Sideman Alissa B, Hernandez de Jesus Alma, Brooks-Smith-Lowe Sharifa, Razon Na'amah, Filippi Melissa K, Wood Julie, Borson Soo
Philip R. Lee Institute for Health Policy Studies, University of California, San Francisco, San Francisco, CA 94158, United States.
Department of Humanities and Social Sciences, University of California, San Francisco, San Francisco, CA 94158, United States.
Health Aff Sch. 2025 Jan 13;3(1):qxae167. doi: 10.1093/haschl/qxae167. eCollection 2025 Jan.
The rapid rise in numbers of people living with Alzheimer's disease and related disorders (ADRD) poses major challenges to health systems and policy. Although primary care clinicians provide ongoing medical care for 80% of affected individuals, they face persistent barriers to providing high-quality dementia care. We conducted qualitative interviews with family physicians ( = 20) to understand what core outcomes they consider most important and what care processes and systems and policy strategies they propose to achieve them. Participants identified processes and outcomes pertaining to their relationships with patients and families, involvement in overall medical care, and efforts to mitigate harm as key components of dementia care. Participants also identified overarching patient care values: making active efforts to maintain continuity in the doctor-patient-family relationship, communicating clearly, building and sustaining trust, and responding to health-related social needs. Policy recommendations included work to create health care systems capable of providing comprehensive dementia care, full integration of caregivers into psychosocial care and medical management, adjustments to care cadence, and payment models that support team-based primary care. Findings could help refocus care improvement efforts on implementing the vital conditions for optimal health that can be achieved in primary care and sustained through the course of dementia.
阿尔茨海默病及相关疾病(ADRD)患者数量的迅速增加给卫生系统和政策带来了重大挑战。尽管初级保健临床医生为80%的受影响个体提供持续的医疗护理,但他们在提供高质量痴呆症护理方面面临持续障碍。我们对20名家庭医生进行了定性访谈,以了解他们认为哪些核心结果最为重要,以及他们提出了哪些护理流程、系统和政策策略来实现这些结果。参与者确定了与他们与患者及家庭的关系、参与整体医疗护理以及减轻伤害的努力相关的流程和结果,这些是痴呆症护理的关键组成部分。参与者还确定了总体患者护理价值观:积极努力保持医患家庭关系的连续性、清晰沟通、建立和维持信任以及回应与健康相关的社会需求。政策建议包括努力创建能够提供全面痴呆症护理的医疗保健系统、将护理人员全面纳入心理社会护理和医疗管理、调整护理节奏以及支持团队初级保健的支付模式。研究结果有助于将改善护理的努力重新聚焦于实施在初级保健中可实现并在痴呆症病程中持续的最佳健康的关键条件。