{"title":"P.065 Understanding treatment barriers and adherence among people living with amyotrophic lateral sclerosis","authors":"G. Matte, D. Blackburn, D. Bolano Del Vecchio","doi":"10.1017/cjn.2024.171","DOIUrl":null,"url":null,"abstract":"Background: Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease with only four approved treatments in North America - sodium phenylbutyrate (PB) and ursodoxicoltaurine (TURSO, also known as taurursodiol), riluzole, edaravone, and tofersen. Poor treatment adherence reduces clinical effectiveness which can adversely impact disease progression and mortality rates. Understanding barriers and adherence to treatment in clinical practice is essential to address these issues. Methods: A scoping review was conducted in PubMed, Medline, Embase, and Web of Science. Retained studies were, (1) published in English, (2) included adults with ALS, (3) explored treatment non-adherence and/or identified barriers associated with non-adherence in ALS in real world clinical practice, (4) focused on ≥1 of the four approved ALS medications, and (5) used a measurement of adherence. Observational studies, real-world data, and case reports were included. Quality assessment was performed. Results: The review illustrated several knowledge gaps, including limited data on the incidence of non-adherence to ALS treatment in clinical practice, a lack of understanding regarding barriers to treatment adherence in ALS, and an absence of studies outside of western societies. Conclusions: We demonstrate a dearth of real-world data on treatment adherence in ALS and highlight opportunities for advancing research into this important area.","PeriodicalId":9571,"journal":{"name":"Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques","volume":"70 18","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-05-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1017/cjn.2024.171","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Background: Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease with only four approved treatments in North America - sodium phenylbutyrate (PB) and ursodoxicoltaurine (TURSO, also known as taurursodiol), riluzole, edaravone, and tofersen. Poor treatment adherence reduces clinical effectiveness which can adversely impact disease progression and mortality rates. Understanding barriers and adherence to treatment in clinical practice is essential to address these issues. Methods: A scoping review was conducted in PubMed, Medline, Embase, and Web of Science. Retained studies were, (1) published in English, (2) included adults with ALS, (3) explored treatment non-adherence and/or identified barriers associated with non-adherence in ALS in real world clinical practice, (4) focused on ≥1 of the four approved ALS medications, and (5) used a measurement of adherence. Observational studies, real-world data, and case reports were included. Quality assessment was performed. Results: The review illustrated several knowledge gaps, including limited data on the incidence of non-adherence to ALS treatment in clinical practice, a lack of understanding regarding barriers to treatment adherence in ALS, and an absence of studies outside of western societies. Conclusions: We demonstrate a dearth of real-world data on treatment adherence in ALS and highlight opportunities for advancing research into this important area.
背景:肌萎缩侧索硬化症(ALS)是一种致命的神经退行性疾病:肌萎缩性脊髓侧索硬化症(ALS)是一种致命的神经退行性疾病,在北美仅有四种获批的治疗方法--苯丁酸钠(PB)和乌索二醇(TURSO,又称牛磺二醇)、利鲁唑、依达拉奉和托福森。治疗依从性差会降低临床疗效,从而对疾病进展和死亡率产生不利影响。要解决这些问题,了解临床实践中的治疗障碍和治疗依从性至关重要。研究方法在 PubMed、Medline、Embase 和 Web of Science 上进行了范围界定审查。保留的研究必须:(1)以英文发表;(2)纳入了 ALS 成人患者;(3)探讨了 ALS 在实际临床实践中的治疗不依从性和/或确定了与不依从性相关的障碍;(4)关注四种获批 ALS 药物中的≥一种;(5)使用了依从性测量方法。研究纳入了观察性研究、真实世界数据和病例报告。进行了质量评估。结果:综述显示了一些知识空白,包括临床实践中不坚持 ALS 治疗的发生率数据有限、对 ALS 患者坚持治疗的障碍缺乏了解,以及缺乏西方社会以外的研究。结论:我们展示了 ALS 治疗依从性方面真实世界数据的匮乏,并强调了推进这一重要领域研究的机会。