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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

Authors :
Musters, A. H.
Broderick, C.
Prieto-Merino, D.
Chiricozzi, Andrea
Damiani, G.
Peris, Ketty
Dhar, S.
De, A.
Freeman, E.
Arents, B. W. M.
Burton, T.
Bosma, A. L. -A. L.
Chi, C. -C.
Fletcher, G.
Drucker, A. M.
Kabashima, K.
de Monchy, E. F.
Panda, M.
Wall, D. R.
Vestergaard, C.
Mahe, E.
Bonzano, L.
Kattach, L.
Napolitano, M.
Ordonez-Rubiano, M. F.
Haufe, E.
Patruno, C.
Irvine, A. D.
Spuls, P. I.
Flohr, C.
Chiricozzi A. (ORCID:0000-0002-6739-0387)
Peris K. (ORCID:0000-0002-5237-0463)
Musters, A. H.
Broderick, C.
Prieto-Merino, D.
Chiricozzi, Andrea
Damiani, G.
Peris, Ketty
Dhar, S.
De, A.
Freeman, E.
Arents, B. W. M.
Burton, T.
Bosma, A. L. -A. L.
Chi, C. -C.
Fletcher, G.
Drucker, A. M.
Kabashima, K.
de Monchy, E. F.
Panda, M.
Wall, D. R.
Vestergaard, C.
Mahe, E.
Bonzano, L.
Kattach, L.
Napolitano, M.
Ordonez-Rubiano, M. F.
Haufe, E.
Patruno, C.
Irvine, A. D.
Spuls, P. I.
Flohr, C.
Chiricozzi A. (ORCID:0000-0002-6739-0387)
Peris K. (ORCID:0000-0002-5237-0463)
Publication Year :
2023

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

Details

Database :
OAIster
Notes :
English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1382660007
Document Type :
Electronic Resource