Children with psoriasis and COVID-19: factors associated with an unfavourable COVID-19 course, and the impact of infection on disease progression (Chi-PsoCov registry).


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 03 2022
accepted: 10 06 2022
pubmed: 25 6 2022
medline: 15 10 2022
entrez: 24 6 2022
Statut: ppublish

Résumé

The COVID-19 pandemic has raised questions regarding the management of chronic skin diseases, especially in patients on systemic treatments. Data concerning the use of biologics in adults with psoriasis are reassuring, but data specific to children are missing. Moreover, COVID-19 could impact the course of psoriasis in children. The aim of this study was therefore to assess the impact of COVID-19 on the psoriasis of children, and the severity of the infection in relation to systemic treatments. We set up an international registry of paediatric psoriasis patients. Children were included if they were under 18 years of age, had a history of psoriasis, or developed it within 1 month of COVID-19 and had COVID-19 with or without symptoms. One hundred and twenty episodes of COVID-19 in 117 children (mean age: 12.4 years) were reported. The main clinical form of psoriasis was plaque type (69.4%). Most children were without systemic treatment (54.2%); 33 (28.3%) were on biologic therapies, and 24 (20%) on non-biologic systemic drugs. COVID-19 was confirmed in 106 children (88.3%) and 3 children had two COVID-19 infections each. COVID-19 was symptomatic for 75 children (62.5%) with a mean duration of 6.5 days, significantly longer for children on non-biologic systemic treatments (P = 0.02) and without systemic treatment (P = 0.006) when compared with children on biologics. The six children who required hospitalization were more frequently under non-biologic systemic treatment when compared with the other children (P = 0.01), and particularly under methotrexate (P = 0.03). After COVID-19, the psoriasis worsened in 17 cases (15.2%). Nine children (8%) developed a psoriasis in the month following COVID-19, mainly a guttate form (P = 0.01). Biologics appear to be safe with no increased risk of severe form of COVID-19 in children with psoriasis. COVID-19 was responsible for the development of psoriasis or the worsening of a known psoriasis for some children.

Sections du résumé

BACKGROUND BACKGROUND
The COVID-19 pandemic has raised questions regarding the management of chronic skin diseases, especially in patients on systemic treatments. Data concerning the use of biologics in adults with psoriasis are reassuring, but data specific to children are missing. Moreover, COVID-19 could impact the course of psoriasis in children.
OBJECTIVES OBJECTIVE
The aim of this study was therefore to assess the impact of COVID-19 on the psoriasis of children, and the severity of the infection in relation to systemic treatments.
METHODS METHODS
We set up an international registry of paediatric psoriasis patients. Children were included if they were under 18 years of age, had a history of psoriasis, or developed it within 1 month of COVID-19 and had COVID-19 with or without symptoms.
RESULTS RESULTS
One hundred and twenty episodes of COVID-19 in 117 children (mean age: 12.4 years) were reported. The main clinical form of psoriasis was plaque type (69.4%). Most children were without systemic treatment (54.2%); 33 (28.3%) were on biologic therapies, and 24 (20%) on non-biologic systemic drugs. COVID-19 was confirmed in 106 children (88.3%) and 3 children had two COVID-19 infections each. COVID-19 was symptomatic for 75 children (62.5%) with a mean duration of 6.5 days, significantly longer for children on non-biologic systemic treatments (P = 0.02) and without systemic treatment (P = 0.006) when compared with children on biologics. The six children who required hospitalization were more frequently under non-biologic systemic treatment when compared with the other children (P = 0.01), and particularly under methotrexate (P = 0.03). After COVID-19, the psoriasis worsened in 17 cases (15.2%). Nine children (8%) developed a psoriasis in the month following COVID-19, mainly a guttate form (P = 0.01).
DISCUSSION CONCLUSIONS
Biologics appear to be safe with no increased risk of severe form of COVID-19 in children with psoriasis. COVID-19 was responsible for the development of psoriasis or the worsening of a known psoriasis for some children.

Identifiants

pubmed: 35748102
doi: 10.1111/jdv.18361
pmc: PMC9349726
doi:

Substances chimiques

Biological Factors 0
Biological Products 0
Methotrexate YL5FZ2Y5U1

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

2076-2086

Subventions

Organisme : Medical Research Council
ID : MR/T02383X/1
Pays : United Kingdom

Informations de copyright

© 2022 European Academy of Dermatology and Venereology.

Références

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Auteurs

J Zitouni (J)

Department of Dermatology, Hôpital Victor Dupouy, Argenteuil, France.

