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1.
Neuro Endocrinol Lett ; 28(1): 33-8, 2007 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-17277734

RESUMO

BACKGROUND: Transcranial magnetic stimulation (rTMS) can modulate cortical activity. The goal of our study was to assess whether rTMS would facilitate effect of serotonin reuptake inhibitors in patients with panic disorder. METHOD: Fifteen patients suffering from panic disorder resistant to serotonin reuptake inhibitor (SRI) therapy were randomly assigned to either active or to sham rTMS. The aim of the study was to compare the 2 and 4 weeks efficacy of the 10 sessions 1 Hz rTMS with sham rTMS add on SRI therapy. We use 1 Hz, 30 minutes rTMS, 110% of motor threshold administered over the right dorso-lateral prefrontal cortex (DLPFC). The same time schedule was used for sham administration. Fifteen patients finished the study,. Psychopathology was assessed using the rating scales CGI, HAMA, PDSS and BAI before the treatment, immediately after the experimental treatment and 2 weeks after the experimental treatment by an independent reviewer. RESULTS: Both groups improved during the study period but the treatment effect did not differ between groups in any of the instruments. CONCLUSION: Low frequency rTMS administered over the right dorso-lateral prefrontal cortex after 10 sessions did not differ from sham rTMS add on serotonin reuptake inhibitors in patients with panic disorder.


Assuntos
Transtorno de Pânico/fisiopatologia , Transtorno de Pânico/terapia , Inibidores Seletivos de Recaptação de Serotonina/uso terapêutico , Estimulação Magnética Transcraniana/métodos , Adulto , Antidepressivos/uso terapêutico , Ansiedade/fisiopatologia , Terapia Combinada , Método Duplo-Cego , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Córtex Pré-Frontal/fisiopatologia , Índice de Gravidade de Doença
2.
Neuro Endocrinol Lett ; 27(4): 473-81, 2006 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-16891998

RESUMO

The aim of the study was to assess the 6-months treatment efficacy and 24-month follow up of three different therapeutic programs (A. moclobemide and supportive guidance, B. group cognitive-behavioral therapy and pill placebo, and C. combination of moclobemide and group cognitive-behavioral therapy) in patients with a generalized form of social phobia. Eighty one patients (38 males and 43 females) were randomly assigned to three different therapeutic programs. Patients were regularly assessed on a monthly basis by an independent rater on the LSAS (Liebowitz Social Anxiety scale), CGI (Clinical Global Impression) for severity and change and BAI (Beck Anxiety Inventory). Altogether, sixty-six patients completed the six month treatment period and 15 patients dropped out. All therapeutic groups showed significant improvement. A combination of CBT and pharmacotherapy yielded the most rapid effect. Moclobemide was superior for the reduction of the subjective general anxiety (BAI) during the first 3 months of treatment, but its influence on avoidant behavior (LSAS avoidance subscale) was less pronounced. Conversely, CBT was the best choice for reduction of avoidant behavior while a reduction of subjective general anxiety appeared later than in moclobemide. After 6 months of treatment there were best results reached in groups treated with CBT and there was no advantage of the combined treatment. The relapse rate during the 24-month follow up was significantly lower in the group treated with CBT in comparison with the group A. formerly treated with moclobemide alone.


Assuntos
Terapia Cognitivo-Comportamental , Moclobemida/uso terapêutico , Inibidores da Monoaminoxidase/uso terapêutico , Transtornos Fóbicos/tratamento farmacológico , Transtornos Fóbicos/psicologia , Adolescente , Adulto , Ansiedade/tratamento farmacológico , Ansiedade/psicologia , Terapia Combinada , Feminino , Seguimentos , Humanos , Masculino , Pessoa de Meia-Idade , Pacientes Desistentes do Tratamento , Placebos , Testes Psicológicos , Índice de Gravidade de Doença , Resultado do Tratamento
3.
Neuro Endocrinol Lett ; 27(3): 327-32, 2006 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-16816829

RESUMO

BACKGROUND: The goal of our study is to assess whether transcranial magnetic stimulation (rTMS) would facilitate the effect of antidepressant in OCD patients. METHOD: The aim of the randomized, double-blind, sham controlled study was to compare the 2 and 4 week efficacy of the 10 sessions rTMS with sham rTMS in serotonin reuptake inhibitor resistant OCD patient. Thirty three right-handed patients were randomly assigned to either active rTMS or to sham rTMS. Active rTMS with the frequency of 1 Hz at 110% of motor threshold (MT) was administered over the left dorso-lateral prefrontal cortex. The same time schedule was used for sham administration. Thirty patients finished the study, three patients' dropped out at the beginning. Psychopathology was assessed by CGI, HAMA, Y-BOCS and BAI before the treatment, immediately after the experimental treatment, and 2 weeks after the experimental treatment by an independent reviewer. RESULTS: Both groups improved during the study period but the treatment effect did not differ between them in any of the instruments. CONCLUSION: Low frequency rTMS administered over the left dorso-lateral prefrontal cortex during 10 daily sessions did not differ from sham rTMS in facilitating the effect of serotonin reuptake inhibitors in OCD patients.


