Systemic treatment of children and adolescents with atopic dermatitis aged ≥2 years: a Delphi consensus project mapping expert opinion in Northern Europe.


Journal

Journal of the European Academy of Dermatology and Venereology : JEADV
ISSN: 1468-3083
Titre abrégé: J Eur Acad Dermatol Venereol
Pays: England
ID NLM: 9216037

Informations de publication

Date de publication:
Nov 2022
Historique:
received: 18 01 2022
accepted: 14 06 2022
pubmed: 7 7 2022
medline: 15 10 2022
entrez: 6 7 2022
Statut: ppublish

Résumé

Paediatric atopic dermatitis (AD) can be burdensome, affecting mental health and impairing quality of life for children and caregivers. Comprehensive guidelines exist for managing paediatric AD, but practical guidance on using systemic therapy is limited, particularly for new therapies including biologics and Janus kinase (JAK) inhibitors, recently approved for various ages in this indication. This expert consensus aimed to provide practical recommendations within this advancing field to enhance clinical decision-making on the use of these and other systemics for children and adolescents aged ≥2 years with moderate-to-severe AD. Nineteen physicians from Northern Europe were selected for their expertise in managing childhood AD. Using a two-round Delphi process, they reached full or partial consensus on 37 statements. Systemic therapy is recommended for children aged ≥2 years with a clear clinical diagnosis of severe AD and persistent disease uncontrolled after optimizing non-systemic therapy. Systemic therapy should achieve long-term disease control and reduce short-term interventions. Recommended are cyclosporine A for short-term use (all ages) and dupilumab or methotrexate for long-term use (ages ≥6 years). Consensus was not reached on the best long-term systemics for children aged 2-6 years, although new systemic therapies will likely become favourable: New biologics and JAK inhibitors will soon be approved for this age group, and more trial and real-world data will become available. This article makes practical recommendations on the use of systemic AD treatments for children and adolescents, to supplement international and regional guidelines. It considers the systemic medication that was available for children and adolescents with moderate-to-severe AD at the time this consensus project was done: azathioprine, cyclosporine A, dupilumab, methotrexate, mycophenolate mofetil and oral glucocorticosteroids. We focus on the geographically similar Northern European countries, whose healthcare systems, local preferences for AD management and reimbursement structures nonetheless differ significantly.

Sections du résumé

BACKGROUND BACKGROUND
Paediatric atopic dermatitis (AD) can be burdensome, affecting mental health and impairing quality of life for children and caregivers. Comprehensive guidelines exist for managing paediatric AD, but practical guidance on using systemic therapy is limited, particularly for new therapies including biologics and Janus kinase (JAK) inhibitors, recently approved for various ages in this indication.
OBJECTIVES OBJECTIVE
This expert consensus aimed to provide practical recommendations within this advancing field to enhance clinical decision-making on the use of these and other systemics for children and adolescents aged ≥2 years with moderate-to-severe AD.
METHODS METHODS
Nineteen physicians from Northern Europe were selected for their expertise in managing childhood AD. Using a two-round Delphi process, they reached full or partial consensus on 37 statements.
RESULTS RESULTS
Systemic therapy is recommended for children aged ≥2 years with a clear clinical diagnosis of severe AD and persistent disease uncontrolled after optimizing non-systemic therapy. Systemic therapy should achieve long-term disease control and reduce short-term interventions. Recommended are cyclosporine A for short-term use (all ages) and dupilumab or methotrexate for long-term use (ages ≥6 years). Consensus was not reached on the best long-term systemics for children aged 2-6 years, although new systemic therapies will likely become favourable: New biologics and JAK inhibitors will soon be approved for this age group, and more trial and real-world data will become available.
CONCLUSIONS CONCLUSIONS
This article makes practical recommendations on the use of systemic AD treatments for children and adolescents, to supplement international and regional guidelines. It considers the systemic medication that was available for children and adolescents with moderate-to-severe AD at the time this consensus project was done: azathioprine, cyclosporine A, dupilumab, methotrexate, mycophenolate mofetil and oral glucocorticosteroids. We focus on the geographically similar Northern European countries, whose healthcare systems, local preferences for AD management and reimbursement structures nonetheless differ significantly.

Identifiants

pubmed: 35793471
doi: 10.1111/jdv.18410
pmc: PMC9796032
doi:

Substances chimiques

Biological Products 0
Janus Kinase Inhibitors 0
Cyclosporine 83HN0GTJ6D
Janus Kinases EC 2.7.10.2
Mycophenolic Acid HU9DX48N0T
Azathioprine MRK240IY2L
Methotrexate YL5FZ2Y5U1

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

2153-2165

Subventions

Organisme : Sanofi Genzyme

Informations de copyright

© 2022 The Authors. Journal of the European Academy of Dermatology and Venereology published by John Wiley & Sons Ltd on behalf of European Academy of Dermatology and Venereology.

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Auteurs

M de Graaf (M)

Department of Dermatology and Allergology, National Expertise Center for Atopic Dermatitis, Wilhelmina Children's Hospital, University Medical Center Utrecht, Utrecht, The Netherlands.

S R Janmohamed (SR)

Department of Dermatology, Unit Pediatric Dermatology, SKIN Research Group, Universitair Ziekenhuis Brussel (UZ Brussel), Vrije Universiteit Brussel (VUB), Brussels, Belgium.

M L A Schuttelaar (MLA)

Department of Dermatology, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.

T Agner (T)

Department of Dermatology and Venereology, Bispebjerg Hospital, Copenhagen, Denmark.

J H Alfonso (JH)

Department of Dermatology, Oslo University Hospital, Rikshospitalet, Oslo, Norway.

S De Schepper (S)

Department of Dermatology, Gent University Hospital, Gent, Belgium.

M Deleuran (M)

Department of Dermatology, Aarhus University Hospital, Aarhus, Denmark.

K Despontin (K)

Department of Dermatology and Venereology, CHU UCL Namur, Namur, Belgium.

V Elenius (V)

Department of Pediatrics, Turku University Hospital, Turku, Finland.

P-D Ghislain (PD)

Department of Dermatology, UCL St-Luc, Louvain University, Brussels, Belgium.

L Huilaja (L)

PEDEGO Research Unit, University of Oulu, Oulu, Finland.
Department of Dermatology and Medical Research Center Oulu, Oulu University Hospital, Oulu, Finland.

E K Johansson (EK)

Dermatology and Venereology Unit, Department of Medicine Solna, Karolinska Institutet, Stockholm, Sweden.
Department of Dermatology, Karolinska University Hospital, Stockholm, Sweden.

B K Kvenshagen (BK)

Department of Paediatrics, Østfold Hospital, Grålum, Norway.

J M Mandelin (JM)

Department of Dermatology, Helsinki University Central Hospital, Helsinki, Finland.

H Olset (H)

Department of Dermatology, Haukeland University Hospital, Bergen, Norway.

A Svensson (A)

Department of Dermatology and Venereology, Malmö University Hospital, Malmö, Sweden.

A M van Tuyll van Serooskerken (AM)

HagaZiekenhuis/Juliana Kinderziekenhuis, The Hague, The Netherlands.

J P Thyssen (JP)

Department of Dermatology and Venereology, Bispebjerg Hospital, Copenhagen, Denmark.

C Vestergaard (C)

Department of Dermatology, Aarhus University Hospital, Aarhus, Denmark.

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Classifications MeSH