Advice regarding COVID‐19 and use of immunomodulators, in patients with severe dermatological diseases

Abstract

Dear Editors, Coronavirus disease 2019 (COVID-19) is the disease caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), as named by the International Committee on Taxonomy of Viruses (ICTV). There is very limited evidence base to formulate specific advice for dermatology patients on immunomodulators with regard to COVID-19. The following is based on expert opinion, taking into account known risks of influenza (a negative-sense single-stranded RNA virus) and other, positive-sense single-stranded, RNA virus infections (such as SARS, MERS and the common cold). An Australia/New Zealand consensus document is in development. This interim advice is for clinicians treating patients with severe inflammatory skin disorders managed on conventional and newer immunomodulators.1 This includes systemic corticosteroids, azathioprine, ciclosporin, methotrexate and mycophenolate mofetil/mycophenolic acid, as well as the newer biologics for eczema and psoriasis including anti-TNF (e.g. adalimumab, certolizumab, etanercept, infliximab), anti-IL4/13 (dupilumab), anti-IL12/23 (ustekinumab), anti-IL17/23 (guselkumab, ixekizumab, risankizumab, secukinumab, tildrakizumab), and small molecules such as PDE inhibitors (apremilast) and JAK inhibitors (abrocitinib, baricitinib, tofacitinib, upatacitinib). There is no evidence of COVID-19 (or any RNA virus)-related harm from systemic retinoids (acetretin, alitretinoin, isotretinoin), so these do not currently need to be stopped/dose adjusted. Currently, most people should continue taking their immunomodulator therapy, but this advice may change as more information becomes available. Any patient with an inflammatory skin disorder being actively managed with an immunomodulator, who is diagnosed with COVID-19, should stop the immunomodulator (s) immediately, with the possible exception of systemic corticosteroids (see below). Whilst there is little specific evidence of COVID-19 infection being aggravated by immunomodulators as used in otherwise healthy dermatology patients, a precautionary approach is mandated, particularly as any secondary bacterial infection as part of COVID-19 may be aggravated by concurrent use of immunomodulators. Patients who are immunosuppressed appear to be at higher risk of a more severe infection or complications from COVID-19, although the extent of this risk is not known. Although median COVID-19 infection duration is in the order of 2 weeks, it would be sensible to discontinue systemic immunomodulators for at least 4 weeks, and until the patient has completely recovered. In any patient with an inflammatory skin disorder being actively managed with an immunomodulator, who develops signs of a winter cold (e.g. mild coughing, sore throat, sneezing and runny nose), but who is not formally diagnosed with COVID-19 disease, it is reasonable to consider lowering the dose of any immunomodulator (see below) or temporarily stopping for 2 weeks. The possible exception is systemic corticosteroids. Doses of predniso(lo)ne >20 mg/day are considered immunosuppressive, but sudden stopping, or significant reduction of dose, in patients on long-term systemic corticosteroids, is unwise, particularly if they have suddenly become physiologically stressed. Note that systemic corticosteroids are part of many adult respiratory distress syndrome (ARDS) protocols, but are not currently recommended for SARS-CoV-2, as there is weak evidence of harm when used in influenza-associated adult respiratory distress syndrome.

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