Assuntos
Antidepressivos de Segunda Geração/uso terapêutico , Transtorno Obsessivo-Compulsivo/terapia , Paroxetina/uso terapêutico , Inibidores Seletivos de Recaptação de Serotonina/uso terapêutico , Estimulação Magnética Transcraniana , Adulto , Terapia Combinada , Método Duplo-Cego , Resistência a Medicamentos , Terapia por Estimulação Elétrica/métodos , Feminino , Humanos , Masculino , Testes Neuropsicológicos , Córtex Pré-Frontal/efeitos dos fármacos , Córtex Pré-Frontal/fisiopatologia , Índice de Gravidade de Doença , Estatísticas não Paramétricas , Resultado do Tratamento
4.
Neuro Endocrinol Lett ; 26(6): 667-74, 2005 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-16380683

RESUMO

UNLABELLED: Most clinicians tend to believe that the occurrence of the anxiety disorder in comorbidity with a personality disorder often leads to longer treatment, worsens the prognosis, and thus increasing treatment costs. The study is designed to compare the short-term effectiveness of combination of cognitive behavioral therapy and pharmacotherapy in patient suffering with panic disorder with and without personality disorder. METHOD: We compare the efficacy of 6th week therapeutic program and 6th week follow up in patients suffering with panic disorder and/or agoraphobia and comorbid personality disorder (29 patients) and panic disorder and/or agoraphobia without comorbid personality disorder (31 patients). Diagnosis was done according to the ICD-10 research diagnostic criteria confirmed with MINI and support with psychological methods: IPDE, MCMI-III and TCI. Patients were treated with CBT and psychopharmacs. They were regularly assessed in week 0, 2, 4, 6 and 12 by an independent reviewer on the CGI (Clinical Global Improvement) for severity and change, PDSS (Panic Disorder Severity Scale), HAMA (Hamilton Anxiety Rating Scale), SDS (Sheehan Disability Scale), HDRS (Hamilton Depression Rating Scale), and in self-assessments BAI (Beck Anxiety Inventory) and BDI (Beck Depression Inventory). RESULTS: A combination of CBT and pharmacotherapy proved to be the effective treatment of patients suffering with panic disorder and/or agoraphobia with or without comorbid personality disorder. The 12th week treatment efficacy in the patients with panic disorder without personality disorder had been showed significantly better compared with the group with panic disorder comorbid with personality disorder in CGI and specific inventory for panic disorder--PDSS. Also the scores in depression inventories HDRS and BDI showed significantly higher decrease during the treatment comparing with group without personality disorder. But the treatment effect between groups did not differ in objective anxiety scale HAMA, and subjective anxiety scale BAI.


Assuntos
Agorafobia/complicações , Terapia Cognitivo-Comportamental , Transtorno de Pânico/complicações , Transtorno de Pânico/terapia , Transtornos da Personalidade/complicações , Inibidores Seletivos de Recaptação de Serotonina/uso terapêutico , Adulto , Agorafobia/terapia , Alprazolam/uso terapêutico , Ansiolíticos/uso terapêutico , Terapia Combinada , Feminino , Seguimentos , Humanos , Masculino , Pessoa de Meia-Idade , Paroxetina/uso terapêutico , Transtornos da Personalidade/terapia , Inventário de Personalidade , Escalas de Graduação Psiquiátrica
5.
Sleep Med ; 6(2): 149-53, 2005 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-15716218

RESUMO

BACKGROUND AND PURPOSE: Disturbed night sleep is a common complaint of patients with panic disorder. The aim of the present study was to demonstrate whether the sleep disturbances can be successively influenced by the standard therapy for treating panic disorder. PATIENTS AND METHODS: Psychiatric examinations of 20 outpatients with panic disorder were supplemented with a study of sleep quality using standardised interviews, sleep logs and polysomnographic recordings. RESULTS: A statistical comparison of data showed that reduced anxiety after successful treatment of panic disorder was not necessarily followed by improved sleep parameters. CONCLUSION: The results suggest that the conventional therapy applied to these patients is not sufficient to treat the co-existing insomnia. Consequently, it seems to be of importance to supplement the treatment of panic disorders with specific treatment of the sleep disturbance.


