Sheehan David V, Meyers Adam L, Prakash Apurva, Robinson Michael J, Swindle Ralph W, Russell James M, Mallinckrodt Craig H
University of South Florida College of Medicine, Tampa, FL, USA.
Curr Med Res Opin. 2008 Sep;24(9):2457-66. doi: 10.1185/03007990802293643. Epub 2008 Jul 24.
To examine the relationship between global functional impairment and the treatment of anxious symptoms and painful somatic symptoms (PSS) in patients with generalized anxiety disorder (GAD).
Data from two double-blind, placebo-controlled trials in adult outpatients meeting DSM-IV criteria for GAD were pooled. In the first trial (9-week, fixed-dose treatment period), patients were randomized to duloxetine 60 mg QD (n=168), duloxetine 120 mg QD (n=170), or placebo (n=175). In the second trial (10-week, flexible-dose treatment period), patients were randomized to 60-120 mg QD of duloxetine (n=168) or placebo (n=159). Path analysis was used to assess the relative contributions of changes in psychic and somatic anxiety and PSS on improved functional outcomes.
Study 1: NCT00122824; Study 2: study completed before registration required.
Sheehan Disability Scale (SDS), Hamilton Anxiety Rating Scale (HAMA), and Visual Analog Scale for overall pain (VAS).
There was a moderate correlation (0.45, p<0.05) at endpoint between changes in global functional impairment and changes in psychic anxiety (controlling for somatic anxiety and PSS); whereas the correlation between changes in global functional impairment and changes in somatic anxiety (controlling for psychic anxiety and PSS) was weak (0.09, p<0.05). The correlation between changes in global functional impairment and changes in PSS (controlling for psychic and somatic anxiety) was weak (0.27, p<0.05). Path analysis revealed that 37% of the total improvement in functional impairment (Sheehan Disability Scale total score) due to duloxetine treatment was independent of improvement in the Hamilton Anxiety Rating Scale (HAMA) psychic and somatic anxiety subscale scores or Visual Analog Scale for overall pain (VAS) score. Improvement in psychic anxiety accounted for 47% of the total treatment effect on improvement of functional impairment, whereas 7% and 9% of the improvement in functional impairment was accounted for by improvements in somatic anxiety and overall pain, respectively.
探讨广泛性焦虑障碍(GAD)患者的整体功能损害与焦虑症状及疼痛性躯体症状(PSS)治疗之间的关系。
汇总两项针对符合DSM-IV标准的成年门诊GAD患者的双盲、安慰剂对照试验的数据。在第一项试验(9周固定剂量治疗期)中,患者被随机分为度洛西汀60mg每日一次(n = 168)、度洛西汀120mg每日一次(n = 170)或安慰剂组(n = 175)。在第二项试验(10周灵活剂量治疗期)中,患者被随机分为度洛西汀60 - 120mg每日一次(n = 168)或安慰剂组(n = 159)。采用路径分析评估心理和躯体焦虑及PSS变化对功能改善结果的相对贡献。
研究1:NCT00122824;研究2:在要求注册之前已完成研究。
希恩残疾量表(SDS)、汉密尔顿焦虑量表(HAMA)以及整体疼痛视觉模拟量表(VAS)。
在终点时,整体功能损害变化与心理焦虑变化之间存在中度相关性(0.45,p<0.05)(控制躯体焦虑和PSS);而整体功能损害变化与躯体焦虑变化之间的相关性较弱(0.09,p<0.05)(控制心理焦虑和PSS)。整体功能损害变化与PSS变化之间的相关性较弱(0.27,p<0.05)(控制心理和躯体焦虑)。路径分析显示,度洛西汀治疗导致的功能损害总改善(希恩残疾量表总分)中有37%独立于汉密尔顿焦虑量表(HAMA)心理和躯体焦虑子量表评分或整体疼痛视觉模拟量表(VAS)评分的改善。心理焦虑的改善占功能损害改善总治疗效果的47%,而躯体焦虑和整体疼痛改善分别占功能损害改善的7%和9%。