Volumetric Absorptive Microsampling to Enhance the Therapeutic Drug Monitoring of Tacrolimus and Mycophenolic Acid: A Systematic Review and Critical Assessment

被引:6
作者
Leino, Abbie D. [1 ]
Takyi-Williams, John [2 ]
Pai, Manjunath P. [1 ,2 ,3 ]
机构
[1] Univ Michigan, Coll Pharm, Dept Clin Pharm, Ann Arbor, MI USA
[2] Univ Michigan, Coll Pharm, Pharmacokinet & Mass Spectrometry Core, Ann Arbor, MI USA
[3] Univ Michigan, Coll Pharm, Dept Clin Pharm, Rm 2568B,428 Church St, Ann Arbor, MI 48108 USA
关键词
volumetric absorptive microsampling; clinical validation; immunosuppression; LIMITED-SAMPLING STRATEGY; DRIED BLOOD SPOTS; TANDEM MASS-SPECTROMETRY; RENAL-TRANSPLANT PATIENTS; WHOLE-BLOOD; CAPILLARY BLOOD; QUANTITATIVE-DETERMINATION; INTERNATIONAL ASSOCIATION; CYCLOSPORINE-A; HEMATOCRIT;
D O I
10.1097/FTD.0000000000001066
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:Volumetric absorptive microsampling (VAMS) is an emerging technique that may support multisample collection to enhance therapeutic drug monitoring in solid organ transplantation. This review aimed to assess whether tacrolimus and mycophenolic acid can be reliably assayed using VAMS and to identify knowledge gaps by providing granularity to existing analytical methods and clinical applications.Methods:A systematic literature search was conducted in accordance with the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines. The PubMed, Embase, and Scopus databases were accessed for records from January 2014 to April 2022 to identify scientific reports on the clinical validation of VAMS for monitoring tacrolimus and mycophenolic acid concentrations. Data on the study population, sample sources, analytical methods, and comparison results were compiled.Results:Data from 12 studies were collected, including 9 studies pertaining to tacrolimus and 3 studies on the concurrent analysis of tacrolimus and mycophenolic acid. An additional 14 studies that provided information relevant to the secondary objectives (analytical validation and clinical application) were also included. The results of the clinical validation studies generally met the method agreement requirements described by regulatory agencies, but in many cases, it was essential to apply correction factors.ConclusionsSCurrent evidence suggests that the existing analytical methods that use VAMS require additional optimization steps for the analysis of tacrolimus and mycophenolic acid. The recommendations put forth in this review can help guide future studies in achieving the goal of improving the care of transplant recipients by simplifying multisample collection for the dose optimization of these drugs.
引用
收藏
页码:463 / 478
页数:16
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