Assuntos
Terapia Cognitivo-Comportamental/métodos , Transtorno de Pânico/epidemiologia , Transtorno de Pânico/terapia , Transtornos do Sono-Vigília/epidemiologia , Adulto , Ansiedade/diagnóstico , Ansiedade/epidemiologia , Manual Diagnóstico e Estatístico de Transtornos Mentais , Eletroencefalografia , Humanos , Pessoa de Meia-Idade , Transtorno de Pânico/diagnóstico , Polissonografia , Índice de Gravidade de Doença , Fases do Sono , Transtornos do Sono-Vigília/diagnóstico , Inquéritos e Questionários
6.
Neuro Endocrinol Lett ; 25(5): 340-8, 2004 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-15580167

RESUMO

BACKGROUND: The goal of our study was to identify brain structures in patients with panic disorder (PD) that show changes in 18FDG PET during the treatment with cognitive behavioral therapy (CBT) or antidepressants. METHOD: Twelve patients suffering from panic disorder were studied with [18F]-2-fluoro-deoxyglucose positron emission tomography (18FDG PET) scanning during resting state (condition of random episodic silent thinking, REST). After PET examination patients were randomly assigned to either cognitive behavioral treatment group (6 patients) or antidepressants treatment group (6 patients). After a 3 month period 18FDG PET examination was repeated in both groups. Psychopathology was assessed using the rating scales HAMA, CGI and Panic Disorder Severity Scale (PDSS). Data were analysed using software for statistical parametric mapping (SPM99). RESULTS: The scores of psychopathology rating scales (CGI, HAMA, PDSS) decreased in both groups. Changes of 18FDG uptake in the pharmacotherapy group: decreases were found in the a priori hypothesized regions in the right hemisphere, in the superior, middle, medial and inferior frontal gyrus, superior and middle temporal gyrus, and increases were detected in the a priori hypothesized regions, mainly in the left hemisphere in medial and middle frontal gyrus, superior, middle and transverse temporal gyrus. Changes of 18FDG uptake in the CBT group: decreases were found in the a priori hypothesized regions of the right hemisphere in the inferior temporal gyrus, superior and inferior frontal gyrus, and increases were detected in the a priori hypothesized region, mostly in the left hemisphere: inferior frontal gyrus, middle temporal gyrus and insula. We did not detect changes in 18FDG uptake in the limbic region (hippocampus, parahippocampal gyrus and amygdala). CONCLUSIONS: Changes in brain metabolism (18FDG uptake) after the treatment either with CBT or with antidepressants were similar in number of brain areas, with prominent right-left difference. This is in concordance with the asymmetry of brain activity noted in patients with PD according to previous PET (and SPECT) studies.


Assuntos
Antidepressivos/uso terapêutico , Córtex Cerebral/metabolismo , Terapia Cognitivo-Comportamental , Lateralidade Funcional , Transtorno de Pânico/metabolismo , Transtorno de Pânico/terapia , Adulto , Mapeamento Encefálico , Córtex Cerebral/diagnóstico por imagem , Córtex Cerebral/fisiopatologia , Feminino , Fluordesoxiglucose F18 , Humanos , Masculino , Testes Neuropsicológicos , Transtorno de Pânico/diagnóstico por imagem , Tomografia por Emissão de Pósitrons , Resultado do Tratamento
7.
Am J Psychiatry ; 159(2): 297-301, 2002 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-11823274

RESUMO

OBJECTIVE: Borrelia burgdorferi infection can affect the CNS and mimic psychiatric disorders. It is not known whether Borrelia burgdorferi contributes to overall psychiatric morbidity. The authors compared the prevalence of antibodies to Borrelia burgdorferi in groups of psychiatric patients and healthy subjects to find out whether there is an association between this infection and psychiatric morbidity. METHOD: Between 1995 and 1999 the authors screened for antibodies to Borrelia burgdorferi in 926 psychiatric patients consecutively admitted to Prague Psychiatric Center. They compared the results of this screening with findings from 884 consecutive healthy subjects who took part in an epidemiological survey of antibodies to Borrelia burgdorferi in the general population of the Czech Republic. Sera were tested by means of enzyme-linked immunosorbent assay. Circulating immune complexes were isolated by polyethylene glycol precipitation. To control for potential confounders, the two groups of patients and healthy subjects were matched according to gender and age. Results were obtained in a sample of 499 matched pairs. RESULTS: Among the matched pairs, 166 (33%) of the psychiatric patients and 94 (19%) of the healthy comparison subjects were seropositive in at least one of the four assays. CONCLUSIONS: These findings support the hypothesis that there is an association between Borrelia burgdorferi infection and psychiatric morbidity. In countries where this infection is endemic, a proportion of psychiatric inpatients may be suffering from neuropathogenic effects of Borrelia burgdorferi.


Assuntos
Anticorpos Antibacterianos/sangue , Borrelia burgdorferi/imunologia , Doença de Lyme/imunologia , Transtornos Mentais/imunologia , Adolescente , Adulto , Idoso , Idoso de 80 Anos ou mais , República Tcheca/epidemiologia , Feminino , Inquéritos Epidemiológicos , Humanos , Doença de Lyme/diagnóstico , Doença de Lyme/epidemiologia , Doença de Lyme/psicologia , Masculino , Programas de Rastreamento , Transtornos Mentais/diagnóstico , Transtornos Mentais/epidemiologia , Transtornos Mentais/psicologia , Pessoa de Meia-Idade , Estudos Soroepidemiológicos
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