Department of Rehabilitation Medicine, University of Washington School of Medicine, Seattle, WA, USA.
PM R. 2022 Dec;14(12):1474-1482. doi: 10.1002/pmrj.12724. Epub 2021 Nov 23.
Falls and their consequences are known to be major contributors to decreased health and well-being in older adults. Several studies suggest that fall rates are higher among individuals with disabling conditions such as multiple sclerosis (MS). However, there is a knowledge gap regarding how individuals with a disability define falls or understand their consequences.
To gain the perspective of community-dwelling adults living with MS about falls and their consequences and to understand the conditions and circumstances surrounding falls, and to identify the specific attributes of a community fall-prevention program that would facilitate participation.
Focus groups or individual interviews were conducted with people with MS.
SETTING/PARTICIPANTS: Community-dwelling adults living with MS (n = 20) (men = 8 [34.7%], mean age 63.2 years [standard deviation (SD) 5.3, range 55-75]). Average time since diagnosis was 20.6 years (SD 9.6, range 9-44).
Not applicable.
Not applicable.
All participants agreed that the definition of a fall required "ending up on the floor." However, the starting point differed depending on mobility ability and device use. When using the most common research definition, individuals reported an increase in their number of falls as compared to when using their personal definition. Most participants considered "fear of falling" to be different from "concern about falling." Participants wanted to learn how to fall and would not join a program with the word "fall" in the title.
Results suggest that fall data for individuals with MS may not be reported accurately. Health care providers would get more accurate data if they provide specific definitions for falls and ask specifically about fear and concern about falling. Patient-centered programming needs to be developed that includes both how to fall and how to engage people with MS, including potential facilitators and barriers to participation.
众所周知,老年人的跌倒及其后果是健康和幸福感下降的主要原因。有几项研究表明,患有多发性硬化症(MS)等致残疾病的人跌倒率更高。然而,对于残疾个体如何定义跌倒或理解其后果,我们知之甚少。
了解社区居住的 MS 患者对跌倒及其后果的看法,了解跌倒的情况和环境,并确定社区预防跌倒计划的具体属性,以促进参与。
对 MS 患者进行焦点小组或个人访谈。
地点/参与者:社区居住的 MS 成年患者(n=20)(男性 8 人[34.7%],平均年龄 63.2 岁[标准差(SD)5.3,范围 55-75])。诊断后平均时间为 20.6 年(SD 9.6,范围 9-44)。
不适用。
不适用。
所有参与者都认为跌倒的定义需要“摔倒在地板上”。然而,起点因移动能力和设备使用而异。当使用最常见的研究定义时,与使用个人定义相比,个体报告跌倒次数增加。大多数参与者认为“害怕跌倒”与“担心跌倒”不同。参与者希望学习如何跌倒,不会加入名称中带有“跌倒”一词的计划。
结果表明,MS 患者的跌倒数据可能报告不准确。如果医疗保健提供者为跌倒提供具体定义并特别询问对跌倒的恐惧和担忧,他们将获得更准确的数据。需要制定以患者为中心的方案,包括如何跌倒以及如何让 MS 患者参与进来,包括参与的潜在促进因素和障碍。