Division of Neurology, The Leslie Dan Faculty of Pharmacy, University of Toronto, Ontario,Canada.
Can J Neurol Sci. 2011 May;38(3):429-33. doi: 10.1017/s0317167100011823.
BACKGROUND/OBJECTIVE: Differences in patient adherence to various disease-modifying drugs (DMDs) in the treatment of multiple sclerosis (MS) are not well understood. The goal of this study was to evaluate adherence of adult MS patients in Ontario with public drug plan coverage to various DMDs: intramuscular interferon beta-1a (i.m. IFNβ-1a, Avonex), subcutaneous interferon beta-1a (s.c. IFNβ-1a, Rebif), subcutaneous interferon beta-1b (IFNβ-1b, Betaseron) or glatiramer acetate (Copaxone).
In this retrospective cohort study, Ontario Public Drug Plan beneficiaries aged 15 or older who were newly treated with i.m. IFNβ-1a, s.c. IFNβ-1a, IFNβ-1b or glatiramer acetate between April 2006 and March 2008 were followed forward until treatment discontinuation, switch to another DMD or a maximum two year follow-up period. Cumulative persistence rates were analyzed by the Kaplan-Meier method. The proportion of patients reaching the study endpoints after the two year follow-up period was also calculated.
Cumulative persistence rates for all four DMDs were similar over time (p=0.80), ranging from 73.6-79.1% at six months, 59.1-63.1% at one year and 41.5-47.4% at two years. After two years, the proportion of patients who had discontinued treatment, switched to another DMD or died was similar among DMDs (p=0.79, Fisher's exact test). Switching between DMD types was low and occurred in 3.4-6.5% of new DMD users.
Adherence to DMDs in adult MS patients in Ontario is poor, which is consistent with previously reported adherence rates to MS DMDs in other regions. No significant differences in adherence exist between the DMDs evaluated in this study.
背景/目的:在多发性硬化症(MS)的治疗中,患者对各种疾病修正药物(DMD)的依从性存在差异,这一点尚未得到充分认识。本研究旨在评估安大略省接受公共药物计划覆盖的成年 MS 患者对各种 DMD 的依从性:肌肉内干扰素 beta-1a(i.m. IFNβ-1a,Avonex)、皮下干扰素 beta-1a(s.c. IFNβ-1a,Rebif)、皮下干扰素 beta-1b(IFNβ-1b,Betaseron)或聚甘酯(Copaxone)。
在这项回顾性队列研究中,2006 年 4 月至 2008 年 3 月期间新接受 i.m. IFNβ-1a、s.c. IFNβ-1a、IFNβ-1b 或聚甘酯治疗的年龄在 15 岁或以上的安大略省公共药物计划受益人被向前随访,直至治疗停止、改用另一种 DMD 或随访期最长两年。采用 Kaplan-Meier 法分析累积持续率。还计算了在两年随访期后达到研究终点的患者比例。
四种 DMD 的累积持续率随时间变化相似(p=0.80),六个月时为 73.6-79.1%,一年时为 59.1-63.1%,两年时为 41.5-47.4%。两年后,DMD 之间停止治疗、改用另一种 DMD 或死亡的患者比例相似(p=0.79,Fisher 精确检验)。DMD 类型之间的转换率较低,新使用 DMD 的患者中为 3.4-6.5%。
安大略省成年 MS 患者对 DMD 的依从性较差,这与之前报道的其他地区 MS DMD 依从率一致。本研究评估的 DMD 之间不存在显著的依从性差异。