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1.
Fortschr Neurol Psychiatr ; 89(7-08): 354-362, 2021 Jul.
Artículo en Alemán | MEDLINE | ID: mdl-33418590

RESUMEN

This study evaluates the usefulness of a modified version of "AMDP Interview Guidance", the established German instrument in simple language for psychopathological examination. A total of 19 patients with intellectual disabilities underwent psychopathological examination with the help of the original version of the AMDP interview guidance, a modified version and a free, non-standardised and the three versions were assessed. With the original version of the AMDP interview guidance, 50% of the patients with intellectual disabilities were able to answer in a proper way and delivered an appropriate result for the psychopathological assessment. Of the remaining patients 85-90% could handle the questions of the modified version with success. The modified version of the AMDP interview guidance in simple language seems to contribute to a better psychopathological examination compared with the original version. Further studies with a statistically appropriate number of patients need to be carried out in the future.


Asunto(s)
Discapacidad Intelectual , Humanos , Discapacidad Intelectual/diagnóstico , Lenguaje , Compuestos Organofosforados , Compuestos Organoplatinos , Escalas de Valoración Psiquiátrica , Psicopatología
2.
Int J Neuropsychopharmacol ; 20(9): 692-697, 2017 09 01.
Artículo en Inglés | MEDLINE | ID: mdl-28911006

RESUMEN

Background: Lithium augmentation of antidepressants is an effective strategy in treatment-resistant depression. The proteohormone ghrelin is thought to be involved in the pathophysiology of depression. The purpose of this study was to investigate the association of treatment response with the course of ghrelin levels during lithium augmentation. Method: Ghrelin serum concentrations and severity of depression were measured in 85 acute depressive patients before and after 4 weeks of lithium augmentation. Results: In a linear mixed model analysis, we found a significant effect of response*time interaction (F1.81=9.48; P=.0028): under treatment, ghrelin levels increased in nonresponders and slightly decreased in responders to lithium augmentation. The covariate female gender had a significant positive effect (F1.83=4.69; P=.033), whereas time, response, appetite, and body mass index (kg/m2) did not show any significant effect on ghrelin levels (P>.05). Conclusion: This is the first study showing that the course of ghrelin levels separates responders and nonresponders to lithium augmentation. Present results support the hypothesis that ghrelin serum concentrations might be involved in response to pharmacological treatment of depression.


Asunto(s)
Antidepresivos/uso terapéutico , Trastorno Depresivo Mayor/sangre , Trastorno Depresivo Mayor/tratamiento farmacológico , Ghrelina/sangre , Litio/uso terapéutico , Adulto , Anciano , Índice de Masa Corporal , Estudios de Cohortes , Femenino , Humanos , Litio/sangre , Masculino , Persona de Mediana Edad , Factores de Tiempo
3.
Z Kinder Jugendpsychiatr Psychother ; 45(2): 141-147, 2017 03.
Artículo en Alemán | MEDLINE | ID: mdl-28320243

RESUMEN

Objective: The study describes the burden of psychosocial risks of mental illnesses and the ways in which children and adolescents with fragile X syndrome (FRX) can be treated. Method: Data from a sample of 34 patients with FRX younger than 18 years stemming from a prospective multicenter (n = 11) registry study (EXPLAIN) were analyzed with regard to psychosocial burden and Treatment. Results: One third of all participants reported having relatives who suffer from FRX. The majority of participants were suffering themselves from one kind or another mental or neurological problems. Younger participants (< 14 years) tended to suffer from atactic disorders, epileptic seizures, and autistic symptoms. These disorders were usually treated by psychotropic drugs supplemented by logopedic therapies and occupational therapies (more than once a month). In our sample, 96.3 % of the younger patients and more than 57.1 % of the older patients were still living with their parents. Conclusions: Patients with FRX often suffer from additional neurological and mental disorders. For that reason, they should be diagnosed and treated early on.


