Bristol-Myers Squibb, Plainsboro, Connecticut, USA.
Int Clin Psychopharmacol. 2013 Mar;28(2):87-90. doi: 10.1097/YIC.0b013e32835ce232.
The aim of this study was to investigate the dosing patterns of adjunctive quetiapine or adjunctive aripiprazole in the treatment of major depressive disorder from 2006 to 2010, and to evaluate the impact of Food and Drug Administration (FDA) approval on these dosing patterns. Patients included in the study were adults diagnosed with major depressive disorder, and treated with adjunctive aripiprazole or quetiapine between the years 2006 and 2010. The average daily dose and dose distribution were calculated and assessed statistically over the same time period. The mean daily dose for patients treated with adjunctive aripiprazole decreased from 13.5 mg/day in 2006 to 6.9 mg/day in 2010, whereas the mean daily dose for patients treated with quetiapine increased from 129 mg/day in 2006 to 139 mg/day in 2007, decreasing to 123 mg/day in 2010. The proportion of patients receiving FDA-recommended doses increased significantly for aripiprazole (86.3% in 2006 to 94.5% in 2010; P<0.001) and remained relatively stable for quetiapine (21.3% in 2006 to 24.0% in 2010; NS). The majority of patients treated with quetiapine received doses below those recommended by the FDA throughout the study period. Aripiprazole was mostly prescribed at therapeutic doses (pre-FDA and post-FDA approval), although the mean dose decreased significantly over time.
本研究旨在调查 2006 年至 2010 年间,辅助喹硫平或辅助阿立哌唑治疗重度抑郁症的给药模式,并评估食品和药物管理局(FDA)批准对这些给药模式的影响。研究纳入了被诊断为重度抑郁症并在 2006 年至 2010 年期间接受阿立哌唑或喹硫平辅助治疗的成年人。在同一时期内计算并评估了平均日剂量和剂量分布,并进行了统计学分析。接受阿立哌唑辅助治疗的患者的平均日剂量从 2006 年的 13.5mg/天降至 2010 年的 6.9mg/天,而接受喹硫平辅助治疗的患者的平均日剂量从 2006 年的 129mg/天增加到 2007 年的 139mg/天,然后在 2010 年降至 123mg/天。阿立哌唑接受 FDA 推荐剂量的患者比例显著增加(2006 年的 86.3%至 2010 年的 94.5%;P<0.001),而喹硫平的比例相对稳定(2006 年的 21.3%至 2010 年的 24.0%;NS)。在整个研究期间,大多数接受喹硫平治疗的患者接受的剂量低于 FDA 推荐的剂量。阿立哌唑主要在治疗剂量下(FDA 批准前和批准后)开具处方,尽管平均剂量随时间显著下降。