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

dc.contributor.coauthorBorradori, L.
dc.contributor.coauthorVan Beek, N.
dc.contributor.coauthorFeliciani, C.
dc.contributor.coauthorTedbirt, B.
dc.contributor.coauthorAntiga, E.
dc.contributor.coauthorBergman, R.
dc.contributor.coauthorBoeckle, B. C.
dc.contributor.coauthorCaproni, M.
dc.contributor.coauthorCaux, F.
dc.contributor.coauthorChandran, N. S.
dc.contributor.coauthorCianchini, G.
dc.contributor.coauthorDaneshpazhooh, M.
dc.contributor.coauthorDe, D.
dc.contributor.coauthorDidona, D.
dc.contributor.coauthorDi Zenzo, G. M.
dc.contributor.coauthorDmochowski, M.
dc.contributor.coauthorDrenovska, K.
dc.contributor.coauthorEhrchen, J.
dc.contributor.coauthorGoebeler, M.
dc.contributor.coauthorGroves, R.
dc.contributor.coauthorGuenther, C.
dc.contributor.coauthorHorvath, B.
dc.contributor.coauthorHertl, M.
dc.contributor.coauthorHofmann, S.
dc.contributor.coauthorIoannides, D.
dc.contributor.coauthorItzlinger-Monshi, B.
dc.contributor.coauthorJedlickova, J.
dc.contributor.coauthorKowalewski, C.
dc.contributor.coauthorKridin, K.
dc.contributor.coauthorLim, Y. L.
dc.contributor.coauthorMarinovic, B.
dc.contributor.coauthorMarzano, A.
dc.contributor.coauthorMascaro, J. -M.
dc.contributor.coauthorMeijer, J. M.
dc.contributor.coauthorMurrell, D.
dc.contributor.coauthorPatsatsi, K.
dc.contributor.coauthorPincelli, C.
dc.contributor.coauthorProst, C.
dc.contributor.coauthorRappersberger, K.
dc.contributor.coauthorSardy, M.
dc.contributor.coauthorSetterfield, J.
dc.contributor.coauthorShahid, M.
dc.contributor.coauthorSprecher, E.
dc.contributor.coauthorTasanen, K.
dc.contributor.coauthorUzun, S.
dc.contributor.coauthorVassileva, S.
dc.contributor.coauthorVestergaard, K.
dc.contributor.coauthorVorobyev, A.
dc.contributor.coauthorVujic, I.
dc.contributor.coauthorWang, G.
dc.contributor.coauthorWozniak, K.
dc.contributor.coauthorZambruno, G.
dc.contributor.coauthorZillikens, D.
dc.contributor.coauthorSchmidt, E.
dc.contributor.coauthorJoly, P.
dc.contributor.kuauthorYaylı, Savaş
dc.contributor.kuprofileFaculty Member
dc.contributor.schoolcollegeinstituteSchool of Medicine
dc.contributor.yokid151352
dc.date.accessioned2024-11-09T12:40:52Z
dc.date.issued2022
dc.description.abstractBackground: 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.
dc.description.fulltextYES
dc.description.indexedbyWoS
dc.description.indexedbyScopus
dc.description.indexedbyPubMed
dc.description.issue10
dc.description.openaccessYES
dc.description.publisherscopeInternational
dc.description.sponsoredbyTubitakEuN/A
dc.description.sponsorshipThe guideline update was partly supported by the European Academy of Dermatology and Venereology (EADV) and the European Network for Rare Skin Disorders (ERN).
dc.description.versionPublisher version
dc.description.volume36
dc.formatpdf
dc.identifier.doi10.1111/jdv.18220
dc.identifier.eissn1468-3083
dc.identifier.embargoNO
dc.identifier.filenameinventorynoIR03814
dc.identifier.issn0926-9959
dc.identifier.linkhttps://doi.org/10.1111/jdv.18220
dc.identifier.quartileQ1
dc.identifier.scopus2-s2.0-85133041862
dc.identifier.urihttps://hdl.handle.net/20.500.14288/2218
dc.identifier.wos818030100001
dc.keywordsAdrenal cortex hormones
dc.keywordsAged
dc.keywordsBlister
dc.keywordsDermatology
dc.keywordsHumans
dc.keywordsPemphigoid, Bullous
dc.keywordsQuality of life
dc.keywordsVenereology
dc.languageEnglish
dc.publisherWiley
dc.relation.grantnoNA
dc.relation.urihttp://cdm21054.contentdm.oclc.org/cdm/ref/collection/IR/id/10672
dc.sourceJournal of the European Academy of Dermatology and Venereology
dc.subjectDermatology
dc.titleUpdated S2 K guidelines for the management of bullous pemphigoid initiated by the European Academy of Dermatology and Venereology (EADV)
dc.typeJournal Article
dspace.entity.typePublication
local.contributor.authorid0000-0001-9402-940X
local.contributor.kuauthorYaylı, Savaş

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