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首页> 外文期刊>International Journal of Integrated Care >Care at the end of life in patients with advanced dementia institutionalized
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Care at the end of life in patients with advanced dementia institutionalized

机译:晚期痴呆患者的临终护理制度化

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Objective : To develop a plan of attention to the terminality in patients with advanced dementia, planning the care through symptomatic control, making decisions with the main caregiver and performing a psychological and spiritual support. Method : Descriptive study of period in the Txara 1 Center of San Sebastian from January 2014 to December 2017, identifying those residents with advanced dementia (GDS 7 and decline syndrome, understood as the presence of total functional dependency and malnutrition). The degree of symptom control (SM-EOLD) is collected quarterly using the PAINAD-Sp scale for pain assessment. At the time of agony, the degree of comfort is determined daily using the scale (CAD-EOLD), establishing with the main caregiver makes decisions based on the palliative care objectives and recording the level of intervention in the electronic medical record. After the death, a satisfaction survey was carried out with the main caregiver (SWC-EOLD) and contact was established with the pastoral for spiritual support. Results : 126 residents with an average age of 87 years are analyzed, 79% are women, and 44% dementia is degenerative. The median of medications is 4.61 and spiritual support is made through the anointing of patients at 70%. In the control of symptoms the pain is evidenced in 8% at least weekly, with a PAINAD-Sp 3 in 20% of the cases, the presence of depression in 4%. In the degree of comfort in situations of agony, the evolution of 64 deaths is recorded (51% of the sample), where the presence of dysphagia is seen in 80%, with the variables of serenity or calm in more than 80 % of the sample. The main cause of death is due to infection of the lower respiratory tract, 93% of the location is in the center itself, with an average of 2.8 incidents, of which 49% are due to dyspnea. Regarding the use of health resources during the last 6 months of life, 12% are referred to the emergency department and 23% require hospital admissions. From the satisfaction survey to the caregivers it is answered by 48%, the overall rating being good at 46% and very good at 54%. Conclusions : The identification of patients with criteria of terminality allows structuring a plan of care in the center, knowing the symptomatic needs, the degree of comfort and reaching decisions regarding the proportionality of care with the family. Care resources must be properly integrated in order to respond to emergency situations and be able to comply with the decisions adopted.
机译:目的:制定一项针对晚期痴呆患者的终末期注意计划,通过对症控制来计划护理,与主要护理者做出决定,并提供心理和精神支持。方法:对2014年1月至2017年12月在圣塞巴斯蒂安的Txara 1中心的期间进行描述性研究,确定患有晚期痴呆症(GDS 7和衰退综合征,被视为存在总功能依赖和营养不良)的居民。每季度使用PAINAD-Sp量表收集症状控制程度(SM-EOLD)进行疼痛评估。在痛苦时,每天使用量表(CAD-EOLD)确定舒适度,并与主要护理人员一起根据姑息治疗目标进行决策并在电子病历中记录干预程度。死后,我们与主要照顾者(SWC-EOLD)进行了满意度调查,并与牧师建立了联系以寻求精神支持。结果:分析了126名平均年龄为87岁的居民,其中女性占79%,变性痴呆症占44%。药物的中位数为4.61,精神支持来自患者的涂膏,占70%。在控制症状方面,至少每周有8%的病例证明疼痛,其中20%的病例中PAINAD-Sp> 3,有4%的人出现抑郁。在痛苦情况下的舒适度方面,记录了64例死亡的演变(占样本的51%),其中80%的人出现吞咽困难,而80%的人则表现出平静或平静。样品。死亡的主要原因是下呼吸道的感染,其中93%的位置在中心本身,平均2.8次,其中49%是由于呼吸困难。关于生命的最后六个月中卫生资源的使用,有12%的人转诊至急诊部门,还有23%的人需要住院。从满意度调查到看护者的回答为48%,总评分为46%,非常好为54%。结论:确定具有终末期标准的患者可以在中心制定护理计划,了解症状需求,舒适程度并就与家人的护理比例做出决定。必须妥善整合护理资源,以应对紧急情况并能够遵守通过的决定。

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