Asunto(s)
Ajuste Emocional , Inteligencia Emocional , Síndrome del Cromosoma X Frágil/diagnóstico , Síndrome del Cromosoma X Frágil/psicología , Trastornos Mentales/psicología , Adolescente , Niño , Terapia Combinada , Comorbilidad , Costo de Enfermedad , Femenino , Síndrome del Cromosoma X Frágil/epidemiología , Síndrome del Cromosoma X Frágil/terapia , Alemania , Humanos , Masculino , Trastornos Mentales/diagnóstico , Trastornos Mentales/epidemiología , Trastornos Mentales/terapia , Examen Neurológico , Proyectos Piloto , Estudios Prospectivos , Factores de Riesgo
4.
BMC Psychiatry ; 16(1): 318, 2016 09 10.
Artículo en Inglés | MEDLINE | ID: mdl-27612457

RESUMEN

BACKGROUND: As data on the phenotype, characteristics and management of patients with Fragile X Syndrome (FXS) are limited, we aimed to collect such data in Germany in experienced centres involved in the treatment of such patients. METHODS: EXPLAIN-FXS is a prospective observational (non-interventional) study (registry) performed between April 2013 and January 2016 at 18 sites in Germany. Requirements for patient participation included confirmed diagnosis of FXS by genetic testing (>200 CGG repeats) and written informed consent. Patients were followed for up to 2 years. RESULTS: Seventy-five patients (84.0 % males, mean age 16.7 ± 14.5 years, ranging from 2 - 82 years) were analysed. The mean 6-item score, determined according to Giangreco (J Pediatr 129:611-614, 1996), was 6.9 ± 2.5 points. At least one neurological finding each was noted in 53 patients (69.7 %). Specifically, ataxia was noted in 5 patients (6.6 %), lack of fine motor skills in 40 patients, (52.6 %), muscle tonus disorder in 4 patients (5.3 %), and other neurological disorders in 39 patients (51.3 %). Spasticity was not noted in any patient. Seizures were reported in 6 patients (8.1 %), anxiety disorders in 22 patients (30.1 %), depression in 7 patients (9.6 %), ADHD/ADD in 36 patients (49.3 %), impairment of social behavior in 39 patients (53.4 %), and other comorbidities in 23 patients (31.5 %). The mean Aberrant Behaviour Checklist Community Edition (ABC-C) score on behavioral symptoms, obtained in 71 patients at first documentation, was 48.4 ± 27.8 (median 45.0, range 5-115). The mean visual analogue scale (VAS) score, obtained in 59 patients at first documentation, was 84.9 ± 14.6 points (median 90; range 50 - 100). CONCLUSIONS: This report describes the largest cohort of patients with FXS in Europe. The reported observations indicate a substantial burden of disease for patients and their caregivers. Based on these observations, an early expert psychiatric diagnosis is recommended for suspected FXS patients. Further recommendations include multimodal and multi-professional management that is tailored to the individual patient's needs. TRIAL REGISTRATION: The ClinTrials.gov identifier is NCT01711606 . Registered on 18 October 2012.


Asunto(s)
Costo de Enfermedad , Síndrome del Cromosoma X Frágil/psicología , Síndrome del Cromosoma X Frágil/terapia , Evaluación del Resultado de la Atención al Paciente , Adolescente , Adulto , Anciano , Anciano de 80 o más Años , Niño , Preescolar , Europa (Continente) , Femenino , Estudios de Seguimiento , Síndrome del Cromosoma X Frágil/complicaciones , Alemania , Humanos , Masculino , Trastornos Mentales/complicaciones , Trastornos Mentales/psicología , Persona de Mediana Edad , Fenotipo , Estudios Prospectivos , Sistema de Registros , Convulsiones/complicaciones , Convulsiones/psicología , Adulto Joven
5.
Psychiatr Prax ; 43(3): 160-4, 2016 Apr.
Artículo en Alemán | MEDLINE | ID: mdl-25643039

RESUMEN

OBJECTIVE: The goal of the study was to describe the burden of psychosocial risks, of mental illnesses and the ways of treatment of patients with fragile X syndrome (FRX). METHOD: Data from a sample of 46 FRX-patients stemming from a prospective multicenter (N = 12) registry study (EXPLAIN) were analyzed with regard to psychosocial burden and treatment. RESULTS: More than 50 % of all participants reported about relatives suffering from FRX, too. The majority of participants did not finish school and was suffering from one or another kind of mental problems. Younger participants (< 18 yrs.) tended to suffer from expansive disorders. Older participants were rather burdened by internalizing symptoms and disorders. Disorders were usually treated by psychotropic drugs added by logopedic therapies and occupational therapies (more than once a month). In our sample 90.6 % of younger and more than 64.3 % of older patients were still living with their parents. CONCLUSIONS: Patients with FRX often suffer from additional mental disorders and should be diagnosed and treated early.


