充血性心力衰竭门诊患者对生活质量和治疗的感知。

S. Paul, N. Sneed
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引用次数: 19

摘要

为了更好地理解患者对生活质量(QOL)的定义,并确定哪些工具最适合用于未来的研究,在一所大学的充血性心力衰竭诊所进行了一项描述性研究。在录制的访谈中,参与者被问及一系列关于他们对生活质量的看法的五个开放式问题。大多数患者将生活质量等同于他们在发生心力衰竭之前行使身体功能的能力。他们为自己以前的能力感到悲伤,并且由于身体上的限制失去了独立性而表现出较低的自尊心。简表36和明尼苏达心衰患者生活问卷解决了对我们患者重要的生活质量问题。在临床实践中使用定量工具测量生活质量时,卫生保健提供者考虑患者对生活质量的感知是很重要的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Patient perceptions of quality of life and treatment in an outpatient congestive heart failure clinic.
In an effort to better understand patients' definitions of quality of life (QOL) and to determine which tools would be most appropriate for use in future studies, a descriptive study was done in a university-based congestive heart failure clinic. Participants were asked a series of five open-ended questions regarding their perceptions of QOL during recorded interviews. Most patients equated QOL with the ability to perform physical functions in the same way they did before developing heart failure. They grieved for their former abilities and expressed lower self-esteem due to loss of independence from physical limitations. The Short Form-36 and the Minnesota Living With Heart Failure Questionnaire addressed the QOL issues important to our patients. It is important for health care providers to consider the patient's perception of QOL when using quantitative tools for QOL measurement in clinical practice.
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