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Clinical Chemistry, Vol 39, 1872-1877, Copyright © 1993 by American Association for Clinical Chemistry
WL Roberts and PM Rainey
Department of Laboratory Medicine, Yale University School of Medicine, New Haven, CT 06510.
Accumulation of phenytoin metabolites in uremia has been shown to interfere with some immunoassay methods for phenytoin measurement. We evaluated the effects of uremia (serum creatinine > 13 mg/L) on free and total phenytoin concentrations measured by the Abbott TDx fluorescence polarization immunoassay, and the DuPont aca and Syva EMIT homogeneous enzyme-multiplied immunoassay methods, using HPLC as the comparison method. In uremic patients, the TDx assay showed both fixed and proportional bias in comparison with the HPLC for both total phenytoin concentration (TDx = 1.24 x HPLC + 1.9 mg/L) and free phenytoin concentration (TDx = 1.52 x HPLC + 0.24 mg/L). The total bias was as great as 100% for both total and free phenytoin. Cross-reactive substances other than 5-(p-hydroxyphenyl)-5-phenylhydantoin (HPPH) and HPPH-glucuronide appeared to be responsible. In contrast, there was minimal interference with aca and EMIT assays.
The following articles in journals at HighWire Press have cited this article:
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W. L. Roberts, B. K. De, J. P. Coleman, and T. M. Annesley Falsely Increased Immunoassay Measurements of Total and Unbound Phenytoin in Critically Ill Uremic Patients Receiving Fosphenytoin Clin. Chem., June 1, 1999; 45(6): 829 - 837. [Abstract] [Full Text] [PDF] |
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P. Datta Oxaprozin and 5-(p-Hydroxyphenyl)- 5-phenylhydantoin Interference in Phenytoin Immunoassays Clin. Chem., August 1, 1997; 43(8): 1468 - 1469. [Full Text] |
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