31 results on '"Canceil O"'
Search Results
2. Quels sont les facteurs limitant le recours à un APAP et comment les dépasser ?
- Author
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Canceil, O., Limosin, F., and Passerieux, C.
- Published
- 2009
- Full Text
- View/download PDF
3. Prise en charge au long cours des schizophrénies
- Author
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Canceil, O.
- Published
- 2007
- Full Text
- View/download PDF
4. Prevalence of antiphospholipid antibodies in psychiatric patients users and non-users of antipsychotics: PB 4.63–5
- Author
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Delluc, A, Rousseau, A, Le Galudec, M, Canceil, O, Woodhams, B, Etienne, S, Walter, M, Mottier, D, Van Dreden, P, and Lacut, K
- Published
- 2013
5. The PREPP program, a french experience in early detection of psychosis: cannabis in at risk mental state: OR060
- Author
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Krebs, M O, Magaud, E, Willard, D, Gut, A, Chauchot, F, Canceil, O, Olié, J P, and Kazes, M
- Published
- 2008
6. La fatigue, un symptôme fréquent chez les aidants familiaux nettement réduit par la participation au programme psychoéducatif Profamille V3.2
- Author
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Hodé, Y., primary, Canceil, O., additional, and Willard, D., additional
- Published
- 2019
- Full Text
- View/download PDF
7. Addictions et troubles psychiatriques
- Author
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Brousse, G., primary, Ballon, N., additional, Dellile, J.M., additional, Canceil, O., additional, Blaise, M., additional, Bernardi, S., additional, Berne, E., additional, Claudepierre, A., additional, Icard, C., additional, Couteron, J.P., additional, Julien, J.P., additional, Revue, P., additional, Vosgien, V., additional, Péquart, C., additional, and Hans, C., additional
- Published
- 2019
- Full Text
- View/download PDF
8. Longitudinal Analyses of Blood Transcriptome During Conversion to Psychosis
- Author
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Chaumette, Boris, Kebir, Oussama, Pouch, Juliette, Ducos, Bertrand, Selimi, Fekrije, Gaillard, Raphael, Krebs, Marie-Odile, Amado, I., Gaillard, C., Plaze, M., Magaud, E., Kazes, M., Mam-Lam-Fook, C., Daban, C., Gay, O., Bourgin, J., Martinez, G., Vacheron, M-N, Viala, A., Laqueille, X., Dervaux, Alain, Petitjean, F., Canceil, O., Garnier, B., Fishmann-Mathis, M., Gal, B., Benoit, J. P., Moro, M. R., Centre Hospitalier Sainte Anne [Paris], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP), Institut de psychiatrie et neurosciences de Paris (IPNP - U1266 Inserm), Institut National de la Santé et de la Recherche Médicale (INSERM)-Université Paris Cité (UPCité), GHU Paris Psychiatrie et Neurosciences, Groupement de recherche en Psychiatrie (GDR Psychiatrie (3557)), Centre National de la Recherche Scientifique (CNRS), Institut de biologie de l'ENS Paris (IBENS), Département de Biologie - ENS Paris, École normale supérieure - Paris (ENS-PSL), Université Paris sciences et lettres (PSL)-Université Paris sciences et lettres (PSL)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)-École normale supérieure - Paris (ENS-PSL), Université Paris sciences et lettres (PSL)-Université Paris sciences et lettres (PSL)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS), ABCD : Biophysique des Biomolécules, Laboratoire de physique de l'ENS - ENS Paris (LPENS (UMR_8023)), Université Paris sciences et lettres (PSL)-Université Paris sciences et lettres (PSL)-Université Paris Diderot - Paris 7 (UPD7)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)-École normale supérieure - Paris (ENS-PSL), Université Paris sciences et lettres (PSL)-Université Paris sciences et lettres (PSL)-Université Paris Diderot - Paris 7 (UPD7)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS), Centre interdisciplinaire de recherche en biologie (CIRB), Labex MemoLife, Université Paris sciences et lettres (PSL)-Université Paris sciences et lettres (PSL)-Collège de France (CdF (institution))-Ecole Superieure de Physique et de Chimie Industrielles de la Ville de Paris (ESPCI Paris), Université Paris sciences et lettres (PSL)-École normale supérieure - Paris (ENS-PSL), Université