Lien Centre for Palliative Care, Duke-NUS Medical School, Singapore.
Program in Health Services and Systems Research, Duke-NUS Medical School, Singapore.
J Alzheimers Dis. 2020;75(2):403-416. doi: 10.3233/JAD-190897.
Although many persons with severe dementia (PWSDs) are cared for at home by their family caregivers, few studies have assessed end of life (EOL) care experiences of PWSDs. We present the protocol for the PISCES study (Panel study Investigating Status of Cognitively impaired Elderly in Singapore) which aims to describe the clinical course, health care utilization, and expenditures for community-dwelling PWSDs; and perceived burden, coping, resilience, anticipatory and prolonged grief among their caregivers. This ongoing multi-center prospective longitudinal study is recruiting primary informal caregivers of 250 PWSDs from major restructured public hospitals, community hospitals, home care foundations, and hospices in Singapore. Caregivers are surveyed every four months for two years or until the PWSD passes away and then at eight weeks and six months post-death to assess the bereavement of the caregiver. Survey questionnaires included validated tools to assess PWSDs' quality of life, suffering, behaviors, functional status, resource utilization; and caregiver's satisfaction with care, awareness of prognosis, care preferences, resilience, coping, perceived burden, distress, positive aspects of caregiving, anticipatory grief, and bereavement adjustment. We also conduct qualitative in-depth interviews with a sub-sample of caregivers. The survey data is being linked with medical and billing records of PWSDs. The study has been approved by an ethics board. Results from the study will be disseminated through publications and presentations targeting researchers, policy makers and clinicians interested in understanding and improving EOL care for PWSDs and their caregivers.
虽然许多患有严重痴呆症(PWSD)的人在家中由其家庭照顾者照顾,但很少有研究评估 PWSD 的临终关怀体验。我们介绍了 PISCES 研究(调查新加坡认知障碍老年人状况的面板研究)的方案,该研究旨在描述居住在社区中的 PWSD 的临床过程、医疗保健利用情况和支出情况;以及他们的照顾者的感知负担、应对方式、适应力、预期性和长期性悲伤。这项正在进行的多中心前瞻性纵向研究正在从新加坡的主要重组公立医院、社区医院、家庭护理基金会和临终关怀机构招募 250 名 PWSD 的主要非正式照顾者。照顾者每四个月接受一次调查,为期两年,或直到 PWSD 去世,然后在去世后八周和六个月进行调查,以评估照顾者的丧亲之痛。调查问卷包括评估 PWSD 生活质量、痛苦、行为、功能状态、资源利用情况的经过验证的工具;以及照顾者对护理的满意度、对预后的认识、护理偏好、适应力、应对方式、感知负担、痛苦、照顾的积极方面、预期性悲伤和丧亲调整。我们还对照顾者的一个亚组进行了深入的定性访谈。正在将调查数据与 PWSD 的医疗和计费记录进行关联。该研究已获得伦理委员会的批准。研究结果将通过针对有兴趣了解和改善 PWSD 及其照顾者临终关怀的研究人员、政策制定者和临床医生的出版物和演示进行传播。