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The effects of systemic immunomodulatory treatments on COVID-19 outcomes in patients with atopic dermatitis: Results from the global SECURE-AD registry.
Musters, Annelie H; Broderick, Conor; Prieto-Merino, David; Chiricozzi, Andrea; Damiani, Giovanni; Peris, Ketty; Dhar, Sandipan; De, Abhishek; Freeman, Esther; Arents, Bernd W M; Burton, Tim; Bosma, Angela Leigh-Ann L; Chi, Ching-Chi; Fletcher, Godfrey; Drucker, Aaron M; Kabashima, Kenji; de Monchy, Emilie F; Panda, Maitreyee; Wall, Dmitri Robert; Vestergaard, Christian; Mahé, Emmanuel; Bonzano, Laura; Kattach, Leila; Napolitano, Maddalena; Ordoñez-Rubiano, María Fernanda; Haufe, Eva; Patruno, Cataldo; Irvine, Alan D; Spuls, Phyllis I; Flohr, Carsten.
  • Musters AH; Department of Dermatology, Amsterdam UMC, location Academic Medical Center, Amsterdam Public Health Infection and Immunity, University of Amsterdam, Amsterdam, The Netherlands.
  • Broderick C; Unit for Population-Based Dermatology Research, Guy's and St Thomas' NHS Foundation Trust and King's College London, London, UK.
  • Prieto-Merino D; Faculty of Epidemiology & Population Health, London School of Hygiene & Tropical Medicine, London, UK.
  • Chiricozzi A; Dermatologia, Fondazione Policlinico Universitario A. Gemelli IRCCS, Rome, Italy.
  • Damiani G; Dermatologia, Università Cattolica del Sacro Cuore, Rome, Italy.
  • Peris K; Clinical Dermatology, IRCCS Istituto Ortopedico Galeazzi, Milan, Italy.
  • Dhar S; Department of Biomedical, Surgical and Dental Sciences, University of Milan, Milan, Italy.
  • De A; Department of Pharmaceutical and Pharmacological Sciences, University of Padua, Padua, Italy.
  • Freeman E; Dermatologia, Dipartimento di Medicina e Chirurgia Traslazionale, Università Cattolica del Sacro Cuore, Rome, Italy.
  • Arents BWM; UOC di Dermatologia, Dipartimento di Scienze Mediche e Chirurgiche, Fondazione Policlinico Universitario A. Gemelli - IRCCS, Rome, Italy.
  • Burton T; Department of Pediatric Dermatology, Institute of Child Health, Kolkata, India.
  • Bosma ALL; Department of Dermatology, Calcutta National Medical College, Kolkata, India.
  • Chi CC; Department of Dermatology, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts, USA.
  • Fletcher G; Medical Practice Evaluation Center, Mongan Institute, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts, USA.
  • Drucker AM; Dutch Association for People with Atopic Dermatitis (VMCE), Nijkerk, The Netherlands.
  • Kabashima K; Patient Representative (independent), Nottingham, UK.
  • de Monchy EF; Department of Dermatology, Amsterdam UMC, location Academic Medical Center, Amsterdam Public Health Infection and Immunity, University of Amsterdam, Amsterdam, The Netherlands.
  • Panda M; Department of Dermatology, Chang Gung Memorial Hospital, Taoyuan, Taiwan.
  • Wall DR; College of Medicine, Chang Gung University, Taoyuan, Taiwan.
  • Vestergaard C; National and International Skin Registry Solutions (NISR), Charles Institute of Dermatology, University College Dublin, Dublin, Ireland.
  • Mahé E; Department of Medicine, University of Toronto, Toronto, Canada; Women's College Research Institute, Women's College Hospital, Toronto, Canada.
  • Bonzano L; Department of Dermatology, Kyoto University Graduate School of Medicine, Kyoto, Japan.
  • Kattach L; Singapore Immunology Network (SIgN) and Skin Research Institute of Singapore (SRIS), Agency for Science Technology and Research (A*STAR) Biopolis, Singapore, Singapore.
  • Napolitano M; Department of Dermatology, Amsterdam UMC, location Academic Medical Center, Amsterdam Public Health Infection and Immunity, University of Amsterdam, Amsterdam, The Netherlands.
  • Ordoñez-Rubiano MF; Department of DVL, Institute of Medical Sciences and SUM Hospital, Bhubaneswar, Odisha, India.
  • Haufe E; National and International Skin Registry Solutions (NISR), Charles Institute of Dermatology, University College Dublin, Dublin, Ireland.
  • Patruno C; Hair Restoration Blackrock, Dublin, Ireland.
  • Irvine AD; Department of Dermatology, Aarhus University Hospital, Aarhus, Denmark.
  • Spuls PI; Service de Dermatologie et Médecine Vasculaire, Centre Hospitalier Victor Dupouy, Argenteuil Cedex, France.
  • Flohr C; Dermatology Unit, Azienda USL-IRCCS di Reggio Emilia, Reggio Emilia, Italy.
J Eur Acad Dermatol Venereol ; 2022 Sep 28.
Article in English | MEDLINE | ID: covidwho-2233605
ABSTRACT

