Rs. Miller et al., MONITORING PLASMA-LEVELS OF FLUPHENAZINE DURING CHRONIC THERAPY WITH FLUPHENAZINE DECANOATE, Journal of clinical pharmacy and therapeutics, 20(2), 1995, pp. 55-62
This study was conducted to examine the interpatient variability in st
eady-state plasma concentrations of fluphenazine by repeat depot intra
muscular administration, and to determine the relationship between the
se concentrations and clinical state. Steady-state pre-dose concentrat
ions of fluphenazine in plasma were measured using a sensitive and spe
cific gas chromatography/mass spectrometry (GC/MS) assay in 24 patient
s with schizophrenia who were receiving continuous treatment with depo
t intramuscular fluphenazine decanoate. Clinical response was measured
using the Andreasen Scale for positive and negative symptoms, Steady-
state plasma concentrations of fluphenazine ranged from undetectable (
<0.1 ng/ml) to 27.9 ng/ml, with a median of 0.5 ng/ml. No significant
associations were found between plasma concentration and dosage, or ag
e and sex of the patient. Steady-state plasma concentrations in patien
ts taking anticholinergic agents were significantly higher than in pat
ients not receiving such drugs (P<0.05 by Mann-Whitney U-test). Poorer
control, expressed as the sum of the negative symptom scores or the s
um of the positive and negative symptom scores, was related to higher
log transformed plasma concentrations of fluphenazine and higher fluph
enazine decanoate dosage. The log transformed plasma concentrations of
fluphenazine and the fluphenazine decanoate dosages were weakly relat
ed. Patients receiving another antipsychotic drug in addition to fluph
enazine decanoate tended to have poorer clinical control and higher do
sages of fluphenazine decanoate. These results indicate the useful rol
e that plasma level monitoring can fulfil in identifying patients who
are therapy-resistant despite high plasma levels.