Patients’, family members’ and healthcare practitioners’experiences of Stevens–Johnson syndrome and toxic epidermal necrolysis: a qualitative descriptive study using emotional touchpoints
posted on 2020-11-30, 15:53authored byPauline O'ReillyPauline O'Reilly, B. Whelan, Bart Ramsay, Catriona Kennedy, Pauline Meskell, Alice Coffey, Donna M. Wilson, Dónal G. Fortune, S. Ryan
Stevens–Johnson syndrome (SJS) and toxic epidermal necrolysis (TEN) are devastating conditions resulting from a severe immune‐mediated mucocutaneous reaction which normally occurs as a result of medication.1 In the acute phase, the patient presents with a febrile illness, followed by skin and mucous membrane necrosis and detachment.2 The patient can quickly become critically ill and is treated as a medical emergency. There may be long‐lasting psychological effects on patients and their significant others.3 However, there is a dearth of research on the experiences of patients with SJS/TEN, those close to them and healthcare practitioners (HCPs) providing care.
History
Publication
Journal of the European Academy of Dermatology and Venereology; 35 (3), pp. e232-e234
Publisher
Wiley and Sons Ltd
Note
peer-reviewed
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