在老年病医院就诊的埃及老年痴呆症患者中,护理人员对护理目标和临终问题的看法

NMarwa Abdel Azeem Abdel Gawad, Nourhan Samy Atta, Sally Adel Hakim, Shereen Moustafa Moussa, Heba Youssif Kamel
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摘要

背景:在埃及,预先讨论痴呆症患者生命末期的护理目标并不常见。目的:本研究旨在确定护理人员对中重度和重度痴呆症患者护理目标和生命终结问题的看法。研究方法对 101 名护理人员进行问卷调查,了解中重度和重度痴呆症患者的护理人员对护理目标和生命终结问题的看法。结果所有护理人员都未接受过痴呆症护理培训,也未与医疗服务提供者讨论过痴呆症护理目标或生命终结问题。对护理目标的看法是,60.4%的护理人员倾向于减少患者的痛苦,39.6%的护理人员倾向于保持患者的功能。没有人选择延长生命作为护理目标。关于生命末期护理,98% 的护理人员接受机械通气,90.1% 接受使用止痛药,74.3% 接受使用喂食管,97% 接受晚期心肺复苏。痴呆症确诊时间(>1 年)与因睡眠问题和喂养问题而选择护理院之间存在明显关系。结论埃及护理人员对护理目标和生命末期问题的看法是,在痴呆症晚期选择减少患者的痛苦和提高他们的生活质量,而不是延长他们的寿命。教育水平和护理人员与患者的关系并不影响护理人员对生命末期问题的看法,但对护理目标略有影响。
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Caregivers’ Perspectives Towards Goals of Care and End-of-Life Issues in Egyptian Elderly with Dementia Attending Geriatric Hospital
Background : Pre-discussion of goals of care specially at end of life in dementia is not a common practice in Egypt. Aim : The aim of the current study is to determine caregivers’ perspectives towards goals of care and end of life issues in moderate to severe and severe dementia patients. Methods: A questionnaire was applied on 101 caregivers about perspectives of caregivers of moderate to severe and severe dementia patients toward goals of care and end of life issues. Results: No one of caregivers had previous training for dementia care or discussed dementia care goals or end of life issues with healthcare providers. Perspectives towards goals of care was 60.4% preferred decreasing patient suffering, 39.6% preferred preserving patient function. No one chose life prolongation as a goal of care. Regarding end of life care, 98% of caregivers accepted mechanical ventilation, 90.1% accepted using pain killers, 74.3% accepted using feeding tube and 97% accepted CPR at late stage. There was significant relation between duration since dementia was diagnosed (>1 year) and choosing nursing home for sleep problems and feeding problems. Conclusions: Egyptians caregivers’ perspectives towards goals of care and end of life issues chose to decrease suffering of patients and improve their quality of life rather than prolonging their life span in late stages of dementia. Educational level and caregivers’ relation with the patients didn’t influence caregivers’ perspectives towards end of life issues yet it slightly affected goals of care .
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