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

Luca Borradori(University Hospital of Bern), Nina van Beek(University of Lübeck), Claudio Feliciani(University of Parma), Billal Tedbirt(Inserm), Emiliano Antiga(University of Florence), Richard N. Bergman(Technion – Israel Institute of Technology), Barbara C. Böckle(Innsbruck Medical University), Marzia Caproni(University of Florence), F. Caux(Université Sorbonne Paris Nord), Nisha Suyien Chandran(National University of Singapore), Giuseppe Cianchini(Ospedale Cristo Re), Maryam Daneshpazhooh(Razi Hospital), Dipankar De(Post Graduate Institute of Medical Education and Research), Dario Didona(Philipps University of Marburg), Giovanni Di Zenzo(Istituto Dermopatico dell'Immacolata), Marian Dmochowski(Poznan University of Medical Sciences), Kossara Drenovska(Medical University of Sofia), Jan Ehrchen(University of Münster), Matthias Goebeler(Universitätsklinikum Würzburg), Richard Groves(Guy's Hospital), Claudia Günther(University Hospital Carl Gustav Carus), Barbara Horváth(University Medical Center Groningen), Michael Hertl(Philipps University of Marburg), Silke Hofmann(Helios Universitätsklinikum Wuppertal), D. Ioannides(Hospital Venereal and Skin Diseases Thessaloniki), Babak Alexander Itzlinger‐Monshi(Sigmund Freud Privatuniversität Wien), J. Jedličková(Masaryk University), Cezary Kowaléwski(Medical University of Warsaw), Khalaf Kridin(National Skin Centre), Yen Loo Lim(University Hospital Centre Zagreb), Branka Marinović(Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico), Angelo Valerio Marzano(University of Milan), José M. Mascaró(Hospital Clínic de Barcelona), Joost M. Meijer(University Medical Center Groningen), Dédée F. Murrell(UNSW Sydney), K. Patsatsi(Papageorgiou General Hospital), Carlo Pincelli(University of Modena and Reggio Emilia), C. Prost(Université Sorbonne Paris Nord), Klemens Rappersberger(Sigmund Freud Privatuniversität Wien), Miklós Sárdy(Semmelweis University), Jane Setterfield(Guy's and St Thomas' NHS Foundation Trust), Martin Shahid(Medical University of Sofia), Eli Sprecher(Tel Aviv University), Kaisa Tasanen(Oulu University Hospital), Soner Uzun(Akdeniz University), Snejina Vassileva(Medical University of Sofia), K. Vestergaard(Aarhus University Hospital), Artem Vorobyev(University of Lübeck), Igor Vujic(Sigmund Freud Privatuniversität Wien), Gang Wang(Xijing Hospital), Krzysztof Woźniak(National Skin Centre), Savaş Yaylı(Koç University), Giovanna Zambruno(Bambino Gesù Children's Hospital), Detlef Zillikens(University of Lübeck), Enno Schmidt(University of Lübeck), P. Joly(Inserm)
Journal of the European Academy of Dermatology and Venereology
June 29, 2022
Cited by 244Open Access
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Abstract

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.


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