Publication details

Updated S2 K guidelines for the management of bullous pemphigoid initiated by the European Academy of Dermatology and Venereology (EADV)

Authors	BORRADORI L. VAN BEEKN N. FELICIANI C. TEDBIRT B. ANTIGA E. BERGMAN R. BOECKLE B. C. CAPRONI M. CAUX F. CHANDRAN N. S. CIANCHINI G. DANESHPAZHOOH M. DE D. DIDONA D. DI ZENZOM M. G. DMOCHOWSKI M. DRENOVSKA K. EHRCHEN J. GOEBELER M. GROVES R. GUENTHER C. HORVATH B. HERTL M. HOFMANN S. IOANNIDES D. ITZLINGER-MONSHI B. JEDLIČKOVÁ Hana KOWALEWSKI C. KRIDIN K. LIM Y. L. MARINOVIC B. MARZANO A. MASCARO J -M. MEIJER J. M. MURRELL D. PATSATSI K. PINCELLI C. PROST C. RAPPERSBERGER K. SARDY M. SETTERFIELD J. SHAHID M. SPRECHER E. TASANEN K. UZUN S. VASSILEVA S. VESTERGAARD K. VOROBYEV A. VUJIC I. WANG G. WOZNIAK K. YAYLI S. ZAMBRUNO G. ZILLIKENS D. SCHMIDT E. JOLY P.
Year of publication	2022
Type	Article in Periodical
Magazine / Source	JEADV - journal of the European Academy of Dermatology and Venereology
MU Faculty or unit	Faculty of Medicine
Citation
web	https://onlinelibrary.wiley.com/doi/10.1111/jdv.18220
Doi	http://dx.doi.org/10.1111/jdv.18220
Keywords	bullous pemphigoid; diagnostics; therapy
Description	Background Bullous pemphigoid (BP) is the most common autoimmune subepidermal blistering disease of the skin and mucous membranes. This disease typically affects the elderly and presents with itch and localized or, most frequently, generalized bullous lesions. A subset of patients only develops excoriations, prurigo-like lesions, and eczematous and/or urticarial erythematous lesions. The disease, which is significantly associated with neurological disorders, has high morbidity and severely impacts the quality of life. Objectives and methodology The Autoimmune blistering diseases Task Force of the European Academy of Dermatology and Venereology sought to update the guidelines for the management of BP based on new clinical information, and new evidence on diagnostic tools and interventions. The recommendations are either evidence-based or rely on expert opinion. The degree of consent among all task force members was included. Results Treatment depends on the severity of BP and patients' comorbidities. High-potency topical corticosteroids are recommended as the mainstay of treatment whenever possible. Oral prednisone at a dose of 0.5 mg/kg/day is a recommended alternative. In case of contraindications or resistance to corticosteroids, immunosuppressive therapies, such as methotrexate, azathioprine, mycophenolate mofetil or mycophenolate acid, may be recommended. The use of doxycycline and dapsone is controversial. They may be recommended, in particular, in patients with contraindications to oral corticosteroids. B-cell-depleting therapy and intravenous immunoglobulins may be considered in treatment-resistant cases. Omalizumab and dupilumab have recently shown promising results. The final version of the guideline was consented to by several patient organizations. Conclusions The guidelines for the management of BP were updated. They summarize evidence- and expert-based recommendations useful in clinical practice.