Michelle Barakat-Johnson, Michelle Lai, Shifa Basjarahil, Jayne Campbell, Michelle Cunich, Gary Disher, Samara Geering, Natalie Ko, Catherine Leahy, Thomas Leong, Eve McClure, Melissa O'Grady, Joan Walsh, Kate White, Fiona Coyer
{"title":"医院环境中患者对大小便失禁和大小便失禁相关皮炎的体验:一项定性研究。","authors":"Michelle Barakat-Johnson, Michelle Lai, Shifa Basjarahil, Jayne Campbell, Michelle Cunich, Gary Disher, Samara Geering, Natalie Ko, Catherine Leahy, Thomas Leong, Eve McClure, Melissa O'Grady, Joan Walsh, Kate White, Fiona Coyer","doi":"10.12968/jowc.2021.0394","DOIUrl":null,"url":null,"abstract":"<p><strong>Objective: </strong>To explore the experience of patients with incontinence and incontinence-associated dermatitis (IAD) in acute care hospitals and their family caregivers, including their perceptions and management, as well as the impact on their wellbeing.</p><p><strong>Method: </strong>A qualitative exploratory study design was employed in 18 wards across six acute/subacute hospitals in New South Wales, Australia. Patients with incontinence (with or without IAD) were invited to participate. Where interviews were not possible with the patient, their family caregiver was invited to participate. Semi-structured interviews were conducted.</p><p><strong>Results: </strong>There were 45 interviewees in the study; 41 were patients with incontinence (11 of whom had IAD) and four were family caregivers. The experience of incontinence was captured by three themes: 'incontinence interrupts every aspect of my life'; 'actively concealing and cloaking'; and 'perceived as irreversible'. Incontinence was expected by the patients at their age and did not come as a surprise. It was normalised and approached with stoicism. As such, patients self-managed their incontinence by developing strategies to ensure they avoided episodes of incontinence during their stay. Incontinence left patients feeling anxious, embarrassed and with a sense of shame, and they did not communicate these feelings, or engage with health professionals about their incontinence, nor did health professionals discuss their incontinence with them. There was a strong sense of resignation that incontinence was irreversible and nothing could be done to improve it. All participants displayed little knowledge of IAD. The experience of having IAD was characterised by the theme 'debilitating and desperate for relief' and was experienced as a particularly painful, itching and burning condition that left patients distressed and irritable.</p><p><strong>Conclusion: </strong>Patients with incontinence in acute settings required further education from health professionals to reduce the stigma of incontinence, and provide further support to manage their incontinence. Health professionals can also play a key role in educating patients about the risks of developing IAD and how it can be prevented.</p>","PeriodicalId":17590,"journal":{"name":"Journal of wound care","volume":null,"pages":null},"PeriodicalIF":1.5000,"publicationDate":"2024-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Patients' experience of incontinence and incontinence-associated dermatitis in hospital settings: a qualitative study.\",\"authors\":\"Michelle Barakat-Johnson, Michelle Lai, Shifa Basjarahil, Jayne Campbell, Michelle Cunich, Gary Disher, Samara Geering, Natalie Ko, Catherine Leahy, Thomas Leong, Eve McClure, Melissa O'Grady, Joan Walsh, Kate White, Fiona Coyer\",\"doi\":\"10.12968/jowc.2021.0394\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Objective: </strong>To explore the experience of patients with incontinence and incontinence-associated dermatitis (IAD) in acute care hospitals and their family caregivers, including their perceptions and management, as well as the impact on their wellbeing.</p><p><strong>Method: </strong>A qualitative exploratory study design was employed in 18 wards across six acute/subacute hospitals in New South Wales, Australia. Patients with incontinence (with or without IAD) were invited to participate. Where interviews were not possible with the patient, their family caregiver was invited to participate. Semi-structured interviews were conducted.</p><p><strong>Results: </strong>There were 45 interviewees in the study; 41 were patients with incontinence (11 of whom had IAD) and four were family caregivers. The experience of incontinence was captured by three themes: 'incontinence interrupts every aspect of my life'; 'actively concealing and cloaking'; and 'perceived as irreversible'. Incontinence was expected by the patients at their age and did not come as a surprise. It was normalised and approached with stoicism. As such, patients self-managed their incontinence by developing strategies to ensure they avoided episodes of incontinence during their stay. Incontinence left patients feeling anxious, embarrassed and with a sense of shame, and they did not communicate these feelings, or engage with health professionals about their incontinence, nor did health professionals discuss their incontinence with them. There was a strong sense of resignation that incontinence was irreversible and nothing could be done to improve it. All participants displayed little knowledge of IAD. The experience of having IAD was characterised by the theme 'debilitating and desperate for relief' and was experienced as a particularly painful, itching and burning condition that left patients distressed and irritable.