首页> 外文期刊>The journal of clinical psychiatry >Combined treatment with methylphenidate and citalopram for accelerated response in the elderly: an open trial.
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Combined treatment with methylphenidate and citalopram for accelerated response in the elderly: an open trial.

机译:哌醋甲酯和西酞普兰联合治疗可提高老年人的反应速度:一项开放试验。

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BACKGROUND: 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. METHOD: 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. RESULTS: Nine patients completed the study. Six patients met criteria for accelerated response (HAM-D score < 10 and Clinical Global Impressions-Improvement scale score of1 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. CONCLUSION: 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.
机译:背景:加速的抗抑郁治疗反应可能对老年患者特别有益,但很少有数据可告知临床实践。我们评估了哌醋甲酯加速对西酞普兰抗抑郁反应的潜​​力,以及在老年重症抑郁症患者中联合治疗的安全性和耐受性。方法:我们在一项为期10周的开放式结构化试验(2001年7月至2002年7月)中研究了11名年龄在70岁以上的老年门诊患者,他们被诊断出患有DSM-IV重度抑郁症。哌醋甲酯在第9周和第10周逐渐减少并停药。缓解定义为汉密尔顿抑郁量表(HAM-D)得分小于10。西酞普兰的日剂量在20到40毫克之间,哌醋甲酯的日剂量在范围介于5到20毫克之间。结果:9名患者完成了研究。 6名患者符合加速反应的标准(到治疗第14天,HAM-D得分<10,临床总体印象-改善量表得分为1或2),另外3例在第3周时有反应。1名患者无反应。所有受试者的西酞普兰平均(SD)剂量为27.5(10.3)mg,哌醋甲酯的平均(SD)剂量为12.2(4.9)mg。观察到的严重程度为轻度至中度,包括镇静,恶心,焦虑,多尿,口干和唾液分泌过多。结论:哌醋甲酯增加西酞普兰可能是一种安全,可行的策略,可提高老年抑郁症患者的抗抑郁反应。该开放标签试验的结果需要在安慰剂对照试验中进行确认。

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