Department of Emergency Medicine, University of Wisconsin-Madison, Madison, Wisconsin.
School of Nursing, University of Wisconsin-Madison, Madison, Wisconsin.
J Am Geriatr Soc. 2019 Apr;67(4):711-718. doi: 10.1111/jgs.15737. Epub 2019 Jan 9.
BACKGROUND/OBJECTIVES: People with dementia (PwD) frequently use emergency care services. To mitigate the disproportionately high rate of emergency care use by PwD, an understanding of contributing factors driving reliance on emergency care services and identification of feasible alternatives are needed. This study aimed to identify clinician, caregiver, and service providers' views and experiences of unmet needs leading to emergency care use among community-dwelling PwD and alternative ways of addressing these needs.
Qualitative, employing semistructured interviews with clinicians, informal caregivers, and aging service providers.
Wisconsin, United States.
Informal caregivers of PwD (n = 4), emergency medicine physicians (n = 4), primary care physicians (n = 5), geriatric healthcare providers (n = 5), aging service providers (n = 6), and community paramedics (n = 3).
Demographic characteristics of participants and data from semistructured interviews.
Four major themes were identified from interviews: (1) system fragmentation influences emergency care use by PwD, (2) informational, decision-making, and social support needs influence emergency care use by PwD, (3) emergency departments (EDs) are not designed to optimally address PwD and caregiver needs, and (4) options to prevent and address emergency care needs of PwD.
Participants identified numerous system and individual-level unmet needs and offered many recommendations to prevent or improve ED use by PwD. These novel findings, aggregating the perspectives of multiple dementia-care stakeholder groups, serve as the first step to developing interventions that prevent the need for emergency care or deliver tailored emergency care services to this vulnerable population through new approaches. J Am Geriatr Soc 67:711-718, 2019.
背景/目的:痴呆症患者(PwD)经常使用急诊护理服务。为了降低 PwD 过度使用急诊护理服务的比率,需要了解导致依赖急诊护理服务的因素,并确定可行的替代方案。本研究旨在确定临床医生、护理人员和服务提供者对导致社区居住的 PwD 使用急诊护理服务的未满足需求的看法和经验,以及解决这些需求的替代方法。
采用半结构化访谈,对临床医生、非正式护理人员和老年服务提供者进行定性研究。
美国威斯康星州。
PwD 的非正式护理人员(n=4)、急诊医学医师(n=4)、初级保健医生(n=5)、老年保健提供者(n=5)、老年服务提供者(n=6)和社区护理人员(n=3)。
参与者的人口统计学特征和半结构化访谈数据。
从访谈中确定了四个主要主题:(1)系统碎片化影响 PwD 使用急诊护理服务,(2)信息、决策和社会支持需求影响 PwD 使用急诊护理服务,(3)急诊部门(EDs)的设计无法最佳满足 PwD 和护理人员的需求,以及(4)预防和满足 PwD 急诊护理需求的选择。
参与者确定了许多系统和个人层面的未满足需求,并提出了许多建议,以预防或改善 PwD 使用 ED 的情况。这些新发现综合了多个痴呆症护理利益相关者群体的观点,是通过新方法为这一脆弱群体开发预防急诊护理需求或提供定制化急诊护理服务的干预措施的第一步。美国老年学会杂志 67:711-718, 2019。