Department of Neurosurgery, Penn State College of Medicine, Hershey, Pennsylvania.
Department of Neurology, University of Michigan, Ann Arbor, Michigan.
Muscle Nerve. 2022 Jun;65(6):659-666. doi: 10.1002/mus.27541. Epub 2022 Apr 13.
INTRODUCTION/AIMS: Riluzole is a glutamate inhibitor approved for the treatment of amyotrophic lateral sclerosis (ALS). There are scant data on factors associated with riluzole initiation and adherence. The goal of this study was to describe the use of riluzole at the Penn State Hershey Medical Center (PSHMC) ALS clinic.
A retrospective medical record review of ALS patients seen at the PSHMC from January 2007 to December 2016. A timeline of riluzole use was established for each patient. Factors contributing to dose changes or discontinuations were recorded. Riluzole adherence was assessed using the proportion of days covered (PDC) calculated by the patient-reported length of riluzole use divided by total time from prescription to death/censor. Multivariable analysis was performed to evaluate the association of demography and clinical course with adherence.
Seven hundred twenty-three records were screened, with 508 (307 men, 201 women) meeting the criteria for inclusion. The median duration of riluzole use was 435 (range, 0-3773) days. The median PDC for the group was 64%. Those with higher initial overall function and slower rate of decline were more likely to have a larger PDC. No trends in patients' demographics, riluzole use, and tracheostomy-free survival were found over time.
A high rate of riluzole initiation and adherence was found in this sample. The most common reasons for dose modification were related to adverse effects, yet social-, economic-, and patient-related factors were also common. The characteristics of riluzole prescription and use have remained relatively unchanged in a single tertiary ALS center over the past 10 years.
简介/目的:利鲁唑是一种谷氨酸抑制剂,已被批准用于治疗肌萎缩侧索硬化症(ALS)。关于与利鲁唑起始和依从性相关的因素的数据很少。本研究的目的是描述宾夕法尼亚州立 Hershey 医疗中心(PSHMC)ALS 诊所使用利鲁唑的情况。
对 2007 年 1 月至 2016 年 12 月在 PSHMC 就诊的 ALS 患者进行回顾性病历回顾。为每位患者建立了利鲁唑使用时间轴。记录了导致剂量变化或停药的因素。通过患者报告的利鲁唑使用时间除以从处方到死亡/删失的总时间,计算出覆盖天数(PDC)来评估利鲁唑的依从性。采用多变量分析评估人口统计学和临床病程与依从性的关系。
筛选了 723 份记录,其中 508 份(307 名男性,201 名女性)符合纳入标准。利鲁唑使用的中位持续时间为 435 天(范围,0-3773 天)。该组的中位 PDC 为 64%。初始整体功能较高且下降速度较慢的患者更有可能具有较大的 PDC。随着时间的推移,未发现患者人口统计学、利鲁唑使用和无气管造口术生存的趋势。
在本样本中发现了较高的利鲁唑起始和依从率。最常见的剂量调整原因与不良反应有关,但社会、经济和患者相关因素也很常见。在过去的 10 年中,在单一的三级 ALS 中心,利鲁唑的处方和使用特点相对保持不变。