TMS Clinical and Research Program, Neuromodulation Division, Semel Institute for Neuroscience and Human Behavior at UCLA, Los Angeles, CA, USA; Department of Psychiatry and Biobehavioral Sciences, David Geffen School of Medicine at UCLA 90024, USA.
TMS Clinical and Research Program, Neuromodulation Division, Semel Institute for Neuroscience and Human Behavior at UCLA, Los Angeles, CA, USA; Department of Psychiatry and Biobehavioral Sciences, David Geffen School of Medicine at UCLA 90024, USA.
Psychiatry Res. 2023 Dec;330:115608. doi: 10.1016/j.psychres.2023.115608. Epub 2023 Nov 14.
Clinical outcomes of repetitive Transcranial Magnetic Stimulation (rTMS) for treatment of Major Depressive Disorder (MDD) vary widely, and no single mood rating scale is standard for assessing rTMS outcomes. This study of 708 subjects undergoing clinical rTMS compared the performance of four scales in measuring symptom change during rTMS treatment. Self-report and observer ratings were examined weekly with the Inventory of Depressive Symptomatology 30-item (IDS), Patient Health Questionnaire 9-item (PHQ), Profile of Mood States 30-item (POMS), and Hamilton Depression Rating Scale 17-item (HDRS). While all scales were correlated and detected significant improvement, the degree of improvement over time as well as response (33-50%) and remission (20-24%) rates varied significantly. Higher baseline severity was associated with lower likelihood of remission, and greater improvement by sessions 5 and 10 predicted response across all scales. Use of only a single scale to assess outcome conferred 14-36% risk of failing to detect response/remission indicated by another scale. The PHQ was most likely to indicate improvement and least likely to miss response or remission. These findings indicate that assessment of symptom burden during rTMS treatment may be most accurately assessed through use of multiple instruments.
经颅重复磁刺激(rTMS)治疗重度抑郁症(MDD)的临床疗效差异很大,没有单一的情绪评分量表可用于评估 rTMS 疗效。本研究对 708 名接受临床 rTMS 的患者进行了研究,比较了四种量表在 rTMS 治疗期间衡量症状变化的表现。采用 30 项抑郁症状清单(IDS)、9 项患者健康问卷(PHQ)、30 项心境状态量表(POMS)和 17 项汉密尔顿抑郁量表(HDRS)每周进行自评和观察评分。虽然所有量表均相关且均检测到明显改善,但随时间的改善程度以及反应(33-50%)和缓解(20-24%)率差异显著。较高的基线严重程度与缓解的可能性降低相关,所有量表中第 5 次和第 10 次治疗时的改善程度更大,预示着对所有量表的反应。仅使用单一量表评估疗效可能会导致 14-36%的风险,无法检测到另一种量表指示的反应/缓解。PHQ 最有可能表明改善,最不可能错过反应或缓解。这些发现表明,在 rTMS 治疗期间评估症状负担可能最准确地通过使用多种仪器进行评估。