Li. Mansur et al., REBOUND OF PLASMA-FREE PHENYTOIN CONCENTRATION FOLLOWING PLASMAPHERESIS IN A PATIENT WITH THROMBOTIC THROMBOCYTOPENIC PURPURA, The Annals of pharmacotherapy, 29(6), 1995, pp. 592-595
OBJECTIVE: To measure the total and free serum phenytoin concentration
s and phenytoin clearance in a patient with thrombotic thrombocytopeni
c purpura undergoing plasmapheresis. CASE SUMMARY: A dose of phenytoin
400 mg iv was administered daily 2.5 hours after the completion of pl
asmapheresis. intravenous samples were obtained to measure the free an
d total phenytoin concentrations on 4 consecutive days. These samples
were obtained before, at the midpoint, upon completion, and 30, 60, an
d 120 minutes after completion of plasmapheresis. The samples were cen
trifuged and stored at 4 degrees C until analysis using the same fluor
escence polarization immunoassay kit. The free phenytoin was separated
by ultracentrifugation. DISCUSSION: Despite a decrease in total and f
ree serum phenytoin concentrations measured during the procedure, a ma
rked rebound in the free phenytoin concentration was noted 30 minutes
after completion of the procedure. However, by 120 minutes after the p
rocedure, the free phenytoin concentration had decreased to thr prepro
cedure value. The total amount of phenytoin removed by the procedure w
as less than 5%. CONCLUSIONS: Despite the decrease in total and foe se
rum phenytoin concentrations observed during plasmapheresis. patients
undergoing plasmapheresis may not need supplemental phenytoin, as a ra
pid reequilibration of the therapeutically active fret: serum phenytoi
n occurs following the completion of the procedure. In addition, less
than 5% of the total body phenytoin is removed. Second if the patient
experiences symptoms of phenytoin toxicity immediately after the proce
dure, a free serum phenytoin concentration may be obtained, as this co
ncentration may reflect the reason for toxicity despite a decreased to
tal phenytoin concentration.