Asunto(s)
Síndrome del Cromosoma X Frágil/psicología , Discapacidad Intelectual/psicología , Trastornos Mentales/psicología , Adolescente , Adulto , Anciano , Anciano de 80 o más Años , Niño , Preescolar , Terapia Combinada , Costo de Enfermedad , Femenino , Síndrome del Cromosoma X Frágil/diagnóstico , Síndrome del Cromosoma X Frágil/genética , Síndrome del Cromosoma X Frágil/terapia , Predisposición Genética a la Enfermedad/genética , Alemania , Humanos , Discapacidad Intelectual/diagnóstico , Discapacidad Intelectual/genética , Discapacidad Intelectual/terapia , Masculino , Trastornos Mentales/diagnóstico , Trastornos Mentales/genética , Trastornos Mentales/terapia , Persona de Mediana Edad , Estudios Prospectivos , Sistema de Registros , Adulto Joven
6.
Psychiatr Prax ; 42(1): 35-41, 2015 Jan.
Artículo en Alemán | MEDLINE | ID: mdl-24089317

RESUMEN

OBJECTIVES: We know from daily experience in the care of people with intellectual disabilities that the usually applied bio-psycho-social model is not sufficient in the psychiatric treatment of that patient-group. A fourth dimension considering cognitive and socio-emotional development should be added. A specific algorithm for evaluating the emotional level of a person (called "SEO") has demonstrated its effectiveness. Aim of this study is to test its feasibility in everyday practice in a hospital team of a psychiatric ward. METHODS: The SEO was used to evaluate 18 patients with intellectual disability by a multi-professional team in a psychiatric hospital ward. The time for completing the SEO was measured within a time period of 8 weeks. Additionally, the influence on patients' problem behaviour in the time period after completion of the SEO was measured. RESULTS: The average time needed for completing one SEO was 11 minutes. After the second week, there was no further shortening of the time necessary for completion of the SEO, nor was their any further improvement in the quality of scoring the SEO by the team. After completion of the SEO, behavioral problems of the patients improved significantly in the following time period. CONCLUSION: The SEO seems to be time-economic and feasible for evaluating the socio-emotional development, which can be well integrated in the routine of a psychiatric hospital team. The benefit for patients is the significant reduction of problem behaviour after SEO-evaluation in general.


Asunto(s)
Algoritmos , Ajuste Emocional , Discapacidad Intelectual/psicología , Discapacidad Intelectual/terapia , Evaluación de Resultado en la Atención de Salud , Grupo de Atención al Paciente , Ajuste Social , Adulto , Comorbilidad , Femenino , Alemania , Humanos , Discapacidad Intelectual/clasificación , Discapacidad Intelectual/diagnóstico , Masculino , Persona de Mediana Edad , Servicio de Psiquiatría en Hospital , Proyectos de Investigación , Trastorno de la Conducta Social/clasificación , Trastorno de la Conducta Social/diagnóstico , Trastorno de la Conducta Social/psicología , Trastorno de la Conducta Social/terapia , Adulto Joven
7.
BMC Psychiatry ; 13: 339, 2013 Dec 19.
Artículo en Inglés | MEDLINE | ID: mdl-24354947

RESUMEN

BACKGROUND: Fragile X syndrome (FXS), caused by a mutation of the FMR1 gene on the X chromosome, is the most common inherited form of intellectual disability and autism spectrum disorders. Comprehensive data are lacking, however, on the characteristics and management patients with FXS in Germany. METHODS/DESIGN: EXPLAIN is a prospective, observational, longitudinal registry with a non-probability sampling approach. It collects data on patient characteristics, therapeutic interventions, psychosocial parameters (including those of family members and caregivers), quality of life of caregiver and patient, caregiver burden, and health economic parameters, such as hospitalisation time. It is designed to include data from 300 patients in ambulatory care from about 50 centres that employ psychiatrists, paediatricians, neurologists, and other relevant specialists, in Germany. The study was initiated in March, 2013. Patients will be followed for at least two years. DISCUSSION: The registry is expected to provide much-needed data on the characteristics and management of patients with FXS in Germany. It will also allow comparisons with other countries, and will enable gap analyses based on current guidelines for management of these patients. TRIAL REGISTRATION: The ClinicalTrials.gov identifier is NCT01711606.