Paris sciences et lettres (PSL)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS), Service de Neuropathologie [Sainte-Anne], Hôpital Sainte-Anne, Unité de Biostatistique et de Recherche Clinique (UBRC), Université de Caen Normandie (UNICAEN), Normandie Université (NU)-Normandie Université (NU)-CHU Caen, Normandie Université (NU)-Tumorothèque de Caen Basse-Normandie (TCBN)-Tumorothèque de Caen Basse-Normandie (TCBN), Université Paris Cité (UPCité), Molecular virology and immunology – Physiopathology and therapeutic of chronic viral hepatitis (Team 18) (Inserm U955), Institut Mondor de Recherche Biomédicale (IMRB), Institut National de la Santé et de la Recherche Médicale (INSERM)-IFR10-Université Paris-Est Créteil Val-de-Marne - Paris 12 (UPEC UP12)-Institut National de la Santé et de la Recherche Médicale (INSERM)-IFR10-Université Paris-Est Créteil Val-de-Marne - Paris 12 (UPEC UP12), Hôpital Louis Mourier - AP-HP [Colombes], Institut de psychiatrie et neurosciences (U894 / UMS 1266), Université Paris Descartes - Paris 5 (UPD5)-Institut National de la Santé et de la Recherche Médicale (INSERM), CHU Amiens-Picardie, Groupe de Recherche sur l'alcool et les pharmacodépendances - UMR INSERM_S 1247 (GRAP), Université de Picardie Jules Verne (UPJV)-Institut National de la Santé et de la Recherche Médicale (INSERM), and Monash University [Clayton]
- Subjects
Adult ,Male ,Risk ,Psychosis ,Longitudinal study ,Adolescent ,[SDV]Life Sciences [q-bio] ,Prodromal Symptoms ,Biology ,Transcriptome ,03 medical and health sciences ,Young Adult ,0302 clinical medicine ,Gene expression ,medicine ,Humans ,Longitudinal Studies ,RNA, Messenger ,Gene ,Genetics ,Sequence Analysis, RNA ,High-Throughput Nucleotide Sequencing ,medicine.disease ,030227 psychiatry ,Psychiatry and Mental health ,Psychotic Disorders ,Schizophrenia ,DNA methylation ,Cohort ,Disease Progression ,Female ,030217 neurology & neurosurgery ,Regular Articles - Abstract
International audience; The biological processes associated with the onset of schizophrenia remain largely unknown. Current hypotheses favor gene x environment interactions as supported by our recent report about DNA methylation changes during the onset of psychosis. Here, we conducted the first longitudinal transcriptomic analysis of blood samples from 31 at-risk individuals who later converted to psychosis and 63 at-risk individuals who did not. Individuals were followed for a maximum of 1 year. Blood samples were collected at baseline and at the end of follow-up and individuals served as their own controls. Differentially expressed genes between the 2 groups were identified using the RNA sequencing of an initial discovery subgroup (n = 15 individuals). The most promising results were replicated using high-throughput real-time qPCR in the whole cohort (n = 94 individuals). We identified longitudinal changes in 4 brain-expressed genes based on RNAseq analysis. One of these genes (CPT1A) was replicated in the whole cohort. The previously observed hypermethylation in NRP1 and GSTM5 during the onset of psychosis correlated with a decrease in corresponding gene expression. RNA sequencing also identified 2 co-expression networks that were impaired after conversion compared with baseline-the Wnt pathway including AKT1, CPT1A and semaphorins, and the Toll-like receptor pathway, related to innate immunity. This longitudinal study of transcriptomic changes in individuals with at-risk mental state revealed alterations during conversion to psychosis in pathways and genes relevant to schizophrenia. These results may be a first step toward better understanding psychosis onset. They may also help to identify new biomarkers and targets for disease-modifying therapeutic strategies.
- Published
- 2018
- Full Text
- View/download PDF
9. CPC-060 Follow-Up of Patients Treated by Prolonged-Release Olanzapine in a Psychiatric Hospital
- Author
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Aldeguer, A, primary, Peloso, C, additional, Moutonnier, C, additional, Canceil, O, additional, Garnier, B, additional, Vacheron, MN, additional, and Advenier-Iakovlev, E, additional
- Published
- 2013
- Full Text
- View/download PDF
10. 266 – Neurological soft signs: Can they predict the outcome?
