Foley Geraldine, Timonen Virpi, Hardiman Orla
1Trinity College Dublin, Dublin, Ireland.
Qual Health Res. 2014 Jan;24(1):67-77. doi: 10.1177/1049732313516545. Epub 2013 Dec 13.
Researchers have explored perceptions of health care services among people with amyotrophic lateral sclerosis (ALS), but little is known about how and why people with ALS engage with services. We undertook a grounded theory study to identify key psychosocial processes that underpin how and why people with ALS engage with health care services. We conducted in-depth interviews with 34 participants sampled from the Irish ALS population-based register. We found that age and life stage shaped participants' decision making about care. Participants in later life were more accepting of ALS and of death than young and middle-aged participants. Family was the primary context to how participants engaged with services, and their decisions about care were shaped by parenthood at different life stages. Health care professionals need to be attuned to the impact of life-course trajectories and family relations on the decisions people with ALS make about their care.
研究人员已经探讨了肌萎缩侧索硬化症(ALS)患者对医疗服务的看法,但对于ALS患者如何以及为何使用这些服务却知之甚少。我们进行了一项扎根理论研究,以确定支撑ALS患者如何以及为何使用医疗服务的关键心理社会过程。我们对从爱尔兰基于人群的ALS登记册中抽取的34名参与者进行了深入访谈。我们发现,年龄和人生阶段影响了参与者对护理的决策。与年轻和中年参与者相比,老年参与者对ALS和死亡的接受度更高。家庭是参与者如何使用服务的主要背景,他们在不同人生阶段的为人父母经历影响了他们对护理的决策。医疗保健专业人员需要了解生命历程轨迹和家庭关系对ALS患者护理决策的影响。