ABSTRACT
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.
Subject(s)
Intellectual Disability , Humans , Intellectual Disability/diagnosis , Language , Organophosphorus Compounds , Organoplatinum Compounds , Psychiatric Status Rating Scales , PsychopathologyABSTRACT
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.
Subject(s)
Antidepressive Agents/therapeutic use , Depressive Disorder, Major/blood , Depressive Disorder, Major/drug therapy , Ghrelin/blood , Lithium/therapeutic use , Adult , Aged , Body Mass Index , Cohort Studies , Female , Humans , Lithium/blood , Male , Middle Aged , Time FactorsABSTRACT
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.
Subject(s)
Emotional Adjustment , Emotional Intelligence , Fragile X Syndrome/diagnosis , Fragile X Syndrome/psychology , Mental Disorders/psychology , Adolescent , Child , Combined Modality Therapy , Comorbidity , Cost of Illness , Female , Fragile X Syndrome/epidemiology , Fragile X Syndrome/therapy , Germany , Humans , Male , Mental Disorders/diagnosis , Mental Disorders/epidemiology , Mental Disorders/therapy , Neurologic Examination , Pilot Projects , Prospective Studies , Risk FactorsABSTRACT
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.
Subject(s)
Cost of Illness , Fragile X Syndrome/psychology , Fragile X Syndrome/therapy , Patient Outcome Assessment , Adolescent , Adult , Aged , Aged, 80 and over , Child , Child, Preschool , Europe , Female , Follow-Up Studies , Fragile X Syndrome/complications , Germany , Humans , Male , Mental Disorders/complications , Mental Disorders/psychology , Middle Aged , Phenotype , Prospective Studies , Registries , Seizures/complications , Seizures/psychology , Young AdultABSTRACT
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 (Nâ=â12) registry study (EXPLAIN) were analyzed with regard to psychosocial burden and treatment. RESULTS: More than 50â% 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 (<â18 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 90.6â% of younger and more than 64.3â% 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.
Subject(s)
Fragile X Syndrome/psychology , Intellectual Disability/psychology , Mental Disorders/psychology , Adolescent , Adult , Aged , Aged, 80 and over , Child , Child, Preschool , Combined Modality Therapy , Cost of Illness , Female , Fragile X Syndrome/diagnosis , Fragile X Syndrome/genetics , Fragile X Syndrome/therapy , Genetic Predisposition to Disease/genetics , Germany , Humans , Intellectual Disability/diagnosis , Intellectual Disability/genetics , Intellectual Disability/therapy , Male , Mental Disorders/diagnosis , Mental Disorders/genetics , Mental Disorders/therapy , Middle Aged , Prospective Studies , Registries , Young AdultABSTRACT
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.
Subject(s)
Algorithms , Emotional Adjustment , Intellectual Disability/psychology , Intellectual Disability/therapy , Outcome Assessment, Health Care , Patient Care Team , Social Adjustment , Adult , Comorbidity , Female , Germany , Humans , Intellectual Disability/classification , Intellectual Disability/diagnosis , Male , Middle Aged , Psychiatric Department, Hospital , Research Design , Social Behavior Disorders/classification , Social Behavior Disorders/diagnosis , Social Behavior Disorders/psychology , Social Behavior Disorders/therapy , Young AdultABSTRACT
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.
Subject(s)
Fragile X Syndrome/diagnosis , Fragile X Syndrome/therapy , Disease Progression , Female , Germany , Humans , Longitudinal Studies , Male , Prospective Studies , Research Design , Treatment OutcomeSubject(s)
Depressive Disorder , Age Factors , Aged , Antidepressive Agents, Tricyclic/administration & dosage , Antidepressive Agents, Tricyclic/therapeutic use , Cognitive Behavioral Therapy , Depressive Disorder/classification , Depressive Disorder/diagnosis , Depressive Disorder/drug therapy , Depressive Disorder/epidemiology , Depressive Disorder/psychology , Depressive Disorder/therapy , Dysthymic Disorder/diagnosis , Family Practice , Female , Humans , Interview, Psychological , Male , Mianserin/administration & dosage , Mianserin/analogs & derivatives , Mianserin/therapeutic use , Mirtazapine , Prevalence , Recurrence , Referral and Consultation , Sex Factors , Surveys and Questionnaires , Time Factors , World Health OrganizationABSTRACT
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.
Subject(s)
Cerebral Cortex/physiopathology , Evoked Potentials/physiology , Functional Laterality/physiology , Obsessive-Compulsive Disorder/diagnosis , Obsessive-Compulsive Disorder/physiopathology , Adult , Brain Mapping , Cerebral Cortex/anatomy & histology , Female , Humans , Magnetoencephalography , Male , Nerve Net/anatomy & histology , Nerve Net/physiopathology , Neural Pathways/anatomy & histology , Neural Pathways/physiopathology , Predictive Value of Tests , Prefrontal Cortex/anatomy & histology , Prefrontal Cortex/physiopathology , Temporal Lobe/anatomy & histology , Temporal Lobe/physiopathology , Time FactorsABSTRACT
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.
Subject(s)
Depression/therapy , Magnetoencephalography , Prefrontal Cortex/physiopathology , Transcranial Magnetic Stimulation/methods , Treatment Outcome , Adult , Brain Mapping , Depression/physiopathology , Functional Laterality/physiology , Humans , Male , Middle Aged , Prefrontal Cortex/radiation effects , Psychiatric Status Rating Scales , Statistics, NonparametricABSTRACT
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.