Center for Epidemiology and Database Analytics, United BioSource Corporation, 430 Bedford Street, Lexington, MA 02420, USA.
J Med Econ. 2010 Mar;13(1):90-8. doi: 10.3111/13696990903579501.
The objective of this study was to explore the cost and utilization in the period following discontinuations or switches of disease modifying drugs (DMDs) for patients with multiple sclerosis (MS). Secondary objectives included an assessment of the time to switch or discontinuation from index DMD treatment.
Cases were defined as a billed MS diagnosis in continuously enrolled patients initiated with interferon-beta1a IM, interferon-beta1b SC, glatiramer acetate, and interferon-beta1a SC found in the PharMetrics Patient-Centric Database. Information on patient demographics, diagnoses, procedures, pharmacy-dispensed drugs, and costs was extracted; reasons for discontinuation and expenses outside of the healthcare system were not available. Treatment discontinuations and switches between study drugs were defined using pharmacy prescription patterns and analyzed by descriptive and regression methods. The non-pharmacy medical costs in the 18 months following switching or discontinuation were compared to the costs in a randomly selected similar period for those patients who did not switch or discontinue these agents.
A total of 5,772 MS patients were continuously enrolled and were treated with one or more of the four drugs of interest, and about half of these patients switched drugs or discontinued treatment for at least 90 days. Patients initiated with interferon-beta1b SC were more likely to discontinue treatment compared to interferon-beta1a IM users. Non-pharmaceutical medical costs were highest for those switching treatments followed by those discontinuing DMDs in the 18 months following a switch or discontinuation, compared to persistent users of these drugs. Interferon beta1b SC initiators had higher costs following changes or discontinuations, while glatiramer acetate and interferon-beta1a SC users had lower subsequent costs compared to interferon-beta1a IM users.
Unfortunately, the reasons for stopping the initial treatment cannot be determined from analysis of an administrative claims database. Also, the MS cases followed in this analysis are billing diagnostic events unconfirmed through a review of medical records or other data sources. The results are unstratified in terms of severity and thus while treatment patterns may vary for patients with different types of MS (e.g., progressive vs. relapsing-remitting), this cannot be examined in this analysis.
Changing or discontinuing DMDs is common among MS patients and is associated with higher non-pharmaceutical medical costs that vary based on the initiating drug and other demographics characteristics.
本研究旨在探讨多发性硬化症(MS)患者停止或更换疾病修正药物(DMD)后的成本和利用情况。次要目标包括评估从索引 DMD 治疗开始转换或停药的时间。
病例定义为在 PharMetrics 患者为中心数据库中发现的连续入组患者中,以肌内注射干扰素-β1a、皮下注射干扰素-β1b、醋酸格拉替雷和皮下注射干扰素-β1a 起始治疗的有 billed MS 诊断的患者。提取患者人口统计学、诊断、程序、药房配药药物和成本信息;无法获得停止治疗和医疗系统以外的费用信息。使用药房处方模式定义治疗中断和研究药物之间的转换,并使用描述性和回归方法进行分析。与未转换或停止使用这些药物的患者随机选择的相似时期相比,比较了转换或停止使用后 18 个月内的非药房医疗费用。
共有 5772 名 MS 患者连续入组,接受了上述四种药物中的一种或多种药物治疗,其中约一半患者至少停止治疗 90 天。与干扰素-β1a IM 使用者相比,开始使用皮下注射干扰素-β1b 的患者更有可能停止治疗。与持续使用这些药物的患者相比,转换治疗或停止 DMD 后 18 个月内的非药物医疗费用最高。与干扰素-β1a IM 使用者相比,干扰素-β1b SC 初始使用者在更改或停药后费用更高,而醋酸格拉替雷和干扰素-β1a SC 使用者的后续费用较低。
不幸的是,从管理索赔数据库的分析中无法确定停止初始治疗的原因。此外,本分析中跟踪的 MS 病例是未经病历或其他数据源审查确认的计费诊断事件。根据严重程度,结果是未分层的,因此,虽然不同类型的 MS(例如,进行性与复发缓解性)的治疗模式可能有所不同,但在本分析中无法检查。
多发性硬化症患者停止或更换 DMD 很常见,与非药物医疗成本增加有关,这些成本因起始药物和其他人口统计学特征而异。