool to cope with the wide pharmacokinetic variability of MMF after liver transplantation.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here