A-C Bursztejn (AC)

Department of Dermatology, Hôpitaux de Brabois, Centre Hospitalier Universitaire de Nancy, Vandœuvre-lès-Nancy, France.

A Belloni Fortina (A)

Pediatric Dermatology Unit, Department of Medicine DIMED, University of Padova, Padova, Italy.

A Beauchet (A)

Department of Public Health, Hôpital Ambroise Paré, Boulogne-Billancourt, France.

V Di Lernia (V)

Dermatology Unit, Arcispedale S. Maria Nuova, Azienda USL-IRCCS di Reggio Emilia, Reggio Emilia, Italy.

A Lesiak (A)

Department of Dermatology, Peadiatric Dermatology and Oncology, Medical Univeristy of Lodz, Lodz, Poland.

J Thomas (J)

J. T. Skin Care Centre, Chennai, Tamil Nadu, India.

Z Topkarci (Z)

Department of Dermatology, Dr. Sadi Konuk Training and Research Hospital, Istanbul, Turkey.

N Murashkin (N)

Department of Dermatology, Federal State Autonomous Institution, Scientific Center of Children's Health of the Ministry of Health of the Russian Federation, Moscow, Russia.

P Brzezinski (P)

Department of Dermatology, Voivodship Specialist Hospital in Slupsk, Ustka, Poland.

T Torres (T)

Department of Dermatology, Centro Hospitalar Universitário do Porto, Porto, Portugal.

A Chiriac (A)

Department of Dermatology, Nicolina Medical Center, P. Poni Institute of Macromolecular Chemistry, Romanian Academy, Iași, Romania.

C Luca (C)

Infectious Disease Department, "Sf. Parascheva" Clinical Hospital, "Gr. T. Popa" University of Medicine, Iasi, Romania.

T McPherson (T)

Department of Dermatology, Oxford University Hospitals NHS Trust, Oxford, UK.

M Akinde (M)

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

A Maruani (A)

Unit of Pediatric Dermatology, Department of Dermatology, University of Tours and Nantes, INSERM 1246 SPHERE - CHRU Tours, Tours, France.

R Epishev (R)

Department of Dermatology, Federal State Autonomous Institution, Scientific Center of Children's Health of the Ministry of Health of the Russian Federation, Moscow, Russia.

H Vidaurri de la Cruz (H)

Servicio de Dermatología Pediátrica, Hospital General de México Dr. Eduardo Liceaga, Secretaría de Salud, Ciudad de México, Mexico.

P C Luna (PC)

Department of Dermatology, Hospital Alemán, Ciudad Autónoma de Buenos Aires, Argentina.

M Amy de la Bretêque (M)

Department of Dermatology, Hôpital Victor Dupouy, Argenteuil, France.

A Lasek (A)

Department of Dermatology, Hôpital Saint Vincent de Paul, Université Catholique de Lille, Lille, France.

E Bourrat (E)

Department of Dermatology, Hôpital Robert Debré, AP-HP, Paris, France.

M Bachelerie (M)

Department of Dermatology, Centre Hospitalier Universitaire, Clermont-Ferrand, France.

S Mallet (S)

Department of Dermatology, Hôpital de la Timone, Assistance-publique-Hôpitaux de Marseille, Marseille, France.

M Steff (M)

Department of Dermatology, Centre Hospitalier Intercommunal Robert Ballanger, Aulnay-sous-Bois, France.

A Bellissen (A)

Department of Dermatology, Centre Hospitalier Edmond Garcin, Aubagne, France.

I Neri (I)

Department of Dermatology, IRCSS Azienda Ospedaliero Universitaria di Bologna, Bologna, Italy.

E Zafiriou (E)

Department of Dermatology, Faculty of Medicine, School of Health Sciences, University of Thessaly, Larissa, Greece.

J M P A van den Reek (JMPA)

Department of Dermatology, Radboud University Medical Center, Nijmegen, The Netherlands.

E Sonkoly (E)

Dermatology and Venereology Division, Department of Medicine Solna, Karolinska Institutet, Stockholm, Sweden.
Center for Molecular Medicine (CMM), Karolinska Institutet, Stockholm, Sweden.
Dermatology, Department of Medical Sciences, Uppsala University, Uppsala, Sweden.

S K Mahil (SK)

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

C H Smith (CH)

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

C Flohr (C)

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

H Bachelez (H)

Department of Dermatology, Hôpital Saint-Louis, AP-HP, Paris, France.
Laboratory of Genetic Skin Diseases, INSERM U1163, Imagine Institute, Université de Paris, Paris, France.

E Mahé (E)

Department of Dermatology, Hôpital Victor Dupouy, Argenteuil, France.

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