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慢性阻塞性肺疾病急性加重后出院和居家时作为自身护理参与者的体验:一项纵向研究。

The experience of being a participant in one's own care at discharge and at home, following a severe acute exacerbation in chronic obstructive pulmonary disease: a longitudinal study.

机构信息

a Odense Patient data Explorative Network, Odense University Hospital/Department of Clinical Research , University of Southern Denmark , Odense , Denmark.

b Department of Medicine , Slagelse Hospital , Slagelse , Denmark.

出版信息

Int J Qual Stud Health Well-being. 2017 Dec;12(1):1371994. doi: 10.1080/17482631.2017.1371994.

Abstract

PURPOSE

In healthcare related to hospital discharge and follow-up, it is acknowledged that patient participation can strengthen self-management in patients with chronic obstructive pulmonary disease. However, the meaning of participation in care following a severe acute exacerbation is less described. Therefore, the aim of this part of a larger study was to explore patients' experiences of participating in their care around discharge and in their subsequent day-to-day care at home.

METHOD

The study was designed as a qualitative, longitudinal study. Data were collected by repeated participant observations and in-depth interviews with 15 patients within a period of 18 months post-discharge. A phenomenological-hermeneutic approach was used to interpret the data.

RESULTS

Before discharge, the patients struggled to regain a sense of control in their efforts to build up strength, and acquire sufficient clarity and confidence to face self-management at home. At home, the patients strived to comply with advice and encouragement in a struggle to stay motivated and confident, and to ask for help.

CONCLUSIONS

With more knowledge about patients' participation in care, healthcare professionals can encounter patients in ways that are sensitive to their specific care and support needs and, thereby, contribute to the promotion of patients' health and well-being.

摘要

目的

在与出院和随访相关的医疗保健中,人们认识到患者参与可以增强慢性阻塞性肺疾病患者的自我管理能力。然而,在严重急性加重后参与护理的意义描述较少。因此,本研究的这一部分旨在探讨患者在出院前后参与护理以及在家中日常护理的体验。

方法

该研究设计为定性、纵向研究。在出院后 18 个月的时间内,通过对 15 名患者进行反复的参与者观察和深入访谈来收集数据。采用现象学-解释学方法对数据进行解释。

结果

在出院前,患者在努力增强体力、获得足够的清晰性和信心以在家中进行自我管理方面,努力恢复控制感。在家中,患者努力遵守建议和鼓励,以保持动力和信心,并寻求帮助。

结论

通过更多地了解患者的参与护理,医护人员可以以对患者特定护理和支持需求敏感的方式与患者接触,从而促进患者的健康和福祉。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/800a/5613917/5d378e81ba07/ZQHW_A_1371994_F0001_B.jpg

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