Calvary Health Care Bethlehem, Caulfield South, VIC, Australia.
Monash Health, Supportive & Palliative Care Department, Clayton, VIC, Australia.
Palliat Med. 2023 Oct;37(9):1402-1412. doi: 10.1177/02692163231191545. Epub 2023 Aug 8.
Motor neurone disease is a rare but debilitating illness with incomplete evidence regarding patients' symptom burden. Palliative care and generalist clinicians are often in-experienced in caring for these patients and assessing their needs.
To identify the symptom prevalence and severity experienced by patients with motor neurone disease. Secondary objectives were to examine differences in symptom burden and clusters according to phenotype, functional status, palliative care provision and those in their last months of life.
A point prevalence study assessing patient-reported symptoms using a modified IPOS-Neuro assessment tool, incorporating 41 symptom items.
SETTING/PARTICIPANTS: Patients with motor neurone disease attending the State-wide Progressive Neurological Disease Service or inpatient unit at Calvary Health Care Bethlehem, Melbourne Australia, from March to December 2021.
A total of 102 patients participated, the majority diagnosed with lumber-onset (30.4%), bulbar-onset (28.4%) and cervical-onset (25.5%) phenotypes. Patients experienced a median of 17 symptoms (range 2-32) with a median of 3 symptoms rated as severe/overwhelming (range 0-13). Motor and functional symptoms predominated, with differences in symptom clusters present according to phenotype. Patients had a higher number of severe/overwhelming symptoms if they were accessing palliative care services ( = 0.005), in their last 6 months of life ( = 0.003) and experiencing moderate or severe functional impairment ( < 0.001).
Patients with motor neurone disease report high symptom burden. A validated motor neurone disease-specific symptom assessment tool is needed to accurately assess patients, including important variations in symptom clusters according to phenotype. Further research must focus on evidence-based treatment guidelines for symptoms experienced commonly and severely.
运动神经元病是一种罕见但使人虚弱的疾病,关于患者的症状负担,证据尚不完整。姑息治疗和全科医生通常在照顾这些患者和评估他们的需求方面经验不足。
确定运动神经元病患者的症状发生率和严重程度。次要目标是根据表型、功能状态、姑息治疗的提供情况以及处于生命最后几个月的患者,检查症状负担和症状群的差异。
一项采用改良的 IPOS-Neuro 评估工具进行的现况研究,该工具纳入了 41 项症状项目,评估了患者报告的症状。
地点/参与者:2021 年 3 月至 12 月期间,澳大利亚墨尔本 Calvary Health Care Bethlehem 的全州进行性神经疾病服务或住院病房的运动神经元病患者。
共有 102 名患者参与了研究,其中大多数患者被诊断为腰椎起病(30.4%)、延髓起病(28.4%)和颈椎起病(25.5%)。患者经历了中位数为 17 种症状(范围 2-32),中位数有 3 种症状被评为严重/难以忍受(范围 0-13)。运动和功能症状为主,根据表型存在不同的症状群。如果患者正在接受姑息治疗服务( = 0.005)、处于生命的最后 6 个月( = 0.003)和经历中度或重度功能障碍( < 0.001),他们会有更多严重/难以忍受的症状。
运动神经元病患者报告的症状负担较高。需要使用经过验证的运动神经元病特异性症状评估工具来准确评估患者,包括根据表型评估重要的症状群变化。进一步的研究必须集中在针对常见和严重症状的基于证据的治疗指南上。