Zusammenfassung
Die Behandlung von Persönlichkeits- und Verhaltensstörungen ist zur Domäne der Psychotherapie geworden. Gleichwohl hat die Psychopharmakotherapie insbesondere im Klinikalltag einen hohen Stellenwert. Einige Verhaltensstörungen werden aufgrund der neuen DSM-5-Strukturen in anderen Kapiteln besprochen, z. B. die Verhaltenssüchte in Kapitel 7.
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Literatur
Amad A, Thomas P, Perez-Rodriguez MM (2015) Borderline personality disorder and oxytocin: review of clinical trials and future directions. Curr Pharm Des 21: 3311–3316
Bellino S, Bozzatello P, Rocca G et al (2014) Efficacy of omega-3 fatty acids in the treatment of borderline personality disorder: a study of the association with valproic acid. J Psychopharmacol 28: 125–132
Black DW, Zanarini MC, Romine A et al (2014) Comparison of low and moderate dosages of extended-release quetiapine in borderline personality disorder: a randomized, double-blind, placebo-controlled trial. Am J Psychiatry 171: 1174–1182
Bolm T (2015) Therapie der Borderline-Persönlichkeitsstörung. DNP – Der Neurologe & Psychiater 16: 34–37
Bozzatello P, Brignolo E, De Grandi E, Bellino S (2016) Supplementation with omega-3 fatty acids in psychiatric disorders: a review of literature data. J Clin Med 5(8): pii: E67
Bozzatello P, Rocca P, Bellino S (2018) Combination of omega-3 fatty acids and valproic acid in treatment of borderline personality disorder: a follow-up study. Clin Drug Investig 38(4): 367–372
Bridler R, Häberle A, Müller ST et al (2015) Psychopharmacological treatment of 2195 in-patients with borderline personality disorder: a comparison with other psychiatric disorders. Eur Neuropsychopharmacol 25: 763–772
Brüne M (2015) On the role of oxytocin in borderline personality disorder. Br J Clin Psychol 55(3): 287–304
Costa AM, Medeiros GC, Redden S et al (2018) Cognitive-behavioral group therapy for intermittent explosive disorder: description and preliminary analysis. Rev Bras Psiquiatr 40(3): 316–319
Crawford MJ, Sanatinia R, Barrett B et al; LABILE study team (2018) The clinical effectiveness and cost-effectiveness of lamotrigine in borderline personality disorder: a randomized placebo-controlled trial. Am J Psychiatry 175(8): 756–764
Cristea IA, Gentili C, Cotet CD et al (2017) Efficacy of psychotherapies for borderline personality disorder: a systematic review and meta-analysis. JAMA Psychiatry 74(4): 319–328
Falkai P, Wittchen HU (Hrsg) (2015) DSM-5. Diagnostisches und Statistisches Manual Psychischer Störungen. Hogrefe, Göttingen
Farde L, Plavén-Sigray P, Borg J, Cervenka S (2018) Brain neuroreceptor density and personality traits: towards dimensional biomarkers for psychiatric disorders. Philos Trans R Soc Lond B Biol Sci 373(1744): pii: 20170156
Gunderson JG, Stout RL, McGlashan TH et al (2011) Ten-year course of borderline personality disorder. Arch Gen Psychiatry 68: 827–837
Hancock-Johnson E, Griffiths C, Picchioni M (2017) A focused systematic review of pharmacological treatment for borderline personality disorder. CNS Drugs 31(5): 345–356
Herpertz SC (2018) Neue Wege der Klassifikation von Persönlichkeitsstörungen in ICD-11. Fortschr Neurol Psychiatr 86(03): 150–155
Herpertz SC, Bertsch K (2015) A new perspective on the pathophysiology of borderline personality disorder: a model of the role of oxytocin. Am J Psychiatry 172: 840–851
Ingenhoven TJ, Duivenvoorden HJ (2011) Differential effectiveness of antipsychotics in borderline personality disorder: meta-analyses of placebo-controlled, randomized clinical trials on symptomatic outcome domains. J Clin Psychopharmacol 31(4): 489–496
Ingenhoven T, Lafay P, Rinne T et al (2010) Effectiveness of pharmacotherapy for severe personality disorders: meta-analyses of randomized controlled trials. J Clin Psychiatry 71: 14–25
Krüger TH, Magid M, Wollmer MA (2016) Can botulinum toxin help patients with borderline personality disorder? Am J Psychiatry 173(9): 940–941
Lischke A, Herpertz SC, Berger C (2017) Divergent effects of oxytocin on (para-)limbic reactivity to emotional and neutral scenes in females with and without borderline personality disorder. Soc Cogn Affect Neurosci 12(11): 1783–1792
Martín-Blanco A, Patrizi B, Soler J et al (2017a) Use of nalmefene in patients with comorbid borderline personality disorder and alcohol use disorder: a preliminary report. Int Clin Psychopharmacol 32(4): 231–234
Martín-Blanco A, Ancochea A, Soler J et al (2017b) Changes over the last 15 years in the psychopharmacological management of persons with borderline personality disorder. Acta Psychiatr Scand 136(3): 323–331
Mielke EL, Neukel C, Bertsch K et al (2018) Alterations of brain volumes in women with early life maltreatment and their associations with oxytocin. Horm Behav 97: 128–136
Naguy A, Al-Enezi N (2017) Lamotrigine uses in psychiatric practice-beyond bipolar prophylaxis a hope or hype? Am J Ther [Epub ahead of print]
Pérez-Pérez B, Cristóbal-Narváez P, Sheinbaum T et al (2018) Interaction between FKBP5 variability and recent life events in the anxiety spectrum: evidence for the differential susceptibility model. PLoS One 13(2): e0193044
Schwerthöffer D, Bäuml J, Rentrop M (2013) Pharmakotherapie der Borderline-Störung: Praxis und Studienlage. Fortschr Neurol Psychiatr 81: 437–443
Stoffers J, Völlm BA, Rücker G et al (2010) Pharmacological interventions for borderline personality disorder. Cochrane Database Syst Rev 6: CD005653
Stoffers JM, Völlm BA, Rücker G et al (2012) Psychological therapies for people with borderline personality disorder. Cochrane Database Syst Rev: CD005652
Stoffers-Winterling J, Lieb K (2015) Pharmakotherapie von Borderline-Persönlichkeitsstörungen – Versorgungsalltag versus aktuelle externe Evidenz. Info Neurol Psychiatrie 17: 51–55
Tebartz van Elst L, Fleck M, Bartels S et al (2016) Increased prevalence of intermittent rhythmic delta or theta activity (IRDA/IRTA) in the electroencephalograms (EEGs) of patients with borderline personality disorder. Front Behav Neurosci 10: 12
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Müller, M.J., Benkert, O. (2019). Medikamente zur Behandlung von Persönlichkeits- und Verhaltensstörungen. In: Benkert, O., Hippius, H. (eds) Kompendium der Psychiatrischen Pharmakotherapie. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-662-57334-1_11
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