Lavretsky Helen, Kim Moon-Doo, Kumar Anand, Reynolds Charles F
Department of Psychiatry and Biobehavioral Sciences, University of California School of Medicine, Los Angeles 90095, USA.
J Clin Psychiatry. 2003 Dec;64(12):1410-4. doi: 10.4088/jcp.v64n1202.
Accelerated antidepressant treatment response may be particularly beneficial for older patients, yet there are few data to inform clinical practice. We evaluated the potential of methylphenidate to accelerate antidepressant response to citalopram and the safety and tolerability of the combined treatment in patients with geriatric major depressive disorder.
We studied 11 elderly outpatients aged 70 years and older who were diagnosed with DSM-IV major depressive disorder in a 10-week, open-label, structured trial (July 2001-July 2002). Methylphenidate was tapered and discontinued during weeks 9 and 10. Response was defined as a Hamilton Rating Scale for Depression (HAM-D) score of less than 10. The daily dose of citalopram ranged between 20 and 40 mg, and the daily dose of methylphenidate ranged between 5 and 20 mg.
Nine patients completed the study. Six patients met criteria for accelerated response (HAM-D score < 10 and Clinical Global Impressions-Improvement scale score of 1 or 2 by treatment day 14), and 2 more patients responded by week 3. One patient was a nonresponder. The mean (SD) citalopram dose for all subjects was 27.5 (10.3) mg and the mean (SD) methylphenidate dose was 12.2 (4.9) mg. The observed side effects were mild to moderate in severity and included sedation, nausea, anxiety, polyuria, dry mouth, and hypersalivation.
Methylphenidate augmentation of citalopram may be a safe and viable strategy for accelerating antidepressant response in elderly depressed patients. The results of this open-label trial need to be confirmed in a placebo-controlled trial.
加速抗抑郁治疗反应可能对老年患者特别有益,但几乎没有数据可指导临床实践。我们评估了哌醋甲酯加速西酞普兰抗抑郁反应的潜力以及联合治疗在老年重度抑郁症患者中的安全性和耐受性。
我们在一项为期10周的开放标签、结构化试验(2001年7月至2002年7月)中研究了11名年龄在70岁及以上、被诊断为DSM-IV重度抑郁症的老年门诊患者。在第9周和第10周逐渐减少并停用哌醋甲酯。反应定义为汉密尔顿抑郁评定量表(HAM-D)得分低于10分。西酞普兰的每日剂量在20至40毫克之间,哌醋甲酯的每日剂量在5至20毫克之间。
9名患者完成了研究。6名患者符合加速反应标准(治疗第14天HAM-D得分<10分且临床总体印象改善量表得分为1或2分),另外2名患者在第3周有反应。1名患者无反应。所有受试者的西酞普兰平均(标准差)剂量为27.5(10.3)毫克,哌醋甲酯平均(标准差)剂量为12.2(4.9)毫克。观察到的副作用严重程度为轻度至中度,包括镇静、恶心、焦虑、多尿、口干和流涎过多。
哌醋甲酯增强西酞普兰可能是加速老年抑郁症患者抗抑郁反应的一种安全可行策略。这项开放标签试验的结果需要在安慰剂对照试验中得到证实。