Global Health Outcomes Strategy and Research, Allergan, 2525 Dupont Drive (T2-2P), Irvine, CA, 92612-1599, USA.
Pharmaceutical Outcomes Research and Policy Program, School of Pharmacy, University of Washington, Seattle, WA, USA.
CNS Drugs. 2017 May;31(5):421-432. doi: 10.1007/s40263-017-0417-0.
Adherence and persistence to therapy, or how well a patient follows provider directions on frequency and time to discontinuation of prescribed medications, is associated with positive health outcomes, including decreased healthcare costs and patient mortality. A clear literature gap exists assessing adherence and persistence to antidepressants (ADs) in the major depressive disorder (MDD) population at clinically relevant time points and at the therapeutic class level.
This study assessed adherence and persistence to specific ADs, therapeutic classes, and AD therapy overall at multiple time points among US individuals from commercial, Medicare supplemental, and Medicaid insurance plans.
Patients with MDD without AD or MDD claims in the prior 6 months who initiated therapy in 2003-2014 with a selective serotonin reuptake inhibitor (SSRI), serotonin and norepinephrine reuptake inhibitor (SNRI), tricyclic AD (TCA), monoamine oxidase inhibitor (MAOI), or other AD were identified using MarketScan databases. These databases contain information on diagnoses, billing codes, and dates of service. Adherence (proportion of days covered) and persistence (days until a 30-day gap in therapy) were calculated to AD medication, AD therapeutic class, and AD therapy overall over the first 3, 6, 9, and 12 months from the index prescription date. Multivariable logistic regression estimated the adjusted odds ratios (ORs) of adherence to initial AD medication comparing AD therapeutic classes.
For 527,907 patients, adherence to initial AD medication decreased over 3, 6, 9, and 12 months (41, 31, 24, and 21%, respectively). Similar patterns were observed for adherence to initial AD therapeutic class, AD therapy overall, and all three persistence calculations. The odds of adherence to SNRIs versus SSRIs were 20-27% greater at 3, 6, 9, and 12 months (ORs 1.20, 1.23, 1.25, 1.27, respectively; p-values all <0.0001). Similar or significantly lower odds of adherence were demonstrated for other classes versus SSRIs at 3, 6, 9, and 12 months [ORs for other ADs 0.80, 0.77, 0.74, 0.72, respectively (p-values all <0.0001); ORs for TCAs 0.46, 0.45, 0.47, 0.49, respectively (p-values all <0.0001); ORs for MAOIs 1.13, 1.0, 0.77, 0.69, respectively (p-values all >0.05)].
We found low adherence and persistence to ADs in the MDD population. Within the limitations of the insurance claims data we analysed, our results suggest that adherence may differ based on therapeutic class, as patients initiating SNRI therapy appeared to have a higher likelihood of adherence versus SSRIs over the year assessed, while the odds of adherence appeared similar or lower for other classes versus SSRIs. Further prospective research is needed to confirm these findings and determine additional drivers of these apparent differences by AD therapeutic class.
患者对治疗的依从性和持久性,即患者遵循提供者关于停药频率和时间的指导的情况,与积极的健康结果相关,包括降低医疗保健成本和患者死亡率。在临床上相关的时间点和治疗类别水平上,评估抗抑郁药(ADs)在重度抑郁症(MDD)人群中的依从性和持久性方面存在明显的文献差距。
本研究评估了美国商业、医疗保险补充和医疗补助计划中的个体在多个时间点使用选择性 5-羟色胺再摄取抑制剂(SSRI)、5-羟色胺和去甲肾上腺素再摄取抑制剂(SNRI)、三环抗抑郁药(TCA)、单胺氧化酶抑制剂(MAOI)或其他 AD 治疗 MDD 时对特定 ADs、AD 治疗类别和 AD 治疗的总体依从性和持久性。
使用 MarketScan 数据库识别了 2003-2014 年期间无 AD 或 MDD 索赔且在前 6 个月内开始使用 SSRI、SNRI、TCA、MAOI 或其他 AD 治疗的 MDD 患者。这些数据库包含有关诊断、计费代码和服务日期的信息。根据索引处方日期,计算 AD 药物、AD 治疗类别和 AD 治疗的总体在第 3、6、9 和 12 个月的依从性(覆盖天数比例)和持久性(30 天治疗间隔的天数)。多变量逻辑回归估计了比较 AD 治疗类别的初始 AD 药物的调整后比值比(OR)。
对于 527,907 名患者,AD 初始药物的依从性在第 3、6、9 和 12 个月时逐渐下降(分别为 41%、31%、24%和 21%)。对初始 AD 治疗类别的依从性、AD 治疗的总体情况以及所有三种持久性计算也观察到了类似的模式。与 SSRIs 相比,SNRIs 的依从性在第 3、6、9 和 12 个月时高出 20-27%(ORs 分别为 1.20、1.23、1.25、1.27;p 值均<0.0001)。在第 3、6、9 和 12 个月时,与 SSRIs 相比,其他类别具有相似或明显较低的依从性(其他 AD 的 OR 分别为 0.80、0.77、0.74、0.72,p 值均<0.0001;TCA 的 OR 分别为 0.46、0.45、0.47、0.49,p 值均<0.0001;MAOI 的 OR 分别为 1.13、1.00、0.77、0.69,p 值均>0.05)。
我们发现 MDD 人群中 AD 的依从性和持久性较低。在我们分析的保险索赔数据的限制范围内,我们的结果表明,依从性可能因治疗类别而异,因为与 SSRIs 相比,开始 SNRI 治疗的患者在评估的一年中似乎更有可能保持依从性,而其他类别的依从性似乎相似或低于 SSRIs。需要进一步的前瞻性研究来证实这些发现,并确定 AD 治疗类别对这些明显差异的其他驱动因素。