- Author
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Krebs, M.O., primary, Ouali, A., additional, Bourdel, M.C., additional, Mouaffak, F., additional, Canceil, O., additional, and Olie, J.P., additional
- Published
- 2008
- Full Text
- View/download PDF
11. Dépistage précoce des schizophrénies
- Author
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Petitjean, F., primary, Canceil, O., additional, Gozlan, G., additional, and Coste, E., additional
- Published
- 2008
- Full Text
- View/download PDF
12. Efficacité et tolérance des antipsychotiques : quelles problématiques actuelles ?
- Author
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Canceil, O., primary
- Published
- 2006
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- View/download PDF
13. 0462 PSYCHIATRIC OUTPATIENT CLINIC FOR EMERGING PSYCHOLOGICAL DISORDERS (PREPP PROGRAM): VALIDATION OF THE FRENCH VERSION OF CAARMS
- Author
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Krebs, M.O., primary, Kazes, M., additional, Willard, D., additional, El Khazen, C., additional, Chauchot, F., additional, Gut, A., additional, Conus, P., additional, MacGorry, P.D., additional, Yung, A.R., additional, and Canceil, O., additional
- Published
- 2006
- Full Text
- View/download PDF
14. 0434 PHARMACOLOGICAL TREATMENTS AMONG SUBJECTS REFERRED TO A PSYCHIATRIC OUTPATIENT CLINIC FOR EMERGING PSYCHOLOGICAL DISORDERS (PREPP RESEARCH PROGRAM)
- Author
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Canceil, O., primary, Fidani, J.P., additional, Sacco, A., additional, and Krebs, M.O., additional
- Published
- 2006
- Full Text
- View/download PDF
15. 0432 THE PREPP PROGRAM AND THE PREPSY HEALTH NETWORK: A CLINICAL AND RESEARCH SETTING FOR EARLY DETECTION OF PSYCHOSIS IN PARIS (FRANCE)
- Author
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Canceil, O., primary, Gozlan, G., additional, and Krebs, M.O., additional
- Published
- 2006
- Full Text
- View/download PDF
16. Assessment of psychopathological and psychosocial adaptation of 145 schizophrenic patients
- Author
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Canceil, O., primary, Attar-Levy, D., additional, Sampaio-Meireles, M., additional, Guedj, F., additional, Bourdel, M.C., additional, Bouhassira, M., additional, Poirier, M.F., additional, and Olie, J.P., additional
- Published
- 1999
- Full Text
- View/download PDF
17. [Prodromal symptoms of schizophrenia]
- Author
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Elkhazen C, Chauchot F, Canceil O, Marie-Odile Krebs, and Fj, Baylé
- Subjects
Diagnosis, Differential ,Diagnostic and Statistical Manual of Mental Disorders ,Schizophrenia ,Humans ,Schizophrenic Psychology - Abstract
The concept of prodromal symptoms of schizophrenia has frequently been subject to debate. Authors widely admit the existence of early specific and non-specific signs preceding the first psychotic episode; however, they have yet to clearly demonstrate their ability to predict and specify the outbreak of a psychosis. These prodromal symptoms consist of behavioral abnormalities, pseudo-neurotic signs, subtle cognitive and affective changes. All these symptoms vary from patient to patient. In general, it is widely believed that future patients go through a variety of abnormal, subjective experiences that progressively develop during their pre-puberty and puberty periods. However, the limit of this assessment is that an individual could present the same prodromal symptoms without necessarily developing a psychotic illness, as a result of toxic intake, a situational crisis, etc. Furthermore, while the prodrome is a retrospective concept, its value and specificity can only be prospective, given that patients' descriptions of pre-morbid changes may be corrupted by inefficient memory reconstruction. DSM III-R included prodromal symptoms; individual presenting such symptoms would potentially present psychopathological vulnerability to psychosis regardless of associated genetic risk. Several investigations have shed doubts on their measurement's reliability; therefore, this classification is no longer present in the latest version (DSM IV). Moreover, recent neurodevelopemental hypothesis on schizophrenia have paved the way for possible early intervention, especially