Abughosh Susan M, Kogut Stephen J
Department of Pharmaceutical Sciences, Massachusetts College of Pharmacy and Health Sciences (MCPHS), MA, USA;
Patient Prefer Adherence. 2008 Feb 2;2:79-85. doi: 10.2147/ppa.s2652.
To compare levels of persistency between cholinesterase inhibitors (ChEIs) among a Medicaid patient population of older adults.
Survival analysis was used to assess differences in discontinuation between ChEIs (donepezil versus rivastigmine and galantamine), and for difference in patient gender, age, race, and care setting.
Rates of discontinuation increased from 42.7% (95% CI = 39.9-45.5) at 12 months to 84.8% (95% CI = 82.3-87.3) at 24 months. In multivariate models, no significant difference in discontinuation existed prior to 365 days. However, patients dispensed donepezil were less likely to discontinue as compared with users of the other two ChEIs after the first year (RR = 0.70; CI = 0.499-0.983; p < 0.04). Patients of white race were less likely to discontinue (RR = 0.549; 95% CI = 0.43-0.82; p = 0.0015), while gender, care setting, and age were not associated with discontinuation.
One-year persistence rates were similar between different ChEIs. Among patients persisting with ChEI medication for at least 12 months, users of donepezil were slightly more likely to continue to persist at 24 months. Nearly half of patients failed to persist with ChEI therapy for at least 12 months. Our findings underscore the limitations of the ChEI medications and the urgent need for effective and tolerable therapeutic options for patients having dementia.
比较医疗补助计划中老年患者群体中胆碱酯酶抑制剂(ChEIs)之间的持续使用水平。
采用生存分析评估ChEIs(多奈哌齐与卡巴拉汀和加兰他敏)之间停药情况的差异,以及患者性别、年龄、种族和护理环境方面的差异。
停药率从12个月时的42.7%(95%置信区间 = 39.9 - 45.5)增至24个月时的84.8%(95%置信区间 = 82.3 - 87.3)。在多变量模型中,365天之前停药情况无显著差异。然而,与其他两种ChEIs的使用者相比,服用多奈哌齐的患者在第一年之后停药的可能性较小(风险比 = 0.70;置信区间 = 0.499 - 0.983;p < 0.04)。白人患者停药的可能性较小(风险比 = 0.549;95%置信区间 = 0.43 - 0.82;p = 0.0015),而性别、护理环境和年龄与停药无关。
不同ChEIs之间的一年持续使用率相似。在持续使用ChEI药物至少12个月的患者中,多奈哌齐使用者在24个月时继续坚持用药的可能性略高。近一半的患者未能坚持ChEI治疗至少12个月。我们的研究结果强调了ChEI药物的局限性,以及为痴呆患者提供有效且可耐受治疗选择的迫切需求。