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      A cross‐sectional study of dermatologists' attitudes towards COVID‐19 vaccination in patients with immunobullous diseases

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          Abstract

          Dear Editor, International experts released recommendations regarding COVID‐19 vaccination for patients with autoimmune bullous diseases (AIBDs) in March 2021. 1 Here, we evaluated knowledge, perceptions and attitudes of dermatologists regarding usage of COVID‐19 vaccines for this patient cohort. Dermatologists taking care of AIBD patients, who were recruited from the database of the International Pemphigus and Pemphigoid Foundation, were asked to complete a COVID‐19 vaccination‐related, web‐based survey between 1 May 2022 and 30 June 2022. The online poll was adapted with minor modifications from Hasseli et al. 2 Electronic informed consent was obtained, and the questionnaire was completed anonymously. The study was granted an exemption by the Institutional Review Board of the University of Southern California. One hundred and eighty‐four emailed invitations were made to complete our survey, and valid questionnaires were collected from a total of 30 dermatologists (16.3%) [19 male and 11 female, aged 33–71 years (median 49.5)] from North America (n = 17, 56.7%), Europe (n = 7, 23.3%), Asia (n = 4, 13.3%), Africa (n = 1, 3.3%) and an unlisted location (n = 1, 3.3%). Workplaces included University hospital (n = 26, 86.7%), private practice (n = 3, 10%) or both (n = 1, 3.3%), with 29 (96.7%) physicians being involved in research. Work experience was 5–10 years (n = 4, 13.3%), 11–20 years (n = 10, 33.3%), 21–30 years (n = 10, 33.3%) and >30 years (n = 6, 20.0%). Twenty‐seven (90)% reported to be at least confident in handling issues of COVID‐19 vaccination, and 29 (96.7%) would recommend COVID‐19 vaccination (preferentially mRNA vaccines), although 12 (40.0%) believed in an association between SARS‐CoV‐2 vaccination and induction/triggering of AIBDs. The majority would continue systemic corticosteroids regardless of the dose during immunization, and half would recommend changes in certain immunomodulatory treatments (i.e. mainly rituximab, methotrexate, mycophenolate and azathioprine) before and/or after COVID‐19 vaccination (Table 1). TABLE 1 Results of the COVID‐19 vaccination questionnaire. Information sources for COVID‐19 vaccination (multiple selection possible) Communication among colleagues 27 (90%) Dermatologic societies (e.g. American Academy of Dermatology, European Academy of Dermatology and Venereology) 25 (83.3%) Centers for Disease Control and Prevention (CDC) or World Health Organization (WHO) 23 (76.6%) Online research 21 (70.0%) General media (newspapers, television, radio) 14 (46.7%) Training 10 (33.3%) Patients asking for information about COVID‐19 vaccination Nearly every patient 13 (43.3%) >50% 10 (33.3%) <50% 6 (20.0%) None 1 (3.3%) Self‐assessment regarding handling COVID‐19 vaccination in AIBD patients Confident 18 (60.0%) Very confident 9 (30.0%) Uncertain/undecided 3 (10.0%) General recommendation of COVID‐19 vaccination for AIBD patients Yes 29 (96.7%) Uncertain 1 (3.3%) Self‐vaccination against COVID‐19 Yes 30 (100%) Preferred type of COVID‐19 vaccines for AIBD patients (multiple selection possible except for ‘no preference’) Pfizer‐BioNTech 23 (76.7%) Moderna 21 (70.0%) AstraZeneca 1 (3.3%) Johnson & Johnson 0 (0%) Other 3 (10.0%) No preference 5 (16.7%) Believe that COVID‐19 vaccines can induce a new‐onset AIBD or trigger a flare of an existing AIBD Yes 12 (40.0%) No 7 (23.3%) Uncertain 11 (36.7%) Recommendation of COVID‐19 vaccination for AIBD patients who are taking systemic corticosteroids such as oral prednisone/prednisolone Yes, regardless of the dose 20 (66.7%) Yes, depending on the dose 10 (33.3%) Recommendation or acceptance of the prednisone/prednisolone dose during COVID‐19 vaccination (multiple selection possible) <5 