because early treatments could well improve illness prognosis. This viewpoint is reinforced by the improved tolerance of new anti-psychotic treatment. In this report, we review the key Articles published over the last 15 Years on this matter. We distinguish two schools of thought: on one hand, the German school referring to the validity of particular neuro-psychological symptoms: attention, perception, proprioperception which can be assessed with many evaluation tools: PAS, TDI, BSABS, SPI-A. The German school points to the fact that patients experimenting such changes could potentially be aware of their state. On the other hand, the Anglo-Saxon school refers to the detection of an "at risk" population. The Anglo-Saxons no longer refer to "prodromal symptoms" but rather to a "prodromal period" that extends to about one Year. This period would begin with the patient's first behavioral changes and extend until the first psychotic episode. Both schools agree that, at this stage, neither the recognition nor the description of the period preceding psychosis allows to effectively predict it. As a result, some Authors continue to refer to psychological changes forming a risk factor for the development of subsequent psychosis, rather than clear predictors of inevitable illness. As for relapses, prodromal signs and symptoms found in schizophrenic patients are both specific and non-specific. In most cases, patients experiment perceptions and behavioral changes before psychosis exacerbation. It is not uncommon for a substantial increase in prodromal symptoms to be followed by degradation in psychotic symptoms. On the other hand, many such increases in psychotic symptoms were not preceded by increases in possible prodromal symptoms; hence their importance in identifying the timing of an intervention, but many relapses will occur regardless of the detection of said symptoms.
18. Family psychoeducation in schizophrenia and schizophrenia related disorder, treatment compliance, and suicidal risk reduction: questions about their relationship from a naturalistic observation.
- Author
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Hode Y, Padovani R, Hikmat W, Guillard-Bouhet N, Attal J, Bralet MC, Biotteau M, Chereau Boudet I, Canceil O, Montagne Larmurier A, Roussel C, Lemestré S, and Willard D
- Abstract
Introduction: The Profamille V3.2 multi-family psycho-educational program directed at caregivers of relatives with schizophrenia or schizophrenia related disorder has been shown to decrease the annual prevalence of suicide attempts. It has been reported that psychoeducation of families can sometimes improve compliance with treatment. This study investigates whether the Profamille program improves compliance and thus reduces the risk of suicide among patients., Method: This is a retrospective study of 179 groups of family caregivers, encompassing 1946 participants enrolled in Module 1 of the Profamille program and followed up one year after completion of the module. Evaluations were conducted using questionnaires filled out by family caregivers at three distinct times: prior to beginning the program, upon its completion, and again one year following its conclusion. The annual prevalence of suicide attempts was measured both before the program began and one year after its conclusion, while compliance to treatment was evaluated at the start and end of the program., Result: After the Profamille program, the annual prevalence of suicide attempts fell by a factor of 2 (p-value = 0.00002) and patient compliance improved (p-value <0.000001). This reduction in suicide attempts was observed independently of improved compliance. Compliance seems to have an additional effect, but only after participation in the program., Conclusion: The Profamille program reduces patients' risk of suicide even when patients are not taking the treatment. When family psychoeducation is not proposed in schizophrenia or schizophrenia related disorder, this can represent a loss of chance for patients., Competing Interests: The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest., (Copyright © 2024 Hode, Padovani, Hikmat, Guillard-Bouhet, Attal, Bralet, Biotteau, Chereau Boudet, Canceil, Montagne Larmurier, Roussel, Lemestré and Willard.)
