Oxford Brookes University, School of Health and Social Care, United Kingdom; University of Oxford, Nuffield Department of Medicine, United Kingdom.
Oxford Brookes University, School of Health and Social Care, United Kingdom; University of Technology Sydney, Faculty of Health, Australia.
Int J Nurs Stud. 2018 Nov;87:149-156. doi: 10.1016/j.ijnurstu.2018.07.017. Epub 2018 Jul 31.
Inflammatory Bowel Disease is a chronic, untreatable condition represented by two illnesses, Crohn's and Ulcerative Colitis. Despite high incidence in well-developed industrialised countries, and the significant impact of symptoms on patient's quality of life, little is known about living with Inflammatory Bowel Disease.
To explore the patients' experiences of living with Inflammatory Bowel Disease.
A qualitative systematic review.
CINAHL, Medline, British Nursing Index and PsycINFO were searched using the following keywords: Inflammatory Bowel Disease AND experiences. We have limited the search to studies published in English from 2000 to 2017.
Thematic synthesis.
Data from 23 studies, identified that fatigue, incontinence and uncertainty about future, body image, and lack of information from healthcare professionals dominated the experiences of those living with Inflammatory Bowel Disease. Also, patients living with Inflammatory Bowel Disease were reluctant to disclose their illness due to lack of public awareness and stigma surrounding symptoms. From these, an overarching theme has been identified: Living in isolation and exclusion.
Patients with Inflammatory Bowel Disease face a variety of problems, often their priorities and those of healthcare professionals differ greatly. Healthcare professionals have little evidence needed to provide adequate, holistic care to this group. With a rise in the Inflammatory Bowel Disease population in newly industrialised countries it is estimated that the condition is turning into a global disease, potentially making long term care unsustainable. More evidence is needed to understand the concerns of this group.
炎症性肠病是一种无法治愈的慢性疾病,由两种疾病组成,即克罗恩病和溃疡性结肠炎。尽管在发达工业化国家发病率很高,且症状对患者的生活质量有重大影响,但人们对炎症性肠病的生活体验知之甚少。
探讨炎症性肠病患者的生活体验。
定性系统综述。
使用以下关键词在 CINAHL、Medline、英国护理索引和 PsycINFO 中进行检索:炎症性肠病和经历。我们将搜索范围限制为 2000 年至 2017 年期间以英语发表的研究。
主题综合。
23 项研究的数据表明,疲劳、失禁和对未来的不确定性、身体形象以及缺乏来自医疗保健专业人员的信息主导了炎症性肠病患者的生活体验。此外,炎症性肠病患者由于公众对症状缺乏认识和污名化,不愿透露自己的病情。由此产生了一个总体主题:孤立和排斥的生活。
炎症性肠病患者面临着各种问题,他们的首要任务和医疗保健专业人员的优先事项往往大不相同。医疗保健专业人员几乎没有提供足够、全面护理所需的证据。随着新工业化国家炎症性肠病患者人数的增加,预计这种疾病将成为一种全球性疾病,这可能使长期护理无法持续。需要更多的证据来了解这一群体的关注点。