mg/day 6 (60.0%) 5–10 mg/day 7 (70.0%) 11–15 mg/day 6 (60.0%) >15 mg/day 5 (50.0%) Recommendation of any changes in at least one immunomodulatory treatment (i.e. azathioprine, colchicine, dapsone, doxycycline, immunoadsorption/plasmapheresis, intravenous immunoglobulins, methotrexate, mycophenolate, and/or rituximab) before and/or after COVID‐19 vaccination Yes 15 (50.0%) No 11 (36.7%) Uncertain 4 (13.3%) Changes in therapy due to COVID‐19 vaccination (i.e. pause before vaccination, pause after vaccination, pause before and after vaccination, dose reduction before vaccination, no changes, respectively; multiple selection possible except for ‘no changes’) Azathioprine 4 (26.7%), 1 (6.7%), 6 (40.0%), 0 (0%), 6 (40.0%) Colchicine 2 (13.3%), 0 (0%), 1 (6.7%), 1 (6.7%), 12 (80.0%) Dapsone 1 (6.7%), 0 (0%), 1 (6.7%), 1 (6.7%), 13 (86.7%) Doxycycline 0 (0%), 0 (0%), 1 (6.7%), 1 (6.7%), 14 (93.3%) Immunoadsorption/plasmapheresis 1 (6.7%), 2 (13.3%), 4 (26.7%), 1 (6.7%), 8 (53.3%) Intravenous immunoglobulins 2 (13.3%), 0 (0%), 2 (13.3%), 1 (6.7%), 11 (73.3%) Methotrexate 4 (26.7%), 4 (26.7%), 7 (46.7%), 1 (6.7%), 3 (20.0%) Mycophenolate 2 (13.3%), 2 (13.3%), 6 (40.0%), 1 (6.7%), 5 (33.3%) Rituximab 6 (40.0%), 3 (20.0%), 8 (53.3%), 1 (6.7%), 1 (6.7%) Although limited by a low number of participants and selection bias (i.e. dermatologists interested in AIBDs), this is the first survey research to investigate the opinion of dermatologists on COVID‐19 vaccines in AIBD patients. It shows that virtually all participating dermatologists across different countries supported SARS‐CoV‐2 vaccination for their AIBD patients, implicating that some concerns of potentially promoting immunobullous disease activity through vaccination were outweighed by the risk of contracting life‐threatening COVID‐19. 3 They advocated COVID‐19 vaccination also during immunosuppressive treatment with some restrictions including rituximab. Those attitudes are generally in accordance with the previously published expert recommendations for the management of AIBDs during the COVID‐19 pandemic. 1 Similar views were shared by rheumatologists regarding COVID‐19 vaccination in patients with inflammatory rheumatic diseases. 2 Surprisingly, however, several dermatologists preferred to temporarily terminate treatment with mycophenolate and azathioprine around the vaccination time to potentially improve the vaccine response. This has neither been specifically recommended for patients with AIBDs nor for those with rheumatic disorders because of the risk of disease exacerbation according to the respective international guidelines and experts' opinions. 1 , 4 In fact, discontinuation of an effective immunosuppressive treatment particularly by patients with chronic inflammatory immune‐mediated skin diseases has been a concern during the COVID‐19 pandemic. 5 In general, there is currently not enough evidence to support modifying treatment of systemic autoimmune diseases before or after SARS‐CoV‐2 vaccination with a few exceptions. 6 In detail, based on viewpoints of the Chinese Rheumatology Association, the American College of Rheumatology and The European League Against Rheumatism, a temporary hold of therapy in the perivaccination period has been limited to patients treated with methotrexate, JAK inhibitors, abatacept, cyclophosphamide (intravenous) and rituximab. 4 Taken together, our preliminary study indicates that basic recommendations on SARS‐CoV‐2 vaccination in AIBD patients were generally well perceived by international dermatologists, but also highlights the need for optimized decision‐making regarding modification of certain immunomodulatory therapies around COVID‐19 vaccination based on most current positions of scientific societies and newly generated objective data. FUNDING INFORMATION None. CONFLICT OF INTEREST R. Strong is a paid employee of the International Pemphigus and Pemphigoid Foundation; all other authors declared no conflicts of interest.

