Dementia Care Specialists Perspectives of Diagnosis and Early Psychosocial Care: A Qualitative Analysis of Focus Groups in Two Large Academic Medical Centers.

Amelia J Hicks, Julie Brewer, Nina Ahmad, Talea Cornelius, Robert A Parker, Kristen Dams-O'Connor, Bradford Dickerson, Christine Ritchie, Ana-Maria Vranceanu, Sarah M Bannon
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Abstract

Background and objective: Alzheimer's disease and related dementias (ADRDs) are progressive conditions that substantially impact individuals and families. Timely diagnosis and early support are critical for long-term adjustment. However, current dementia care models do not meet needs of patients and families. Dementia care specialists treating individuals with dementia offer unique insight into care needs of diverse groups of patients, families, and healthcare systems that can be used to identify opportunities to improve care.To understand dementia care specialists' impressions of factors impacting ADRD diagnosis and post-diagnosis support. We aimed to identify factors that impact: (1) timely and accurate diagnosis, (2) diagnostic disclosure and provision of post-diagnosis support, and (3) patient and care-partner adjustment after diagnosis.

Research design and methods: We recruited dementia care specialists treating persons living with dementia (n=19) from two academic medical centers. Participants completed 60-minute qualitative focus groups or individual interviews. Data were analyzed using a hybrid inductive-deductive approach to thematic analysis.

Results: We identified subthemes within three overarching a-priori determined themes. Participants highlighted the presence of delays in referrals, time constraints, specialist discomfort, and lack of training as factors impacting the timeliness and accuracy of diagnosis. They also highlighted information needed in disclosure visits, ways of coordinating care, and identifying early support needs. Finally, participants highlighted factors impacting adjustment including families' insight and acceptance, distress, and available resources.

Discussion and implications: Our study highlights the challenges dementia care specialist specialists face in delivering early support for individuals and families impacted by ADRDs and suggests avenues for revising existing care models.

痴呆症护理专家对诊断和早期社会心理护理的看法:两个大型学术医疗中心焦点小组的定性分析。
背景和目的:阿尔茨海默病和相关痴呆症(ADRDs)是一种渐进性疾病,对个人和家庭都有重大影响。及时诊断和早期支持对长期调整至关重要。然而,目前的痴呆症护理模式并不能满足患者和家属的需求。治疗痴呆症患者的痴呆症护理专家对不同患者群体、家庭和医疗保健系统的护理需求有着独特的见解,可用于确定改善护理的机会。我们旨在确定影响以下方面的因素:(1)及时准确的诊断;(2)诊断披露和提供诊断后支持;(3)诊断后患者和护理伙伴的适应:我们从两所学术医疗中心招募了治疗痴呆症患者的痴呆症护理专家(19 人)。参与者完成了 60 分钟的定性焦点小组或个人访谈。我们采用归纳-演绎混合法对数据进行了主题分析:我们确定了三个先验主题中的次主题。参与者强调,转诊延误、时间限制、专家不适和缺乏培训是影响诊断及时性和准确性的因素。他们还强调了披露访问所需的信息、协调护理的方法以及识别早期支持需求。最后,参与者强调了影响适应的因素,包括家人的洞察力和接受度、痛苦和可用资源:我们的研究强调了痴呆症护理专科专家在为受 ADRDs 影响的个人和家庭提供早期支持时所面临的挑战,并提出了修改现有护理模式的途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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