Division of Geriatrics, Department of Medicine, University of California, San Francisco, San Francisco, CA, USA.
Department of Veterans Affairs Medical Center, San Francisco, CA, USA.
J Alzheimers Dis. 2022;86(2):787-800. doi: 10.3233/JAD-215203.
After a diagnosis of Alzheimer's disease and related disorders, people living with dementia (PWD) and caregivers wonder what disease trajectory to expect and how to plan for functional and cognitive decline. This qualitative study aimed to identify patient and caregiver experiences receiving anticipatory guidance about dementia from a specialty dementia clinic.
To examine PWD and caregiver perspectives on receiving anticipatory guidance from a specialty dementia clinic.
We conducted semi-structured interviews with PWD, and active and bereaved family caregivers, recruited from a specialty dementia clinic. Interviews were recorded, transcribed, and systematically summarized. Thematic analysis identified anticipatory guidance received from clinical or non-clinical sources and areas where respondents wanted additional guidance.
Of 40 participants, 9 were PWD, 16 were active caregivers, and 15 were bereaved caregivers. PWD had a mean age of 75 and were primarily male (n = 6/9); caregivers had a mean age of 67 and were primarily female (n = 21/31). Participants felt they received incomplete or "hesitant" guidance on prognosis and expected disease course via their clinicians and filled the gap with information they found via the internet, books, and support groups. They appreciated guidance on behavioral, safety, and communication issues from clinicians, but found more timely and advance guidance from other non-clinical sources. Guidance on legal and financial planning was primarily identified through non-clinical sources.
PWD and caregivers want more information about expected disease course, prognosis, and help planning after diagnosis. Clinicians have an opportunity to improve anticipatory guidance communication and subsequent care provision.
在被诊断出患有阿尔茨海默病及相关疾病后,痴呆患者(PWD)及其照护者想知道他们会经历怎样的疾病进程,以及如何为功能和认知能力下降做计划。本项定性研究旨在确定患者和照护者从专业痴呆诊所获得预期性指导的体验。
检验 PWD 和照护者从专业痴呆诊所获得预期性指导的观点。
我们从一家专业的痴呆诊所招募了痴呆患者和有活力的、已去世的照护者,对他们进行半结构化访谈。访谈进行录音、转写,并进行系统总结。主题分析确定了从临床或非临床来源获得的预期性指导,以及受访者希望获得更多指导的领域。
40 名参与者中,有 9 名是痴呆患者,16 名是有活力的照护者,15 名是已去世的照护者。痴呆患者的平均年龄为 75 岁,主要为男性(n=6/9);照护者的平均年龄为 67 岁,主要为女性(n=21/31)。患者表示,他们从临床医生那里获得的关于预后和预期疾病进程的指导不完整或“犹豫不决”,并通过互联网、书籍和支持小组来填补信息空白。他们欣赏临床医生在行为、安全和沟通问题上提供的指导,但更希望从其他非临床来源获得更及时和提前的指导。法律和财务规划方面的指导主要是通过非临床来源获得的。
PWD 和照护者希望获得更多关于预期疾病进程、预后以及诊断后帮助计划的信息。临床医生有机会改善预期性指导沟通,并随后提供更好的护理。