不成熟的防御机制预示着合并B型人格障碍的重度抑郁症患者对心理治疗的不良反应。

Carolina Rheingantz Scaini, Igor Soares Vieira, Rosiene Machado, Taiane de Azevedo Cardoso, Thaise Mondin, Luciano Souza, Mariane Lopez Molina, Karen Jansen, Ricardo Azevedo da Silva
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引用次数: 0

摘要

目的:评价防御机制对伴有和不伴有B类人格障碍(pd)的抑郁症患者在接受简短心理治疗及随访6个月后抑郁症状的影响。方法:这项准实验研究嵌套在随机临床试验中,包括使用迷你国际神经精神病学访谈诊断为重度抑郁症的成年人(18-60岁)的临床样本。采用百万临床多轴量表(million Clinical Multiaxial Inventory- iii)评估PD,采用防御风格问卷40分析防御机制,采用贝克抑郁量表(Beck Depression Inventory)测量抑郁症状的严重程度。采用线性回归进行校正分析。结果:最终样本包括177例诊断为重度抑郁症的患者,其中39.5%为B类pd。仅在pd患者干预后和随访6个月时,基线不成熟防御显著预测抑郁症状的持续存在。结论:在B类pd抑郁症患者中,不成熟的防御预示着对短期治疗的不良反应。在基线时对不成熟防御的评估可以帮助识别治疗效果差的风险较大的患者,并使其能够选择更适当的治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Immature defense mechanisms predict poor response to psychotherapy in major depressive patients with comorbid cluster B personality disorder.

Immature defense mechanisms predict poor response to psychotherapy in major depressive patients with comorbid cluster B personality disorder.

Immature defense mechanisms predict poor response to psychotherapy in major depressive patients with comorbid cluster B personality disorder.

Objective: To evaluate the impact of defense mechanisms at baseline on depressive symptoms after brief psychotherapies and after 6-months of follow-up among depressed patients with and without cluster B personality disorders (PDs).

Methods: This quasi-experimental study nested within a randomized clinical trial included a clinical sample of adults (18-60 years) diagnosed with major depressive disorder using the Mini-International Neuropsychiatric Interview. The Millon Clinical Multiaxial Inventory-III was applied to assess PD, the Defense Style Questionnaire 40 was used to analyze defense mechanisms, and the Beck Depression Inventory was used to measure the severity of depressive symptoms. Adjusted analysis was performed by linear regression.

Results: The final sample consisted of 177 patients diagnosed with major depressive disorder, of whom 39.5% had cluster B PDs. Immature defenses at baseline significantly predicted the persistence of depressive symptoms at post-intervention and at 6-months of follow-up only in patients with PDs.

Conclusion: In depressed patients with cluster B PDs, immature defenses predicted a poor response to brief therapies. The assessment of immature defenses at baseline can help identify patients at greater risk of poor therapeutic results and enable more appropriate treatment choices.

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