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在澳大利亚的日常生活背景下,人们如何构建他们对继发性淋巴水肿的生活体验。

How people construct their experience of living with secondary lymphoedema in the context of their everyday lives in Australia.

机构信息

School of Public Health and Social Work, Queensland University of Technology, Kelvin Grove, 4059, Brisbane, Australia.

出版信息

Support Care Cancer. 2013 Feb;21(2):459-66. doi: 10.1007/s00520-012-1534-4. Epub 2012 Jul 18.

Abstract

PURPOSE

The purpose of this work was to explore how men and women construct their experiences living with lymphoedema following treatment for any cancer in the context of everyday life.

METHODS

The design and conduct of this qualitative study was guided by Charmaz' social constructivist grounded theory. To collect data, focus groups and telephone interviews were conducted. Audiotapes were transcribed verbatim and imported into NVivo8 to organize data and codes. Data were analyzed using key grounded theory principles of constant comparison, data saturation, and initial, focused, and theoretical coding.

RESULTS

Participants were 3 men and 26 women who had developed upper- or lower-limb lymphoedema following cancer treatment. Three conceptual categories were developed during data analysis and were labeled "accidental journey," "altered normalcy," and "ebb and flow of control." "Altered normalcy" reflects the physical and psychosocial consequences of lymphoedema and its relationship to everyday life. "Accidental journey" explains the participants' experiences with the health care system, including the prevention, treatment, and management of their lymphoedema. "Ebb and flow of control" draws upon a range of individual and social elements that influenced the participants' perceived control over lymphoedema. These conceptual categories were interrelated and contributed to the core category of "sense of self," which describes their perceptions of their identity and roles.

CONCLUSIONS

Results highlight the need for greater clinical and public awareness of lymphoedema as a chronic condition requiring prevention and treatment, and one that has far-reaching effects on physical and psychosocial well-being as well as overall quality of life.

摘要

目的

本研究旨在探讨男性和女性在日常生活背景下,如何构建其在癌症治疗后患有淋巴水肿的体验。

方法

本定性研究的设计和实施以 Charmaz 的社会建构主义扎根理论为指导。为了收集数据,进行了焦点小组和电话访谈。将录音逐字转录并导入 NVivo8 以组织数据和编码。使用扎根理论的关键原则,如持续比较、数据饱和和初始、聚焦和理论编码,对数据进行分析。

结果

参与者为 3 名男性和 26 名女性,他们在癌症治疗后出现了上肢或下肢淋巴水肿。在数据分析过程中,确定了三个概念类别,分别命名为“意外之旅”、“改变的常态”和“控制的起伏”。“改变的常态”反映了淋巴水肿的身体和心理社会后果及其与日常生活的关系。“意外之旅”解释了参与者的医疗保健系统体验,包括淋巴水肿的预防、治疗和管理。“控制的起伏”借鉴了一系列个体和社会因素,这些因素影响了参与者对淋巴水肿的控制感。这些概念类别相互关联,并促成了核心类别“自我意识”,描述了他们对自身身份和角色的看法。

结论

研究结果强调了临床和公众对淋巴水肿作为一种需要预防和治疗的慢性疾病的认识的重要性,因为它对身体和心理社会健康以及整体生活质量都有深远的影响。

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