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Antipsychotics, Antidepressants, Anticonvulsants, and Placebo on the Symptom Dimensions of Borderline Personality Disorder A Meta-Analysis of Randomized Controlled and Open-Label Trials

期刊

JOURNAL OF CLINICAL PSYCHOPHARMACOLOGY
卷 31, 期 5, 页码 613-624

出版社

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1097/JCP.0b013e31822c1636

关键词

borderline personality disorder; antidepressants; antipsychotics; anticonvulsants; placebo; meta-analysis

资金

  1. Health Authority of Lombardy Region
  2. Ministry of Research
  3. University of Brescia
  4. Stroder
  5. European Psychiatric Association
  6. University of Brescia School of Medicine
  7. Janssen Cilag
  8. Lundbeck
  9. Rottapharm
  10. Servier
  11. Health Authority of Lombardy [153]
  12. Eulo University Study of Brescia
  13. MIUR
  14. AstraZeneca
  15. Eli Lilly

向作者/读者索取更多资源

The aim of this study was to quantitatively review randomized controlled trials (RCTs) and open-label trials analyzing the efficacy of antidepressants, mood stabilizers, and antipsychotics for the treatment of the core symptoms of borderline personality disorder (BPD). Using a similar meta-analytic approach, the efficacy of placebo on the same core symptoms of BPD was evaluated. The risk of discontinuation of each of the medication classes reported in the studies was also analyzed to establish the major causes of discontinuation. MEDLINE (1966 to June 2010) and EMBASE (1980 to June 2010) databases were systematically searched to identify relevant RCTs and open studies. The primary outcome was improvement in the specific core symptoms of the disorder: affective dysregulation, impulsive-behavioral dyscontrol, and cognitive-perceptual symptoms. Evidence from RCTs and open studies suggests that drug treatment, especially with mood stabilizers and antipsychotics, may be effective for treating affective dysregulation and impulsive-behavioral dyscontrol. Antipsychotics were also effective in reducing cognitive-perceptual symptoms. Antidepressants failed to show efficacy in treating BPD symptom dimensions other than affective dysregulation. Our analyses of the placebo arm of RCTs showed a significant improvement of symptomatology in these patients also. There were no significant differences in overall dropout rates between patients on medications and those on placebo. In conclusion, the efficacy of pharmacological treatment on the symptom dimensions of BPD has been shown by various independent meta-analyses, with a positive effect of drug treatment on the core symptoms of BPD and some documentable differences in terms of efficacy between different drug classes in each of the symptom domains.

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