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          Most cited references6

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          The first dose of COVID‐19 vaccine may trigger pemphigus and bullous pemphigoid flares: is the second dose therefore contraindicated?

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            Updated international expert recommendations for the management of autoimmune bullous diseases during the COVID‐19 pandemic

            Dear Editor, The SARS‐CoV‐2 pandemic has worsened since the publication of our initial recommendations for the management of autoimmune bullous diseases (AIBDs) during the COVID‐19 outbreak in April 2020. 1 Based on the rapidly emerging increase in knowledge, this consensus of an expanded panel of international AIBD experts proposes updated recommendations to promote the optimal care of AIBD patients during the pandemic. The updated scientifically based guidance specifically pertains to the following questions: What do we recommend for AIBD patients considering the effects of immunomodulating therapy on SARS‐CoV‐2 infection? Patients with AIBDs treated with immunosuppressive therapies are generally prone to develop opportunistic infections, 2 , 3 which raised concerns that they could be more susceptible to SARS‐CoV‐2 infection and/or have worse COVID‐19 outcomes. Nevertheless, patients with AIBDs receiving immunomodulating therapies do not appear to have higher rates of manifest SARS‐CoV‐2 infection or more severe COVID‐19 than the general population according to a systematic review of 732 AIBD patients on various immunomodulating treatments including rituximab. 4 While overall 9.5% of them had COVID‐19 symptoms, 0.8% showed severe symptoms requiring hospitalization and 0.4% died of COVID‐19, with the latter being elderly people and/or having comorbidities. 4 However, since it has been also reported that patients with AIBDs or rheumatic diseases diagnosed with and dying of COVID‐19 were more likely to be receiving rituximab treatment and that each passing month from the last rituximab dose decreased the risk of getting COVID‐19 and related hospitalization, 5 , 6 , 7 we currently do not recommend the use of rituximab as maintenance therapy to prevent relapses. This particularly applies to individuals who have not received a SARS‐CoV‐2 vaccine (see below). Therefore, while the decision to initiate B‐cell depletion therapy remains to be made on a case‐by‐case basis, delays or obstructions in other important immunomodulatory treatments should be avoided during the pandemic, supporting our initial advice. Temporary changes in some immunosuppressive medications are still recommended in patients who have active COVID‐19, as detailed in our previously suggested guidelines. 1 What should patients with AIBDs do to protect themselves from SARS‐CoV‐2 infection? Patients should continuously follow generally recommended measures to prevent SARS‐CoV‐2 infection (www.who.int, www.cdc.gov) and preferentially be managed with telemedicine instead of in‐person visits where appropriate. The major advance in protection from COVID‐19 is the recent advent of mRNA vaccines [from Pfizer‐BioNTech and Moderna, authorized by the European Medicines Agency (EMA) and US Food and Drug Administration (FDA)] and adenoviral vector vaccines (from AstraZeneca and Johnson & Johnson, authorized by EMA and/or FDA), which induce an immune response to the SARS‐CoV‐2 spike protein, while additional vaccines are pending authorization or undergoing testing (www.who.int, www.cdc.gov). Therefore, it is recommended that every AIBD patient without contraindications to vaccination is immunized with one of the authorized vaccines to prevent COVID‐19. Since the effect of AIBD treatment on the efficacy of COVID‐19 vaccines is widely unknown, it is preferred to vaccinate patients while in remission or before planned immunosuppression, if feasible. In the case of rituximab, it is suggested to complete the entire vaccination series ≥4 weeks prior to the initiation of infusions or 12–20 weeks after completion of a rituximab cycle, 8 but the optimal time points are not clearly defined. Although vaccination is expected to be most effective when immunosuppression is low, we do not advise deliberately decreasing the patients’ immunomodulatory medications before or during the vaccination period because of the risk of disease exacerbation. Finally, it is worth mentioning that the European Academy of Dermatology and Venereology task force has initiated a registry for AIBD patients with confirmed COVID‐19 (https://recovab.umcg.nl). This online registry, which is open to physicians worldwide, will help determine how the SARS‐CoV‐2 infection impacts patients with AIBDs and provide future recommendations. Conflicts of interest Dr. Schmidt reports grants and personal fees from UCB, grants and personal fees from Biotest, grants from Incyte, grants from Euroimmun, personal fees from Novartis, grants and personal fees from ArgenX, personal fees from Astra Zeneca, grants and personal fees from Fresenius Medical Care, grants from Dompe, grants from Synthon, grants from Admirx and personal fees from Thermo Fisher, outside the submitted work; Dr. Amagai reports grants from Ono Pharmaceutical Company, grants from MBL and grants from RegCell, outside the submitted work; Dr. Fairley reports grants from National Institutes of Health and other from AstraZeneca, outside the submitted work; Dr. Murrell has served as a Principal Investigator and Advisor for trials with Principia Biopharma, Roche and Sanofi; Dr. Payne reports grants, personal fees and non‐financial support from Cabaletta Bio and personal fees from Villaris Therapeutics, outside the submitted work; in addition, Dr. Payne has a patent Compositions and methods of chimeric autoantibody receptor T cells with royalties paid from Cabaletta Bio, a patent Compositions and methods for selective protein expression with royalties paid from Novartis, and a patent Method of redirecting T cells to treat HIV infection with royalties paid from Tmunity; Dr. Zillikens reports personal fees from UCB, Almirall, ArGEN‐x, grants from Biotest, Euroimmun, Fresenius, personal fees from Biotest, Fresenius, Miltenyi, Roche, Biogen, Abbvie, UCB, Janssen, Novartis, outside the submitted work; Mr. Yale and Drs. Kasperkiewicz, Joly and Woodley have nothing to disclose.
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              Impact of the COVID-19 pandemic on the course and management of chronic inflammatory immune-mediated skin diseases: What's the evidence?

