8 results on '"Holtzmann, Jérôme"'
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2. Dépression résistante : les autres stratégies thérapeutiques
- Author
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Saba, Ghassen, Nieto, Isabel, Bation, Rémy, Allaïli, Najib, Bennabi, Djamila, Moliere, Fanny, Richieri, Raphaëlle, Holtzmann, Jérôme, Bubrovszky, Maxime, Camus, Vincent, Charpeaud, Thomas, Courtet, Philippe, Courvoisier, Pierre, Haesebaert, Frédéric, Doumy, Olivier, El-Hage, Wissam, Garnier, Marion, d’Amato, Thierry, Bougerol, Thierry, Lançon, Christophe, Haffen, Emmanuel, Llorca, Pierre-Michel, Vaiva, Guillaume, Bellivier, Frank, Leboyer, Marion, and Aouizerate, Bruno
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- 2016
- Full Text
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3. Dépression résistante : les stratégies de changement et d’association de médicaments antidépresseurs
- Author
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Charpeaud, Thomas, Moliere, Fanny, Bubrovszky, Maxime, Haesebaert, Frédéric, Allaïli, Najib, Bation, Rémy, Nieto, Isabel, Richieri, Raphaëlle, Saba, Ghassen, Bellivier, Frank, Bennabi, Djamila, Holtzmann, Jérôme, Camus, Vincent, Courtet, Philippe, Courvoisier, Pierre, d’Amato, Thierry, Doumy, Olivier, Garnier, Marion, Bougerol, Thierry, Lançon, Christophe, Haffen, Emmanuel, Leboyer, Marion, Llorca, Pierre-Michel, Vaiva, Guillaume, El-Hage, Wissam, and Aouizerate, Bruno
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- 2016
- Full Text
- View/download PDF
4. Quelle définition pour la dépression résistante ?
- Author
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Holtzmann, Jérôme, Richieri, Raphaëlle, Saba, Ghassen, Allaïli, Najib, Bation, Rémy, Moliere, Fanny, Nieto, Isabel, Bellivier, Frank, Bennabi, Djamila, Bubrovszky, Maxime, Camus, Vincent, Charpeaud, Thomas, Courvoisier, Pierre, Haesebaert, Frédéric, Doumy, Olivier, Courtet, Philippe, El-Hage, Wissam, Garnier, Marion, d’Amato, Thierry, Lançon, Christophe, Leboyer, Marion, Llorca, Pierre-Michel, Vaiva, Guillaume, Bougerol, Thierry, Aouizerate, Bruno, and Haffen, Emmanuel
- Published
- 2016
- Full Text
- View/download PDF
5. [Switching and combining strategies of antidepressant medications].
- Author
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Charpeaud T, Moliere F, Bubrovszky M, Haesebaert F, Allaïli N, Bation R, Nieto I, Richieri R, Saba G, Bellivier F, Bennabi D, Holtzmann J, Camus V, Courtet P, Courvoisier P, d'Amato T, Doumy O, Garnier M, Bougerol T, Lançon C, Haffen E, Leboyer M, Llorca PM, Vaiva G, El-Hage W, and Aouizerate B
- Subjects
- Antidepressive Agents adverse effects, Antidepressive Agents classification, Antidepressive Agents pharmacokinetics, Drug Administration Schedule, Drug Interactions, Drug Resistance, Drug Substitution, Drug Therapy, Combination, Humans, Practice Guidelines as Topic, Antidepressive Agents therapeutic use, Depressive Disorder drug therapy
- Abstract
Switching antidepressant medication may be helpful in depressed patients having no benefit from the initial antidepressant treatment. Before considering switching strategy, the initial antidepressant treatment should produce no therapeutic effect after at least 4 weeks of administration at adequate dosage. Choosing an antidepressant of pharmacologically distinct profile fails to consistently demonstrate a significant superiority in terms of effectiveness over the switching to another antidepressant within the same pharmacological class. Augmenting SSRI/SNRIs with mirtazapine/mianserin has become the most recommended strategy of antidepressant combinations. Augmenting SSRI with tricyclic drugs is now a less recommended strategy of antidepressant combinations given the increased risk for the occurrence of pharmacokinetic drug-drug interactions and adverse effects., (Copyright © 2016 Elsevier Masson SAS. All rights reserved.)
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- 2016
- Full Text
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6. [How to define treatment-resistant depression?].
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Holtzmann J, Richieri R, Saba G, Allaïli N, Bation R, Moliere F, Nieto I, Bellivier F, Bennabi D, Bubrovszky M, Camus V, Charpeaud T, Courvoisier P, Haesebaert F, Doumy O, Courtet P, El-Hage W, Garnier M, d'Amato T, Lançon C, Leboyer M, Llorca PM, Vaiva G, Bougerol T, Aouizerate B, and Haffen E
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- Antidepressive Agents classification, Antidepressive Agents pharmacokinetics, Antidepressive Agents therapeutic use, Avitaminosis diagnosis, Chronic Pain diagnosis, Comorbidity, Depressive Disorder classification, Depressive Disorder epidemiology, Diagnosis, Differential, Drug Interactions, Drug Resistance, Drug Substitution, Electroconvulsive Therapy, Endocrine System Diseases diagnosis, Humans, Mental Disorders diagnosis, Patient Compliance, Psychometrics, Quality of Life, Recurrence, Socioeconomic Factors, Stress, Psychological epidemiology, Stress, Psychological psychology, Depressive Disorder diagnosis
- Abstract
The most largely used definition of the treatment-resistant depression relies on the failure of two successive trials of antidepressant treatment at an adequate dose and duration. The absence of response to previous antidepressant treatments should be assessed using specific and appropriate clinical instruments enabling a correct staging of the therapeutic resistance. A wide range of socio-demographic and clinical factors (i.e. psychiatric/somatic comorbidities) are classically associated with the therapeutic resistance. The aim of the treatment of major depression is to achieve a complete clinical remission. The presence of residual symptoms increases the risk for the subsequent occurrence of relapses and recurrences, hence facilitating the development of therapeutic resistance. The treatment-resistant depression has a deleterious impact on the social, familial or professional functioning, thereby leading to an impaired quality of life with serious socioeconomic consequences and costs., (Copyright © 2016. Published by Elsevier Masson SAS.)
