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本文引用的文献

1
Implementing Measurement-Based Care for Depression: Practical Solutions for Psychiatrists and Primary Care Physicians.实施基于测量的抑郁症护理:精神科医生和初级保健医生的实用解决方案。
Neuropsychiatr Dis Treat. 2021 Jan 14;17:79-90. doi: 10.2147/NDT.S283731. eCollection 2021.
2
Meaningful Change in Depression Symptoms Assessed with the Patient Health Questionnaire (PHQ-9) and Montgomery-Åsberg Depression Rating Scale (MADRS) Among Patients with Treatment Resistant Depression in Two, Randomized, Double-blind, Active-controlled Trials of Esketamine Nasal Spray Combined With a New Oral Antidepressant.在两项使用 Esketamine 鼻喷雾剂联合新型口服抗抑郁药的随机、双盲、活性对照试验中,对于治疗抵抗性抑郁症患者,使用患者健康问卷(PHQ-9)和蒙哥马利-Åsberg 抑郁评定量表(MADRS)评估抑郁症状的有意义变化。
J Affect Disord. 2021 Feb 15;281:767-775. doi: 10.1016/j.jad.2020.11.066. Epub 2020 Nov 14.
3
Clinically meaningful changes on depressive symptom measures and patient-reported outcomes in patients with treatment-resistant depression.难治性抑郁症患者抑郁症状测量和患者报告结局方面具有临床意义的变化。
Acta Psychiatr Scand. 2021 Mar;143(3):253-263. doi: 10.1111/acps.13260. Epub 2021 Jan 22.
4
Esketamine Nasal Spray Plus Oral Antidepressant in Patients With Treatment-Resistant Depression: Assessment of Long-Term Safety in a Phase 3, Open-Label Study (SUSTAIN-2).依他佐辛鼻喷剂联合口服抗抑郁药治疗难治性抑郁症患者:3 期、开放标签研究(SUSTAIN-2)的长期安全性评估。
J Clin Psychiatry. 2020 Apr 28;81(3):19m12891. doi: 10.4088/JCP.19m12891.
5
Efficacy and Safety of Esketamine Nasal Spray Plus an Oral Antidepressant in Elderly Patients With Treatment-Resistant Depression-TRANSFORM-3.依他佐辛鼻喷剂联合口服抗抑郁药治疗老年难治性抑郁症的疗效和安全性-TRANSFORM-3。
Am J Geriatr Psychiatry. 2020 Feb;28(2):121-141. doi: 10.1016/j.jagp.2019.10.008. Epub 2019 Oct 17.
6
Adaptation of the Clinical Global Impression for Use in Correctional Settings: The CGI-C.适用于惩教环境的临床总体印象量表:CGI-C
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7
Efficacy and Safety of Fixed-Dose Esketamine Nasal Spray Combined With a New Oral Antidepressant in Treatment-Resistant Depression: Results of a Randomized, Double-Blind, Active-Controlled Study (TRANSFORM-1).依他佐辛鼻喷剂固定剂量联合新型抗抑郁药治疗难治性抑郁症的疗效和安全性:一项随机、双盲、阳性对照研究(TRANSFORM-1)的结果。
Int J Neuropsychopharmacol. 2019 Oct 1;22(10):616-630. doi: 10.1093/ijnp/pyz039.
8
Efficacy of Esketamine Nasal Spray Plus Oral Antidepressant Treatment for Relapse Prevention in Patients With Treatment-Resistant Depression: A Randomized Clinical Trial.依他佐辛鼻喷剂联合口服抗抑郁药治疗治疗抵抗性抑郁症患者预防复发的疗效:一项随机临床试验。
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9
Efficacy and Safety of Flexibly Dosed Esketamine Nasal Spray Combined With a Newly Initiated Oral Antidepressant in Treatment-Resistant Depression: A Randomized Double-Blind Active-Controlled Study.灵活剂量依他佐辛鼻喷雾剂联合新起始口服抗抑郁药治疗难治性抑郁症的疗效和安全性:一项随机、双盲、活性对照研究。
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10
Chronic Vagus Nerve Stimulation Significantly Improves Quality of Life in Treatment-Resistant Major Depression.慢性迷走神经刺激显著改善治疗抵抗性重度抑郁症患者的生活质量。
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使用临床总体印象-严重程度(CGI-S)评估难治性抑郁症患者对抗抑郁治疗的反应。

Use of Clinical Global Impressions-Severity (CGI-S) to Assess Response to Antidepressant Treatment in Patients with Treatment-Resistant Depression.