Asunto(s)
Síndrome del Cromosoma X Frágil/diagnóstico , Síndrome del Cromosoma X Frágil/terapia , Progresión de la Enfermedad , Femenino , Alemania , Humanos , Estudios Longitudinales , Masculino , Estudios Prospectivos , Proyectos de Investigación , Resultado del Tratamiento
9.
Brain Res ; 1129(1): 200-5, 2007 Jan 19.
Artículo en Inglés | MEDLINE | ID: mdl-17156764

RESUMEN

Non-invasive functional imaging techniques have begun to delineate the underlying neurophysiological basis of obsessive-compulsive disorder (OCD). In the present study, we investigated slow (2-6 Hz) and fast (12.5-30 Hz) spontaneous magnetoencephalographic (MEG) activity in ten patients with obsessive-compulsive disorders compared to ten healthy control subjects. Fast MEG activity was significantly elevated in OCD patients. The corresponding dipole density maxima were concentrated on the left superior temporal gyrus. Although no differences were detected in the absolute dipole numbers between controls and OCD patients regarding slow MEG activity, only the latter showed a clustering of slow MEG activity over their left dorsolateral prefrontal cortex. We conclude that alterations of spontaneous MEG activity in prefrontal and temporal cortices may be linked to the pathogenesis of OCD. Therefore, we provide further functional neuroimaging evidence that the complex features of OCD have neural correlates, which may help in a future understanding of this disease.


Asunto(s)
Corteza Cerebral/fisiopatología , Potenciales Evocados/fisiología , Lateralidad Funcional/fisiología , Trastorno Obsesivo Compulsivo/diagnóstico , Trastorno Obsesivo Compulsivo/fisiopatología , Adulto , Mapeo Encefálico , Corteza Cerebral/anatomía & histología , Femenino , Humanos , Magnetoencefalografía , Masculino , Red Nerviosa/anatomía & histología , Red Nerviosa/fisiopatología , Vías Nerviosas/anatomía & histología , Vías Nerviosas/fisiopatología , Valor Predictivo de las Pruebas , Corteza Prefrontal/anatomía & histología , Corteza Prefrontal/fisiopatología , Lóbulo Temporal/anatomía & histología , Lóbulo Temporal/fisiopatología , Factores de Tiempo
10.
Neuroreport ; 16(16): 1839-42, 2005 Nov 07.
Artículo en Inglés | MEDLINE | ID: mdl-16237338

RESUMEN

Recently, repetitive transcranial magnetic stimulation has evolved as a potential therapeutic tool to interfere with brain changes associated with neurological and psychiatric diseases. Little is known about its mode of action, however. Here, we investigated effects of repetitive transcranial magnetic stimulation on spontaneous magnetoencephalographic activity in patients with major depression. Before treatment, depressed patients showed a significant increase in slow magnetoencephalographic activity (2-6 Hz) over the left prefrontal cortex, compared with healthy controls. This activity significantly decreased during 10 days of repetitive transcranial magnetic stimulation, paralleled by clinical improvement. We conclude that therapeutic repetitive transcranial magnetic stimulation effects can be mirrored by changes of spontaneous magnetoencephalographic activity.


Asunto(s)
Depresión/terapia , Magnetoencefalografía , Corteza Prefrontal/fisiopatología , Estimulación Magnética Transcraneal/métodos , Resultado del Tratamiento , Adulto , Mapeo Encefálico , Depresión/fisiopatología , Lateralidad Funcional/fisiología , Humanos , Masculino , Persona de Mediana Edad , Corteza Prefrontal/efectos de la radiación , Escalas de Valoración Psiquiátrica , Estadísticas no Paramétricas
14.
Neuroreport ; 15(3): 523-6, 2004 Mar 01.
Artículo en Inglés | MEDLINE | ID: mdl-15094516

RESUMEN

Auditory hallucinations are one the most enigmatic and hampering symptoms associated with schizophrenia. Non-invasive functional imaging techniques have begun to delineate the underlying neuronal basis. We investigated the spontaneous magnetoencephalographic activity in a 33-year-old male schizophrenic patient and compared the results to those obtained from 13 healthy controls. Despite current neuroleptic medication (clozapine) the patient was still suffering from auditory hallucinations. Using the dipole density method, we were able to demonstrate an increase of fast MEG activity (12.5-30 Hz) in the left auditory cortex associated with hallucinations. This activity was absent in healthy controls. We conclude that an increase in fast MEG activity in the auditory cortex is a neurophysiologic correlate for auditory hallucinations in schizophrenia.


Asunto(s)
Corteza Cerebral/fisiopatología , Alucinaciones/fisiopatología , Psicología del Esquizofrénico , Adulto , Antipsicóticos/uso terapéutico , Ritmo beta , Clozapina/uso terapéutico , Lateralidad Funcional/fisiología , Alucinaciones/tratamiento farmacológico , Humanos , Magnetoencefalografía , Masculino , Lóbulo Temporal/fisiopatología
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