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在 STAR*D 试验中,安非他酮-SR 与丁螺环酮增强西酞普兰的药物心理计量三角结局。

Outcomes on the pharmacopsychometric triangle in bupropion-SR vs. buspirone augmentation of citalopram in the STAR*D trial.

机构信息

Psychiatric Research Unit, Mental Health Centre North Zealand, Copenhagen University, Hillerød, Denmark.

出版信息

Acta Psychiatr Scand. 2012 Apr;125(4):342-8. doi: 10.1111/j.1600-0447.2011.01791.x. Epub 2011 Nov 12.

DOI:10.1111/j.1600-0447.2011.01791.x
PMID:22077211
Abstract

OBJECTIVE

To compare within the framework of a novel pharmacopsychometric triangle, augmentation treatment with bupropion vs. buspirone in the acute therapy of major depression in the STAR*D study. The triangle provides a composite view in three domains of antidepressive activity, side effects, and quality of life.

METHOD

Within the pharmacopsychometric triangle, the short six-item subscales of the Hamilton Depression Scale (HAM-D(17)) and of the Inventory of Depressive Symptomatology (IDS-C(30)), referred to as HAM-D(6) and IDS-C(6), were focussed on pure antidepressive effect. Side-effects (tolerable vs. intolerable) and quality of life were measured using patient-administered questionnaires. A modified intention to treat sample was used.

RESULTS

Within the pharmacopsychometric triangle, bupropion-SR (sustained release) was superior to buspirone when augmented to the current citalopram treatment. Thus, in the domain of pure antidepressive effect, bupropion-SR was superior (P = 0.05) on the HAM-D(6), IDS-C(6), and IDS-C(30), but not on the HAM-D(17). In the domain of side effects, the total scores on the Patient Rated Inventory of Side Effects (PRISE) were reduced significantly more by bupropion-SR than by buspirone (P = 0.03). In the domain of quality of life, the total scores on the Quality of Life Enjoyment and Satisfaction Questionnaire (QLES-Q) showed a trend (P = 0.10) from baseline to endpoint of a superiority for bupropion-SR compared with buspirone.

CONCLUSION

In all domains of the pharmacopsychometric triangle, bupropion-SR was superior to buspirone as augmentation therapy in depressed outpatients not responding to citalopram.

摘要

目的

在新型精神药理学三角的框架内,比较 STAR*D 研究中,安非他酮与丁螺环酮分别作为增效治疗药物,对重度抑郁症急性期的疗效。该三角提供了抗抑郁活性、副作用和生活质量三个领域的综合视图。

方法

在精神药理学三角内,我们重点关注汉密尔顿抑郁量表(HAM-D(17))和抑郁症状自评量表(IDS-C(30))的简短六分量表(HAM-D(6)和 IDS-C(6)),它们代表了纯粹的抗抑郁作用。使用患者自评问卷来测量副作用(可耐受与不可耐受)和生活质量。采用修改后的意向治疗样本。

结果

在精神药理学三角内,安非他酮持续释放(bupropion-SR)与丁螺环酮相比,在增强当前西酞普兰治疗方面更为有效。因此,在纯粹的抗抑郁作用领域,bupropion-SR 在 HAM-D(6)、IDS-C(6)和 IDS-C(30)上均优于丁螺环酮(P = 0.05),但在 HAM-D(17)上则不然。在副作用领域,患者自评的副作用量表(PRISE)的总分显著降低,bupropion-SR 比丁螺环酮更为显著(P = 0.03)。在生活质量领域,生活质量享受和满意度问卷(QLES-Q)的总分显示出 bupropion-SR 相对于丁螺环酮的优势趋势(P = 0.10)。

结论

在精神药理学三角的所有领域,与丁螺环酮相比,安非他酮-SR 作为增效治疗药物,对未对西酞普兰产生反应的门诊重度抑郁症患者更为有效。

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