From the Mood Disorders Center and Beijing Key Laboratory of Mental Disorders, Beijing Anding Hospital, Capital Medical University, Beijing; the Center of Depression, Beijing Institute for Brain Disorders and China Clinical Research Center for Mental Disorders, Beijing; the Unit of Psychiatry, Faculty of Health Sciences, University of Macau; the Department of Psychiatry, Chinese University of Hong Kong, Hong Kong; the University of Notre Dame Australia, Marian Centre, Perth; the School of Psychiatry and Clinical Neurosciences, University of Western Australia, Perth; and the Division of Psychiatry Research, Zucker Hillside Hospital, North Shore-Long Island Jewish Health System, Glen Oaks, N.Y.
Am J Psychiatry. 2015 Oct;172(10):1004-13. doi: 10.1176/appi.ajp.2015.14050652. Epub 2015 Aug 28.
The authors compared measurement-based care with standard treatment in major depression.
Outpatients with moderate to severe major depression were consecutively randomized to 24 weeks of either measurement-based care (guideline- and rating scale-based decisions; N=61), or standard treatment (clinicians' choice decisions; N=59). Pharmacotherapy was restricted to paroxetine (20-60 mg/day) or mirtazapine (15-45 mg/day) in both groups. Depressive symptoms were measured with the Hamilton Depression Rating Scale (HAM-D) and the Quick Inventory of Depressive Symptomatology-Self-Report (QIDS-SR). Time to response (a decrease of at least 50% in HAM-D score) and remission (a HAM-D score of 7 or less) were the primary endpoints. Outcomes were evaluated by raters blind to study protocol and treatment.
Significantly more patients in the measurement-based care group than in the standard treatment group achieved response (86.9% compared with 62.7%) and remission (73.8% compared with 28.8%). Similarly, time to response and remission were significantly shorter with measurement-based care (for response, 5.6 weeks compared with 11.6 weeks, and for remission, 10.2 weeks compared with 19.2 weeks). HAM-D scores decreased significantly in both groups, but the reduction was significantly larger for the measurement-based care group (-17.8 compared with -13.6). The measurement-based care group had significantly more treatment adjustments (44 compared with 23) and higher antidepressant dosages from week 2 to week 24. Rates of study discontinuation, adverse effects, and concomitant medications did not differ between groups.
The results demonstrate the feasibility and effectiveness of measurement-based care for outpatients with moderate to severe major depression, suggesting that this approach can be incorporated in the clinical care of patients with major depression.
作者比较了基于测量的护理与重度抑郁症的标准治疗。
连续将中度至重度重度抑郁症门诊患者随机分为 24 周的基于测量的护理(基于指南和评定量表的决策;N=61)或标准治疗(临床医生的选择决策;N=59)。两组均限制使用帕罗西汀(20-60mg/天)或米氮平(15-45mg/天)进行药物治疗。使用汉密尔顿抑郁评定量表(HAM-D)和抑郁症状快速自评量表(QIDS-SR)测量抑郁症状。反应时间(HAM-D 评分至少下降 50%)和缓解(HAM-D 评分 7 或更低)是主要终点。结果由对研究方案和治疗方案盲法的评估者进行评估。
基于测量的护理组患者的反应率(86.9%比 62.7%)和缓解率(73.8%比 28.8%)明显高于标准治疗组。同样,基于测量的护理组反应和缓解的时间明显更短(反应时间为 5.6 周,而标准治疗组为 11.6 周;缓解时间为 10.2 周,而标准治疗组为 19.2 周)。两组 HAM-D 评分均显著下降,但基于测量的护理组的下降幅度更大(-17.8 比-13.6)。基于测量的护理组的治疗调整次数(44 次比 23 次)和 2 周至 24 周的抗抑郁药剂量更高。两组的研究中断率、不良反应率和伴随药物治疗率无差异。
结果表明,基于测量的护理对于中度至重度抑郁症门诊患者是可行且有效的,这表明该方法可以纳入重度抑郁症患者的临床护理。