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1.
BMC Psychiatry ; 19(1): 262, 2019 08 28.
Article de Anglais | MEDLINE | ID: mdl-31455302

RÉSUMÉ

BACKGROUND: Clear guidance for successive antidepressant pharmacological treatments for non-responders in major depression is not well established. METHOD: Based on the RAND/UCLA Appropriateness Method, the French Association for Biological Psychiatry and Neuropsychopharmacology and the fondation FondaMental developed expert consensus guidelines for the management of treatment-resistant depression. The expert guidelines combine scientific evidence and expert clinicians' opinions to produce recommendations for treatment-resistant depression. A written survey comprising 118 questions related to highly-detailed clinical presentations was completed on a risk-benefit scale ranging from 0 to 9 by 36 psychiatrist experts in the field of major depression and its treatments. Key-recommendations are provided by the scientific committee after data analysis and interpretation of the results of the survey. RESULTS: The scope of these guidelines encompasses the assessment of pharmacological resistance and situations at risk of resistance, as well as the pharmacological and psychological strategies in major depression. CONCLUSION: The expert consensus guidelines will contribute to facilitate treatment decisions for clinicians involved in the daily assessment and management of treatment-resistant depression across a number of common and complex clinical situations.


Sujet(s)
Psychiatrie biologique/normes , Trouble dépressif résistant aux traitements/thérapie , Expertise/normes , Guides de bonnes pratiques cliniques comme sujet/normes , Psychiatrie/normes , Psychopharmacologie/normes , Antidépresseurs/usage thérapeutique , Psychiatrie biologique/méthodes , Trouble dépressif majeur/épidémiologie , Trouble dépressif majeur/psychologie , Trouble dépressif majeur/thérapie , Trouble dépressif résistant aux traitements/épidémiologie , Trouble dépressif résistant aux traitements/psychologie , Expertise/méthodes , Femelle , Fondations/normes , France/épidémiologie , Humains , Mâle , Psychiatrie/méthodes , Psychopharmacologie/méthodes
2.
BMC Psychiatry ; 19(1): 50, 2019 01 30.
Article de Anglais | MEDLINE | ID: mdl-30700272

RÉSUMÉ

BACKGROUND: Recommendations for pharmacological treatments of major depression with specific comorbid psychiatric conditions are lacking. METHOD: The French Association for Biological Psychiatry and Neuropsychopharmacology and the fondation FondaMental developed expert consensus guidelines for the management of depression based on the RAND/UCLA Appropriatneness Method. Recommendations for lines of treatment are provided by the scientific committee after data analysis and interpretation of the results of a survey of 36 psychiatrist experts in the field of major depression and its treatments. RESULTS: The expert guidelines combine scientific evidence and expert clinician's opinion to produce recommendations for major depression with comorbid anxiety disorders, personality disorders or substance use disorders and in geriatric depression. CONCLUSION: These guidelines provide direction addressing common clinical dilemmas that arise in the pharmacologic treatment of major depression with comorbid psychiatric conditions.


Sujet(s)
Psychiatrie biologique/normes , Trouble dépressif majeur/thérapie , Expertise/normes , Guides de bonnes pratiques cliniques comme sujet/normes , Psychiatrie/normes , Psychopharmacologie/normes , Sujet âgé , Troubles anxieux/épidémiologie , Troubles anxieux/psychologie , Troubles anxieux/thérapie , Psychiatrie biologique/méthodes , Comorbidité , Trouble dépressif majeur/épidémiologie , Trouble dépressif majeur/psychologie , Expertise/méthodes , Femelle , Fondations/normes , France/épidémiologie , Humains , Mâle , Troubles de la personnalité/épidémiologie , Troubles de la personnalité/psychologie , Troubles de la personnalité/thérapie , Psychopharmacologie/méthodes , Troubles liés à une substance/épidémiologie , Troubles liés à une substance/psychologie , Troubles liés à une substance/thérapie
3.
Encephale ; 43(4S): S1-S24, 2017 Sep.
Article de Français | MEDLINE | ID: mdl-28822460

