American Journal of Clinical Pathology · 1991 · 12 citations · 3 references
PharmacyPharmacokineticsPharmacologyClinical PharmacologyEpilepsyTherapeutic Drug MonitoringAntiepileptic Drug MonitoringDrug Concentration InterpretationAlbumin QuantificationClinical Value AssessmentCorrelationFree Drug Concentration MeasurementFree Drug Concentration MonitoringFree Drug SamplesPhenytoin TherapySerum Drug Concentration Measurement
Therapeutic monitoring of the pharmacologically active (free drug) fraction of protein-bound medications (e.g., phenytoin) represents a major diagnostic challenge in clinical and laboratory medicine. While free drug levels may be beneficial in many clinical situations, current methods for predicting free phenytoin concentrations are unreliable and not recommended for general use. The authors have demonstrated a linear relationship (r2 = 0.98) between serum levels of total and bound phenytoin in 56 patients with seizure disorders. No significant correlations were observed when total phenytoin and albumin levels were compared independently to measured concentrations of free phenytoin or percent free phenytoin. A good correlation (r2 = 0.89) existed between free phenytoin levels and [total phenytoin]/[albumin] ratios in patients with normal or elevated albumin levels, but significantly weaker correlations were found in patients with hypoalbuminemia. Thus, [total phenytoin]/[albumin] ratios may have clinical value in predicting free phenytoin levels in uncomplicated patients without hypoalbuminemia.
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Accuracy of three methods for predicting concentrations of free phenytoin.
D E Beck, John A. Farringer, William R. Ravis et al. · PubMed · 1987 · 18 citations