Stang Paul, Suppapanaya Nittaya, Hogue Susan L, Park Daniel, Rigney Una
West Chester University College of Health Sciences, West Chester, Pennsylvania, USA.
Am J Ther. 2007 May-Jun;14(3):241-6. doi: 10.1097/MJT.0b013e31802b59e4.
In this study, the impact of dosing frequency [once daily with bupropion extended-release (XL) versus twice daily with bupropion sustained-release (SR)] on medication persistence was assessed over a 9-month period in a large cohort of patients with depression in a managed-care setting. Administrative claims data from the Integrated Health Care Information Services National Managed Care Benchmark database were analyzed for patients 18 to 64 years old with a documented diagnosis of depression who began treatment with bupropion XL or SR between September 2003 and February 2004. Persistence of use was higher with once-daily bupropion XL (n = 1074) than with twice-daily bupropion SR (n = 1917) across measures assessed by univariate tests of proportions. The mean (+/-SD) number of days between the first and last prescription claims was longer with bupropion XL (128.37 +/- 103.46 days) than with bupropion SR (82.31 +/- 96.86 days) (P < 0.0001). The bupropion XL cohort had higher persistency of use than the bupropion SR cohort (mean +/- SD = 0.47 +/- 0.38 versus 0.30 +/- 0.36) (P < 0.0001) and a higher medication possession ratio (mean +/- SD = 0.50 +/- 0.33 versus 0.36 +/- 0.31) (P < 0.0001). Medication persistency >0.7 and a medication possession ratio >0.7 were almost twice as likely in the bupropion XL cohort (38.5% and 32.0%, respectively) than in the bupropion SR cohort (21.5% and 17.0%, respectively). Results of multivariate analyses adjusted for age, gender, and index date support the univariate analyses. Because better persistence and adherence may be associated with less likelihood of relapse and lower depression-associated health care utilization and economic burden, health care providers should consider the potential benefits of initiating treatment with bupropion XL for bupropion candidates and for switching bupropion SR recipients to treatment with bupropion XL.
在本研究中,在一个管理式医疗环境下的大量抑郁症患者队列中,评估了给药频率[安非他酮缓释剂(XL)每日一次与安非他酮缓释剂(SR)每日两次]对药物持续性的影响,为期9个月。分析了综合医疗保健信息服务国家管理式医疗基准数据库中的管理式医疗索赔数据,这些数据来自于2003年9月至2004年2月期间开始使用安非他酮XL或SR治疗且有抑郁症诊断记录的18至64岁患者。在通过比例单变量检验评估的各项指标中,安非他酮XL每日一次组(n = 1074)的用药持续性高于安非他酮SR每日两次组(n = 1917)。安非他酮XL组首次和最后一次处方索赔之间的平均(±标准差)天数(128.37 ± 103.46天)比安非他酮SR组(82.31 ± 96.86天)更长(P < 0.0001)。安非他酮XL组的用药持续性高于安非他酮SR组(平均±标准差 = 0.47 ± 0.38对0.30 ± 0.36)(P < 0.0001),且药物持有率更高(平均±标准差 = 0.50 ± 0.33对0.36 ± 0.31)(P < 0.0001)。安非他酮XL组药物持续性>0.7和药物持有率>0.7的可能性几乎是安非他酮SR组(分别为21.5%和17.0%)的两倍(分别为38.5%和32.0%)。针对年龄、性别和索引日期进行调整后的多变量分析结果支持单变量分析。由于更好的持续性和依从性可能与复发可能性降低以及与抑郁症相关的医疗保健利用率和经济负担降低相关,医疗保健提供者应考虑对于适合使用安非他酮的患者起始使用安非他酮XL治疗以及将安非他酮SR使用者转换为安非他酮XL治疗的潜在益处。