Article ID Journal Published Year Pages File Type
1971512 Clinical Biochemistry 2008 4 Pages PDF
Abstract

ObjectivesThe aim of this work was to compare a validated liquid chromatography–mass spectrometry (LC–MS) method with the commercial enzyme multiplied immunoassay technique (EMIT) for cyclosporine and tacrolimus whole blood quantification.Design and methodsSamples of transplant patients receiving cyclosporine (n = 38) or tacrolimus (n = 41) were analyzed successively by LC–MS and EMIT. Several statistical approaches for method comparison were evaluated and Passing–Bablok and Bland–Altman analyses chosen.ResultsOverestimations of the concentrations measured with EMIT compared to LC–MS were observed with means of 23% (range: 6% to 46%) for cyclosporine and 30% (range: − 3% to 73%) for tacrolimus.ConclusionThe EMIT demonstrated significant positive biases due to cross-reactions with metabolites. This indicates that, in some clinical situations, a selective method such as LC–MS is preferable for therapeutic drug monitoring in transplant patients.

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