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1.
Encephale ; 43(5): 409-415, 2017 Oct.
Article in French | MEDLINE | ID: mdl-28641816

ABSTRACT

BACKGROUND: Violence is a common issue in psychiatry and has multiple determiners. The aim of this study is to assess the psychotic inpatients' violence in association with the violence of the neighborhood from which the patients are drawn and to estimate the impact of this environmental factor with regard to other factors. METHOD: A prospective multicenter study was led in nine French cities. Eligible patients were psychotic involuntary patients hospitalized in the cities' psychiatric wards. During their treatments, any kind of aggressive behavior by the patients has been reported by the Overt Aggression Scale (OAS). RESULTS: From June 2010 to May 2011, 95 patients have been included. Seventy-nine per cent of the patients were violent during their hospitalizations. In a bivariate analysis, inpatient violence was significantly associated with different factors: male gender, patient violence history, substance abuse, manic or mixed disorder, the symptoms severity measured by the BPRS, the insight degree and the city crime rate. In a multivariate analysis, the only significant factors associated with the patients' violence were substance abuse, the symptoms severity and the crime rates from the different patients' cities. CONCLUSION: These results suggest that violence within the psychotic patients' neighborhood could represent a risk of violence during their treatments.


Subject(s)
Hospitalization/statistics & numerical data , Psychotic Disorders/psychology , Psychotic Disorders/therapy , Residence Characteristics , Violence/statistics & numerical data , Adolescent , Adult , Aggression/psychology , Female , Humans , Middle Aged , Psychiatric Department, Hospital/statistics & numerical data , Psychotic Disorders/complications , Psychotic Disorders/epidemiology , Residence Characteristics/statistics & numerical data , Violence/psychology , Young Adult
2.
Schizophr Res ; 159(2-3): 411-4, 2014 Nov.
Article in English | MEDLINE | ID: mdl-25278103

ABSTRACT

Schizophrenia is a chronic illness with a progressive course that can be marked by resistance to antipsychotic treatment. This can make therapeutic support challenging for the practitioner, with results that are partial and unsatisfactory. In the literature, treatment with high-dose olanzapine (>20mg/day) appears to be a good alternative to clozapine, the gold standard for treatment-resistant schizophrenia. In the present observational prospective study, we studied the clinical and biological profiles of patients treated with olanzapine doses up to 100mg/day. In total, 50 patients were clinically and biologically assessed. We found a linear relationship between oral dose and serum concentration (Pearson's r=0.83, p<0.001) with effects of tobacco (p<0.05) and of coffee and tea consumption (p<0.01). Tolerance seemed to be good regardless of dose. No link was found between concentration and efficiency. Despite a nonexhaustive assessment of pharmacokinetic parameters, not least pharmacogenetic data (e.g., genotyping of cytochrome P450-1A2 or glycoprotein P Abcb1a), pharmacokinetic aspects alone cannot account for why the disease may sometimes be resistant to 20mg of olanzapine but respond to higher doses. A nuclear imaging study exploring brain occupancy by high-dose olanzapine, coupled with the abovementioned pharmacokinetic assessment, may prove a relevant experimental paradigm for studying the pathophysiological mechanisms of resistant schizophrenia.


Subject(s)
Antipsychotic Agents , Benzodiazepines , Psychotic Disorders/drug therapy , Schizophrenia/drug therapy , Adult , Antipsychotic Agents/administration & dosage , Antipsychotic Agents/pharmacokinetics , Antipsychotic Agents/pharmacology , Benzodiazepines/administration & dosage , Benzodiazepines/pharmacokinetics , Benzodiazepines/pharmacology , Drug Resistance , Female , Humans , Male , Middle Aged , Olanzapine , Treatment Outcome , Young Adult
3.
Phys Rev Lett ; 63(9): 919-922, 1989 Aug 28.
Article in English | MEDLINE | ID: mdl-10041222
4.
Phys Rev A Gen Phys ; 38(2): 930-938, 1988 Jul 15.
Article in English | MEDLINE | ID: mdl-9900457
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