- Published
- 2024
- Full Text
- View/download PDF
19. Prevalence of antiphospholipid antibodies in psychiatric patients users and non-users of antipsychotics.
- Author
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Delluc A, Rousseau A, Le Galudec M, Canceil O, Woodhams B, Etienne S, Walter M, Mottier D, Van Dreden P, and Lacut K
- Subjects
- Adult, Aged, Aged, 80 and over, Antibodies, Antiphospholipid blood, Antipsychotic Agents therapeutic use, Cross-Sectional Studies, Female, Humans, Male, Middle Aged, Prevalence, Psychotic Disorders blood, Psychotic Disorders diagnosis, Psychotic Disorders drug therapy, Psychotic Disorders immunology, Young Adult, Antibodies, Antiphospholipid immunology, Antipsychotic Agents adverse effects, Seroepidemiologic Studies
- Abstract
Past reports have suggested that antiphospholipid (aPL) antibodies may emerge as a response to antipsychotics treatment, as a high prevalence of aPL antibodies in antipsychotics users has been observed. However, no control group of non-medicated psychiatric patients was included in these reports. In a cross sectional study we determined the prevalence of aPL antibodies in 333 psychiatric inpatients. We compared the proportions of positive aPL antibodytests between users and non-users of antipsychotics with adjustments for potential confounders. The proportion of antipsychotics users carrying at least one aPL antibody ranged from 10·8% to 27·0% compared with 6·8% to 27·2% in non-users (P = 0·24, P = 0·24) depending on the method of detection of lupus anticoagulant (LA). The prevalence of LA detected by dilute Russell viper venom time or partial thromboplastin time-LA was not different between antipsychotics users and non-users (8·1% vs. 5·4%, P = 0·53 and 18·4% vs. 18·2%, P = 0·22), as well as the prevalence of IgM and IgG anti-β2-glycoprotein-I antibodies, IgM and IgG anti-cardiolipin antibodies(3·8% vs. 2·0%, P = 0·75, 0·0% vs. 0·0%, P = not applicable, 1·1 vs. 1·4%, P = 0·91, 2·7% vs. 3·4%, P = 0·71). In conclusion, aPL antibodies were frequently found in patients with psychiatric diseases and no significant increase in the prevalence of aPL antibodies was observed in antipsychotics users., (© 2013 John Wiley & Sons Ltd.)
- Published
- 2014
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- View/download PDF
20. Incidence of venous thromboembolism in psychiatric units.
- Author
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Delluc A, Montavon S, Canceil O, Carpentier M, Nowak E, Mercier B, Bressollette L, Etienne S, Walter M, Mottier D, and Lacut K
- Subjects
- Adult, Aged, Cohort Studies, Female, France epidemiology, Hospitalization, Humans, Incidence, Male, Middle Aged, Prospective Studies, Psychiatric Department, Hospital statistics & numerical data, Risk Factors, Mental Disorders blood, Mental Disorders epidemiology, Venous Thromboembolism epidemiology, Venous Thromboembolism psychology
- Abstract
Introduction: Incidence and risk factors of venous thromboembolism (VTE) are well established in surgical and medical settings, but data in psychiatric units are lacking. The aim of this study was to estimate the incidence of VTE in hospitalized psychiatric patients, and to assess the risk factors for VTE in this specific population., Materials and Methods: All consecutive adult patients, admitted for a psychiatric disorder for at least seven days in psychiatric units were considered for inclusion. Patients were evaluated for signs and symptoms of VTE during hospitalization. At Day 10, all participants were interviewed and a systematic compression ultrasonography of the lower limbs was performed. Patients were followed-up until Day 90., Results: Among the 471 included patients, 449 were evaluable at Day 10, and 458 were followed-up until Day 90. Ten deep vein thromboses (DVT) were diagnosed by Day 10 leading to an incidence of VTE of 2.2% (95% CI, 1.1%-4.1%). Six additional symptomatic VTE occurred between Day 10 and Day 90, leading to a 3.5% incidence at Day 90 (95% CI, 2.0%-5.6%). The main factors associated with VTE were age, bed rest, and diagnosis of dementia. The incidence of VTE in patients aged 75 or over with a diagnosis of dementia reached 8.2% at Day 10 and 12.5% at Day 90., Conclusions: The incidence of VTE in psychiatric units appeared low. However, in older patients, especially those with dementia, the incidence of VTE increased considerably. Further studies are needed to confirm these results., (Copyright © 2012 Elsevier Ltd. All rights reserved.)
- Published
- 2012
- Full Text
- View/download PDF
21. Sensory dysfunction is correlated to cerebellar volume reduction in early schizophrenia.
- Author
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Mouchet-Mages S, Canceil O, Willard D, Krebs MO, Cachia A, Martinot JL, Rodrigo S, Oppenheim C, and Meder JF
- Subjects
- Adolescent, Adult, Diagnostic and Statistical Manual of Mental Disorders, Female, Humans, Magnetic Resonance Imaging, Male, Schizophrenia diagnosis, Severity of Illness Index, Cerebellum anatomy & histology, Schizophrenia epidemiology, Schizophrenia physiopathology, Sensation Disorders diagnosis, Sensation Disorders epidemiology
- Published
- 2007
- Full Text
- View/download PDF
22. [Physiological adolescence, pathological adolescence].
