Impact of treatment burden on medication adherence and quality of life in amyotrophic lateral sclerosis: a prospective multicentre study.

IF 2.8
Andrea Lizio, Matteo Farè, Francesca Gerardi, Marianna Collesi, Valeria Ada Sansone, Christian Lunetta, Luca Diamanti, Federica Cerri
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Abstract

Background: Patients with amyotrophic lateral sclerosis (ALS) face substantial barriers to medication adherence as disease progression necessitates complex drug formulation adjustments, such as crushing tablets, mixing with liquids, or delivering via feeding tubes. These modifications may not only increase the time and effort required but could also impact drug efficacy and safety.

Objective: To evaluate the prevalence and the impact of treatment burden on medication adherence and patient-reported quality of life (QoL) in ALS.

Methods: This prospective multicenter study enrolled ALS patients across three Italian reference centers, with assessments at baseline, 6, and 12 months. Key measures included the Multimorbidity Treatment Burden Questionnaire (MTBQ), ALSFRS-R, DYALS (dysphagia), Morisky Medication Adherence Scale, SSS-8 (somatic symptoms), INQoL (QoL), SWAMECO (swallowing/medication difficulties), alongside comorbidities and current therapies. Associations between treatment burden, QoL, and adherence were analyzed using multivariable models.

Results: A total of 114 consecutive ALS patients were enrolled. Clinically significant treatment burden was observed in 69.3% of patients, with over half reporting moderate-to-high levels according to the MTBQ classification. Elevated burden was independently related to greater somatic symptom severity and formulation modification needs. Moreover, higher burden associated with poorer QoL and diminished adherence after confounder adjustment. Longitudinally, patients experiencing worsening burden over 1 year showed accelerated QoL decline compared to those remaining stable, though adherence trajectories were unaffected.

Conclusion: Treatment burden, particularly driven by drug formulation complexities and somatic symptoms, emerges as a pivotal, modifiable determinant of adherence and QoL in ALS. Targeted interventions to alleviate modifiable burden components hold promise for optimizing clinical outcomes and enhancing patient-centred care.

肌萎缩性侧索硬化症患者治疗负担对药物依从性和生活质量的影响:一项前瞻性多中心研究。
背景:肌萎缩性侧索硬化症(ALS)患者在药物依从性方面面临重大障碍,因为疾病进展需要复杂的药物配方调整,如粉碎片剂、与液体混合或通过饲管给药。这些修改不仅可能增加所需的时间和精力,而且可能影响药物的疗效和安全性。目的:评价ALS患者的患病率及治疗负担对药物依从性和患者报告生活质量(QoL)的影响。方法:这项前瞻性多中心研究纳入了三个意大利参考中心的ALS患者,分别在基线、6个月和12个月进行评估。主要测量指标包括多病治疗负担问卷(MTBQ)、ALSFRS-R、DYALS(吞咽困难)、Morisky药物依从性量表、SSS-8(躯体症状)、INQoL (QoL)、SWAMECO(吞咽/用药困难)以及合并症和当前治疗。使用多变量模型分析治疗负担、生活质量和依从性之间的关系。结果:共有114例连续ALS患者入组。69.3%的患者有临床显著的治疗负担,根据MTBQ分类,超过一半的患者报告中至高水平。加重的负担与躯体症状的严重程度和制剂修改需求独立相关。此外,在混杂因素调整后,较高的负担与较差的生活质量和降低的依从性相关。纵向上,与保持稳定的患者相比,1年内负担加重的患者的生活质量下降加快,尽管依从性轨迹未受影响。结论:治疗负担,特别是由药物配方复杂性和躯体症状驱动的负担,成为ALS患者依从性和生活质量的关键、可改变的决定因素。有针对性的干预措施,以减轻可改变的负担组成部分,有望优化临床结果和加强以患者为中心的护理。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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