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Persistence and adherence to disease modifying drugs among patients with multiple sclerosis

机译:多发性硬化症患者对疾病改变药物的坚持和坚持

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This retrospective database study aimed to evaluate the adherence of multiple sclerosis (MS) patients on immunomodulatory treatments using claims data, and to identify differences between compliance and persistency measurements in the context of this disease. Continuously enrolled MS patients treated with subcutaneous IFNβ-1b (Betaseron*Currency sign), subcutaneous IFNβ-1a (Rebif?Currency sign), intramuscular IFNβ-1a (Avonex?Currency sign), and subcutaneous glatiramer acetate (Copaxone§Currency sign).) were identified from the PharMetrics patient-centric database, and all information related to patient demographics and pharmacy claims for the drugs of interest were extracted. The main outcomes were treatment switches and discontinuations for patients initiated on the drugs of interest. Various compliance and persistency metrics including the proportion of days covered, treatment prevalence at 6-monthly time points after initiation, and the continuous time on drug were also examined. A total of 6134 MS patients were started on one of the four drugs of interest. The number of patients switching or discontinuing therapy rose over the study period. The proportion of patients switching was similar between study drugs, by the different metrics, with the highest switch rates for subcutaneous IFNβ-1b and the lowest for subcutaneous glatiramer acetate. Discontinuation rates were highest for subcutaneous IFNβ-1b and lowest for intramuscular IFNβ-1a. Regression models showed that intramuscular IFNβ-1a and subcutaneous IFNβ-1a had similar and higher persistency compared to subcutaneous IFNβ-1b and subcutaneous glatiramer acetate. Although treatment switching and discontinuation is common in MS patients, there is some noticeable variability between drugs and across measures of persistency and adherence. Also, claims data do not allow distinguishing between clinical patterns of MS, direct estimation of disease severity and observation of care that occurs outside of insurance coverage, and results need to be cautiously interpreted. The compliance to the various MS drugs was 80 or higher at all times for all four drugs. The highest rate of treatment persistency existed in the intramuscular IFNβ-1a initiator group, while subcutaneous IFNβ-1b was associated with a significantly lower persistence (p<0.0001).
机译:这项回顾性数据库研究旨在使用索赔数据评估多发性硬化症(MS)患者在免疫调节治疗中的依从性,并确定在该疾病背景下依从性和持久性测量之间的差异。连续纳入MS患者,分别接受皮下IFNβ-1b(贝他塞隆*货币符号),皮下IFNβ-1a(Rebif?Currency符号),肌内IFNβ-1a(Avonex?Currency符号)和皮下醋酸格拉替雷(Copaxone§Currency符号)治疗。 )从以患者为中心的PharMetrics数据库中进行了识别,并提取了与所关注药物的患者人口统计信息和药房声明有关的所有信息。主要结局是采用目标药物治疗后患者的治疗切换和停药。还检查了各种依从性和持久性指标,包括覆盖天数的比例,开始后6个月时间点的治疗患病率以及药物持续服用时间。共有6134名MS患者开始使用四种感兴趣的药物之一。在研究期间,转用或终止治疗的患者人数有所增加。根据不同的指标,研究药物之间的患者转换比例相似,皮下IFNβ-1b的转换率最高,而醋酸格拉替雷的皮下转换率最低。皮下IFNβ-1b的停药率最高,而肌内IFNβ-1a的停药率最低。回归模型显示,与皮下IFNβ-1b和醋酸格拉替雷相比,肌内IFNβ-1a和皮下IFNβ-1a具有相似且更高的持久性。尽管治疗切换和停药在MS患者中很常见,但是药物之间以及持续性和依从性的测量之间存在明显的差异。此外,理赔数据不允许区分MS的临床模式,疾病严重程度的直接估计以及在保险范围之外进行的护理观察,因此需要谨慎解释结果。所有四种药物对各种MS药物的依从性始终都达到80或更高。肌肉注射IFNβ-1a引发剂组的治疗持久性最高,而皮下IFNβ-1b的持久性则显着降低(p <0.0001)。

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