RÉSUMÉ

Major depression represents among the most frequent psychiatric disorders in the general population with an estimated lifetime prevalence of 16-17%. It is characterized by high levels of comorbidities with other psychiatric conditions or somatic diseases as well as a recurrent or chronic course in 50 to 80% of the cases leading to negative repercussions on the daily functioning, with an impaired quality of life, and to severe direct/indirect costs. Large cohort studies have supported that failure of a first-line antidepressant treatment is observed in more than 60% of patients. In this case, several treatment strategies have been proposed by classical evidence-based guidelines from internationally recognized scientific societies, referring primarily on: I) the switch to another antidepressant of the same or different class; II) the combination with another antidepressant of complementary pharmacological profile; III) the addition of a wide range of pharmacological agents intending to potentiate the therapeutic effects of the ongoing antidepressant medication; IV) the association with appropriate psychological therapies; and, V) the use of non-invasive brain stimulation techniques. However, although based on the most recently available data and rigorous methodology, standard guidelines have the significant disadvantage of not covering a large variety of clinical conditions, while currently observed in everyday clinical practice. From these considerations, formalized recommendations by a large panel of French experts in the management of depressed patients have been developed under the shared sponsorship of the French Association of Biological Psychiatry and Neuropsychopharmacology (AFPBN) and the Fondation FondaMental. These French recommendations are presented in this special issue in order to provide relevant information about the treatment choices to make, depending particularly on the clinical response to previous treatment lines or the complexity of clinical situations (clinical features, specific populations, psychiatric comorbidities, etc.). Thus, the present approach will be especially helpful for the clinicians enabling to substantially facilitate and guide their clinical decision when confronted to difficult-to-treat forms of major depression in the daily clinical practice. This will be expected to significantly improve the poor prognosis of the treatment-resistant depression thereby lowering the clinical, functional and costly impact owing directly to the disease.


Sujet(s)
Antidépresseurs/usage thérapeutique , Psychiatrie biologique/normes , Trouble dépressif résistant aux traitements/thérapie , Neuropsychologie/normes , Comités consultatifs/organisation et administration , Comités consultatifs/normes , Neuroleptiques/usage thérapeutique , Psychiatrie biologique/organisation et administration , Comorbidité , Consensus , Trouble dépressif résistant aux traitements/classification , Trouble dépressif résistant aux traitements/diagnostic , Trouble dépressif résistant aux traitements/épidémiologie , Association de médicaments , Expertise , France/épidémiologie , Humains , Neuropsychologie/organisation et administration , Qualité de vie , Sociétés médicales/normes
4.
Vet Immunol Immunopathol ; 178: 88-98, 2016 Oct 01.
Article de Anglais | MEDLINE | ID: mdl-27496747

