BORRADORI, L., N. VAN BEEKN, C. FELICIANI, B. TEDBIRT, E. ANTIGA, R. BERGMAN, B. C. BOECKLE, M. CAPRONI, F. CAUX, N. S. CHANDRAN, G. CIANCHINI, M. DANESHPAZHOOH, D. DE, D. DIDONA, M. G. DI ZENZOM, M. DMOCHOWSKI, K. DRENOVSKA, J. EHRCHEN, M. GOEBELER, R. GROVES, C. GUENTHER, B. HORVATH, M. HERTL, S. HOFMANN, D. IOANNIDES, B. ITZLINGER-MONSHI, Hana JEDLIČKOVÁ, C. KOWALEWSKI, K. KRIDIN, Y. L. LIM, B. MARINOVIC, A. MARZANO, J -M. MASCARO, J. M. MEIJER, D. MURRELL, K. PATSATSI, C. PINCELLI, C. PROST, K. RAPPERSBERGER, M. SARDY, J. SETTERFIELD, M. SHAHID, E. SPRECHER, K. TASANEN, S. UZUN, S. VASSILEVA, K. VESTERGAARD, A. VOROBYEV, I. VUJIC, G. WANG, K. WOZNIAK, S. YAYLI, G. ZAMBRUNO, D. ZILLIKENS, E. SCHMIDT a P. JOLY. Updated S2 K guidelines for the management of bullous pemphigoid initiated by the European Academy of Dermatology and Venereology (EADV). JEADV - journal of the European Academy of Dermatology and Venereology. HOBOKEN: WILEY, 2022, roč. 36, č. 10, s. 1689-1704. ISSN 0926-9959. Dostupné z: https://dx.doi.org/10.1111/jdv.18220.
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Základní údaje
Originální název Updated S2 K guidelines for the management of bullous pemphigoid initiated by the European Academy of Dermatology and Venereology (EADV)
Autoři BORRADORI, L. (garant), N. VAN BEEKN, C. FELICIANI, B. TEDBIRT, E. ANTIGA, R. BERGMAN, B. C. BOECKLE, M. CAPRONI, F. CAUX, N. S. CHANDRAN, G. CIANCHINI, M. DANESHPAZHOOH, D. DE, D. DIDONA, M. G. DI ZENZOM, M. DMOCHOWSKI, K. DRENOVSKA, J. EHRCHEN, M. GOEBELER, R. GROVES, C. GUENTHER, B. HORVATH, M. HERTL, S. HOFMANN, D. IOANNIDES, B. ITZLINGER-MONSHI, Hana JEDLIČKOVÁ (203 Česká republika, domácí), C. KOWALEWSKI, K. KRIDIN, Y. L. LIM, B. MARINOVIC, A. MARZANO, J -M. MASCARO, J. M. MEIJER, D. MURRELL, K. PATSATSI, C. PINCELLI, C. PROST, K. RAPPERSBERGER, M. SARDY, J. SETTERFIELD, M. SHAHID, E. SPRECHER, K. TASANEN, S. UZUN, S. VASSILEVA, K. VESTERGAARD, A. VOROBYEV, I. VUJIC, G. WANG, K. WOZNIAK, S. YAYLI, G. ZAMBRUNO, D. ZILLIKENS, E. SCHMIDT a P. JOLY.
Vydání JEADV - journal of the European Academy of Dermatology and Venereology, HOBOKEN, WILEY, 2022, 0926-9959.
Další údaje
Originální jazyk angličtina
Typ výsledku Článek v odborném periodiku
Obor 30216 Dermatology and venereal diseases
Stát vydavatele Spojené státy
Utajení není předmětem státního či obchodního tajemství
WWW URL
Impakt faktor Impact factor: 9.200
Kód RIV RIV/00216224:14110/22:00128444
Organizační jednotka Lékařská fakulta
Doi http://dx.doi.org/10.1111/jdv.18220
UT WoS 000818030100001
Klíčová slova anglicky bullous pemphigoid; diagnostics; therapy
Štítky 14110125, rivok
Příznaky Mezinárodní význam, Recenzováno
Změnil Změnila: Mgr. Tereza Miškechová, učo 341652. Změněno: 3. 2. 2023 08:53.
Anotace
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.
VytisknoutZobrazeno: 9. 10. 2024 01:41