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Patients’, family members’ and healthcare practitioners’experiences of Stevens–Johnson syndrome and toxic epidermal necrolysis: a qualitative descriptive study using emotional touchpoints

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posted on 2020-11-30, 15:53 authored by Pauline 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 Please see link to podcast linked to this paper: https://open.spotify.com/episode/3wtcDxQebURXG8cybAHFHK?si=EqP0ovECS6eFl1qQ9ZDXoA&utm_source=copy-link

Language

English

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