Østergaard Søren D, Meyers Barnett S, Flint Alastair J, Mulsant Benoit H, Whyte Ellen M, Ulbricht Christine M, Bech Per, Rothschild Anthony J
Unit for Psychiatric Research, Aalborg Psychiatric Hospital, Aalborg University Hospital, Mølleparkvej 10, DK-9000 Aalborg, Denmark; Institute of Clinical Medicine, Aarhus University Hospital, Aarhus, Denmark; Depression Clinical and Research Program, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA.
Department of Psychiatry, Weill Medical College of Cornell University and New York Presbyterian Hospital, Westchester Division, White Plains, NY, USA.
J Affect Disord. 2014 May;160:68-73. doi: 10.1016/j.jad.2013.12.020. Epub 2014 Jan 2.
There is no established psychometric instrument dedicated to the measurement of severity in psychotic depression (PD). The aim of this study was to investigate whether a new composite rating scale, the Psychotic Depression Assessment Scale (PDAS), covering both the psychotic and the depressive domains of PD, could detect differences in effect between two psychopharmacological treatment regimens.
We reanalyzed the data from the Study of Pharmacotherapy of Psychotic Depression (STOP-PD), which compared the effect of Olanzapine+Sertraline (n=129) versus Olanzapine+Placebo (n=130). The response to the two regimens was compared using both a mixed effects model and effect size statistics on the total scores of three rating scales: the 17-item Hamilton Depression Rating Scale (HAM-D17), its 6-item melancholia subscale (HAM-D6), and the 11-item PDAS consisting of the HAM-D6 plus five items from the Brief Psychiatric Rating Scale covering psychotic symptoms.
According to both statistical approaches, the PDAS, the HAM-D17 and the HAM-D6 were all able to detect significant differences in treatment effect between Olanzapine+Sertraline and Olanzapine+Placebo (Olanzapine+Sertraline being superior). Notably, 45% of the trial participants were at least "probable psychotic" at their last assessment in the trial.
The STOP-PD was not designed specifically to answer the research questions of the present study.
The Psychotic Depression Assessment Scale (PDAS) is a sensitive measure of treatment response in PD. The fact that 45% of the patients still experienced psychotic symptoms at their last trial assessment emphasizes the need to include items pertaining to psychotic symptoms in rating scales for PD.
目前尚无专门用于测量精神病性抑郁(PD)严重程度的心理测量工具。本研究的目的是调查一种新的综合评定量表——精神病性抑郁评估量表(PDAS),该量表涵盖了PD的精神病性和抑郁两个领域,是否能够检测出两种精神药物治疗方案在疗效上的差异。
我们重新分析了精神病性抑郁药物治疗研究(STOP-PD)的数据,该研究比较了奥氮平+舍曲林(n = 129)与奥氮平+安慰剂(n = 130)的疗效。使用混合效应模型和效应量统计方法,对三个评定量表的总分进行比较,以评估两种治疗方案的反应:17项汉密尔顿抑郁评定量表(HAM-D17)、其6项抑郁亚型量表(HAM-D6)以及由HAM-D6加上简明精神病评定量表中涵盖精神病性症状的5项组成的11项PDAS。
根据两种统计方法,PDAS、HAM-D17和HAM-D6均能够检测出奥氮平+舍曲林与奥氮平+安慰剂在治疗效果上的显著差异(奥氮平+舍曲林更优)。值得注意的是,45%的试验参与者在试验的最后一次评估中至少为“可能的精神病性”。
STOP-PD并非专门为回答本研究的研究问题而设计。
精神病性抑郁评估量表(PDAS)是PD治疗反应的敏感测量工具。45%的患者在试验的最后一次评估中仍有精神病性症状,这一事实强调了在PD评定量表中纳入与精神病性症状相关条目的必要性。