- Author
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Olié JP, Gourion D, Canceil O, and Lôo H
- Subjects
- Adolescent physiology, Age Factors, Female, Humans, Male, Mental Disorders epidemiology
- Abstract
The uncertainties of looming adulthood, nostalgia for childhood, and a general malaise explain the crisis of adolescence. Rebellion, conflict, occasional failure at school or in society, and at-risk behaviors are not always signs of future psychiatric illness. In contrast, the physician must be in a position to identify tell-tale signs such as dysmorphophobia, existential anxiety, a feeling of emptiness, and school or social breakdown. Most psychiatric disorders that begin in adolescence are only diagnosed several years after onset. Yet early diagnosis is of utmost importance, as treatment becomes less effective and the long-term prognosis worsens with time. Suicide is the second cause of death during adolescence. All signs of suicidal behavior require hospitalization and evaluation in a psychiatric unit. Antidepressants may be necessary in adolescence. The recent controversy concerning a possible increase in the suicidal risk during antidepressant treatment should not mask the fact that the real public health issue is depression, and not antidepressants. Eating disorders are especially frequent among adolescent girls; it is important to identify psychiatric comorbidities such as schizophrenia, depression and obsessive-compulsive disorders, and to assess the vital risk. Illicit drug and alcohol consumption are frequent during adolescence; for example, close to half of all French adolescents have tried cannabis at least once. Once again, it is important to detect psychiatric comorbidities in substance-abusing adolescents. Phobia is an underdiagnosed anxiety disorder among adolescents; it may become chronic if proper treatment is not implemented, leading to suffering and disability. Finally, two major psychiatric disorders--schizophrenia and bipolar disorder--generally begin in adolescence. Treatment efficacy and the long-term prognosis both depend on early diagnosis. Treatment must be tailored to the individual patient. "Borderline" states are over-diagnosed, hindering more precise diagnosis and delaying appropriate treatment.
- Published
- 2006
23. [Prodromal symptoms of schizophrenia].
- Author
-
Elkhazen C, Chauchot F, Canceil O, Krebs MO, and Baylé FJ
- Subjects
- Diagnosis, Differential, Diagnostic and Statistical Manual of Mental Disorders, Humans, Schizophrenic Psychology, Schizophrenia diagnosis
- Abstract
The concept of prodromal symptoms of schizophrenia has frequently been subject to debate. Authors widely admit the existence of early specific and non-specific signs preceding the first psychotic episode; however, they have yet to clearly demonstrate their ability to predict and specify the outbreak of a psychosis. These prodromal symptoms consist of behavioral abnormalities, pseudo-neurotic signs, subtle cognitive and affective changes. All these symptoms vary from patient to patient. In general, it is widely believed that future patients go through a variety of abnormal, subjective experiences that progressively develop during their pre-puberty and puberty periods. However, the limit of this assessment is that an individual could present the same prodromal symptoms without necessarily developing a psychotic illness, as a result of toxic intake, a situational crisis, etc. Furthermore, while the prodrome is a retrospective concept, its value and specificity can only be prospective, given that patients' descriptions of pre-morbid changes may be corrupted by inefficient memory reconstruction. DSM III-R included prodromal symptoms; individual presenting such symptoms would potentially present psychopathological vulnerability to psychosis regardless of associated genetic risk. Several investigations have shed doubts on their measurement's reliability; therefore, this classification is no longer present in the latest version (DSM IV). Moreover, recent neurodevelopemental hypothesis on schizophrenia have paved the way for possible early intervention, especially because early treatments could well improve illness prognosis. This viewpoint is reinforced by the improved tolerance of new anti-psychotic treatment. In this report, we review the key Articles published over the last 15 Years on this matter. We distinguish two schools of thought: on one hand, the German school referring to the validity of particular neuro-psychological symptoms: attention, perception, proprioperception which can be assessed with many evaluation tools: PAS, TDI, BSABS, SPI-A. The German school points to the fact that patients experimenting such changes could potentially be aware of their state. On the other hand, the Anglo-Saxon school refers to the detection of an "at risk" population. The Anglo-Saxons no longer refer to "prodromal symptoms" but rather to a "prodromal period" that extends to about one Year. This period would begin with the patient's first behavioral changes and extend until the first psychotic episode. Both schools agree that, at this stage, neither the recognition nor the description of the period preceding psychosis allows to effectively predict it. As a result, some Authors continue to refer to psychological changes forming a risk factor for the development of subsequent psychosis, rather than clear predictors of inevitable illness. As for relapses, prodromal signs and symptoms found in schizophrenic patients are both specific and non-specific. In most cases, patients experiment perceptions and behavioral changes before psychosis exacerbation. It is not uncommon for a substantial increase in prodromal symptoms to be followed by degradation in psychotic symptoms. On the other hand, many such increases in psychotic symptoms were not preceded by increases in possible prodromal symptoms; hence their importance in identifying the timing of an intervention, but many relapses will occur regardless of the detection of said symptoms.
