A Qualitative Study to Characterize the Experiences of Patients and Caregivers With Dementia Diagnostic Disclosure Communication and Care Planning.

IF 2.5 4区 医学 Q2 CLINICAL NEUROLOGY
Joanna Paladino, Heily Chavez Granados, Jade A Connor Eruchalu, Carine Davila, Liliana Ramirez Gomez, Alissa Bernstein Sideman, Daniel Dohan, Elizabeth Lindenberger, Lindsay Dow, Ana-Maria Vranceanu, Deborah Blacker, Christine S Ritchie
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Abstract

BackgroundClinician communication at the time of a dementia diagnosis often inadequately addresses patient and caregiver needs. We aimed to characterize the communication experiences of patients and caregivers affected by dementia using an evidence-based serious illness communication framework.MethodsWe conducted semi-structured interviews of patients with dementia and caregivers. An interdisciplinary research team used thematic content analysis to identify themes.ResultsParticipants included 6 patients and 15 caregivers recruited from the community and health care settings (n = 21; 17/21 female; n = 13 White (61%); n = 4 Black or African American (19%); n = 4 Latino/a (19%); n = 2 Asian; n = 2 other). Five themes were identified. First, perceptions of respectful or disrespectful communication affect the relationship with clinicians and contributes to positive or negative communication experiences. Second, participants described the emotional impact of sudden or unsupported disclosures, in which they felt unprepared to receive the news or emotionally abandoned after diagnosis. Third, the absence of, or ambiguity around, a definitive dementia diagnosis contributes to patient and caregiver distress and to feeling dismissed by clinicians. Fourth, mixed responses to illness education and clinician recommendations after disclosure reveals the need for more personalized and comprehensive care planning. Fifth, careful consideration around the timing of prognostic communication and advance care planning discussions is necessary to meet the needs of patients and caregivers with different emotional readiness, illness beliefs, and information preferences.ConclusionDementia diagnostic disclosure would benefit from a structured yet tailored communication approach that prioritizes respectful communication, emotional support, and comprehensive care planning to meet the needs of patients and caregivers.

失智症病患与照护者诊断、揭露、沟通与照护计划经验之定性研究。
临床医生在痴呆症诊断时的沟通往往不能充分解决患者和护理人员的需求。我们的目的是利用基于证据的严重疾病沟通框架来描述痴呆症患者和护理人员的沟通经历。方法对痴呆患者和护理人员进行半结构化访谈。一个跨学科的研究团队使用主题内容分析来确定主题。结果从社区和卫生保健机构招募6名患者和15名护理人员(n = 21; 17/21女性;n = 13白人(61%);n = 4黑人或非裔美国人(19%);n = 4拉丁裔/a (19%);n = 2亚洲;N = 2 other)。确定了五个主题。首先,尊重或不尊重沟通的感知影响与临床医生的关系,并有助于积极或消极的沟通经验。其次,参与者描述了突然或无证据支持的信息披露对情绪的影响,在这种情况下,他们感到没有准备好接受这个消息,或者在诊断后被情感抛弃。第三,明确的痴呆诊断的缺失或模糊会导致患者和护理人员的痛苦,并使临床医生感到被忽视。第四,对疾病教育和临床医生建议的反应不一,这表明需要更个性化和全面的护理计划。第五,仔细考虑预后沟通和预先护理计划讨论的时机是必要的,以满足具有不同情绪准备,疾病信念和信息偏好的患者和护理人员的需求。结论痴呆诊断信息披露将受益于结构化且量身定制的沟通方式,优先考虑尊重沟通、情感支持和全面的护理计划,以满足患者和护理人员的需求。
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来源期刊
CiteScore
6.20
自引率
0.00%
发文量
40
审稿时长
>12 weeks
期刊介绍: Journal of Geriatric Psychiatry and Neurology (JGP) brings together original research, clinical reviews, and timely case reports on neuropsychiatric care of aging patients, including age-related biologic, neurologic, and psychiatric illnesses; psychosocial problems; forensic issues; and family care. The journal offers the latest peer-reviewed information on cognitive, mood, anxiety, addictive, and sleep disorders in older patients, as well as tested diagnostic tools and therapies.
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