Increasing number of unmanaged distressing symptoms in people living with dementia associated with family carer burden and distress following an unplanned hospital admission: A longitudinal cohort study.
Sophie Crawley, Victoria Vickerstaff, Clare Ellis-Smith, Charlotte Kenten, Emel Yorganci, Catherine J Evans, Elizabeth L Sampson, Nuriye Kupeli
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引用次数: 0
Abstract
Background: People living with dementia (PLWD) often have high symptom burden, exacerbated by comorbidities and experience unplanned hospital admissions that increase towards the end of life. Unmanaged symptoms and unplanned hospital admissions are distressing for the person living with dementia and family carers and expensive for the healthcare system.
Objective: To explore the relationship between unmanaged symptoms of PLWD following an unplanned hospital admission and carer health and wellbeing outcomes over time.
Design: Prospective longitudinal cohort study.
Methods: Physical, psychosocial and spiritual symptoms of the PLWD and carer burden, distress and pre-death grief were assessed over 12 months following an unplanned hospital admission. Descriptive statistics and multilevel linear regression analyses were used to examine the relationships between PLWD unmanaged symptoms and carer outcomes.
Results: A total of 51 carers of PLWD with a mean age of 59.6 participated. Carer burden was significantly associated with increasing PLWD unmanaged symptoms (coefficient = 0.07, 95% CI [0.03, 0.12], p = 0.002) and agitation (coefficient = 0.08, 95%CI [0.02, 0.14], p = 0.009). Carer psychological distress showed a positive trend in its association with increasing PLWD unmanaged symptoms (coefficient = 0.07, 95% CI [-0.00, 0.13], p = 0.059) and agitation (coefficient = 0.06, 95% CI [-0.01, 0.14], p = 0.090), but both analyses did not reach statistical significance. Carer pre-death grief was not associated with PLWD symptoms or agitation.
Conclusion: Identifying and addressing symptoms in PLWD following an unplanned hospital admission is essential in enhancing the wellbeing of PLWD and carers. Hospital discharge planning should incorporate carer perspectives, provide support for carer burden and distress, and ensure continuity of care to reduce symptoms and improve outcomes for both PLWD and their carers.
背景:痴呆症(PLWD)患者通常有很高的症状负担,并因合并症而加重,并且在生命末期经历计划外住院。对于痴呆症患者和家庭护理人员来说,症状失控和未经计划的住院治疗是痛苦的,对医疗保健系统来说也是昂贵的。目的:探讨计划外住院后PLWD的未处理症状与护理人员健康和幸福结局之间的关系。设计:前瞻性纵向队列研究。方法:在计划外入院后的12个月内,评估PLWD患者的身体、社会心理和精神症状以及照顾者负担、痛苦和死前悲伤。使用描述性统计和多水平线性回归分析来检验PLWD未控制症状与护理结果之间的关系。结果:共有51名PLWD护理人员参与,平均年龄59.6岁。护理人员负担与PLWD失控症状增加(系数= 0.07,95%CI [0.03, 0.12], p = 0.002)和躁动(系数= 0.08,95%CI [0.02, 0.14], p = 0.009)显著相关。护理人员心理困扰与PLWD无控制症状增加(系数= 0.07,95% CI [-0.00, 0.13], p = 0.059)和躁动(系数= 0.06,95% CI [-0.01, 0.14], p = 0.090)呈正相关,但两项分析均无统计学意义。护理人员临终前悲伤与PLWD症状或躁动无关。结论:识别和处理计划外住院后PLWD的症状对于提高PLWD及其护理人员的福祉至关重要。出院计划应纳入护理人员的观点,为护理人员的负担和痛苦提供支持,并确保护理的连续性,以减轻PLWD及其护理人员的症状并改善结果。