- Published
- 2003
24. [The Swedish model].
- Author
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Canceil O
- Subjects
- Humans, Models, Organizational, Sweden, Mental Disorders therapy, Mental Health Services organization & administration
- Published
- 2002
25. Prevalence of smoking in psychiatric patients.
- Author
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Poirier MF, Canceil O, Baylé F, Millet B, Bourdel MC, Moatti C, Olié JP, and Attar-Lévy D
- Subjects
- Adult, Age Factors, Aged, Analysis of Variance, Chi-Square Distribution, Female, France epidemiology, Humans, Male, Mental Disorders psychology, Middle Aged, Patients statistics & numerical data, Prevalence, Sex Factors, Smoking psychology, Socioeconomic Factors, Mental Disorders epidemiology, Smoking epidemiology
- Abstract
Compelling evidence that tobacco-smoking is a form of drug addiction exists. The aim of this study is to determine the following: (1) prevalence of tobacco-smoking and of nicotine dependence in French psychiatric patients; (2) rates and patterns of tobacco smoking and of nicotine dependence according to diagnosis; (3) relationship between current smoking status and antipsychotic medications; and (4) relationship between cigarette smoking and neurological side effects induced by neuroleptics. A population of 711 psychiatric in- and outpatients was assessed using: (1) a detailed smoking self-questionnaire for smoking history and nicotine dependence; and (2) a questionnaire for staff covering treatments and DSMIII-R diagnoses. Data were analyzed using chi2 analysis of variance (ANOVA) tests (one factor) for quantitative comparisons between groups of patients, and analysis of covariance (ANCOVA) test with age covariate was performed for age-dependent variables. Prevalence of smoking in the population of psychiatric patients was significantly higher than in the French general population. Diagnoses among current smokers were mainly substance-related disorder and schizophrenia. The authors established correlations between prevalence of smoking and age, sex, marital and socioeconomic status, alcohol use, coffee consumption and other psychoactive substance use or abuse. The authors did not find relationship between smoking prevalence and institutionalization. Neuroleptic neurological side effects were significantly fewer among smokers compared to nonsmokers. However, the rate of smokers was significantly higher in psychiatric patients receiving neuroleptic drugs. Nicotine abuse in psychiatric patients, and especially in schizophrenic patients, could support the hypothesis that smoking is consistent with self-medication.
- Published
- 2002
- Full Text
- View/download PDF
26. Principal-component analysis of the Positive and Negative Syndrome Scale in patients with schizophrenia: does a 5-factor model apply to published data?
- Author
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Canceil O, Sampaio-Meireles M, Poirier-Littre MF, Bourdel MC, Olie JP, Attar-Levy D, and Olivier V
- Subjects
- Adult, Female, Humans, Male, Severity of Illness Index, Schizophrenia diagnosis
- Published
- 2002
27. [Antipsychotic drugs and cardiovascular safety: current studies of prolonged QT interval and risk of ventricular arrhythmia].
