Objective: The aim of this study was to evaluate the benefit of mirtazapine plasma concentration
monitoring in a typical clinical setting. Methods: The relationship between mirtazapine plasma concentration, dose, response, and side
effects was studied in 65 inpatients presenting with a depressive episode according
to ICD-10. Plasma concentrations, the 17-item Hamilton Depression Rating (HAMD), and
the UKU side effect rating were performed weekly. A subgroup of 45 patients was evaluated
for a concentration-response relationship. Results: We found a low positive correlation between plasma concentration and dose. A low
negative correlation between plasma concentration and increased duration of sleep
was noted in the first week of mirtazapine treatment, but not during the entire observation
time. Responders to mirtazapine treatment presented with higher plasma concentrations
than non-responders, revealing a threshold concentration of 30 ng/mL. Conclusion: The mirtazapine dose is a weak predictor of mirtazapine plasma concentrations. Plasma
concentration measurements may therefore be useful to adjust mirtazapine doses in
non-responders with plasma concentrations below 30 ng/mL. Sedative effects appear
temporary and require no plasma concentration control when standard doses are administered.
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Dr. Katja Grasmäder
Department of Psychiatry
University of Bonn
Sigmund-Freud-Str. 25
53121 Bonn
Germany
eMail: kgrasmae@uni-bonn.de