Institute of Geriatric Psychiatry, Weill Cornell Medical College, White Plains, NY 10605, USA.
Bipolar Disord. 2010 Feb;12(1):56-67. doi: 10.1111/j.1399-5618.2009.00779.x.
This report considers the conceptual and methodological concerns confronting clinical investigators seeking to generate knowledge regarding the tolerability and benefits of pharmacotherapy in geriatric bipolar disorder (BD) patients.
There is continuing need for evidence-based guidelines derived from randomized controlled trials that will enhance drug treatment of geriatric BD patients. Therefore, we present the complex conceptual and methodological choices encountered in designing a multisite clinical trial and the decisions reached by the investigators with the intention that study findings be pertinent to, and can facilitate, routine treatment decisions.
Guided by a literature review and input from peers, the tolerability and antimanic effects of lithium and valproate were judged to be the key mood stabilizers to investigate with regard to treating bipolar I disorder manic, mixed, and hypomanic states. The patient selection criteria are intended to generate a sample that not only experiences common treatment needs but also represents the variety of older patients seen in university-based clinical settings. The clinical protocol guides titration of lithium and valproate to target serum concentrations, with lower levels allowed when necessitated by limited tolerability. The protocol emphasizes initial monotherapy. However, augmentation with risperidone is permitted after three weeks when indicated by operational criteria.
A randomized, controlled trial that both investigates commonly prescribed mood stabilizers and maximizes patient participation can meaningfully address high-priority clinical concerns directly relevant to the routine pharmacologic treatment of geriatric BD patients.
本报告考虑了寻求生成有关老年双相情感障碍(BD)患者药物治疗耐受性和益处的知识的临床研究人员所面临的概念和方法学问题。
需要继续从随机对照试验中得出基于证据的指南,以增强对老年 BD 患者的药物治疗。因此,我们介绍了在设计多中心临床试验中遇到的复杂概念和方法学选择,以及研究人员为使研究结果与常规治疗决策相关并能为其提供便利而做出的决策。
在文献综述和同行意见的指导下,锂盐和丙戊酸盐的耐受性和抗躁狂作用被认为是治疗双相 I 型障碍躁狂、混合和轻躁狂状态的关键心境稳定剂,需要进行研究。患者选择标准旨在生成一个不仅经历常见治疗需求,而且代表大学临床环境中所见的各种老年患者的样本。临床方案指导锂盐和丙戊酸盐的滴定至目标血清浓度,当耐受性有限时允许降低水平。该方案强调初始单药治疗。然而,当根据操作标准表明需要时,在第三周后可以允许使用利培酮进行增效治疗。
一项既调查常用处方心境稳定剂又最大限度地提高患者参与度的随机对照试验,可以有意义地直接解决与老年 BD 患者常规药物治疗直接相关的高优先级临床问题。