              Since the beginning of the coronavirus disease 2019 (COVID-19) pandemic, medical professionals have been overwhelmed by questions beyond the infection itself. In dermatology practice, clinicians have been facing difficulties about the management of chronic immune-mediated skin diseases. Issues arose, such as the grade of immunosuppression or immunomodulation, discontinuation or modification of treatment, and initiation of new treatments. In this comprehensive review, we present the current evidence about the course and management of chronic inflammatory dermatoses during the COVID-19 pandemic, focusing on psoriasis, atopic dermatitis, and hidradenitis suppurativa.
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                Author and article information

                Contributors
                michael.kasperkiewicz@med.usc.edu
                Journal
                J Eur Acad Dermatol Venereol
                J Eur Acad Dermatol Venereol
                10.1111/(ISSN)1468-3083
                JDV
                Journal of the European Academy of Dermatology and Venereology
                John Wiley and Sons Inc. (Hoboken )
                0926-9959
                1468-3083
                29 October 2022
                February 2023
                29 October 2022
                : 37
                : 2 ( doiID: 10.1111/jdv.v37.2 )
                : e132-e134
                Affiliations
                [ 1 ] Department of Dermatology, Keck School of Medicine University of Southern California Los Angeles California USA
                [ 2 ] International Pemphigus and Pemphigoid Foundation Roseville California USA
                Author notes
                [*] [* ] Correspondence

                Michael Kasperkiewicz, Department of Dermatology, Keck School of Medicine, University of Southern California, Los Angeles, California, USA.

                Email: michael.kasperkiewicz@ 123456med.usc.edu

                Author information
                https://orcid.org/0000-0003-0146-1661
                Article
                JDV18674 JEADV-2022-1966.R1
                10.1111/jdv.18674
                9874519
                36268687
                4db0ad50-9e0e-4e74-a9bd-606d44953d5c
                © 2022 European Academy of Dermatology and Venereology.

                This article is being made freely available through PubMed Central as part of the COVID-19 public health emergency response. It can be used for unrestricted research re-use and analysis in any form or by any means with acknowledgement of the original source, for the duration of the public health emergency.

                History
                : 18 July 2022
                : 13 October 2022
                Page count
                Figures: 0, Tables: 1, Pages: 3, Words: 978
                Categories
                Covid‐19 Special Forum ‐ Letter to the Editor
                Covid‐19 Special Forum ‐ Letter to the Editor
                Custom metadata
                2.0
                February 2023
                Converter:WILEY_ML3GV2_TO_JATSPMC version:6.2.4 mode:remove_FC converted:26.01.2023

                Dermatology
                Dermatology

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