International consensus on methotrexate dosing for patients with atopic dermatitis: An eDelphi study

Author:

Caron Anouk G. M.12ORCID,van Huizen Astrid M.12ORCID,Musters Annelie A. H.12ORCID,Gerbens Louise A. A.12ORCID,Middelkamp Hup Maritza A.12,Flohr Carsten3ORCID,Irvine Alan D.4ORCID,Vestergaard Christian5ORCID,Peris Ketty67ORCID,Brandling‐Bennett Heather A.8,Drucker Aaron M.9ORCID,Spuls Phyllis I.12ORCID,

Affiliation:

1. Dermatology Amsterdam UMC Location University of Amsterdam Amsterdam The Netherlands

2. Amsterdam Public Health, Infection and Immunity University of Amsterdam Amsterdam The Netherlands

3. Department of Paediatric Dermatology St John's Institute of Dermatology, King's College London and Guy's and St Thomas' NHS Foundation Trust London UK

4. Clinical Medicine Trinity College Dublin Dublin Ireland

5. Department of Dermatology Aarhus University Hospital Aarhus Denmark

6. Dipartimento di Scienze Mediche Chirurgiche, Fondazione Policlinico Universitario A. Gemelli ‐ IRCCSUOC di Dermatologia Rome Italy

7. Dipartimento di Medicina Chirurgia Traslazionale, Università Cattolica del Sacro CuoreDermatologia Rome Italy

8. Division of Dermatology, Department of Pediatrics University of Washington Seattle Washington USA

9. Division of Dermatology, Department of Medicine University of Toronto and Women's College Hospital, and the Women's College Research Institute, Women's College Hospital Toronto Ontario Canada

Abstract

AbstractBackgroundDespite the widespread off‐label use of methotrexate (MTX) for the treatment of atopic dermatitis (AD), there is limited high‐quality evidence on dosing regimens and existing guidelines do not provide clear recommendations regarding dosing strategies.ObjectiveThe aim of this study was to achieve international consensus among AD experts to standardize the dosing regimen for MTX treatment in adults and children with AD.MethodsAn electronic Delphi (eDelphi) study was conducted from October 2021 to September 2022. Recruitment was conducted through dermatology societies and AD interest groups. Participation was open to dermatologists and dermatology residents experienced in treating AD patients with MTX. The study consisted of three online rounds. The first round was informed by a systematic review of relevant literature, and subsequent rounds were adjusted based on the results of the previous round. Participants voted on 19 proposals using a 9‐point scale (1–3 disagree, 4–6 neither agree nor disagree, 7–9 agree). Consensus was achieved when at least 70% of participants agreed, and less than 15% disagreed. Proposals that did not reach consensus in the first three rounds were discussed in a consensus meeting, where consensus was defined as less than 30% disagreement.ResultsIn total, 152 participants completed Round 1, 104 (68%) completed all survey rounds, and 43 (28%) joined the consensus meeting. Consensus was achieved on 7 proposals in Round 1, 4 in Round 2 and 6 in Round 3. The final 2 proposals reached consensus during the consensus meeting. Consensus topics include test dose, start dose, maximum dose, administration route, dosing schedule, management of stopping treatment, treatment duration and folic acid supplementation.ConclusionsThis eDelphi study achieved consensus on 19 proposals related to MTX dosing for adults and children with AD. These results aim to guide prescribing decisions and encourage a standardized global approach to MTX use in AD.

Funder

European Academy of Dermatology and Venereology

Publisher

Wiley

Reference43 articles.

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