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Self-report and clinician-rated measures of depression severity: Can one replace the other?

机译:自我报告和临床医师评估的抑郁症严重程度:一种可以替代另一种吗?

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Background It has been suggested that clinician-rated scales and self-report questionnaires may be interchangeable in the measurement of depression severity, but it has not been tested whether clinically significant information is lost when assessment is restricted to either clinician-rated or self-report instruments. The aim of this study is to test whether self-report provides information relevant to short-term treatment outcomes that is not captured by clinician-rating and vice versa. Methods In genome-based drugs for depression (GENDEP), 811 patients with major depressive disorder treated with escitalopram or nortriptyline were assessed with the clinician-rated Montgomery-?sberg Depression Rating Scale (MADRS), Hamilton Rating Scale for Depression (HRSD), and the self-report Beck Depression Inventory (BDI). In sequenced treatment alternatives to relieve depression (STAR*D), 4,041 patients treated with citalopram were assessed with the clinician-rated and self-report versions of the Quick Inventory of Depressive Symptomatology (QIDS-C and QIDS-SR) in addition to HRSD. Results In GENDEP, baseline BDI significantly predicted outcome on MADRS/HRSD after adjusting for baseline MADRS/HRSD, explaining additional 3 to 4% of variation in the clinician-rated outcomes (both P <.001). Likewise, each clinician-rated scale significantly predicted outcome on BDI after adjusting for baseline BDI and explained additional 1% of variance in the self-reported outcome (both P <.001). The results were confirmed in STAR*D, where self-report and clinician-rated versions of the same instrument each uniquely contributed to the prediction of treatment outcome. Conclusions Complete assessment of depression should include both clinician-rated scales and self-reported measures.
机译:背景有人建议,在评估抑郁症严重程度时,临床医师评定的量表和自我报告问卷可以互换使用,但是当评估仅限于临床医师评定或自我报告时,尚未检验是否会丢失临床上重要的信息仪器。这项研究的目的是检验自我报告是否提供了与短期治疗结果相关的信息,而临床医生未对此进行评估,反之亦然。方法在基于基因组的抑郁症药物(GENDEP)中,对811例接受依西酞普兰或去甲替林治疗的重度抑郁症患者进行了临床医师评估的蒙哥马利-伯格伯格抑郁量表(MADRS),汉密尔顿抑郁量表(HRSD),以及自我报告的贝克抑郁量表(BDI)。在缓解抑郁症的按顺序治疗替代方案(STAR * D)中,除HRSD以外,还对4,041名接受西酞普兰治疗的患者进行了临床评估和自我报告的抑郁症状快速调查表(QIDS-C和QIDS-SR)评估。 。结果在GENDEP中,基线BDI在调整了基线MADRS / HRSD后可显着预测MADRS / HRSD的结局,解释了临床医师评估结局的3%至4%的变化(均P <.001)。同样,每个临床医生评定的量表在调整基线BDI后均能显着预测BDI的结局,并解释了自我报告结局中方差的1%(均P <.001)。 STAR * D证实了结果,其中同一仪器的自我报告版本和临床医师评定版本各自独特地有助于预测治疗结果。结论对抑郁症的完整评估应包括临床医师评定的量表和自我报告的措施。

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