Zacker Christopher, Puckett Justin T, Kamal-Bahl Sachin
Cerevel Therapeutics, LLC, Cambridge, MA, USA.
COVIA Health Solutions, Ambler, PA, USA.
Clinicoecon Outcomes Res. 2024 Aug 14;16:567-579. doi: 10.2147/CEOR.S469001. eCollection 2024.
Little is known about adherence to and discontinuation of newly initiated oral antipsychotics (OAPs) as well as associated factors among Medicare beneficiaries with schizophrenia. This study aimed to examine rates of OAP adherence and discontinuation and associated factors in a national sample of fee-for-service Medicare beneficiaries with schizophrenia.
This retrospective study used 100% fee-for-service Medicare claims data to identify adult beneficiaries with schizophrenia, initiating a new OAP between 01/01/2017 and 12/31/2019 (index date = date of new OAP prescription). Outcomes included adherence and discontinuation. Factors associated with adherence were assessed using logistic and linear regressions; Cox regressions were used to assess factors associated with discontinuation.
In our final sample of 46,452 Medicare beneficiaries with schizophrenia, 35.4% were adherent to their newly initiated OAP (mean [SD] PDC: 0.52 [0.37]) over 12 months after initiation. Most patients (79.4%) discontinued their new OAP (median [IQR] time to discontinuation: 3.6 (1.0, 9.9) months). Factors associated with lower odds of adherence included younger age (OR: 0.43; 95% CI: 0.40-0.47, p <0.001 for patients aged 18-35 relative to patients aged ≥65 years); non-White race (OR: 0.72; 95% CI: 0.69-0.75, p <0.001 relative to White patients); and evidence of prior schizophrenia-related hospitalization (OR: 0.80; 95% CI: 0.77-0.83, p <0.001 relative to patients without evidence of prior schizophrenia-related hospitalization). Similar associations were observed for discontinuation outcomes. Twice-daily dosing frequency was also associated with lower odds of adherence (odds ratio [OR]: 0.93; 95% CI: 0.89-0.97, p = 0.0014) and higher hazard of discontinuation (hazard ratio [HR]: 1.03; 95% CI: 1.00-1.05, p = 0.0244) relative to once-daily dosing frequency.
We found high rates of non-adherence and discontinuation among Medicare beneficiaries initiated on currently available OAPs. We also identified risk factors that contribute to increased odds of medication non-adherence. By identifying at-risk patient populations, targeted interventions can be initiated to facilitate treatment continuity.
对于新启用的口服抗精神病药物(OAPs)的依从性和停药情况以及医疗保险受益的精神分裂症患者的相关因素,我们知之甚少。本研究旨在调查按服务收费的医疗保险受益精神分裂症患者全国样本中OAPs的依从率和停药率以及相关因素。
这项回顾性研究使用了100%按服务收费的医疗保险理赔数据,以识别2017年1月1日至2019年12月31日期间开始使用新OAP的成年精神分裂症受益患者(索引日期=新OAP处方日期)。结局包括依从性和停药情况。使用逻辑回归和线性回归评估与依从性相关的因素;使用Cox回归评估与停药相关的因素。
在我们最终纳入的46452名医疗保险受益精神分裂症患者样本中,35.4%的患者在开始使用新OAP后的12个月内对其保持依从(平均[标准差]持续治疗率:0.52[0.37])。大多数患者(79.4%)停用了他们的新OAP(停药的中位[四分位间距]时间:3.6(1.0,9.9)个月)。与较低依从可能性相关的因素包括年龄较小(比值比[OR]:0.43;95%置信区间[CI]:0.40 - 0.47,18 - 35岁患者相对于≥65岁患者,p<0.001);非白人种族(OR:0.72;95%CI:0.69 - 0.75,相对于白人患者,p<0.001);以及有先前精神分裂症相关住院治疗的证据(OR:0.80;95%CI:0.77 - 0.83,相对于没有先前精神分裂症相关住院治疗证据的患者,p<0.001)。在停药结局方面也观察到类似的关联。与每日一次给药频率相比,每日两次给药频率也与较低的依从可能性相关(比值比[OR]:0.93;95%CI:0.89 - 0.97,p = 0.0014)以及较高的停药风险(风险比[HR]:1.03;95%CI:1.00 - 1.05,p = 0.0244)。
我们发现开始使用现有OAPs的医疗保险受益患者中存在高不依从率和停药率。我们还确定了导致药物不依从可能性增加的风险因素。通过识别高危患者群体,可以启动有针对性的干预措施以促进治疗的连续性。