Monteiro Andreia, Ali Amira Mohammed, Laranjeira Carlos
School of Health Sciences, Polytechnic University of Leiria, Campus 2, Morro do Lena, Alto do Vieiro, Apartado 4137, 2411-901 Leiria, Portugal.
Integrated Continuing Care Unit of Manuel Fanha Vieira, Rua da Barroca 60, 2330-108 Entroncamento, Portugal.
Behav Sci (Basel). 2025 Apr 10;15(4):510. doi: 10.3390/bs15040510.
Amyotrophic lateral sclerosis (ALS) is a disease that has a multidimensional impact on a person's life, with symptoms associated with a significant loss of autonomy. Specialized palliative care (PC) should be provided early and throughout the course of the disease. Indeed, physiotherapists should be understood as integral members of the multidisciplinary team in PC, in the care and improvement of the quality of life of these people. This study aimed to describe the lived experience of physiotherapists in the context of intervention in people with advanced ALS and their families. Descriptive phenomenology was employed as a framework for conducting semi-structured interviews to reveal experiences. Sixteen physiotherapists who performed interventions on at least one person with advanced ALS in the last 2 years were included in the study. The study involved conducting semi-structured individual interviews, through the Zoom videoconferencing platform (version 6.4.3). Data were analyzed according to Giorgi's five-stage approach and managed using webQDA software (Version 3.0, University of Aveiro, Aveiro, Portugal). The COREQ checklist was applied in the study. Participants were mostly female (n = 12) and aged between 26 and 55 years (M = 36.81; SD = 6.75). Four constituents were identified: (1) undulating course of a complex disease; (2) barriers to person-centered care; (3) enablers of person-centered care; (4) transition between curative and palliative care. The findings illustrate the multidimensional impact of the disease trajectory on the person and their family. This study highlights the need to invest in specialized training for physiotherapists, contributing to a person-centered PC practice with an impact on promoting comfort and quality of life.
肌萎缩侧索硬化症(ALS)是一种对人的生活有多方面影响的疾病,其症状与自主性的显著丧失相关。应在疾病早期及整个病程中提供专业的姑息治疗(PC)。事实上,物理治疗师应被视为PC多学科团队的重要成员,参与这些患者的护理并改善其生活质量。本研究旨在描述物理治疗师在对晚期ALS患者及其家属进行干预的背景下的生活经历。描述性现象学被用作进行半结构化访谈以揭示经历的框架。研究纳入了16名在过去2年中至少对一名晚期ALS患者进行过干预的物理治疗师。该研究通过Zoom视频会议平台(版本6.4.3)进行半结构化个人访谈。数据根据 Giorgi 的五阶段方法进行分析,并使用 webQDA 软件(版本3.0,葡萄牙阿威罗大学)进行管理。研究应用了COREQ清单。参与者大多为女性(n = 12),年龄在26至55岁之间(M = 36.81;SD = 6.75)。确定了四个组成部分:(1)复杂疾病的起伏病程;(2)以患者为中心的护理障碍;(3)以患者为中心的护理促进因素;(4)治愈性护理与姑息治疗之间的过渡。研究结果说明了疾病轨迹对患者及其家庭的多方面影响。本研究强调需要为物理治疗师提供专业培训,以促进以患者为中心的PC实践,从而对提升舒适度和生活质量产生影响。