- Author
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Gury C, Canceil O, and Iaria P
- Subjects
- Antipsychotic Agents therapeutic use, Humans, Risk Factors, Antipsychotic Agents adverse effects, Electrocardiography drug effects, Long QT Syndrome chemically induced, Schizophrenia drug therapy, Torsades de Pointes chemically induced
- Abstract
Cardiovascular mortality is higher among schizophrenic patients than in the general population, and it is possible that most unexplained sudden deaths among these patients are due to ventricular arrhythmias for which antipsychotic drugs are either the cause or a predisposing factor. Most antipsychotic agents show electrophysiological effects resembling those of class 1a antiarrhythmic agents, and may be responsible for prolonging the QT interval, potentially going on to cause torsades de pointes. Some of the antipsychotic agents carry a high risk of arrhythmias, related to their effects on the QT interval. These include thioridazine, pimozide, sultopride, droperidol, and to a lesser extent haloperidol and chlorpromazine. In the case of the new atypical antipsychotic agents, it is possible to rank the risks of different drugs, with sertindole (now withdrawn from sale) having the highest risk, and ziprasidone somewhat lower, followed by risperidone and finally by quetiapine, clozapine and olanzapine which have negligible effects on the QT interval. A number of risk factors have been demonstrated, particularly: hypokalaemia and hypomagnesaemia, bradycardia, congenital long QT syndrome, and any underlying cardiac pathology. Lastly, the risk associated with any given antipsychotic agent is increased if it is combined either with any other drug known to prolong the QT interval and provoke torsades de pointes, or with any drug capable of inhibiting the hepatic metabolism of the antipsychotic agent. A list of such drugs is provided, together with advice on the action to be taken when prescribing an antipsychotic agent to a patient with a long QT interval.
- Published
- 2000
28. [Epidemiology of humor perception disorders in schizophrenia].
- Author
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Canceil O and Rouillon F
- Subjects
- Adult, Female, Humans, Male, Bipolar Disorder complications, Bipolar Disorder epidemiology, Mood Disorders complications, Mood Disorders epidemiology, Schizophrenia complications
- Published
- 1999
29. [First clinical episode of bipolar disorders: a study within a population of bipolar I and bipolar II French patients].
- Author
-
Canceil O, Bouzid R, Olíe JP, Lôo H, and Poirier MF
- Subjects
- Adolescent, Adult, Age of Onset, Aged, Aged, 80 and over, Bipolar Disorder diagnosis, Bipolar Disorder rehabilitation, Female, France epidemiology, Hospitalization, Humans, Male, Middle Aged, Retrospective Studies, Sex Distribution, Surveys and Questionnaires, Bipolar Disorder epidemiology
- Abstract
Clinical symptoms of bipolar disorders onset act as a prognostic risk-factor. Discrepancies of data are related with geographical or cultural conditions. Within a patient population of bipolar (ICD 10) in and out patients of a psychiatric department, manic or hypomanic disorders initiate the space disease in 33% of the cases theses features are similar within the western psychiatric population. In a maghrebian population this proportion reaches 50%. A percentage of 65% of bipolar 1 patients was found within our sample. Sex ratio is 1 for bipolar 1, when, for bipolar 2 disorders sex-ratio was superior to 1, in favor of females. Mean age of the first episode of the disease was younger for patients with a familial history of the disease.
- Published
- 1999
30. [Effect of sertraline on blood clozapine].
- Author
-
Darchy A, Fdhil H, and Canceil O
- Subjects
- 1-Naphthylamine administration & dosage, 1-Naphthylamine adverse effects, Adult, Antidepressive Agents administration & dosage, Antipsychotic Agents administration & dosage, Clozapine administration & dosage, Depressive Disorder, Major blood, Dose-Response Relationship, Drug, Drug Therapy, Combination, Female, Humans, Schizophrenia blood, Sertraline, 1-Naphthylamine analogs & derivatives, Antidepressive Agents adverse effects, Antipsychotic Agents pharmacokinetics, Clozapine pharmacokinetics, Depressive Disorder, Major drug therapy, Schizophrenia drug therapy
- Published
- 1998
31. [Response to antidepressive drugs: a useful trait marker for genetic characterization of depressed patients?].
- Author
-
Canceil O
- Subjects
- Antidepressive Agents adverse effects, Antimanic Agents adverse effects, Antimanic Agents therapeutic use, Bipolar Disorder drug therapy, Bipolar Disorder psychology, Depressive Disorder drug therapy, Depressive Disorder psychology, Humans, Lithium adverse effects, Lithium therapeutic use, Prognosis, Treatment Outcome, Antidepressive Agents therapeutic use, Bipolar Disorder genetics, Depressive Disorder genetics, Genetic Markers genetics
- Published
- 1995
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