</p><p><strong>Conclusion: </strong>Patients with incontinence in acute settings required further education from health professionals to reduce the stigma of incontinence, and provide further support to manage their incontinence. Health professionals can also play a key role in educating patients about the risks of developing IAD and how it can be prevented.</p>\",\"PeriodicalId\":17590,\"journal\":{\"name\":\"Journal of wound care\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":1.5000,\"publicationDate\":\"2024-08-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of wound care\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.12968/jowc.2021.0394\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"DERMATOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of wound care","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.12968/jowc.2021.0394","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"DERMATOLOGY","Score":null,"Total":0}
引用次数: 0
摘要
目的探讨急症护理医院中大小便失禁和大小便失禁相关皮炎(IAD)患者及其家庭护理人员的经历,包括他们的认知和管理,以及对他们福祉的影响:在澳大利亚新南威尔士州 6 家急症/亚急性医院的 18 个病房中采用了定性探索性研究设计。尿失禁患者(伴有或不伴有尿失禁)受邀参与研究。如果无法与患者进行访谈,则邀请其家庭护理人员参与。访谈采用半结构式访谈:研究共有 45 位受访者,其中 41 位是尿失禁患者(其中 11 位患有 IAD),4 位是家庭护理人员。尿失禁的经历可归纳为三个主题:"尿失禁干扰了我生活的方方面面";"积极隐瞒和掩饰";以及 "被认为是不可逆转的"。尿失禁在患者这个年龄段是意料之中的事,并不感到意外。他们将尿失禁视为正常现象,并委曲求全。因此,患者通过制定策略来自我管理大小便失禁,以确保在住院期间避免大小便失禁的发生。尿失禁让患者感到焦虑、尴尬和羞耻,他们不会将这些感受告诉医护人员,也不会与医护人员讨论他们的尿失禁问题。他们有一种强烈的逆反心理,认为尿失禁是不可逆转的,没有任何办法可以改善。所有参与者对 IAD 都知之甚少。患有 IAD 的经历以 "令人衰弱、急需缓解 "为主题,并被认为是一种特别痛苦、瘙痒和灼热的症状,令患者感到痛苦和烦躁:结论:急诊环境中的尿失禁患者需要医疗专业人员提供进一步的教育,以减少尿失禁的耻辱感,并提供进一步的支持来管理他们的尿失禁。医护人员还可以在教育患者了解患上尿失禁的风险以及如何预防尿失禁方面发挥关键作用。
Patients' experience of incontinence and incontinence-associated dermatitis in hospital settings: a qualitative study.
Objective: To explore the experience of patients with incontinence and incontinence-associated dermatitis (IAD) in acute care hospitals and their family caregivers, including their perceptions and management, as well as the impact on their wellbeing.
Method: A qualitative exploratory study design was employed in 18 wards across six acute/subacute hospitals in New South Wales, Australia. Patients with incontinence (with or without IAD) were invited to participate. Where interviews were not possible with the patient, their family caregiver was invited to participate. Semi-structured interviews were conducted.
Results: There were 45 interviewees in the study; 41 were patients with incontinence (11 of whom had IAD) and four were family caregivers. The experience of incontinence was captured by three themes: 'incontinence interrupts every aspect of my life'; 'actively concealing and cloaking'; and 'perceived as irreversible'. Incontinence was expected by the patients at their age and did not come as a surprise. It was normalised and approached with stoicism. As such, patients self-managed their incontinence by developing strategies to ensure they avoided episodes of incontinence during their stay. Incontinence left patients feeling anxious, embarrassed and with a sense of shame, and they did not communicate these feelings, or engage with health professionals about their incontinence, nor did health professionals discuss their incontinence with them. There was a strong sense of resignation that incontinence was irreversible and nothing could be done to improve it. All participants displayed little knowledge of IAD. The experience of having IAD was characterised by the theme 'debilitating and desperate for relief' and was experienced as a particularly painful, itching and burning condition that left patients distressed and irritable.
Conclusion: Patients with incontinence in acute settings required further education from health professionals to reduce the stigma of incontinence, and provide further support to manage their incontinence. Health professionals can also play a key role in educating patients about the risks of developing IAD and how it can be prevented.
期刊介绍:
Journal of Wound Care (JWC) is the definitive wound-care journal and the leading source of up-to-date research and clinical information on everything related to tissue viability. The journal was first launched in 1992 and aimed at catering to the needs of the multidisciplinary team. Published monthly, the journal’s international audience includes nurses, doctors and researchers specialising in wound management and tissue viability, as well as generalists wishing to enhance their practice.
In addition to cutting edge and state-of-the-art research and practice articles, JWC also covers topics related to wound-care management, education and novel therapies, as well as JWC cases supplements, a supplement dedicated solely to case reports and case series in wound care. All articles are rigorously peer-reviewed by a panel of international experts, comprised of clinicians, nurses and researchers.
Specifically, JWC publishes:
High quality evidence on all aspects of wound care, including leg ulcers, pressure ulcers, the diabetic foot, burns, surgical wounds, wound infection and more
The latest developments and innovations in wound care through both preclinical and preliminary clinical trials of potential new treatments worldwide
In-depth prospective studies of new treatment applications, as well as high-level research evidence on existing treatments
Clinical case studies providing information on how to deal with complex wounds
Comprehensive literature reviews on current concepts and practice, including cost-effectiveness
Updates on the activities of wound care societies around the world.