The British Journal of Psychiatry (2010) 196: 4-12. doi: 10.1192/bjp.bp.108.062984
© 2010 The Royal College of Psychiatrists
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REVIEW ARTICLE

Pharmacotherapy for borderline personality disorder: Cochrane systematic review of randomised trials

Klaus Lieb, MD

Department of Psychiatry and Psychotherapy, University Medical Centre, Mainz, Germany

Birgit Völlm, MRCPsych, MD, PhD

Section of Forensic Mental Health, Division of Psychiatry, Institute of Mental Health, University of Nottingham, UK

Gerta Rücker, MSc

German Cochrane Centre, University Medical Centre Freiburg, Department of Medical Biometry and Statistics, Freiburg

Antje Timmer, MD, MSc, PhD

Institute of Epidemiology, Helmholtz Centre Munich, Neuherberg

Jutta M. Stoffers, MA

Department of Psychiatry and Psychotherapy, University Medical Centre, Mainz, and Department of Psychiatry and Psychotherapy, University Medical Centre Freiburg, Freiburg, Germany

Correspondence: Correspondence: Dr Klaus Lieb, Department of Psychiatry and Psychotherapy, University Medical Centre Mainz, Untere Zahlbacher Str. 8, D–55131 Mainz, Germany. Email: Klaus.lieb{at}ukmainz.de

Declaration of interest

None.

Background

Many patients with borderline personality disorder receive pharmacological treatment, but there is uncertainty about the usefulness of such therapies.

Aims

To evaluate the evidence of effectiveness of pharmacotherapy in treating different facets of the psychopathology of borderline personality disorder.

Method

A Cochrane Collaboration systematic review and meta-analysis of randomised comparisons of drug v. placebo, drug v. drug, or single drug v. combined drug treatment in adult patients with borderline personality disorder was conducted. Primary outcomes were overall disorder severity as well as specific core symptoms. Secondary outcomes comprised associated psychiatric pathology and drug tolerability.

Results

Twenty-seven trials were included in which first- and second-generation antipsychotics, mood stabilisers, antidepressants and omega-3 fatty acids were tested. Most beneficial effects were found for the mood stabilisers topiramate, lamotrigine and valproate semisodium, and the second-generation antipsychotics aripiprazole and olanzapine. However, the robustness of findings is low, since they are based mostly on single, small studies. Selective serotonin reuptake inhibitors so far lack high-level evidence of effectiveness.

Conclusions

The current evidence from randomised controlled trials suggests that drug treatment, especially with mood stabilisers and second-generation antipsychotics, may be effective for treating a number of core symptoms and associated psychopathology, but the evidence does not currently support effectiveness for overall severity of borderline personality disorder. Pharmacotherapy should therefore be targeted at specific symptoms.


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