Cardiotonic steroids (CTSs), such as digoxin, are used for heart failure treatment. However, digoxin permeates the brain-blood barrier (BBB), affecting central nervous system (CNS) functions. Finding a CTS that does not pass through the BBB would increase CTSs' applicability in the clinic and decrease the risk of side effects on the CNS.
View Article and Find Full Text PDFZh Nevrol Psikhiatr Im S S Korsakova
June 2023
Objective: To evaluate the relationship between daily doses of antipsychotic drugs, their serum concentrations, and characteristics of patients treated for schizophrenia or schizophreniform disorder in day-to-day clinical practice.
Material And Methods: A total of 187 patients were included in the study, 77 (41.1%) patients were on monotherapy, and 110 (58.
Zh Nevrol Psikhiatr Im S S Korsakova
February 2022
Objective: To personalize pharmacotherapy with aripiprazole in patients with schizophrenia via therapeutic drug monitoring (TDM).
Material And Methods: TDM of aripiprazole (ARI) and its active metabolite dehydroaripiprazole (DHA) was performed for patients diagnosed with schizophrenia (ICD-10 F20.00; F20.
Zh Nevrol Psikhiatr Im S S Korsakova
August 2019
Aim: To conduct a routine therapeutic drug monitoring (TDM) and analyze its results for the optimization of pharmacotherapy.
Material And Methods: Fifty-six inpatients (in total 68 samples) with various forms of schizophrenia were enrolled. High performance liquid chromatography with mass-spectrometric detection was used for quantitative determination of risperidone and 9-hydroxyrisperidone in the serum.
Zh Nevrol Psikhiatr Im S S Korsakova
April 2016
Objective: To study a relationship between plasma levels of antipsychotics (AP) and severity of side-effects (SE) during the treatment of inpatients with exacerbation of schizophrenia.
Material And Methods: The study included 39 patients treated with risperidone, haloperidol, zuclopenthixol, clozapine, aripiprazole or olanzapine as monotherapy or in combination of two AP. Blood sampling to measure the AP plasma level was performed twice (at 7-10 and 26-30 day from start of treatment), the levels of prolactin and glucose were determined once (at 26-30 day from start of treatment).