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- 2016
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7. [Potentiation strategies].
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Doumy O, Bennabi D, El-Hage W, Allaïli N, Bation R, Bellivier F, Holtzmann J, Bubrovszky M, Camus V, Charpeaud T, Courvoisier P, d'Amato T, Garnier M, Haesebaert F, Bougerol T, Lançon C, Moliere F, Nieto I, Richieri R, Saba G, Courtet P, Vaiva G, Leboyer M, Llorca PM, Aouizerate B, and Haffen E
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- Anticonvulsants pharmacokinetics, Anticonvulsants therapeutic use, Antidepressive Agents classification, Antidepressive Agents pharmacokinetics, Antipsychotic Agents adverse effects, Antipsychotic Agents pharmacokinetics, Antipsychotic Agents therapeutic use, Bipolar Disorder drug therapy, Double-Blind Method, Drug Resistance, Drug Synergism, Drug Therapy, Combination, Humans, Lithium Carbonate pharmacokinetics, Lithium Carbonate therapeutic use, Meta-Analysis as Topic, Practice Guidelines as Topic, Randomized Controlled Trials as Topic, Thyroid Hormones pharmacokinetics, Thyroid Hormones therapeutic use, Thyrotropin blood, Treatment Outcome, Antidepressive Agents therapeutic use, Depressive Disorder drug therapy
- Abstract
Lithium is among the most classically recommended add-on therapeutic strategy for the management of depressive patients showing unsuccessful response to standard antidepressant medications. The effectiveness of the add-on strategy with lithium requires achieving plasma levels above 0.5 mEq/L. Mood-stabilizing antiepileptic drugs such as carbamazepine, valproate derivatives or lamotrigine have not demonstrated conclusive therapeutic effects for the management of depressive patients showing unsuccessful response to standard antidepressant medications. Thyroid hormones are considered among the currently recommended add-on therapeutic strategy for the management of depressive patients showing unsuccessful response to standard antidepressant medications. The effectiveness of the add-on strategy with thyroid hormones requires achieving plasma concentration of TSH close to the lower limits at the normal range (0.4 μUI/L) or even below it. Second-generation antipsychotics such as aripiprazole or quetiapine have consistently demonstrated significant therapeutic effects for the management of depressive patients showing unsuccessful response to standard antidepressant medications. Second-generation antipsychotics however require the careful monitoring of both cardiovascular and metabolic adverse effects., (Copyright © 2016. Published by Elsevier Masson SAS.)
- Published
- 2016
- Full Text
- View/download PDF
8. [Other therapeutic strategies].
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Saba G, Nieto I, Bation R, Allaïli N, Bennabi D, Moliere F, Richieri R, Holtzmann J, Bubrovszky M, Camus V, Charpeaud T, Courtet P, Courvoisier P, Haesebaert F, Doumy O, El-Hage W, Garnier M, d'Amato T, Bougerol T, Lançon C, Haffen E, Llorca PM, Vaiva G, Bellivier F, Leboyer M, and Aouizerate B
- Subjects
- Antidepressive Agents pharmacokinetics, Double-Blind Method, Drug Interactions, Drug Resistance, Drug Therapy, Combination, Fatty Acids, Omega-3 therapeutic use, Folic Acid therapeutic use, Food-Drug Interactions, Humans, Monoamine Oxidase Inhibitors pharmacokinetics, Randomized Controlled Trials as Topic, S-Adenosylmethionine therapeutic use, Adrenergic alpha-Agonists therapeutic use, Antidepressive Agents therapeutic use, Central Nervous System Stimulants therapeutic use, Depressive Disorder drug therapy, Dietary Supplements, Dopamine Agonists therapeutic use, Excitatory Amino Acid Antagonists therapeutic use, Ketamine therapeutic use, Monoamine Oxidase Inhibitors therapeutic use
- Abstract
Non-selective and irreversible MAOI have become as third or fourth-line strategy for the management of treatment-resistant depression. Non-selective and irreversible MAOI requires careful monitoring of drug interactions and dietary restrictions. Nutritional supplements such as omega-3 have been found to produce beneficial effects in the management of treatment-resistant depression when administered in combination with the ongoing antidepressant treatment. The glutamate antagonist ketamine has been found to produce beneficial effects in the management of treatment-resistant depression while administered alone. Dopamine and/or norepinephrine agonists, such as methylphenidate, modafinil or pramipexole, have been found to produce beneficial effects in the management of treatment-resistant depression when administered in combination with the ongoing antidepressant treatment., (Copyright © 2016. Published by Elsevier Masson SAS.)
- Published
- 2016
- Full Text
- View/download PDF
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