[无论是好是坏——描述长期护理患者的老年配偶所经历的问题]。

Hoitotiede Pub Date : 1998-01-01
T Jykylä, P Astedt-Kurki
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引用次数: 0

摘要

这篇文章的目的是描述永久性机构病人的配偶在他们的生活中感受到的问题。这项研究的性质是定性的。数据收集自在两个初级卫生保健医院病房接受护理的患者的6对配偶。资料收集方法为主题访谈。采用定性含量分析法进行分析。研究结果显示了夫妻的经历。他们将其分为六类:1)对自己和配偶命运的怨恨;2)配偶在医院接受治疗时自由生活的负罪感;3)与病人捆绑在一起的感觉,失去了自己生活的可能性;4)失去配偶的感觉;5)与家人以外的人失去联系;6)对未来的愿景缺失。研究结果为医院长期护理向以家庭为中心的护理发展提供了多种途径。患者的家庭成员不仅构成了患者或护理的背景。他们还需要信息和情感支持来管理他们的日常生活。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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[For better or worse--description of the problems experienced by elderly spouses of long-term care patients].

The aim of this article is to describe, what problems the spouses of permanently institutionalised patients feel in their lives. The nature of the study is qualitative. Data were collected from six spouses of patients cared for in two hospital wards in primary health care. The data collection method was theme interview. Analysis was made by qualitative content analysis method. The results of the study showed the spouses' experiences. They formed six categories: 1) embitterment of the fate of their own and their spouses, 2) feeling of guilt when living free while the spouse is in a hospital care, 3) feeling of being bound to the patient and losing own possibilities in life, 4) feeling of loss of the spouse, 5) losing contacts to other people outside the family, and 6) missing visions for the future. The results showed many ways how to develop the long-term hospital care toward family-centered care. The family members of the patients do not only form background of the patients or the care. They also need informational and emotional support to manage in their everyday lives.

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