Greene Mallik, Yan Tingjian, Chang Eunice, Hartry Ann, Touya Maëlys, Broder Michael S
a Otsuka Pharmaceutical Development & Commercialization Inc. , Princeton , NJ , USA.
b Partnership for Health Analytic Research LLC , Beverly Hills , CA , USA.
J Med Econ. 2018 Feb;21(2):127-134. doi: 10.1080/13696998.2017.1379412. Epub 2017 Sep 29.
To examine medication adherence and discontinuation in two separate groups of patients with schizophrenia or bipolar disorder (BD), who began receiving a long-acting injectable antipsychotic (LAI) versus those who changed to a different oral antipsychotic monotherapy.
The Truven Health Analytics MarketScan Multi-State Medicaid claims database was used to identify patients with schizophrenia; Truven Health Analytics MarketScan Commercial and Medicaid claims databases were used to identify patients with BD. The analyses included adult patients (≥18 years) who either began receiving an LAI (no prior LAI therapy) or changed to a different oral antipsychotic (monotherapy). The first day of initiating an LAI or changing to a new oral antipsychotic was the index date. Linear and Cox regression models were conducted to estimate medication adherence (proportion of days covered [PDC]) and time to medication discontinuation (continuous medication gap ≥60 days), respectively. Models adjusted for patient demographic and clinical characteristics, baseline medication use, and baseline ED or hospitalizations.
Patients with schizophrenia (N = 5638) who began receiving LAIs had better medication adherence (5% higher adjusted mean adherence) during the 1 year post-index period and were 20% less likely to discontinue their medication during the entire follow-up period than patients who changed to a different oral antipsychotic monotherapy, adjusting for differences between LAI users and oral users. Similarly, patients with BD (N = 11,344) who began receiving LAIs also had 5% better medication adherence and were 19% less likely to discontinue their medication than those using oral antipsychotics.
Clinical differences unmeasurable in this database may have been responsible for the choice of LAI versus oral antipsychotics, and these differences may be responsible for some of the adherence advantages observed.
This real-world study suggests that patients with schizophrenia or BD who began receiving LAIs had better medication adherence and lower discontinuation risk than those who changed to a different oral antipsychotic monotherapy.
研究两组分别患有精神分裂症或双相情感障碍(BD)的患者的药物依从性和停药情况,一组开始接受长效注射用抗精神病药物(LAI)治疗,另一组改用不同的口服抗精神病药物单一疗法。
使用Truven Health Analytics MarketScan多州医疗补助索赔数据库识别精神分裂症患者;使用Truven Health Analytics MarketScan商业和医疗补助索赔数据库识别双相情感障碍患者。分析包括开始接受长效注射用抗精神病药物(此前未接受过长效注射用抗精神病药物治疗)或改用不同口服抗精神病药物(单一疗法)的成年患者(≥18岁)。开始使用长效注射用抗精神病药物或改用新的口服抗精神病药物的第一天为索引日期。分别进行线性回归模型和Cox回归模型,以估计药物依从性(覆盖天数比例[PDC])和停药时间(连续停药间隔≥60天)。模型对患者人口统计学和临床特征、基线用药情况以及基线急诊科就诊或住院情况进行了调整。
与改用不同口服抗精神病药物单一疗法的患者相比,开始接受长效注射用抗精神病药物治疗的精神分裂症患者(N = 5638)在索引日期后的1年内药物依从性更好(调整后的平均依从性高5%),并且在整个随访期间停药的可能性低20%,对长效注射用抗精神病药物使用者和口服药物使用者之间的差异进行了调整。同样,开始接受长效注射用抗精神病药物治疗的双相情感障碍患者(N = 11344)的药物依从性也比使用口服抗精神病药物的患者高5%,停药的可能性低19%。
该数据库中无法衡量的临床差异可能导致了长效注射用抗精神病药物与口服抗精神病药物的选择,这些差异可能是观察到的一些依从性优势的原因。
这项真实世界研究表明,与改用不同口服抗精神病药物单一疗法的患者相比,开始接受长效注射用抗精神病药物治疗的精神分裂症或双相情感障碍患者具有更好的药物依从性和更低的停药风险。