The impact of personality disorder pathology on the effectiveness of Cognitive Therapy and Interpersonal Psychotherapy for Major Depressive Disorder

被引:14
|
作者
van Bronswijk, Suzanne C. [1 ]
Lemmens, Lotte H. J. M. [2 ]
Viechtbauer, Wolfgang [1 ]
Huibers, Marcus J. H. [3 ,4 ]
Arntz, Arnoud [2 ,5 ]
Peeters, Frenk P. M. L. [1 ]
机构
[1] Maastricht Univ, Fac Hlth Med & Life Sci, Dept Psychiat & Neuropsychol, POB 616, NL-6200 MD Maastricht, Netherlands
[2] Maastricht Univ, Fac Psychol & Neurosci, Dept Clin Psychol Sci, POB 616, NL-6200 MD Maastricht, Netherlands
[3] Vrije Univ Amsterdam, Dept Clin Psychol, Van der Boechorststr 1, NL-1081 BT Amsterdam, Netherlands
[4] Univ Penn, Dept Psychol, 3720 Walnut St, Philadelphia, PA 19104 USA
[5] Univ Amsterdam, Dept Clin Psychol, POB 19268, NL-1000 GG Amsterdam, Netherlands
关键词
Depression; Personality; Cognitive Therapy; Interpersonal Psychotherapy; Psychotherapy; REMISSION; PHARMACOTHERAPY; PREDICTORS; EFFICACY; QUALITY; CLUSTER; WORSE;
D O I
10.1016/j.jad.2017.08.043
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: Despite extensive research, there is no consensus how Personality Disorders (PD) and PD features affect outcome for Major Depressive Disorder (MDD). The present study evaluated the effects of PD (features) on treatment continuation and effectiveness in Cognitive Therapy (CT) and Interpersonal Psychotherapy (IPT) for MDD. Methods: Depressed outpatients were randomized to CT (n= 72) and IPT (n= 74). Primary outcome was depression severity measured repeatedly with the Beck Depression Inventory-II (BDI-II) at baseline, three months, at the start of each therapy session, at post-treatment and monthly during five months follow-up. Results: Comorbid PD and PD features did not affect dropout. Multilevel and Cox regression models indicated no negative effect of PD on BDI-II change and remission rates during treatment and follow-up, irrespective of the treatment received. For both therapies, higher dependent PD features predicted overall lower BDI-II scores during treatment, however this effect did not sustain through follow-up. Cluster A PD features moderated treatment outcome during treatment and follow-up: individuals with high cluster A PD features had greater BDIII reductions over time in CT as compared to IPT. Limitations: Not all therapists and participants were blind to the assessment of PD (features), and assessments were performed by one rater. Further research must investigate the state and trait dependent changes of PD and MDD over time. Conclusions: We found no negative impact of PD on the effectiveness and treatment retention of CT and IPT for MDD during treatment and follow-up. If replicated, cluster A PD features can be used to optimize treatment selection.
引用
收藏
页码:530 / 538
页数:9
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