Denyer Jacqueline
Department of Dermatology, Great Ormond Street Hospital, London.
Nurs Times. 2012;108(29):21-3.
Epidermolysis bullosa is a rare genetic skin fragility disorder, with several types of varying severity. While research is progressing towards effective treatments, management remains symptomatic. One of the most distressing symptoms is pain, which may be multifactorial in origin. This article focuses on managing procedural pain during dressing changes and includes a case study.
大疱性表皮松解症是一种罕见的遗传性皮肤脆性疾病,有几种严重程度不同的类型。虽然针对有效治疗方法的研究正在取得进展,但治疗仍以对症处理为主。最令人痛苦的症状之一是疼痛,其成因可能是多方面的。本文重点关注换药过程中程序性疼痛的处理,并包括一个病例研究。