RESUMEN
The study was focused on the clinico-pharmacological analysis of differences between subjective and objective assessment of the effects of antiasthenic drug ladasten and placebo effects in patients with neurasthenia with different individual patterns manifested in their EEG alpha rhythms and MMPI findings. It is established that, in patients with neurasthenia characterized by reduced EEG alpha activity combined with emotional lability and inertness, the therapeutic action and effectiveness of ladasten and placebo was more robust (the subjective estimation was higher) than in patients with prominent alpha rhythm and sthenic personal traits. The self-assessment of the effect of single test doses of ladasten and placebo was independent of the individual differences of EEG alpha rhythm organization and personal traits with respect to tolerability, wish to continue the treatment, activating and calming effects. In long-term treatment, higher subjective estimations of the ladasten and placebo effect appeared in patients with reduced EEG alpha rhythm, and the difference corresponded to objective indices of the psychotropic action and effectiveness of the drug.
Asunto(s)
Adamantano/análogos & derivados , Ritmo alfa/efectos de los fármacos , Neurastenia/tratamiento farmacológico , Psicotrópicos/uso terapéutico , Adamantano/uso terapéutico , Adolescente , Adulto , Autoevaluación Diagnóstica , Femenino , Humanos , Masculino , Persona de Mediana Edad , Neurastenia/fisiopatología , Efecto Placebo , Psicotrópicos/farmacologíaRESUMEN
The spectral-coherence analysis of phenazepam single-dose action in patients with anxiety disorder was performed. Significant changes in coherence parameters indicating the generalized character of reorganizations of interzonal connections with the involvement of delta, alpha, theta and beta-1 to beta-3 rhythms, including both their strengthening and weakening, were revealed. Correlations between the character of reorganizations of interzonal relations and subjective assessments of the drug effect were observed: activating and antianxiety drug effects were correlated with tolerability and the wish to continue treatment with the drug. Results suggest that drug effect on EEG spectra is more informative when subjective assessments are taken into account.
Asunto(s)
Ansiedad/tratamiento farmacológico , Ansiedad/fisiopatología , Benzodiazepinas/administración & dosificación , Encéfalo/efectos de los fármacos , Electroencefalografía , Sentido de Coherencia/efectos de los fármacos , Adulto , Encéfalo/fisiopatología , Relación Dosis-Respuesta a Droga , Femenino , Humanos , Masculino , Persona de Mediana Edad , Adulto JovenRESUMEN
Self-evaluation of the effect of single-dose (15 mg) ladasten administration versus placebo has been studied in patients with neurasthenia diagnosis. Relationships between self-evaluation parameters and personal features, psychopathological and psychophysiological parameters of patients, drug action characteristics, and course treatment effectiveness have been analyzed. Results suggest that the self-rated high tolerability of ladasten treatment is comparable with that of placebo. No relationships are found between the self-evaluated single-dose effects of ladasten and personal features of patients. Correlations of the self-estimations and some psychopathological and psychophysiological parameters before treatment, main drug effects, and overall course treatment effectiveness are revealed, whereas the self-evaluation of placebo effect was related to personal features.
Asunto(s)
Adamantano/análogos & derivados , Afecto/efectos de los fármacos , Ansiolíticos/uso terapéutico , Actividad Motora/efectos de los fármacos , Neurastenia/tratamiento farmacológico , Adamantano/administración & dosificación , Adamantano/uso terapéutico , Administración Oral , Adulto , Ansiolíticos/administración & dosificación , Autoevaluación Diagnóstica , Esquema de Medicación , Femenino , Humanos , Masculino , Persona de Mediana Edad , Neurastenia/diagnóstico , Neurastenia/fisiopatología , Examen Físico , Efecto Placebo , Psicofisiología , Proyectos de Investigación , Trastornos del Inicio y del Mantenimiento del Sueño , Fases del Sueño , Resultado del TratamientoRESUMEN
Self-evaluation of single-dose (15 mg) action and course treatment (30 mg daily) results were studied in patients with anxiety and asthenic disorders treated with the new anxiolytic afobazole. Also, relationships between self-evaluated parameters and personal features, clinician-rated therapeutic changes, and treatment effectiveness were analyzed. The study was conducted according to formalized protocol using standard scales and methods. Results suggest that higher self-rated tolerability and patient acceptability were associated with afobazole treatment in comparison to benzodiazepines. The results revealed relationships between self-evaluated single-dose effects of afobazole and other parameters, personal features, cognitive impairments severity, main drug effects, and overall treatment effectiveness.
Asunto(s)
Ansiolíticos/uso terapéutico , Ansiedad/tratamiento farmacológico , Astenia/tratamiento farmacológico , Bencimidazoles/uso terapéutico , Autoevaluación Diagnóstica , Morfolinas/uso terapéutico , Adolescente , Adulto , Ansiolíticos/administración & dosificación , Ansiedad/psicología , Astenia/psicología , Bencimidazoles/administración & dosificación , Trastornos del Conocimiento/etiología , Trastornos del Conocimiento/psicología , Relación Dosis-Respuesta a Droga , Femenino , Humanos , Masculino , Persona de Mediana Edad , Morfolinas/administración & dosificación , Pruebas Neuropsicológicas , Cooperación del Paciente , Satisfacción del Paciente , Índice de Severidad de la Enfermedad , Resultado del Tratamiento , Adulto JovenRESUMEN
An aim of a randomized blind study was to assess therapeutic efficacy and safety of ladasten used as an antiastenic drug in patients with neurasthenia. Tasks of the study included the investigation of characteristics of therapeutical actions, efficacy of the drug comparing to placebo, possible side-effects and probability of the development of "withdrawal syndromes". The design of the study included a wash-out period, a monotherapy with ladasten and placebo during 28 days and a final 1-week period of receiving placebo. Standartisized objective and subjective methods of mental state evaluation in patients were administered. The results obtained suggest that a combination of psychostimulant and anxiolytic actions in the spectrum of psychotropic activity of ladasten determines the its high therapeutic efficacy in asthenic disorders. It has been found that ladasten is superior in the rate and degree of reduction of main symptoms of asthenic syndrome compared to placebo. The absence of "withdrawal syndrome" after the drug withdrawal reveals the lack of addictive potential in this drug.