南非脊髓损伤患者对继发性健康问题的体验:定性研究。

IF 1 Q4 REHABILITATION
South African Journal of Physiotherapy Pub Date : 2021-04-06 eCollection Date: 2021-01-01 DOI:10.4102/sajp.v77i1.1530
Sonti I Pilusa, Hellen Myezwa, Joanne Potterton
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引用次数: 0

摘要

背景:在脊髓损伤(SCI)患者的整个生命周期中,疼痛、压疮、性问题、肠道和膀胱问题等继发性健康问题(SHC)十分普遍。研究报告显示,SHC 会缩短脊髓损伤患者的预期寿命并增加医疗费用。然而,有关脊髓损伤患者生活经历的研究却十分有限:目的:探讨南非一家公立康复医院的 SCI 患者的 SHC 体验:从 2018 年 8 月到 2019 年 7 月,对 SCI 患者进行了面对面的半结构化访谈。所有访谈均逐字记录,并采用内容分析法进行分析:17 名 SCI 患者接受了访谈。参与者经历了一系列的 SHC。最常见的 SHC 是疼痛(94%)。分析得出的主要主题是 "继发性健康状况对健康和幸福的影响"。与影响相关的类别包括:继发性健康问题的共同发生,以及继发性健康问题如何限制功能、限制参与、影响心理健康和扰乱生活:我们发现,SHC 对参与者的生活和健康产生了巨大的影响,他们讲述的恐惧、尴尬和羞耻的故事就说明了这一点。了解重症肌无力患者在特殊健康问题上的经历可以加强重症肌无力患者与医疗专业人员之间的沟通,并有助于制定预防策略:为加强以患者为中心的护理,鼓励医疗专业人员积极倾听患者的患病经历及其对健康和幸福的影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Experiences of secondary health conditions amongst people with spinal cord injury in South Africa: A qualitative study.

Background: Secondary health conditions (SHCs) such as pain, pressure sores, sexual problems, bowel and bladder problems are prevalent throughout the lifespan of people with spinal cord injury (SCI). Studies have reported that SHCs decrease life expectancy and increase health care costs. Studies on the lived experience of SHCs are, however, limited.

Objectives: To explore the experiences of SHCs amongst people with SCI in a public rehabilitation hospital in South Africa.

Method: Face-to-face semi-structured interviews were conducted with people with SCI from August 2018 to July 2019. All interviews were transcribed verbatim and analysed using a content analysis approach.

Results: Seventeen people with SCI were interviewed. Participants experienced a range of SHCs. The most common experienced SHC was pain (94%). The main theme that emerged from the analysis was 'the impact of secondary health conditions on health and well-being'. The categories linked to the impact were SHCs co-occurrence and how SHCs limit function, restrict participation, affect mental health and disrupt lives.

Conclusion: We found that SHCs were enormously impactful on our participants' lives and health, as illustrated by their stories of fear, embarrassment and shame. Understanding people with SCI experiences of SHCs can enhance communication between people with SCI and health professionals and may help develop prevention strategies.

Clinical implications: To enhance patient-centred care, health professionals are encouraged to actively listen to patients' experiences of illness and the impact on health and wellbeing.

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来源期刊
CiteScore
1.70
自引率
9.10%
发文量
35
审稿时长
30 weeks
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