Jykylä T, Astedt-Kurki P
Hoitotiede. 1998;10(4):191-8.
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.
本文旨在描述长期住院患者的配偶在生活中感受到哪些问题。该研究性质为定性研究。数据收集自初级卫生保健机构中两个医院病房所护理患者的六位配偶。数据收集方法为主题访谈。采用定性内容分析法进行分析。研究结果展示了配偶们的经历。这些经历形成了六个类别:1)对自身及配偶命运的怨愤;2)配偶住院治疗期间自己享受自由时产生的愧疚感;3)感觉被患者束缚,失去了自己的生活可能性;4)配偶离世的感觉;5)与家庭之外其他人失去联系;6)对未来失去憧憬。结果显示了多种将长期住院护理发展为以家庭为中心护理的方法。患者的家庭成员不仅构成患者或护理的背景。他们在日常生活中也需要信息和情感支持。