Psychopharmacology Unit, University of Bristol, Bristol, UK.
J Psychopharmacol. 2009 Nov;23(8):867-73. doi: 10.1177/0269881108094722. Epub 2008 Jul 17.
To evaluate acute onset of anxiolytic activity using a dental anxiety model, 89 patients were randomised to double-blind single dose pregabalin 150 mg, alprazolam 0.5 mg or placebo 4 h before a scheduled dental procedure. A Dental Anxiety Total score >12 (moderate-to-severe) without meeting Diagnostic and Statistical Manual of Mental Disorders (Fourth edition) (DSM-IV) anxiety disorder criteria was required. Efficacy and safety, assessed 2, 2.5, 3, 3.5 and 4 h postdose, included 100 mm Visual Analogue Scale for Anxiety (VAS-Anxiety; primary outcome), 100 mm VAS-Sedation and Time-to-Onset of Action Scale (TOAS), a patient-rated anti-anxiety drug-benefit scale (no [0] to full benefit [10]). Mixed model analysis found significantly greater VAS-A improvement slopes for pregabalin (t = -2.47; P = 0.014) and alprazolam (t = -2.39; P = 0.018). There was a significant improvement versus placebo in the TOAS from 2 h through endpoint in alprazolam patients and from 3 h onward in pregabalin patients. Pregabalin produced significantly greater increases in VAS-Sedation versus placebo from 2.5 h through 4 h (2 h onward for alprazolam). Notably, there was a higher correlation between TOAS and VAS-Sedation (r = +0.58) than VAS-Anxiety (r = -0.50) on Spearman's analysis. The majority of Adverse Effects (AEs) were mild, and the most frequent for pregabalin, alprazolam, and placebo, respectively, were fatigue (N = 7, 7, 3), dizziness (N = 6, 3, 3), attention disturbance (N = 3, 1, 0), somnolence (N = 3, 0, 0), feeling abnormal (N = 0, 2, 0) and balance disorder (N = 0, 2, 0). These results suggest that onset of clinically meaningful anxiolytic effect after single-dose pregabalin occurs within the first 3-4 h. Additional research is needed to determine whether anxiolytic effect occurs in generalized anxiety disorder populations by day 1 or within 3-4 h post-first dose.
为了评估使用牙科焦虑模型的抗焦虑作用的急性发作,将 89 名患者随机分配至双盲单次剂量普瑞巴林 150mg、阿普唑仑 0.5mg 或安慰剂,在预定的牙科手术前 4 小时。需要有牙科焦虑总分>12(中重度),但不符合精神障碍诊断与统计手册(第四版)(DSM-IV)焦虑障碍标准。疗效和安全性评估包括:给药后 2、2.5、3、3.5 和 4 小时的 100mm 视觉模拟焦虑量表(VAS-Anxiety;主要终点)、100mm VAS 镇静量表和起效时间量表(TOAS)、患者自评抗焦虑药物获益量表(0 无获益至 10 完全获益)。混合模型分析发现普瑞巴林(t = -2.47;P = 0.014)和阿普唑仑(t = -2.39;P = 0.018)的 VAS-Anxiety 改善斜率显著更大。阿普唑仑患者在 2 小时至终点和普瑞巴林患者在 3 小时后,TOAS 与安慰剂相比有显著改善。普瑞巴林从 2.5 小时到 4 小时的 VAS 镇静评分显著高于安慰剂(阿普唑仑从 2 小时开始)。值得注意的是,Spearman 分析显示,TOAS 与 VAS 镇静之间的相关性(r = +0.58)明显高于 VAS-Anxiety(r = -0.50)。大多数不良事件(AE)为轻度,普瑞巴林、阿普唑仑和安慰剂的最常见 AE 分别为疲劳(N = 7、7、3)、头晕(N = 6、3、3)、注意力障碍(N = 3、1、0)、嗜睡(N = 3、0、0)、感觉异常(N = 0、2、0)和平衡障碍(N = 0、2、0)。这些结果表明,单次剂量普瑞巴林后 3-4 小时内出现有临床意义的抗焦虑作用。需要进一步研究以确定在广泛性焦虑障碍人群中,是否在第 1 天或首次给药后 3-4 小时内出现抗焦虑作用。