作者信息

Morrens Joachim, Mathews Maju, Popova Vanina, Borentain Stephane, Rive Benoit, Gonzalez Martin Moro Beatriz, Jamieson Carol, Zhang Qiaoyi

机构信息

Janssen Research & Development, Beerse, Belgium.

Janssen Global Services, LLC, Titusville, NJ, USA.

出版信息

Neuropsychiatr Dis Treat. 2022 Jun 7;18:1127-1132. doi: 10.2147/NDT.S358367. eCollection 2022.

DOI:10.2147/NDT.S358367
PMID:35707064
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9189368/
Abstract

BACKGROUND

This post-hoc analysis evaluated the agreement between Clinical Global Impressions-Severity (CGI-S) score- and Montgomery-Åsberg Depression Rating Scale (MADRS) total score-based assessment of response in patients with treatment-resistant depression (TRD) treated with esketamine nasal spray plus a newly initiated oral antidepressant (ESK-NS + AD).

METHODS

Data were analyzed from a phase 3, randomized, double-blind study (TRANSFORM-2) of flexibly dosed esketamine or placebo nasal spray plus a newly initiated oral-AD in adults with moderate-to-severe TRD. Patients with ≥50% reduction in MADRS from baseline at the end of the 4-week acute treatment phase were defined as responders. For the CGI-S-based assessment of response, patients with ≥2 points decrease from baseline or a CGI-S score of ≤3 (mildly depressed to normal) were considered responders. Cohen's kappa coefficient was calculated to assess level of agreement between MADRS and CGI-S-based assessments.

RESULTS

At the end of 4-week treatment, the proportion of responders among all study patients (n=201) was similar when assessed using the MADRS (61%) and CGI-S (62%) methods, with substantial agreement (Cohen's kappa=0.76; sensitivity=92%; specificity=84%) between both methods. When restricting analysis to ESK-NS + AD-treated patients (n=101) who had a higher response rate (on MADRS: 69%; on CGI-S: 68%), the agreement remained substantial (Cohen's kappa=0.75; sensitivity=91%; specificity=84%).

CONCLUSION

The CGI-S may be a practical and reliable alternative to the MADRS to assess response to ESK-NS + AD in patients with TRD and can be used in real-world practice to support informed treatment decisions.

摘要

背景

本事后分析评估了在难治性抑郁症(TRD)患者中,使用艾氯胺酮鼻喷雾剂加新启用的口服抗抑郁药(ESK-NS + AD)治疗时,基于临床总体印象-严重程度(CGI-S)评分和蒙哥马利-艾斯伯格抑郁量表(MADRS)总分的疗效评估之间的一致性。

方法

对一项3期随机双盲研究(TRANSFORM-2)的数据进行分析,该研究中,中度至重度TRD成人患者接受灵活剂量的艾氯胺酮或安慰剂鼻喷雾剂加新启用的口服抗抑郁药治疗。在4周急性治疗期结束时,MADRS较基线降低≥50%的患者被定义为有反应者。对于基于CGI-S的疗效评估,较基线降低≥2分或CGI-S评分为≤3(轻度抑郁至正常)的患者被视为有反应者。计算Cohen's kappa系数以评估基于MADRS和CGI-S的评估之间的一致性水平。

结果

在4周治疗结束时,使用MADRS(61%)和CGI-S(62%)方法评估时,所有研究患者(n = 201)中有反应者的比例相似,两种方法之间具有高度一致性(Cohen's kappa = 0.76;敏感性 = 92%;特异性 = 84%)。当将分析限制在反应率较高的ESK-NS + AD治疗患者(n = 101)时(基于MADRS:69%;基于CGI-S:68%),一致性仍然很高(Cohen's kappa = 0.75;敏感性 = 91%;特异性 = 84%)。

结论

对于评估TRD患者对ESK-NS + AD的反应,CGI-S可能是MADRS的一种实用且可靠的替代方法,可用于实际临床实践以支持明智的治疗决策。