Personality Trait Dimensions and the Pharmacological Treatment of Borderline Personality Disorder

被引:25
作者
Saunder, Erika F. H. [1 ,2 ]
Silk, Kenneth R. [1 ]
机构
[1] Univ Michigan, Dept Psychiat, Ann Arbor, MI 48109 USA
[2] Penn State Univ, Dept Psychiat, Coll Med, Hershey, PA USA
关键词
borderline personality disorder; personality traits; pharmacotherapy; treatment; psychiatry; DIALECTICAL BEHAVIOR-THERAPY; DOUBLE-BLIND; PLACEBO; HALOPERIDOL; AMITRIPTYLINE; PHARMACOTHERAPY; AGGRESSION; TRIAL; FLUOXETINE; OLANZAPINE;
D O I
10.1097/JCP.0b013e3181b2b9f3
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The number of well-designed placebo-controlled Studies on pharmacological treatment of borderline personality disorder has been small. We present a breakdown of results of placebo-controlled pharmacological studies, sorting target symptoms into the trait dimensions of affective instability, anxiety inhibition, cognitive-perceptual disturbances, and impulsivity-aggression. Twenty randomized placebo-controlled pharmacological trials studying typical and atypical antipsychotics, selective serotonin reuptake and monoamine oxidase inhibitors, tricyclic antidepressants, mood stabilizers, and benzodiazepines were included. A relative measure of the weight of an outcome was determined by (1) dividing the number of positive comparison, for a drug class by the total number of comparisons of all drugs of all classes for each dimension and (2) dividing the number of positive comparisons for a drug class by the total number of comparisons for that particular drug class for that trait dimension. Antipsychotics (neuroleptics and atypicals) had the most evidence for each of the traits with both methods. Our results are compared with the results of 2 meta-analyses, 1 guideline set, and 1 other systematic review. We found little concordance across these Studies, We propose a consortium to discuss guidelines for future studies, including agreement as to what should be measured to determine the outcome and adoption of standardized instruments to measure that outcome.
引用
收藏
页码:461 / 467
页数:7
相关论文
共 46 条
[41]  
TAYLOR MA, 2003, APA M MAY 17 22 SAN
[42]   Lamotrigine treatment of aggression in female borderline-patients: a randomized, double-blind, placebo-controlled study [J].
Tritt, K ;
Nickel, C ;
Lahmann, C ;
Leiberich, PK ;
Rother, WK ;
Loew, TH ;
Nickel, MK .
JOURNAL OF PSYCHOPHARMACOLOGY, 2005, 19 (03) :287-291
[43]  
ZANARINI M, 2006, 25 BIENN C COLL INT
[44]   Axis II comorbidity of borderline personality disorder [J].
Zanarini, MC ;
Frankenburg, FR ;
Dubo, ED ;
Sickel, AE ;
Trikha, A ;
Levin, A ;
Reynolds, V .
COMPREHENSIVE PSYCHIATRY, 1998, 39 (05) :296-302
[45]   Axis I comorbidity of borderline personality disorder [J].
Zanarini, MC ;
Frankenburg, FR ;
Dubo, ED ;
Sickel, AE ;
Trikha, A ;
Levin, A ;
Reynolds, V .
AMERICAN JOURNAL OF PSYCHIATRY, 1998, 155 (12) :1733-1739
[46]   Olanzapine treatment of female borderline personality disorder patients: A double-blind, placebo-controlled pilot study [J].
Zanarini, MC ;
Frankenburg, FR .
JOURNAL OF CLINICAL PSYCHIATRY, 2001, 62 (11) :849-854