RÉSUMÉ

Our objective was to evaluate the effect of an injectable trace mineral (ITM) supplement containing zinc, manganese, selenium, and copper on the humoral and cell mediated immune (CMI) responses to vaccine antigens in dairy calves receiving a modified-live viral (MLV) vaccine containing BVDV, BHV1, PI3V and BRSV. A total of 30 dairy calves (3.5 months of age) were administered a priming dose of the MLV vaccine containing BHV1, BVDV1 & 2, BRSV, PI3V, and an attenuated-live Mannheimia-Pasteurella bacterin subcutaneously (SQ). Calves were randomly assigned to 1 of 2 groups: (1) administration of ITM SQ (ITM, n=15) or (2) injection of sterile saline SQ (Control; n=15). Three weeks later, calves received a booster of the same vaccine combination SQ, and a second administration of ITM, or sterile saline, according to the treatment group. Blood samples were collected on days 0, 7, 14, 21, 28, 42, 56, and 90 post-vaccination for determination of antibody titer, viral recall antigen-induced IFN-γ production, and viral antigen-induced proliferation by peripheral blood mononuclear cells (PBMC). Administration of ITM concurrently with MLV vaccination resulted in higher antibody titers to BVDV1 on day 28 after priming vaccination compared to the control group (P=0.03). Calves treated with ITM showed an earlier enhancement in PBMC proliferation to BVDV1 following vaccination compared to the control group. Proliferation of PBMC after BVDV stimulation tended to be higher on day 14 after priming vaccination in calves treated with ITM than in the control group (P=0.08). Calves that received ITM showed higher PBMC proliferation to BRSV stimulation on day 7 after priming vaccination compared to the control group (P=0.01). Moreover, calves in the ITM group also had an enhanced production IFN-γ by PBMC after stimulation with BRSV on day 21 after priming vaccination compared to day 0 (P<0.01). In conclusion, administration of ITM concurrently with MLV vaccination in dairy calves resulted in increased antibody titer to BVDV1, and greater PBMC proliferation to BVDV1 and BRSV recall stimulation compared to the control group, suggesting that ITM might represent a promising tool to enhance the humoral and CMI responses to MLV vaccines in cattle.


Sujet(s)
Maladies des bovins/immunologie , Maladies des bovins/prévention et contrôle , Virus de la diarrhée virale bovine/immunologie , Herpèsvirus bovin de type 1/immunologie , Virus respiratoire syncytial bovin/immunologie , Oligoéléments/administration et posologie , Vaccins antiviraux/administration et posologie , Animaux , Anticorps neutralisants/sang , Anticorps antiviraux/sang , Diarrhée virale bovine-maladie des muqueuses/immunologie , Diarrhée virale bovine-maladie des muqueuses/prévention et contrôle , Bovins , Infections à Herpesviridae/immunologie , Infections à Herpesviridae/prévention et contrôle , Infections à Herpesviridae/médecine vétérinaire , Immunité cellulaire/effets des médicaments et des substances chimiques , Immunité humorale/effets des médicaments et des substances chimiques , Mâle , Infections à virus respiratoire syncytial/immunologie , Infections à virus respiratoire syncytial/prévention et contrôle , Infections à virus respiratoire syncytial/médecine vétérinaire , Vaccins atténués/administration et posologie
5.
J Affect Disord ; 171: 137-41, 2015 Jan 15.
Article de Anglais | MEDLINE | ID: mdl-25305428

RÉSUMÉ

BACKGROUND: Treatment resistant depression is a complex disorder and an important source of morbidity and mortality. Identification of risk factors of resistance may be useful to improve early recognition as well as treatment selection and prediction of outcome in patients with depression. METHODS: The aim of this paper was to review the current status of knowledge regarding risk factors of treatment resistance in unipolar depression, in patients who failed to respond to at least two successive and adequate antidepressant treatments. RESULTS: Systematic literature search yielded 8 publications exploring clinical and biological factors. Specific psychiatric comorbidities, psychosocial factors, clinical characteristics of the depressive episode and biological markers emerge as possible risk factor for treatment resistant depression. LIMITATIONS: Due to the lack of objective definition and diagnostic criteria for treatment resistant depression, and the paucity of reports on risk factors, our review only summarized a small number of studies. CONCLUSION: Future investigations of risk factors should help to improve the understanding of the mechanisms underlying resistance in mood disorders and contribute to improve their therapeutic management.


Sujet(s)
Trouble dépressif résistant aux traitements/psychologie , Antidépresseurs/usage thérapeutique , Trouble dépressif résistant aux traitements/complications , Trouble dépressif résistant aux traitements/traitement médicamenteux , Humains , Adhésion au traitement médicamenteux/psychologie , Adhésion au traitement médicamenteux/statistiques et données numériques , Troubles mentaux/complications , Troubles mentaux/psychologie , Facteurs de risque
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