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本文引用的文献

1
Evaluation of wound care options in patients with recessive dystrophic epidermolysis bullosa: a costly necessity.隐性营养不良型大疱性表皮松解症患者伤口护理选择的评估:一项代价高昂但必要的工作。
Pediatr Dermatol. 2014 Jan-Feb;31(1):33-7. doi: 10.1111/pde.12243. Epub 2013 Nov 14.
2
Specialist home-based nursing services for children with acute and chronic illnesses.为患有急慢性疾病的儿童提供的专科居家护理服务。
Cochrane Database Syst Rev. 2013 Jun 15;2013(6):CD004383. doi: 10.1002/14651858.CD004383.pub3.
3
Epidermolysis bullosa and chronic wounds: a model for wound bed preparation of fragile skin.大疱性表皮松解症与慢性创面:一种脆弱皮肤的创面床准备模型。
Adv Skin Wound Care. 2013 Apr;26(4):177-88; quiz 189-90. doi: 10.1097/01.ASW.0000428864.72412.b7.
4
Access to wound dressings for patients living with epidermolysis bullosa - an Australian perspective.大疱性表皮松解症患者获得伤口敷料的情况——澳大利亚视角
Int Wound J. 2014 Oct;11(5):505-8. doi: 10.1111/j.1742-481X.2012.01116.x. Epub 2012 Nov 22.
5
The evaluation of family impact of recessive dystrophic epidermolysis bullosa using the Italian version of the Family Dermatology Life Quality Index.使用家庭皮肤病生活质量指数意大利版评估隐性营养不良型大疱性表皮松解症的家庭影响。
J Eur Acad Dermatol Venereol. 2013 Sep;27(9):1151-5. doi: 10.1111/j.1468-3083.2012.04682.x. Epub 2012 Aug 11.
6
A consensus approach to wound care in epidermolysis bullosa.大疱性表皮松解症伤口护理的共识方法。
J Am Acad Dermatol. 2012 Nov;67(5):904-17. doi: 10.1016/j.jaad.2012.01.016. Epub 2012 Mar 2.
7
The psychosocial impact of epidermolysis bullosa.大疱性表皮松解症的心理社会影响。
Qual Health Res. 2011 Jun;21(6):771-82. doi: 10.1177/1049732311400431. Epub 2011 Feb 22.
8
Family burden in epidermolysis bullosa is high independent of disease type/subtype.大疱性表皮松解症患者的家庭负担不论疾病类型/亚型都很高。
Acta Derm Venereol. 2010 Nov;90(6):607-11. doi: 10.2340/00015555-0947.
9
'You're whatever the patient needs at the time': the impact on health and social care professionals of supporting people with epidermolysis bullosa.“患者当时需要什么,你就得成为什么”:支持大疱性表皮松解症患者对健康和社会护理专业人员的影响
Chronic Illn. 2010 Sep;6(3):215-27. doi: 10.1177/1742395310377006. Epub 2010 Jul 27.
10
Epidemiology of epidermolysis bullosa in the antipodes: the Australasian Epidermolysis Bullosa Registry with a focus on Herlitz junctional epidermolysis bullosa.澳大拉西亚地区大疱性表皮松解症的流行病学:以澳大利亚大疱性表皮松解症登记处为重点,聚焦于赫利茨交界型大疱性表皮松解症。
Arch Dermatol. 2010 Jun;146(6):635-40. doi: 10.1001/archdermatol.2010.109.

从澳大利亚视角看大疱性表皮松解症患者家庭护理项目的成效

Understanding the outcomes of a home nursing programme for patients with epidermolysis bullosa: an Australian perspective.

作者信息

Stevens Louise J, McKenna Sue, Marty Jennifer, Cowin Allison J, Kopecki Zlatko

机构信息

Brightsky Australia, Sydney, NSW, Australia.

Dystrophic Epidermolysis Bullosa Research Association - Australia, Pittsworth, QLD, Australia.

出版信息

Int Wound J. 2016 Oct;13(5):863-9. doi: 10.1111/iwj.12394. Epub 2014 Dec 3.

DOI:10.1111/iwj.12394
PMID:25469719
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7950174/
Abstract

Epidermolysis bullosa (EB) consists of a spectrum of genodermatoses characterised by skin fragility and various degrees of skin and mucous membrane blistering. Minimal trauma and friction can cause extensive blistering in patients with EB, resulting in a number of complications. However, wound management is the main challenge for these patients because of a high risk of infection, fluid loss and potential development of aggressive squamous cell carcinoma (SCC). Indeed, patients with EB have an increased risk for developing skin cancers compared to the general population. In 2012, a home nursing programme was established in Australia to provide assistance to families or patients with severe forms of EB. Nursing care was provided to patients with severe EB during dressing changes in their homes over a period of 2 years. Both families of patients and nurses were surveyed periodically using a developed questionnaire to assess the benefits of this home nursing and its impact on the patients, their families and the nurses. Key findings included a perceived improvement in quality of life, a better provision of support and improved family life management. These findings are the first to highlight the benefits of this national home nursing programme for EB patients within Australia and demonstrate the continued need and benefit of home nursing for patients with severe skin blistering disorders.

摘要

大疱性表皮松解症(EB)是一系列遗传性皮肤病,其特征为皮肤脆弱以及不同程度的皮肤和黏膜水疱形成。轻微的创伤和摩擦即可导致EB患者出现广泛的水疱,进而引发多种并发症。然而,由于感染风险高、体液流失以及侵袭性鳞状细胞癌(SCC)发生的可能性,伤口处理是这些患者面临的主要挑战。事实上,与普通人群相比,EB患者患皮肤癌的风险更高。2012年,澳大利亚设立了一项家庭护理计划,为患有严重形式EB的家庭或患者提供帮助。在两年时间里,为严重EB患者在家中换药时提供护理服务。定期使用一份编制好的问卷对患者家属和护士进行调查,以评估这种家庭护理的益处及其对患者、其家庭和护士的影响。主要发现包括生活质量得到改善、支持更加充分以及家庭生活管理得到改善。这些发现首次凸显了澳大利亚这项全国性家庭护理计划对EB患者的益处,并证明了家庭护理对于患有严重皮肤水疱性疾病患者的持续需求和益处。