BACKGROUND:

Limited data are available on the effects of systemic immunomodulatory treatments on COVID-19 outcomes in patients with atopic dermatitis (AD).

OBJECTIVE:

To investigate COVID-19 outcomes in patients with AD treated with or without systemic immunomodulatory treatments, using a global registry platform.

METHODS:

Clinicians were encouraged to report cases of COVID-19 in their patients with AD in the Surveillance Epidemiology of Coronavirus Under Research Exclusion for Atopic Dermatitis (SECURE-AD) registry. Data entered from 1 April 2020 to 31 October 2021 were analysed using multivariable logistic regression. The primary outcome was hospitalization from COVID-19, according to AD treatment groups.

RESULTS:

442 AD patients (mean age 35.9 years, 51.8% male) from 27 countries with strongly suspected or confirmed COVID-19 were included in analyses. 428 (96.8%) patients were treated with a single systemic therapy (n = 297 [67.2%]) or topical therapy only (n = 131 [29.6%]). Most patients treated with systemic therapies received dupilumab (n = 216). Fourteen patients (3.2%) received a combination of systemic therapies. Twenty-six patients (5.9%) were hospitalized. No deaths were reported. Patients treated with topical treatments had significantly higher odds of hospitalization, compared with those treated with dupilumab monotherapy (odds ratio (OR) 4.65 [95%CI 1.71-14.78]), including after adjustment for confounding variables (adjusted OR (aOR) 4.99 [95%CI 1.4-20.84]). Combination systemic therapy which did not include systemic corticosteroids was associated with increased odds of hospitalization, compared with single agent non-steroidal immunosuppressive systemic treatment (OR 8.09 [95%CI 0.4-59.96], aOR 37.57 [95%CI 1.05-871.11]). Hospitalization was most likely in patients treated with combination systemic therapy which included systemic corticosteroids (OR 40.43 [95%CI 8.16-207.49], aOR 45.75 [95%CI 4.54-616.22]).

CONCLUSIONS:

Overall, the risk of COVID-19 complications appears low in patients with AD, even when treated with systemic immunomodulatory agents. Dupilumab monotherapy was associated with lower hospitalization than other therapies. Combination systemic treatment, particularly combinations including systemic corticosteroids, was associated with the highest risk of severe COVID-19.

Full text: Available Collection: International databases Database: MEDLINE Type of study: Experimental Studies / Prognostic study / Randomized controlled trials Language: English Journal subject: Dermatology / Sexually Transmitted Diseases Year: 2022 Document Type: Article Affiliation country: Jdv.18613

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Full text: Available Collection: International databases Database: MEDLINE Type of study: Experimental Studies / Prognostic study / Randomized controlled trials Language: English Journal subject: Dermatology / Sexually Transmitted Diseases Year: 2022 Document Type: Article Affiliation country: Jdv.18613